-
1
-
-
0034935071
-
Lipid, sugar and liposaccharide based delivery systems
-
Wong, A.; Toth, I., Lipid, sugar and liposaccharide based delivery systems. Curr. Med. Chem., 2001, 8(9), 1123-1136.
-
(2001)
Curr. Med. Chem.
, vol.8
, Issue.9
, pp. 1123-1136
-
-
Wong, A.1
Toth, I.2
-
2
-
-
0028210276
-
Lipidic conjugates of luteinizing-hormone-releasing hormone (LHRH)+ and thyrotropin-releasing-hormone (TRH)+ that release and protect the native hormones in homogenates of humane intestinal epithelial (CACO-2) cells
-
Toth, I.; Flinn, N.; Hillery, A.; Gibbons, W.A.; Artursson, P., Lipidic conjugates of luteinizing-hormone-releasing hormone (LHRH)+ and thyrotropin-releasing-hormone (TRH)+ that release and protect the native hormones in homogenates of humane intestinal epithelial (CACO-2) cells. Int. J. Pharm., 1994, 105(3), 241-247.
-
(1994)
Int. J. Pharm.
, vol.105
, Issue.3
, pp. 241-247
-
-
Toth, I.1
Flinn, N.2
Hillery, A.3
Gibbons, W.A.4
Artursson, P.5
-
3
-
-
34848907786
-
Protein lipidation
-
Nadolski, M.J.; Linder, M.E., Protein lipidation. FEBS J., 2007, 274(20), 5202-5210.
-
(2007)
FEBS J.
, vol.274
, Issue.20
, pp. 5202-5210
-
-
Nadolski, M.J.1
Linder, M.E.2
-
4
-
-
0037329141
-
Maturation of dendritic cells with lipopeptides that represent vaccine candidates for hepatitis C virus
-
Chua, B.Y.; Healy, A.; Cameron, P.U.; Stock, O.; Rizkalla, M.; Zeng, W.G.; Torresi, J.; Brown, L.E.; Fowler, N.L.; Gowans, E.J.; Jackson, D.C., Maturation of dendritic cells with lipopeptides that represent vaccine candidates for hepatitis C virus. Immunol. Cell Biol., 2003, 81(1), 67-72.
-
(2003)
Immunol. Cell Biol.
, vol.81
, Issue.1
, pp. 67-72
-
-
Chua, B.Y.1
Healy, A.2
Cameron, P.U.3
Stock, O.4
Rizkalla, M.5
Zeng, W.G.6
Torresi, J.7
Brown, L.E.8
Fowler, N.L.9
Gowans, E.J.10
Jackson, D.C.11
-
5
-
-
49749110778
-
A self-adjuvanting lipopeptidebased vaccine candidate for the treatment of hepatitis C virus infection
-
Chua, B.Y.; Eriksson, E.M.; Brown, L.E.; Zeng, W.G.; Gowans, E.J.; Torresi, J.; Jackson, D.C., A self-adjuvanting lipopeptidebased vaccine candidate for the treatment of hepatitis C virus infection. Vaccine, 2008, 26(37), 4866-4875.
-
(2008)
Vaccine
, vol.26
, Issue.37
, pp. 4866-4875
-
-
Chua, B.Y.1
Eriksson, E.M.2
Brown, L.E.3
Zeng, W.G.4
Gowans, E.J.5
Torresi, J.6
Jackson, D.C.7
-
6
-
-
68249133732
-
A novel synthetic adjuvant enhances dendritic cell function
-
Phillipps, K.S.M.; Wykes, M.N.; Liu, X.Q.; Brown, M.; Blanchfield, J.; Toth, I., A novel synthetic adjuvant enhances dendritic cell function. Immunology, 2009, 128(1), e582-e588.
-
(2009)
Immunology
, vol.128
, Issue.1
-
-
Phillipps, K.S.M.1
Wykes, M.N.2
Liu, X.Q.3
Brown, M.4
Blanchfield, J.5
Toth, I.6
-
7
-
-
33845508580
-
Paclitaxel prodrugs: Toward smarter delivery of anticancer agents
-
Skwarczynski, M.; Hayashi, Y.; Kiso, Y., Paclitaxel prodrugs: Toward smarter delivery of anticancer agents. J. Med. Chem., 2006, 49(25), 7253-7269.
-
(2006)
J. Med. Chem.
, vol.49
, Issue.25
, pp. 7253-7269
-
-
Skwarczynski, M.1
Hayashi, Y.2
Kiso, Y.3
-
8
-
-
4444244953
-
Lipid, sugar and liposaccharide based delivery systems 2
-
Blanchfield, J.; Toth, I., Lipid, sugar and liposaccharide based delivery systems 2. Curr. Med. Chem., 2004, 11(17), 2375-2382.
-
(2004)
Curr. Med. Chem.
, vol.11
, Issue.17
, pp. 2375-2382
-
-
Blanchfield, J.1
Toth, I.2
-
9
-
-
0026352791
-
Lipidic peptides.3. Lipidic amino-acids and oligomer conjugates of morphine
-
Hughes, R.A.; Toth, I.; Ward, P.; Ireland, S.J.; Gibbons, W.A., Lipidic peptides.3. Lipidic amino-acids and oligomer conjugates of morphine. J. Pharm. Sci., 1991, 80(12), 1103-1105.
-
(1991)
J. Pharm. Sci.
, vol.80
, Issue.12
, pp. 1103-1105
-
-
Hughes, R.A.1
Toth, I.2
Ward, P.3
Ireland, S.J.4
Gibbons, W.A.5
-
10
-
-
0025785677
-
Lipidic peptides.4. Penicillin and cephalosporin amide conjugates with lipidic aminoacids and their oligomers
-
Toth, I.; Hughes, R.A.; Ward, P.; Baldwin, M.A.; Welham, K.J.; McColm, A.M.; Cox, D.M.; Gibbons, W.A., Lipidic peptides.4. Penicillin and cephalosporin amide conjugates with lipidic aminoacids and their oligomers. Int. J. Pharm., 1991, 73(3), 259-266.
-
(1991)
Int. J. Pharm.
, vol.73
, Issue.3
, pp. 259-266
-
-
Toth, I.1
Hughes, R.A.2
Ward, P.3
Baldwin, M.A.4
Welham, K.J.5
McColm, A.M.6
Cox, D.M.7
Gibbons, W.A.8
-
11
-
-
0032498638
-
Synthesis and in vitro evaluation of lipoamino acid and carbohydrate-modified enkephalins as potential antinociceptive agents
-
Kellam, B.; Drouillat, B.; Dekany, G.; Starr, M.S.; Toth, I., Synthesis and in vitro evaluation of lipoamino acid and carbohydrate-modified enkephalins as potential antinociceptive agents. Int. J. Pharm., 1998, 161(1), 55-64.
-
(1998)
Int. J. Pharm.
, vol.161
, Issue.1
, pp. 55-64
-
-
Kellam, B.1
Drouillat, B.2
Dekany, G.3
Starr, M.S.4
Toth, I.5
-
12
-
-
0026329336
-
Mucosal penetration enhancers for facilitation of peptide and protein drug absorption
-
Lee, V.H.L.; Yamamoto, A.; Kompella, U.B., Mucosal penetration enhancers for facilitation of peptide and protein drug absorption. Crit. Rev. Ther. Drug Carrier Syst., 1991, 8(2), 91-192.
-
(1991)
Crit. Rev. Ther. Drug Carrier Syst.
, vol.8
, Issue.2
, pp. 91-192
-
-
Lee, V.H.L.1
Yamamoto, A.2
Kompella, U.B.3
-
13
-
-
0030983071
-
Applications of the ion-pair concept to hydrophilic substances with special emphasis on peptides
-
QuintanarGuerrero, D.; Allemann, E.; Fessi, H.; Doelker, E., Applications of the ion-pair concept to hydrophilic substances with special emphasis on peptides. Pharm. Res., 1997, 14(2), 119-127.
-
(1997)
Pharm. Res.
, vol.14
, Issue.2
, pp. 119-127
-
-
QuintanarGuerrero, D.1
Allemann, E.2
Fessi, H.3
Doelker, E.4
-
14
-
-
0037123701
-
Microemulsion formulation for enhanced absorption of poorly soluble drugs-II. In vivo study
-
Kawakami, K.; Yoshikawa, T.; Hayashi, T.; Nishihara, Y.; Masuda, K., Microemulsion formulation for enhanced absorption of poorly soluble drugs-II. In vivo study. J. Controlled Release, 2002, 81(1-2), 75-82.
-
(2002)
J. Controlled Release
, vol.81
, Issue.1-2
, pp. 75-82
-
-
Kawakami, K.1
Yoshikawa, T.2
Hayashi, T.3
Nishihara, Y.4
Masuda, K.5
-
15
-
-
0028067744
-
A novel chemical approach to drug-delivery-lipidic amino-acid conjugates
-
Toth, I., A novel chemical approach to drug-delivery-lipidic amino-acid conjugates. J. Drug Targeting, 1994, 2(3), 217-239.
-
(1994)
J. Drug Targeting
, vol.2
, Issue.3
, pp. 217-239
-
-
Toth, I.1
-
16
-
-
78449236368
-
Pro-apoptotic activity of lipidic alpha-amino acids isolated from Protopalythoa variabilis
-
Wilke, D.V.; Jimenez, P.C.; Araujo, R.M.; Barbosa da Silva, W.M.; Loiola Pessoa, O.D.; Silveira, E.R.; Pessoa, C.; de Moraes, M.O.; Skwarczynski, M.; Simerska, P.; Toth, I.; Costa-Lotufo, L.V., Pro-apoptotic activity of lipidic alpha-amino acids isolated from Protopalythoa variabilis. Bioorg. Med. Chem., 2010, 18(22), 7997-8004.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, Issue.22
, pp. 7997-8004
-
-
Wilke, D.V.1
Jimenez, P.C.2
Araujo, R.M.3
Barbosa da Silva, W.M.4
Loiola Pessoa, O.D.5
Silveira, E.R.6
Pessoa, C.7
de Moraes, M.O.8
Skwarczynski, M.9
Simerska, P.10
Toth, I.11
Costa-Lotufo, L.V.12
-
17
-
-
0035977612
-
Isolation and structure elucidation of chlorofusin, a novel p53-MDM2 antagonist from a Fusarium sp
-
Duncan, S.J.; Gruschow, S.; Williams, D.H.; McNicholas, C.; Purewal, R.; Hajek, M.; Gerlitz, M.; Martin, S.; Wrigley, S.K.; Moore, M., Isolation and structure elucidation of chlorofusin, a novel p53-MDM2 antagonist from a Fusarium sp. J. Am. Chem. Soc., 2001, 123(4), 554-560.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, Issue.4
, pp. 554-560
-
-
Duncan, S.J.1
Gruschow, S.2
Williams, D.H.3
McNicholas, C.4
Purewal, R.5
Hajek, M.6
Gerlitz, M.7
Martin, S.8
Wrigley, S.K.9
Moore, M.10
-
18
-
-
0011169144
-
Component amino-acids of antibiotic longicatenamycin-isolation of 5-chloro-d-tryptophan
-
Shiba, T.; Mukunoki, Y.; Akiyama, H., Component amino-acids of antibiotic longicatenamycin-isolation of 5-chloro-d-tryptophan. Bull. Chem. Soc. Jpn., 1975, 48(6), 1902-1906.
-
(1975)
Bull. Chem. Soc. Jpn.
, vol.48
, Issue.6
, pp. 1902-1906
-
-
Shiba, T.1
Mukunoki, Y.2
Akiyama, H.3
-
19
-
-
0015298713
-
Myriocin, a new antifungal antibiotic from myriococcum-albomyces
-
Kluepfel, D.; Vezina, C.; Sehgal, S.N.; Kudelski, A.; Charest, M.P.; Bagli, J., Myriocin, a new antifungal antibiotic from myriococcum-albomyces. J. Antibiot., 1972, 25(2), 109-&.
-
(1972)
J. Antibiot.
, vol.25
, Issue.2
, pp. 109
-
-
Kluepfel, D.1
Vezina, C.2
Sehgal, S.N.3
Kudelski, A.4
Charest, M.P.5
Bagli, J.6
-
20
-
-
0028205909
-
Fungal metabolites.12. potent immunosuppressant, 14-deoxomyriocin, (2s, 3r, 4r)-(e)-2-amino-3, 4-dihydroxy-2-hydroxymethyleicos-6-enoic acid and structure-activityrelationships of myriocin derivatives
-
Fujita, T.; Inoue, K.; Yamamoto, S.; Ikumoto, T.; Sasaki, S.; Toyama, R.; Yoneta, M.; Chiba, K.; Hoshino, Y.; Okumoto, T., Fungal metabolites.12. potent immunosuppressant, 14-deoxomyriocin, (2s, 3r, 4r)-(e)-2-amino-3, 4-dihydroxy-2-hydroxymethyleicos-6-enoic acid and structure-activityrelationships of myriocin derivatives. J. Antibiot., 1994, 47(2), 216-224.
-
(1994)
J. Antibiot.
, vol.47
, Issue.2
, pp. 216-224
-
-
Fujita, T.1
Inoue, K.2
Yamamoto, S.3
Ikumoto, T.4
Sasaki, S.5
Toyama, R.6
Yoneta, M.7
Chiba, K.8
Hoshino, Y.9
Okumoto, T.10
-
21
-
-
0028372227
-
Fungal metabolites.11. a potent immunosuppressive activity found in isaria-sinclairii metabolite
-
Fujita, T.; Inoue, K.; Yamamoto, S.; Ikumoto, T.; Sasaki, S.; Toyama, R.; Chiba, K.; Hoshino, Y.; Okumoto, T., Fungal metabolites.11. a potent immunosuppressive activity found in isaria-sinclairii metabolite. J. Antibiot., 1994, 47(2), 208-215.
-
(1994)
J. Antibiot.
, vol.47
, Issue.2
, pp. 208-215
-
-
Fujita, T.1
Inoue, K.2
Yamamoto, S.3
Ikumoto, T.4
Sasaki, S.5
Toyama, R.6
Chiba, K.7
Hoshino, Y.8
Okumoto, T.9
-
22
-
-
0026499739
-
Sphingofungin-E and sphingofungin-F-novel serinepalmitoyl transferase inhibitors from paecilomyces-variotii
-
Horn, W.S.; Smith, J.L.; Bills, G.F.; Raghoobar, S.L.; Helms, G.L.; Kurtz, M.B.; Marrinan, J.A.; Frommer, B.R.; Thornton, R.A.; Mandala, S.M., Sphingofungin-E and sphingofungin-F-novel serinepalmitoyl transferase inhibitors from paecilomyces-variotii. J. Antibiot., 1992, 45(10), 1692-1696.
-
(1992)
J. Antibiot.
, vol.45
, Issue.10
, pp. 1692-1696
-
-
Horn, W.S.1
Smith, J.L.2
Bills, G.F.3
Raghoobar, S.L.4
Helms, G.L.5
Kurtz, M.B.6
Marrinan, J.A.7
Frommer, B.R.8
Thornton, R.A.9
Mandala, S.M.10
-
23
-
-
0026570297
-
Determination of the relative and absolute stereochemistry of sphingofungin-A, sphingofungin-B, sphingofungin-C, and sphingofungin-D
-
Vanmiddlesworth, F.; Dufresne, C.; Wincott, F.E.; Mosley, R.T.; Wilson, K.E., Determination of the relative and absolute stereochemistry of sphingofungin-A, sphingofungin-B, sphingofungin-C, and sphingofungin-D. Tetrahedron Lett., 1992, 33(3), 297-300.
-
(1992)
Tetrahedron Lett.
, vol.33
, Issue.3
, pp. 297-300
-
-
Vanmiddlesworth, F.1
Dufresne, C.2
Wincott, F.E.3
Mosley, R.T.4
Wilson, K.E.5
-
24
-
-
0026648309
-
Sphingofungin-A, sphingofungin-B, sphingofungin-C, and sphingofungin-D-a new family of antifungal agents.1. fermentation, isolation, and biological-activity
-
Vanmiddlesworth, F.; Giacobbe, R.A.; Lopez, M.; Garrity, G.; Bland, J.A.; Bartizal, K.; Fromtling, R.A.; Polishook, J.; Zweerink, M.; Edison, A.M.; Rozdilsky, W.; Wilson, K.E.; Monaghan, R.L., Sphingofungin-A, sphingofungin-B, sphingofungin-C, and sphingofungin-D-a new family of antifungal agents.1. fermentation, isolation, and biological-activity. J. Antibiot., 1992, 45(6), 861-867.
-
(1992)
J. Antibiot.
, vol.45
, Issue.6
, pp. 861-867
-
-
Vanmiddlesworth, F.1
Giacobbe, R.A.2
Lopez, M.3
Garrity, G.4
Bland, J.A.5
Bartizal, K.6
Fromtling, R.A.7
Polishook, J.8
Zweerink, M.9
Edison, A.M.10
Rozdilsky, W.11
Wilson, K.E.12
Monaghan, R.L.13
-
25
-
-
0030708812
-
Chemoenzymatic synthesis of fluorescent N-ras lipopeptides and their use in membrane localization studies in vivo
-
Waldmann, H.; Schelhaas, M.; Nagele, E.; Kuhlmann, J.; Wittinghofer, A.; Schroeder, H.; Silvius, J.R., Chemoenzymatic synthesis of fluorescent N-ras lipopeptides and their use in membrane localization studies in vivo. Angew. Chem., Int. Ed., 1997, 36(20), 2238-2241.
-
(1997)
Angew. Chem., Int. Ed.
, vol.36
, Issue.20
, pp. 2238-2241
-
-
Waldmann, H.1
Schelhaas, M.2
Nagele, E.3
Kuhlmann, J.4
Wittinghofer, A.5
Schroeder, H.6
Silvius, J.R.7
-
26
-
-
0032986772
-
Synthesis of the N-terminal lipohexapeptide of human GαO-protein and fluorescent-labeled analogs for biological studies
-
Cotte, A.; Bader, B.; Kuhlmann, J.; Waldmann, H., Synthesis of the N-terminal lipohexapeptide of human GαO-protein and fluorescent-labeled analogs for biological studies. Chem.--Eur. J., 1999, 5, 922-936.
-
(1999)
Chem.--Eur. J.
, vol.5
, pp. 922-936
-
-
Cotte, A.1
Bader, B.2
Kuhlmann, J.3
Waldmann, H.4
-
27
-
-
28044433451
-
Jr., Protein posttranslational modifications: The chemistry of proteome diversifications
-
Walsh, C.T.; Garneau-Tsodikova, S.; Gatto, G.J., Jr., Protein posttranslational modifications: The chemistry of proteome diversifications. Angew. Chem., Int. Ed., 2005, 44, 7342-7372.
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 7342-7372
-
-
Walsh, C.T.1
Garneau-Tsodikova, S.2
Gatto, G.J.3
-
28
-
-
26644431626
-
The structure, synthesis, and immunomodulating activity of bacterial lipopeptides and their analogues
-
Ousanova, M.P.; Sebyakin, Y.L., The structure, synthesis, and immunomodulating activity of bacterial lipopeptides and their analogues. Russ. Chem. Rev., 1997, 66(10), 889-900.
-
(1997)
Russ. Chem. Rev.
, vol.66
, Issue.10
, pp. 889-900
-
-
Ousanova, M.P.1
Sebyakin, Y.L.2
-
29
-
-
26844498856
-
A study of the possible asymmetry of the aliphatic diazo compounds
-
Marvel, C.S.; Noyes, W.A., A study of the possible asymmetry of the aliphatic diazo compounds. J. Am. Chem. Soc., 1920, 42, 2259-2278.
-
(1920)
J. Am. Chem. Soc.
, vol.42
, pp. 2259-2278
-
-
Marvel, C.S.1
Noyes, W.A.2
-
30
-
-
0018543934
-
Some aspects of the catalytic synthesis of n-acyl-alpha-aminoacids by carbonylation of aldehydes in the presence of amides
-
Parnaud, J.J.; Campari, G.; Pino, P., Some aspects of the catalytic synthesis of n-acyl-alpha-aminoacids by carbonylation of aldehydes in the presence of amides. J. Mol. Catal., 1979, 6(5), 341-350.
-
(1979)
J. Mol. Catal.
, vol.6
, Issue.5
, pp. 341-350
-
-
Parnaud, J.J.1
Campari, G.2
Pino, P.3
-
31
-
-
0032934226
-
First amidocarbonylation with nitriles for the synthesis of N-acyl amino acids
-
Beller, M.; Eckert, M.; Moradi, W.A., First amidocarbonylation with nitriles for the synthesis of N-acyl amino acids. Synlett, 1999(1), 108-110.
-
(1999)
Synlett
, Issue.1
, pp. 108-110
-
-
Beller, M.1
Eckert, M.2
Moradi, W.A.3
-
32
-
-
84866945147
-
Prosteni. M, Preparation of alpha-arylamidoketones from alpha-amino acids
-
Gerencev N; Castek, A.; Sateva, M.; Pluscec, J.; Prosteni. M, Preparation of alpha-arylamidoketones from alpha-amino acids. Monatshefte Fur Chemie Und Verwandte Teile Anderer Wissenschaften, 1966, 97(2), 331-&.
-
(1966)
Monatshefte Fur Chemie Und Verwandte Teile Anderer Wissenschaften
, vol.97
, Issue.2
, pp. 331
-
-
Gerencev, N.1
Castek, A.2
Sateva, M.3
Pluscec, J.4
-
34
-
-
73649160461
-
Studies on acylase activity and microorganisms.21. Optical resolution of higher amino acids by acylase of soil bacteria
-
Kimura, Y., Studies on acylase activity and microorganisms.21. Optical resolution of higher amino acids by acylase of soil bacteria. Chem. Pharm. Bull., 1962, 10(12), 1154-1157.
-
(1962)
Chem. Pharm. Bull.
, vol.10
, Issue.12
, pp. 1154-1157
-
-
Kimura, Y.1
-
35
-
-
0000270614
-
Synthesis of 2-amino acids via selective mono-N-alkylation of trichloroacetamide by 2-bromo carboxylic esters under solid-liquid phase-transfer catalysis conditions
-
Albanese, D.; Landini, D.; Penso, M., Synthesis of 2-amino acids via selective mono-N-alkylation of trichloroacetamide by 2-bromo carboxylic esters under solid-liquid phase-transfer catalysis conditions. J. Org. Chem., 1992, 57, 1603-1605.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 1603-1605
-
-
Albanese, D.1
Landini, D.2
Penso, M.3
-
36
-
-
0001600886
-
Resolution of the racemic alpha-amino derivatives of heptylic, caprylic, nonylic, decylic, and undecylic acids
-
Birnbaum, S.M.; Fu, S.C.J.; Greenstein, J.P., Resolution of the racemic alpha-amino derivatives of heptylic, caprylic, nonylic, decylic, and undecylic acids. J. Biol. Chem., 1953, 203(1), 333-338.
-
(1953)
J. Biol. Chem.
, vol.203
, Issue.1
, pp. 333-338
-
-
Birnbaum, S.M.1
Fu, S.C.J.2
Greenstein, J.P.3
-
37
-
-
0025615838
-
N-alkylation of trifluoroacetamide with 2-bromo carboxylic esters under PTC conditions: A new procedure for the synthesis of α-amino acids
-
Landini, D.; Penso, M., N-alkylation of trifluoroacetamide with 2-bromo carboxylic esters under PTC conditions: a new procedure for the synthesis of α-amino acids. J. Org. Chem., 1991, 56, 420-423.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 420-423
-
-
Landini, D.1
Penso, M.2
-
38
-
-
0001699572
-
The synthesis of amino acids from ethyl acetamidomalonate and ethyl acetamidocyanoacetate.3. The use of primary halides
-
Albertson, N.F., The synthesis of amino acids from ethyl acetamidomalonate and ethyl acetamidocyanoacetate.3. The use of primary halides. J. Am. Chem. Soc., 1946, 68(3), 450-453.
-
(1946)
J. Am. Chem. Soc.
, vol.68
, Issue.3
, pp. 450-453
-
-
Albertson, N.F.1
-
39
-
-
84977821270
-
Lipidic peptides. 1. Synthesis, resolution and structural elucidation of lipidic amino-acids and their homo-oligomers and heterooligomers
-
Gibbons, W.A.; Hughes, R.A.; Charalambous, M.; Christodoulou, M.; Szeto, A.; Aulabaugh, A.E.; Mascagni, P.; Toth, I., Lipidic peptides.1. Synthesis, resolution and structural elucidation of lipidic amino-acids and their homo-oligomers and heterooligomers Liebigs Ann. Chem., 1990(12), 1175-1183.
-
(1990)
Liebigs Ann. Chem.
, Issue.12
, pp. 1175-1183
-
-
Gibbons, W.A.1
Hughes, R.A.2
Charalambous, M.3
Christodoulou, M.4
Szeto, A.5
Aulabaugh, A.E.6
Mascagni, P.7
Toth, I.8
-
40
-
-
0017308082
-
Alkylation and Michael additions of glycine ethyl ester. Use in α-amino acid synthesis and as acyl carbanion equivalent
-
Stork, G.; Leong, A.Y.W.; Touzin, A.M., Alkylation and Michael additions of glycine ethyl ester. Use in α-amino acid synthesis and as acyl carbanion equivalent. J. Org. Chem., 1976, 41, 3491-3493.
-
(1976)
J. Org. Chem.
, vol.41
, pp. 3491-3493
-
-
Stork, G.1
Leong, A.Y.W.2
Touzin, A.M.3
-
41
-
-
0033532005
-
Ru-centered coordination complexes as a new phase transfer catalyst for alkylation of enolates and Michael additions
-
Tzalis, D.; Knochel, P., Ru-centered coordination complexes as a new phase transfer catalyst for alkylation of enolates and Michael additions. Tetrahedron Lett., 1999, 40, 3685-3688.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 3685-3688
-
-
Tzalis, D.1
Knochel, P.2
-
42
-
-
0001147034
-
Synthesis of amino acids. Alkylation of aldimine and ketimine derivatives of glycine ethyl ester under various phase-transfer conditions
-
Ghosez, L.; Antoine, J.P.; Deffense, E.; Navarro, M.; Libert, V.; O'Donnell, M.J.; Bruder, W.A.; Willey, K.; Wojciechowski, K., Synthesis of amino acids. Alkylation of aldimine and ketimine derivatives of glycine ethyl ester under various phase-transfer conditions. Tetrahedron Lett., 1982, 23, 4255-4258.
-
(1982)
Tetrahedron Lett.
, vol.23
, pp. 4255-4258
-
-
Ghosez, L.1
Antoine, J.P.2
Deffense, E.3
Navarro, M.4
Libert, V.5
O'Donnell, M.J.6
Bruder, W.A.7
Willey, K.8
Wojciechowski, K.9
-
43
-
-
0030658103
-
Solid-phase synthesis of unnatural amino acids using unactivated alkyl halides
-
O'Donnell, M.J.; Lugar, C.W.; Pottorf, R.S.; Zhou, C.; Scott, W.L.; Cwi, C.L., Solid-phase synthesis of unnatural amino acids using unactivated alkyl halides. Tetrahedron Lett., 1997, 38, 7163-7166.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 7163-7166
-
-
O'Donnell, M.J.1
Lugar, C.W.2
Pottorf, R.S.3
Zhou, C.4
Scott, W.L.5
Cwi, C.L.6
-
44
-
-
10044225569
-
Solid-phase synthetic method for (±)-α-amino acids via phasetransfer catalytic alkylation
-
Park, H.-G.; Kim, M.-J.; Park, M.-K.; Jung, H.-J.; Lee, J.; Lee, Y.-J.; Jeong, B.-S.; Lee, J.-H.; Yoo, M.-S.; Ku, J.-M.; Jew, S.-s., Solid-phase synthetic method for (±)-α-amino acids via phasetransfer catalytic alkylation. Tetrahedron Lett., 2005, 46, 93-95.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 93-95
-
-
Park, H.-G.1
Kim, M.-J.2
Park, M.-K.3
Jung, H.-J.4
Lee, J.5
Lee, Y.-J.6
Jeong, B.-S.7
Lee, J.-H.8
Yoo, M.-S.9
Ku, J.-M.10
Jew, S.-S.11
-
45
-
-
0001082956
-
Oxidative cleavage of mono-, di-, and trisubstituted olefins to methyl esters through ozonolysis in methanolic sodium hydroxide
-
Marshall, J.A.; Garofalo, A.W., Oxidative cleavage of mono-, di-, and trisubstituted olefins to methyl esters through ozonolysis in methanolic sodium hydroxide. J. Org. Chem., 1993, 58, 3675-3680.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 3675-3680
-
-
Marshall, J.A.1
Garofalo, A.W.2
-
46
-
-
0002263265
-
Porcine pancreatic lipase catalyzed enantioselective hydrolysis of esters of N-protected unusual amino acids
-
Miyazawa, T.; Iwanaga, H.; Ueji, S.; Yamada, T.; Kuwata, S., Porcine pancreatic lipase catalyzed enantioselective hydrolysis of esters of N-protected unusual amino acids. Chem. Lett., 1989, 2219-2222.
-
(1989)
Chem. Lett.
, pp. 2219-2222
-
-
Miyazawa, T.1
Iwanaga, H.2
Ueji, S.3
Yamada, T.4
Kuwata, S.5
-
47
-
-
0037094115
-
Solution-Phase Parallel Synthesis of a Pharmacophore Library of HUN-7293 Analogues: A General Chemical Mutagenesis Approach To Defining Structure-Function Properties of Naturally Occurring Cyclic Depsipeptides
-
Chen, Y.; Bilban, M.; Foster, C.A.; Boger, D.L., Solution-Phase Parallel Synthesis of a Pharmacophore Library of HUN-7293 Analogues: A General Chemical Mutagenesis Approach To Defining Structure-Function Properties of Naturally Occurring Cyclic Depsipeptides. J. Am. Chem. Soc., 2002, 124, 5431-5440.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 5431-5440
-
-
Chen, Y.1
Bilban, M.2
Foster, C.A.3
Boger, D.L.4
-
48
-
-
4644279027
-
Potent Inhibitors of the Hepatitis C Virus NS3 Protease: Design and Synthesis of Macrocyclic Substrate-Based β-Strand Mimics
-
Goudreau, N.; Brochu, C.; Cameron, D.R.; Duceppe, J.-S.; Faucher, A.-M.; Ferland, J.-M.; Grand-Maitre, C.; Poirier, M.; Simoneau, B.; Tsantrizos, Y.S., Potent Inhibitors of the Hepatitis C Virus NS3 Protease: Design and Synthesis of Macrocyclic Substrate-Based β-Strand Mimics. J. Org. Chem., 2004, 69, 6185-6201.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 6185-6201
-
-
Goudreau, N.1
Brochu, C.2
Cameron, D.R.3
Duceppe, J.-S.4
Faucher, A.-M.5
Ferland, J.-M.6
Grand-Maitre, C.7
Poirier, M.8
Simoneau, B.9
Tsantrizos, Y.S.10
-
49
-
-
0029865173
-
A general approach to the enantiomeric synthesis of lipidic α-amino acids, peptides and vicinal amino alcohols
-
Kokotos, G.; Padron, J.M.; Noula, C.; Gibbons, W.A.; Martin, V.S., A general approach to the enantiomeric synthesis of lipidic α-amino acids, peptides and vicinal amino alcohols. Tetrahedron-Asymmetry, 1996, 7, 857-866.
-
(1996)
Tetrahedron-Asymmetry
, vol.7
, pp. 857-866
-
-
Kokotos, G.1
Padron, J.M.2
Noula, C.3
Gibbons, W.A.4
Martin, V.S.5
-
50
-
-
0032575206
-
Practical synthesis of α-amino acids using cis-aminoindanol derived hippuric acid amide as a glycine enolate equivalent
-
Lee, J.; Choi, W.-B.; Lynch, J.E.; Volante, R.P.; Reider, P.J., Practical synthesis of α-amino acids using cis-aminoindanol derived hippuric acid amide as a glycine enolate equivalent. Tetrahedron Lett., 1998, 39, 3679-3682.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 3679-3682
-
-
Lee, J.1
Choi, W.-B.2
Lynch, J.E.3
Volante, R.P.4
Reider, P.J.5
-
51
-
-
84987287394
-
Asymmetric syntheses via heterocyclic intermediates. XII. Enantioselective synthesis of (R)-α-amino acids using tert-leucine as chiral auxiliary reagent
-
Schoellkopf, U.; Neubauer, H.J., Asymmetric syntheses via heterocyclic intermediates. XII. Enantioselective synthesis of (R)-α-amino acids using tert-leucine as chiral auxiliary reagent. Synthesis, 1982, 861-864.
-
(1982)
Synthesis
, pp. 861-864
-
-
Schoellkopf, U.1
Neubauer, H.J.2
-
52
-
-
0036678164
-
Diastereoselective alkylation of Schiff bases for the synthesis of lipidic unnatural Fmoc-protected α-amino acids
-
Papini, A.M.; Nardi, E.; Nuti, F.; Uziel, J.; Ginanneschi, M.; Chelli, M.; Brandi, A., Diastereoselective alkylation of Schiff bases for the synthesis of lipidic unnatural Fmoc-protected α-amino acids. Eur. J. Org. Chem., 2002, 2736-2741.
-
(2002)
Eur. J. Org. Chem.
, pp. 2736-2741
-
-
Papini, A.M.1
Nardi, E.2
Nuti, F.3
Uziel, J.4
Ginanneschi, M.5
Chelli, M.6
Brandi, A.7
-
53
-
-
0023838839
-
A short and efficient synthesis of (3S, 4S)-4-[(tert-Butyloxycarbonyl)amino]-5-cyclohexyl-3-hydroxypentanoic acid ethyl ester
-
Schuda, P.F.; Greenlee, W.J.; Chakravarty, P.K.; Eskola, P., A short and efficient synthesis of (3S, 4S)-4-[(tert-Butyloxycarbonyl)amino]-5-cyclohexyl-3-hydroxypentanoic acid ethyl ester. J. Org. Chem., 1988, 53, 873-875.
-
(1988)
J. Org. Chem.
, vol.53
, pp. 873-875
-
-
Schuda, P.F.1
Greenlee, W.J.2
Chakravarty, P.K.3
Eskola, P.4
-
54
-
-
0033553459
-
Enantioselective solidphase synthesis of α-amino acid derivatives
-
O'Donnell, M.J.; Delgado, F.; Pottorf, R.S., Enantioselective solidphase synthesis of α-amino acid derivatives. Tetrahedron, 1999, 55, 6347-6362.
-
(1999)
Tetrahedron
, vol.55
, pp. 6347-6362
-
-
O'Donnell, M.J.1
Delgado, F.2
Pottorf, R.S.3
-
55
-
-
0032569863
-
An efficient homogeneous catalytic enantioselective synthesis of α-amino acid derivatives
-
O'Donnell, M.J.; Delgado, F.; Hostettler, C.; Schwesinger, R., An efficient homogeneous catalytic enantioselective synthesis of α-amino acid derivatives. Tetrahedron Lett., 1998, 39, 8775-8778.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 8775-8778
-
-
O'Donnell, M.J.1
Delgado, F.2
Hostettler, C.3
Schwesinger, R.4
-
56
-
-
20044376663
-
Highly Enantioselective Phase-Transfer Catalytic Alkylation in the Preparation of Non-natural α-Amino Acids via Solid Phase Synthesis Using Aldimine Linker
-
Park, H.-g.; Kim, M.-J.; Park, M.-K.; Jung, H.-J.; Lee, J.; Choi, S.-h.; Lee, Y.-J.; Jeong, B.-S.; Lee, J.-H.; Yoo, M.-S.; Ku, J.-M.; Jew, S.-S., Highly Enantioselective Phase-Transfer Catalytic Alkylation in the Preparation of Non-natural α-Amino Acids via Solid Phase Synthesis Using Aldimine Linker. J. Org. Chem., 2005, 70, 1904-1906.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 1904-1906
-
-
Park, H.-G.1
Kim, M.-J.2
Park, M.-K.3
Jung, H.-J.4
Lee, J.5
Choi, S.-H.6
Lee, Y.-J.7
Jeong, B.-S.8
Lee, J.-H.9
Yoo, M.-S.10
Ku, J.-M.11
Jew, S.-S.12
-
57
-
-
4444290482
-
Asymmetric alkylation of glycine imine esters using solid supports preloaded with base
-
Yu, H.; Takigawa, S.; Koshima, H., Asymmetric alkylation of glycine imine esters using solid supports preloaded with base. Tetrahedron, 2004, 60, 8405-8410.
-
(2004)
Tetrahedron
, vol.60
, pp. 8405-8410
-
-
Yu, H.1
Takigawa, S.2
Koshima, H.3
-
58
-
-
20444475056
-
Cinchona alkaloid phase-transfer catalysts revisited: Influence of substituted aryl groups on the enantioselectivity of glycine ester enolate alkylation
-
Kumar, S.; Ramachandran, U., Cinchona alkaloid phase-transfer catalysts revisited: influence of substituted aryl groups on the enantioselectivity of glycine ester enolate alkylation. Tetrahedron, 2005, 61, 7022-7028.
-
(2005)
Tetrahedron
, vol.61
, pp. 7022-7028
-
-
Kumar, S.1
Ramachandran, U.2
-
59
-
-
0037008633
-
C2-symmetric chiral pentacyclic guanidine: A phase-transfer catalyst for the asymmetric alkylation of tert-butyl glycinate Schiff base
-
Kita, T.; Georgieva, A.; Hashimoto, Y.; Nakata, T.; Nagasawa, K., C2-symmetric chiral pentacyclic guanidine: A phase-transfer catalyst for the asymmetric alkylation of tert-butyl glycinate Schiff base. Angew. Chem., Int. Ed., 2002, 2832-2834.
-
(2002)
Angew. Chem., Int. Ed.
, pp. 2832-2834
-
-
Kita, T.1
Georgieva, A.2
Hashimoto, Y.3
Nakata, T.4
Nagasawa, K.5
-
60
-
-
0037459867
-
Highly efficient ortho-fluoro-dimeric cinchonaderived phase-transfer catalysts
-
Park, H.-g.; Jeong, B.-S.; Yoo, M.-S.; Lee, J.-H.; Park, B.-s.; Kim, M.G.; Jew, S.-s., Highly efficient ortho-fluoro-dimeric cinchonaderived phase-transfer catalysts. Tetrahedron Lett., 2003, 44, 3497-3500.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 3497-3500
-
-
Park, H.-G.1
Jeong, B.-S.2
Yoo, M.-S.3
Lee, J.-H.4
Park, B.-S.5
Kim, M.G.6
Jew, S.-S.7
-
61
-
-
0000536458
-
Lithium diorganocuprate reactions with l-serine derivatives
-
Bajgrowicz, J.A.; El Hallaoui, A.; Jacquier, R.; Pigiere, C.; Viallefont, P., Lithium diorganocuprate reactions with l-serine derivatives. Tetrahedron Lett., 1984, 25(26.), 2759-2762.
-
(1984)
Tetrahedron Lett.
, vol.25
, Issue.26
, pp. 2759-2762
-
-
Bajgrowicz, J.A.1
El Hallaoui, A.2
Jacquier, R.3
Pigiere, C.4
Viallefont, P.5
-
62
-
-
0001523153
-
Organocuprates in a novel synthesis of optically pure amino acids
-
Bajgrowicz, J.A.; El, H.A.; Jacquier, R.; Pigiere, C.; Viallefont, P., Organocuprates in a novel synthesis of optically pure amino acids. Tetrahedron, 1985, 41, 1833-1843.
-
(1985)
Tetrahedron
, vol.41
, pp. 1833-1843
-
-
Bajgrowicz, J.A.1
El, H.A.2
Jacquier, R.3
Pigiere, C.4
Viallefont, P.5
-
63
-
-
1942535633
-
Use of organocuprates in amino acid synthesis
-
Bernardini, A.; El, H.A.; Jacquier, R.; Pigiere, C.; Viallefont, P.; Bajgrowicz, J., Use of organocuprates in amino acid synthesis. Tetrahedron Lett., 1983, 24, 3717-3720.
-
(1983)
Tetrahedron Lett.
, vol.24
, pp. 3717-3720
-
-
Bernardini, A.1
El, H.A.2
Jacquier, R.3
Pigiere, C.4
Viallefont, P.5
Bajgrowicz, J.6
-
64
-
-
0041819645
-
Combined application of organozinc chemistry and one-pot hydroboration-Suzuki coupling to the synthesis of amino acids
-
Rodriguez, A.; Miller, D.D.; Jackson, R.F.W., Combined application of organozinc chemistry and one-pot hydroboration-Suzuki coupling to the synthesis of amino acids. Org. Biomol. Chem., 2003, 1, 973-977.
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 973-977
-
-
Rodriguez, A.1
Miller, D.D.2
Jackson, R.F.W.3
-
65
-
-
0032476172
-
Enantiospecific synthesis of α-amino acid semialdehydes: A key step for the synthesis of unnatural unsaturated and saturated α-amino acids
-
Padron, J.M.; Kokotos, G.; Martin, T.; Markidis, T.; Gibbons, W.A.; Martin, V.S., Enantiospecific synthesis of α-amino acid semialdehydes: a key step for the synthesis of unnatural unsaturated and saturated α-amino acids. Tetrahedron-Asymmetry, 1998, 9, 3381-3394.
-
(1998)
Tetrahedron-Asymmetry
, vol.9
, pp. 3381-3394
-
-
Padron, J.M.1
Kokotos, G.2
Martin, T.3
Markidis, T.4
Gibbons, W.A.5
Martin, V.S.6
-
66
-
-
0001340433
-
A General Approach to the Asymmetric Synthesis of Unsaturated Lipidic α-Amino Acids. The First Synthesis of α-Aminoarachidonic Acid
-
Kokotos, G.; Padron, J.M.; Martin, T.; Gibbons, W.A.; Martin, V.S., A General Approach to the Asymmetric Synthesis of Unsaturated Lipidic α-Amino Acids. The First Synthesis of α-Aminoarachidonic Acid. J. Org. Chem., 1998, 63, 3741-3744.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 3741-3744
-
-
Kokotos, G.1
Padron, J.M.2
Martin, T.3
Gibbons, W.A.4
Martin, V.S.5
-
67
-
-
0033574553
-
Catalytic asymmetric hydrogenation of β-substituted α, β, γ, δ-unsaturated amino acids
-
Burk, M.J.; Bedingfield, K.M.; Kiesman, W.F.; Allen, J.G., Catalytic asymmetric hydrogenation of β-substituted α, β, γ, δ-unsaturated amino acids. Tetrahedron Lett., 1999, 40, 3093-3096.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 3093-3096
-
-
Burk, M.J.1
Bedingfield, K.M.2
Kiesman, W.F.3
Allen, J.G.4
-
68
-
-
0032481423
-
Highly Regio-and Enantioselective Catalytic Hydrogenation of Enamides in Conjugated Diene Systems: Synthesis and Application of γ, δ-Unsaturated Amino Acids
-
Burk, M.J.; Allen, J.G.; Kiesman, W.F., Highly Regio-and Enantioselective Catalytic Hydrogenation of Enamides in Conjugated Diene Systems: Synthesis and Application of γ, δ-Unsaturated Amino Acids. J. Am. Chem. Soc., 1998, 120, 657-663.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 657-663
-
-
Burk, M.J.1
Allen, J.G.2
Kiesman, W.F.3
-
69
-
-
0000740766
-
Preparation and use of C2-symmetric bis(phospholanes): Production of α-amino acid derivatives via highly enantioselective hydrogenation reactions
-
Burk, M.J.; Feaster, J.E.; Nugent, W.A.; Harlow, R.L., Preparation and use of C2-symmetric bis(phospholanes): production of α-amino acid derivatives via highly enantioselective hydrogenation reactions. J. Am. Chem. Soc., 1993, 115, 10125-10138.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 10125-10138
-
-
Burk, M.J.1
Feaster, J.E.2
Nugent, W.A.3
Harlow, R.L.4
-
70
-
-
33748666441
-
Cross-metathesis of unsaturated α-amino acid derivatives
-
Biagini, S.C.G.; Gibson, S.E.; Keen, S.P., Cross-metathesis of unsaturated α-amino acid derivatives. J. Chem. Soc., Perkin Trans. 1, 1998, 2485-2500.
-
(1998)
J. Chem. Soc., Perkin Trans. 1
, pp. 2485-2500
-
-
Biagini, S.C.G.1
Gibson, S.E.2
Keen, S.P.3
-
71
-
-
0002268913
-
Cross metathesis of the amino acid homoallylglycine
-
Gibson, S.E.; Gibson, V.C.; Keen, S.P., Cross metathesis of the amino acid homoallylglycine. Chem. Commun. (Cambridge), 1997, 1107-1108.
-
(1997)
Chem. Commun. (Cambridge)
, pp. 1107-1108
-
-
Gibson, S.E.1
Gibson, V.C.2
Keen, S.P.3
-
72
-
-
0033816196
-
Intestinal permeation enhancers
-
Aungst, B.J., Intestinal permeation enhancers. J. Pharm. Sci., 2000, 89(4), 429-442.
-
(2000)
J. Pharm. Sci.
, vol.89
, Issue.4
, pp. 429-442
-
-
Aungst, B.J.1
-
73
-
-
0027207689
-
A combined adjuvant and carrier system for enhancing synthetic peptides immunogenicity utilizing lipidic amino-acids
-
Toth, I.; Danton, M.; Flinn, N.; Gibbons, W.A., A combined adjuvant and carrier system for enhancing synthetic peptides immunogenicity utilizing lipidic amino-acids. Tetrahedron Lett., 1993, 34(24), 3925-3928.
-
(1993)
Tetrahedron Lett.
, vol.34
, Issue.24
, pp. 3925-3928
-
-
Toth, I.1
Danton, M.2
Flinn, N.3
Gibbons, W.A.4
-
74
-
-
84858013364
-
Biological Applications of Dendrimers
-
Patri, A.K.; Simanek, E., Biological Applications of Dendrimers. Mol. Pharm., 2012, 9(3), 341-341.
-
(2012)
Mol. Pharm.
, vol.9
, Issue.3
, pp. 341-342
-
-
Patri, A.K.1
Simanek, E.2
-
75
-
-
44449179814
-
Synthesis and in vitro evaluation of a library of modified endomorphin 1 peptides
-
Koda, Y.; Del Borgo, M.; Wessling, S.T.; Lazarus, L.H.; Okada, Y.; Toth, I.; Blanchfield, J.T., Synthesis and in vitro evaluation of a library of modified endomorphin 1 peptides. Bioorg. Med. Chem., 2008, 16(11), 6286-6296.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, Issue.11
, pp. 6286-6296
-
-
Koda, Y.1
Del Borgo, M.2
Wessling, S.T.3
Lazarus, L.H.4
Okada, Y.5
Toth, I.6
Blanchfield, J.T.7
-
76
-
-
42649132468
-
In vitro stability and permeability studies of liposomal delivery systems for a novel lipophilic endomorphin 1 analogue
-
Koda, Y.; Liang, M.T.; Blanchfield, J.T.; Toth, I., In vitro stability and permeability studies of liposomal delivery systems for a novel lipophilic endomorphin 1 analogue. Int. J. Pharm., 2008, 356(1-2), 37-43.
-
(2008)
Int. J. Pharm.
, vol.356
, Issue.1-2
, pp. 37-43
-
-
Koda, Y.1
Liang, M.T.2
Blanchfield, J.T.3
Toth, I.4
-
77
-
-
70349318055
-
Lipid Core Peptide System for Gene, Drug, and Vaccine Delivery
-
Zhong, W.; Skwarczynski, M.; Toth, I., Lipid Core Peptide System for Gene, Drug, and Vaccine Delivery. Aust. J. Chem., 2009, 62(9), 956-967.
-
(2009)
Aust. J. Chem.
, vol.62
, Issue.9
, pp. 956-967
-
-
Zhong, W.1
Skwarczynski, M.2
Toth, I.3
-
78
-
-
0037453176
-
The interaction of cationic dendrons with albumin and their diffusion through cellulose membranes
-
Purohit, G.; Sakthivel, T.; Florence, A.T., The interaction of cationic dendrons with albumin and their diffusion through cellulose membranes. Int. J. Pharm., 2003, 254(1), 37-41.
-
(2003)
Int. J. Pharm.
, vol.254
, Issue.1
, pp. 37-41
-
-
Purohit, G.1
Sakthivel, T.2
Florence, A.T.3
-
79
-
-
0035910882
-
Interaction of cationic partial dendrimers with charged and neutral liposomes
-
Purohit, G.; Sakthivel, T.; Florence, A.T., Interaction of cationic partial dendrimers with charged and neutral liposomes. Int. J. Pharm., 2001, 214(1-2), 71-76.
-
(2001)
Int. J. Pharm.
, vol.214
, Issue.1-2
, pp. 71-76
-
-
Purohit, G.1
Sakthivel, T.2
Florence, A.T.3
-
80
-
-
0037453172
-
Adsorption of amphipathic dendrons on polystyrene nanoparticles
-
Sakthivel, T.; Florence, A.T., Adsorption of amphipathic dendrons on polystyrene nanoparticles. Int. J. Pharm., 2003, 254(1), 23-26.
-
(2003)
Int. J. Pharm.
, vol.254
, Issue.1
, pp. 23-26
-
-
Sakthivel, T.1
Florence, A.T.2
-
81
-
-
16644372928
-
Investigation of the association and flexibility of cationic lipidic peptide dendrons by NMR spectroscopy
-
Zloh, M.; Ramaswamy, C.; Sakthivel, T.; Wilderspin, A.; Florence, A.T., Investigation of the association and flexibility of cationic lipidic peptide dendrons by NMR spectroscopy. Magn. Reson. Chem., 2005, 43(1), 47-52.
-
(2005)
Magn. Reson. Chem.
, vol.43
, Issue.1
, pp. 47-52
-
-
Zloh, M.1
Ramaswamy, C.2
Sakthivel, T.3
Wilderspin, A.4
Florence, A.T.5
-
82
-
-
0031783590
-
Synthesis and physicochemical properties of lipophilic polyamide dendrimers
-
Sakthivel, T.; Toth, I.; Florence, A.T., Synthesis and physicochemical properties of lipophilic polyamide dendrimers. Pharm. Res., 1998, 15(5), 776-782.
-
(1998)
Pharm. Res.
, vol.15
, Issue.5
, pp. 776-782
-
-
Sakthivel, T.1
Toth, I.2
Florence, A.T.3
-
83
-
-
0026172588
-
Synthesis and characterization of new polysiloxane starburst polymers
-
Morikawa, A.; Kakimoto, M.; Imai, Y., Synthesis and characterization of new polysiloxane starburst polymers Macromolecules, 1991, 24(12), 3469-3474.
-
(1991)
Macromolecules
, vol.24
, Issue.12
, pp. 3469-3474
-
-
Morikawa, A.1
Kakimoto, M.2
Imai, Y.3
-
84
-
-
84989592700
-
Nanoarchitectures.1. Controlled synthesis of phenylacetylene sequences
-
Zhang, J.S.; Moore, J.S.; Xu, Z.F.; Aguirre, R.A., Nanoarchitectures.1. Controlled synthesis of phenylacetylene sequences J. Am. Chem. Soc., 1992, 114(6), 2273-2274.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, Issue.6
, pp. 2273-2274
-
-
Zhang, J.S.1
Moore, J.S.2
Xu, Z.F.3
Aguirre, R.A.4
-
85
-
-
0033061971
-
Distribution of a lipidic 2.5 nm diameter dendrimer carrier after oral administration
-
Sakthivel, T.; Toth, I.; Florence, A.T., Distribution of a lipidic 2.5 nm diameter dendrimer carrier after oral administration. Int. J. Pharm., 1999, 183(1), 51-55.
-
(1999)
Int. J. Pharm.
, vol.183
, Issue.1
, pp. 51-55
-
-
Sakthivel, T.1
Toth, I.2
Florence, A.T.3
-
86
-
-
0034000927
-
Oral uptake and translocation of a polylysine dendrimer with a lipid surface
-
Florence, A.T.; Sakthivel, T.; Toth, I., Oral uptake and translocation of a polylysine dendrimer with a lipid surface. J. Controlled Release, 2000, 65(1-2), 253-259.
-
(2000)
J. Controlled Release
, vol.65
, Issue.1-2
, pp. 253-259
-
-
Florence, A.T.1
Sakthivel, T.2
Toth, I.3
-
87
-
-
0037453170
-
Dendrisomes: Cationic lipidic dendron vesicular assemblies
-
Al-Jamal, K.T.; Sakthivel, T.; Florence, A.T., Dendrisomes: cationic lipidic dendron vesicular assemblies. Int. J. Pharm., 2003, 254(1), 33-36.
-
(2003)
Int. J. Pharm.
, vol.254
, Issue.1
, pp. 33-36
-
-
Al-Jamal, K.T.1
Sakthivel, T.2
Florence, A.T.3
-
88
-
-
26844472149
-
Solubilisation and transformation of amphipathic lipidic dendron vesicles (dendrisomes) into mixed micelles
-
Al-Jamal, K.T.; Sakthivel, T.; Florence, A.T., Solubilisation and transformation of amphipathic lipidic dendron vesicles (dendrisomes) into mixed micelles. Colloids and Surfaces a-Physicochemical and Engineering Aspects, 2005, 268(1-3), 52-59.
-
(2005)
Colloids and Surfaces a-Physicochemical and Engineering Aspects
, vol.268
, Issue.1-3
, pp. 52-59
-
-
Al-Jamal, K.T.1
Sakthivel, T.2
Florence, A.T.3
-
89
-
-
33745055241
-
Protein transduction by lipidic peptide dendrimers
-
Bayele, H.K.; Ramaswamy, C.; Wilderspin, A.F.; Srai, K.S.; Toth, I.; Florence, A.T., Protein transduction by lipidic peptide dendrimers. J. Pharm. Sci., 2006, 95(6), 1227-1237.
-
(2006)
J. Pharm. Sci.
, vol.95
, Issue.6
, pp. 1227-1237
-
-
Bayele, H.K.1
Ramaswamy, C.2
Wilderspin, A.F.3
Srai, K.S.4
Toth, I.5
Florence, A.T.6
-
90
-
-
0035910881
-
Interfacial behaviour and micelle formation of novel amphiphilic sequential lipid-lysine oligomers
-
Yanai, S.; Sakthivel, T.; Florence, A.T., Interfacial behaviour and micelle formation of novel amphiphilic sequential lipid-lysine oligomers. Int. J. Pharm., 2001, 214(1-2), 49-53.
-
(2001)
Int. J. Pharm.
, vol.214
, Issue.1-2
, pp. 49-53
-
-
Yanai, S.1
Sakthivel, T.2
Florence, A.T.3
-
91
-
-
28744439003
-
Supramolecular structures from dendrons and dendrimers
-
Al-Jamal, K.T.; Ramaswamy, C.; Florence, A.T., Supramolecular structures from dendrons and dendrimers. Adv. Drug Delivery Rev., 2005, 57(15), 2238-2270.
-
(2005)
Adv. Drug Delivery Rev.
, vol.57
, Issue.15
, pp. 2238-2270
-
-
Al-Jamal, K.T.1
Ramaswamy, C.2
Florence, A.T.3
-
92
-
-
1142297405
-
The sugar code in drug delivery
-
Gabius, H.J., The sugar code in drug delivery. Adv. Drug Delivery Rev., 2004, 56(4), 421-424.
-
(2004)
Adv. Drug Delivery Rev.
, vol.56
, Issue.4
, pp. 421-424
-
-
Gabius, H.J.1
-
93
-
-
0036181219
-
Design and synthesis of glycodendrimers
-
Turnbull, W.B.; Stoddart, J.F., Design and synthesis of glycodendrimers. J. Biotechnol., 2002, 90(3-4), 231-255.
-
(2002)
J. Biotechnol.
, vol.90
, Issue.3-4
, pp. 231-255
-
-
Turnbull, W.B.1
Stoddart, J.F.2
-
94
-
-
0036182796
-
Glycodendrimers: Novel glycotope isosteres unmasking sugar coding. case study with T-antigen markers from breast cancer MUC1 glycoprotein
-
Roy, R.; Baek, M.-G., Glycodendrimers: novel glycotope isosteres unmasking sugar coding. case study with T-antigen markers from breast cancer MUC1 glycoprotein. J. Biotechnol., 2002, 90(3-4), 291-309.
-
(2002)
J. Biotechnol.
, vol.90
, Issue.3-4
, pp. 291-309
-
-
Roy, R.1
Baek, M.-G.2
-
95
-
-
68949137329
-
-
In, Lindhorst, T.K.O.S., Ed
-
Lahmann, M. In Glycoscience and Microbial Adhesion. Lindhorst, T.K.O.S., Ed., 2009; 288, 17-65.
-
(2009)
Glycoscience and Microbial Adhesion
, vol.288
, pp. 17-65
-
-
Lahmann, M.1
-
96
-
-
77249174795
-
Recent Developments in Carbohydrate-Decorated Targeted Drug/Gene Delivery
-
Zhang, H.; Ma, Y.; Sun, X.-L., Recent Developments in Carbohydrate-Decorated Targeted Drug/Gene Delivery. Med. Res. Rev., 2010, 30(2), 270-289.
-
(2010)
Med. Res. Rev.
, vol.30
, Issue.2
, pp. 270-289
-
-
Zhang, H.1
Ma, Y.2
Sun, X.-L.3
-
97
-
-
0031936866
-
Novel liposaccharide conjugates for drug and peptide delivery
-
Drouillat, B.; Hillery, A.M.; Dekany, G.; Falconer, R.; Wright, K.; Toth, I., Novel liposaccharide conjugates for drug and peptide delivery. J. Pharm. Sci., 1998, 87(1), 25-30.
-
(1998)
J. Pharm. Sci.
, vol.87
, Issue.1
, pp. 25-30
-
-
Drouillat, B.1
Hillery, A.M.2
Dekany, G.3
Falconer, R.4
Wright, K.5
Toth, I.6
-
98
-
-
0035828883
-
Carbohydrate-based templates for synthetic vaccines and drug delivery
-
McGeary, R.P.; Jablonkai, I.; Toth, I., Carbohydrate-based templates for synthetic vaccines and drug delivery. Tetrahedron, 2001, 57(41), 8733-8742.
-
(2001)
Tetrahedron
, vol.57
, Issue.41
, pp. 8733-8742
-
-
McGeary, R.P.1
Jablonkai, I.2
Toth, I.3
-
99
-
-
21144477910
-
Synthesis, structure and reactions of glycosyl azides
-
Gyorgydeak, Z.; Szilagyi, L.; Paulsen, H., Synthesis, structure and reactions of glycosyl azides. J. Carbohydr. Chem., 1993, 12(2), 139-163.
-
(1993)
J. Carbohydr. Chem.
, vol.12
, Issue.2
, pp. 139-163
-
-
Gyorgydeak, Z.1
Szilagyi, L.2
Paulsen, H.3
-
100
-
-
27744527586
-
Polycationic lipophilic-core dendrons as penetration enhancers for the oral administration of low molecular weight heparin
-
Hayes, P.Y.; Ross, B.P.; Thomas, B.G.; Toth, I., Polycationic lipophilic-core dendrons as penetration enhancers for the oral administration of low molecular weight heparin. Bioorg. Med. Chem., 2006, 14(1), 143-152.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, Issue.1
, pp. 143-152
-
-
Hayes, P.Y.1
Ross, B.P.2
Thomas, B.G.3
Toth, I.4
-
101
-
-
0026527091
-
Lipidic Peptides.10. Synthesis, structural and physico-chemical elucidation of lipidic amino acid conjugates with hydrophilic compounds
-
Toth, I.; Anderson, G.J.; Hussain, R.; Wood, I.P.; Fernandez, E.D.; Ward, P.; Gibbons, W.A., Lipidic Peptides.10. Synthesis, structural and physico-chemical elucidation of lipidic amino acid conjugates with hydrophilic compounds Tetrahedron, 1992, 48(5), 923-930.
-
(1992)
Tetrahedron
, vol.48
, Issue.5
, pp. 923-930
-
-
Toth, I.1
Anderson, G.J.2
Hussain, R.3
Wood, I.P.4
Fernandez, E.D.5
Ward, P.6
Gibbons, W.A.7
-
102
-
-
1242318785
-
Design, synthesis, and evaluation of a liposaccharide drug delivery agent: Application to the gastrointestinal absorption of gentamicin
-
Ross, B.P.; DeCruz, S.E.; Lynch, T.B.; Davis-Goff, K.; Toth, I., Design, synthesis, and evaluation of a liposaccharide drug delivery agent: Application to the gastrointestinal absorption of gentamicin. J. Med. Chem., 2004, 47(5), 1251-1258.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.5
, pp. 1251-1258
-
-
Ross, B.P.1
DeCruz, S.E.2
Lynch, T.B.3
Davis-Goff, K.4
Toth, I.5
-
103
-
-
12644286573
-
Design of compounds that increase the absorption of polar molecules
-
Bowe, C.L.; Mokhtarzadeh, L.; Venkatesan, P.; Babu, S.; Axelrod, H.R.; Sofia, M.J.; Kakarla, R.; Chan, T.Y.; Kim, J.S.; Lee, H.J.; Amidon, G.L.; Choe, S.Y.; Walker, S.; Kahne, D., Design of compounds that increase the absorption of polar molecules. Proc. Natl. Acad. Sci. USA, 1997, 94(22), 12218-12223.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, Issue.22
, pp. 12218-12223
-
-
Bowe, C.L.1
Mokhtarzadeh, L.2
Venkatesan, P.3
Babu, S.4
Axelrod, H.R.5
Sofia, M.J.6
Kakarla, R.7
Chan, T.Y.8
Kim, J.S.9
Lee, H.J.10
Amidon, G.L.11
Choe, S.Y.12
Walker, S.13
Kahne, D.14
-
104
-
-
17144407394
-
Micellar aggregation and membrane partitioning of bile salts, fatty acids, sodium dodecyl sulfate, and sugar-conjugated fatty acids: Correlation with hemolytic potency and implications for drug delivery
-
Ross, B.P.; Braddy, A.C.; McGeary, R.P.; Blanchfield, J.T.; Prokai, L.; Toth, I., Micellar aggregation and membrane partitioning of bile salts, fatty acids, sodium dodecyl sulfate, and sugar-conjugated fatty acids: Correlation with hemolytic potency and implications for drug delivery. Mol. Pharm., 2004, 1(3), 233-245.
-
(2004)
Mol. Pharm.
, vol.1
, Issue.3
, pp. 233-245
-
-
Ross, B.P.1
Braddy, A.C.2
McGeary, R.P.3
Blanchfield, J.T.4
Prokai, L.5
Toth, I.6
-
105
-
-
84860753358
-
Development and characterization of anionic liposaccharides for enhanced oral drug delivery
-
Abdelrahim, A.S.; Simerska, P.; Toth, I., Development and characterization of anionic liposaccharides for enhanced oral drug delivery. Int. J. Pharm. (Amsterdam, Neth.), 2012, 430, 120-128.
-
(2012)
Int. J. Pharm. (Amsterdam, Neth.)
, vol.430
, pp. 120-128
-
-
Abdelrahim, A.S.1
Simerska, P.2
Toth, I.3
-
106
-
-
70349759486
-
Design and synthesis of a series of novel, cationic liposaccharide derivatives as potential penetration enhancers for oral drug delivery
-
Abdelrahim, A.S.; Ziora, Z.M.; Bergeon, J.A.; Moss, A.R.; Toth, I., Design and synthesis of a series of novel, cationic liposaccharide derivatives as potential penetration enhancers for oral drug delivery. Tetrahedron, 2009, 65(45), 9436-9442.
-
(2009)
Tetrahedron
, vol.65
, Issue.45
, pp. 9436-9442
-
-
Abdelrahim, A.S.1
Ziora, Z.M.2
Bergeon, J.A.3
Moss, A.R.4
Toth, I.5
-
107
-
-
34748885101
-
Design, synthesis and biological evaluation of novel lipoamino acid-based glycolipids for oral drug delivery
-
Falconer, R.A.; Toth, I., Design, synthesis and biological evaluation of novel lipoamino acid-based glycolipids for oral drug delivery. Bioorg. Med. Chem., 2007, 15(22), 7012-7020.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, Issue.22
, pp. 7012-7020
-
-
Falconer, R.A.1
Toth, I.2
-
108
-
-
0035171364
-
Carbohydrate mimetics-based glycosyltransferase inhibitors
-
Compain, P.; Martin, O.R., Carbohydrate mimetics-based glycosyltransferase inhibitors. Bioorg. Med. Chem., 2001, 9(12), 3077-3092.
-
(2001)
Bioorg. Med. Chem.
, vol.9
, Issue.12
, pp. 3077-3092
-
-
Compain, P.1
Martin, O.R.2
-
109
-
-
84866934324
-
Lipopeptides for the fragment-based pharmaceutics design
-
Ziora, Z.M.; Wimmer, N.; New, R.; Skwarczynski, M.; Toth, I., Lipopeptides for the fragment-based pharmaceutics design. Int. J. Org. Chem., 2012, 1(2), 75-81.
-
(2012)
Int. J. Org. Chem.
, vol.1
, Issue.2
, pp. 75-81
-
-
Ziora, Z.M.1
Wimmer, N.2
New, R.3
Skwarczynski, M.4
Toth, I.5
-
110
-
-
79959932564
-
Synthesis of glycolipopeptidic building blocks for carbohydrate receptor discovery
-
Ziora, Z.M.; Wimmer, N.; New, R.; Skwarczynski, M.; Toth, I., Synthesis of glycolipopeptidic building blocks for carbohydrate receptor discovery. Carbohydr. Res., 2011, 346(12), 1439-1444.
-
(2011)
Carbohydr. Res.
, vol.346
, Issue.12
, pp. 1439-1444
-
-
Ziora, Z.M.1
Wimmer, N.2
New, R.3
Skwarczynski, M.4
Toth, I.5
-
111
-
-
77951800778
-
Thymine, adenine and lipoamino acid based gene delivery systems
-
Skwarczynski, M.; Ziora, Z.M.; Coles, D.J.; Lin, I.C.; Toth, I., Thymine, adenine and lipoamino acid based gene delivery systems. Chem. Commun. (Cambridge, U. K.), 2010, 46(18), 3140-3142.
-
(2010)
Chem. Commun. (Cambridge, U. K.)
, vol.46
, Issue.18
, pp. 3140-3142
-
-
Skwarczynski, M.1
Ziora, Z.M.2
Coles, D.J.3
Lin, I.C.4
Toth, I.5
-
112
-
-
79955619433
-
Uptake and Transport of Novel Amphiphilic Polyelectrolyte-Insulin Nanocomplexes by Caco-2 Cells-Towards Oral Insulin
-
Thompson, C.; Cheng, W.P.; Gadad, P.; Skene, K.; Smith, M.; Smith, G.; McKinnon, A.; Knott, R., Uptake and Transport of Novel Amphiphilic Polyelectrolyte-Insulin Nanocomplexes by Caco-2 Cells-Towards Oral Insulin. Pharm. Res., 2011, 28(4), 886-896.
-
(2011)
Pharm. Res.
, vol.28
, Issue.4
, pp. 886-896
-
-
Thompson, C.1
Cheng, W.P.2
Gadad, P.3
Skene, K.4
Smith, M.5
Smith, G.6
McKinnon, A.7
Knott, R.8
-
113
-
-
3843150602
-
Development of solid lipid nanoparticles containing lonically complexed chemotherapeutic drugs and chemosensitizers
-
Wong, H.L.; Bendayan, R.; Rauth, A.M.; Wu, X.Y., Development of solid lipid nanoparticles containing lonically complexed chemotherapeutic drugs and chemosensitizers. J. Pharm. Sci., 2004, 93(8), 1993-2008.
-
(2004)
J. Pharm. Sci.
, vol.93
, Issue.8
, pp. 1993-2008
-
-
Wong, H.L.1
Bendayan, R.2
Rauth, A.M.3
Wu, X.Y.4
-
114
-
-
33746626869
-
Solid lipid nanoparticles for enhancing vinpocetine's oral bioavailability
-
Luo, Y.; Chen, D.; Ren, L.; Zhao, X.; Qin, J., Solid lipid nanoparticles for enhancing vinpocetine's oral bioavailability. J. Controlled Release, 2006, 114(1), 53-59.
-
(2006)
J. Controlled Release
, vol.114
, Issue.1
, pp. 53-59
-
-
Luo, Y.1
Chen, D.2
Ren, L.3
Zhao, X.4
Qin, J.5
-
115
-
-
33745588040
-
A new polymerlipid hybrid nanoparticle system increases cytotoxicity of doxorubicin against multidrug-resistant human breast cancer cells
-
Wong, H.L.; Rauth, A.M.; Bendayan, R.; Manias, J.L.; Ramaswamy, M.; Liu, Z.; Erhan, S.Z.; Wu, X.Y., A new polymerlipid hybrid nanoparticle system increases cytotoxicity of doxorubicin against multidrug-resistant human breast cancer cells. Pharm. Res., 2006, 23(7), 1574-1585.
-
(2006)
Pharm. Res.
, vol.23
, Issue.7
, pp. 1574-1585
-
-
Wong, H.L.1
Rauth, A.M.2
Bendayan, R.3
Manias, J.L.4
Ramaswamy, M.5
Liu, Z.6
Erhan, S.Z.7
Wu, X.Y.8
-
116
-
-
33646798446
-
A mechanistic study of enhanced doxorubicin uptake and retention in multidrug resistant breast cancer cells using a polymer-lipid hybrid nanoparticle system
-
Wong, H.L.; Bendayan, R.; Rauth, A.M.; Xue, H.Y.; Babakhanian, K.; Wu, X.Y., A mechanistic study of enhanced doxorubicin uptake and retention in multidrug resistant breast cancer cells using a polymer-lipid hybrid nanoparticle system. J. Pharmacol. Exp. Ther., 2006, 317(3), 1372-1381.
-
(2006)
J. Pharmacol. Exp. Ther.
, vol.317
, Issue.3
, pp. 1372-1381
-
-
Wong, H.L.1
Bendayan, R.2
Rauth, A.M.3
Xue, H.Y.4
Babakhanian, K.5
Wu, X.Y.6
-
117
-
-
33847284493
-
In vivo evaluation of a new polymer-lipid hybrid nanoparticle (PLN) formulation of doxorubicin in a murine solid tumor model
-
Wong, H.L.; Rauth, A.M.; Bendayan, R.; Wu, X.Y., In vivo evaluation of a new polymer-lipid hybrid nanoparticle (PLN) formulation of doxorubicin in a murine solid tumor model. Eur. J. Pharmaceut. Biopharmaceut., 2007, 65(3), 300-308.
-
(2007)
Eur. J. Pharmaceut. Biopharmaceut.
, vol.65
, Issue.3
, pp. 300-308
-
-
Wong, H.L.1
Rauth, A.M.2
Bendayan, R.3
Wu, X.Y.4
-
118
-
-
37849185909
-
Simultaneous delivery of doxorubicin and GG918 (Elacridar) by new Polymer-Lipid Hybrid Nanoparticles (PLN) for enhanced treatment of multidrug-resistant breast cancer
-
Wong, H.L.; Bendayan, R.; Rauth, A.M.; Wu, X.Y., Simultaneous delivery of doxorubicin and GG918 (Elacridar) by new Polymer-Lipid Hybrid Nanoparticles (PLN) for enhanced treatment of multidrug-resistant breast cancer. J. Controlled Release, 2006, 116(3), 275-284.
-
(2006)
J. Controlled Release
, vol.116
, Issue.3
, pp. 275-284
-
-
Wong, H.L.1
Bendayan, R.2
Rauth, A.M.3
Wu, X.Y.4
-
119
-
-
42749088606
-
Molecular interactions, internal structure and drug release kinetics of rationally developed polymer-lipid hybrid nanoparticles
-
Li, Y.; Wong, H.L.; Shuhendler, A.J.; Rauth, A.M.; Wu, M.Y., Molecular interactions, internal structure and drug release kinetics of rationally developed polymer-lipid hybrid nanoparticles. J. Controlled Release, 2008, 128(1), 60-70.
-
(2008)
J. Controlled Release
, vol.128
, Issue.1
, pp. 60-70
-
-
Li, Y.1
Wong, H.L.2
Shuhendler, A.J.3
Rauth, A.M.4
Wu, M.Y.5
-
120
-
-
59049088106
-
Silica-lipid hybrid (SLH) microcapsules: A novel oral delivery system for poorly soluble drugs
-
Tan, A.; Simovic, S.; Davey, A.K.; Rades, T.; Prestidge, C.A., Silica-lipid hybrid (SLH) microcapsules: A novel oral delivery system for poorly soluble drugs. J. Controlled Release, 2009, 134(1), 62-70.
-
(2009)
J. Controlled Release
, vol.134
, Issue.1
, pp. 62-70
-
-
Tan, A.1
Simovic, S.2
Davey, A.K.3
Rades, T.4
Prestidge, C.A.5
-
121
-
-
80051666394
-
Pharmaceutical drug transport: The issues and the implications that it is essentially carrier-mediated only
-
Kell, D.B.; Dobson, P.D.; Oliver, S.G., Pharmaceutical drug transport: the issues and the implications that it is essentially carrier-mediated only. Drug Discov. Today, 2011, 16(15-16), 704-714.
-
(2011)
Drug Discov. Today
, vol.16
, Issue.15-16
, pp. 704-714
-
-
Kell, D.B.1
Dobson, P.D.2
Oliver, S.G.3
-
122
-
-
84864612910
-
Evidence-based approach to assess passive diffusion and carrier-mediated drug transport
-
Di, L.; Artursson, P.; Avdeef, A.; Ecker, G.F.; Faller, B.; Fischer, H.; Brian, H.J.; Kansy, M.; Kerns, E.H.; Kramer, S.D.; Lennernas, H.; Sugano, K., Evidence-based approach to assess passive diffusion and carrier-mediated drug transport. Drug Discov. Today, 2012, http://dx.doi.org/10.1016/j.drudis.2012.03.015.
-
(2012)
Drug Discov. Today
-
-
Di, L.1
Artursson, P.2
Avdeef, A.3
Ecker, G.F.4
Faller, B.5
Fischer, H.6
Brian, H.J.7
Kansy, M.8
Kerns, E.H.9
Kramer, S.D.10
Lennernas, H.11
Sugano, K.12
-
123
-
-
84942257852
-
-
Lowe, D., In the Pipeline. http://pipeline.corante.com/ archives/2012/04/27/how_do_drugs_get_into_cells_a_vicious_ debate.php, 2012.
-
(2012)
In the Pipeline
-
-
Lowe, D.1
-
124
-
-
28044461993
-
Strategies to improve oral drug bioavailability
-
Gomez-Orellana, I., Strategies to improve oral drug bioavailability. Expert opinion on drug delivery, 2005, 2(3), 419-433.
-
(2005)
Expert opinion on drug delivery
, vol.2
, Issue.3
, pp. 419-433
-
-
Gomez-Orellana, I.1
-
125
-
-
0020556575
-
1, 3-Dipalmitoylglycerol ester of chlorambucil as a lymphotropic, orally administrable anti-neoplastic agent
-
Garzonaburbeh, A.; Poupaert, J.H.; Claesen, M.; Dumont, P.; Atassi, G., 1, 3-Dipalmitoylglycerol ester of chlorambucil as a lymphotropic, orally administrable anti-neoplastic agent. J. Med. Chem., 1983, 26(8), 1200-1203.
-
(1983)
J. Med. Chem.
, vol.26
, Issue.8
, pp. 1200-1203
-
-
Garzonaburbeh, A.1
Poupaert, J.H.2
Claesen, M.3
Dumont, P.4
Atassi, G.5
-
126
-
-
0031455129
-
Drug delivery to the lymphatic system
-
Porter, C.J.H., Drug delivery to the lymphatic system. Crit. Rev. Ther. Drug Carrier Syst., 1997, 14(4), 333-393.
-
(1997)
Crit. Rev. Ther. Drug Carrier Syst.
, vol.14
, Issue.4
, pp. 333-393
-
-
Porter, C.J.H.1
-
127
-
-
34447265979
-
A lipid-based liquid crystalline matrix that provides sustained release and enhanced oral bioavailability for a model poorly water soluble drug in rats
-
Boyd, B.J.; Khoo, S.-M.; Whittaker, D.V.; Davey, G.; Porter, C.J.H., A lipid-based liquid crystalline matrix that provides sustained release and enhanced oral bioavailability for a model poorly water soluble drug in rats. Int. J. Pharm., 2007, 340(1-2), 52-60.
-
(2007)
Int. J. Pharm.
, vol.340
, Issue.1-2
, pp. 52-60
-
-
Boyd, B.J.1
Khoo, S.-M.2
Whittaker, D.V.3
Davey, G.4
Porter, C.J.H.5
-
128
-
-
0346098043
-
Invitro and in-vivo studies of cefpirom using bile salts as absorption enhancers
-
Mrestani, Y.; Bretschneider, B.; Hartl, A.; Neubert, R.H.H., Invitro and in-vivo studies of cefpirom using bile salts as absorption enhancers. J. Pharm. Pharmacol., 2003, 55(12), 1601-1606.
-
(2003)
J. Pharm. Pharmacol.
, vol.55
, Issue.12
, pp. 1601-1606
-
-
Mrestani, Y.1
Bretschneider, B.2
Hartl, A.3
Neubert, R.H.H.4
-
129
-
-
1842523977
-
Influence of enhancers on the absorption and on the pharmacokinetics of cefodizime using in-vitro and in-vivo models
-
Mrestani, Y.; Bretschneider, B.; Hartl, A.; Brandsch, M.; Neubert, R.H.H., Influence of enhancers on the absorption and on the pharmacokinetics of cefodizime using in-vitro and in-vivo models. J. Pharm. Pharmacol., 2004, 56(4), 485-493.
-
(2004)
J. Pharm. Pharmacol.
, vol.56
, Issue.4
, pp. 485-493
-
-
Mrestani, Y.1
Bretschneider, B.2
Hartl, A.3
Brandsch, M.4
Neubert, R.H.H.5
-
130
-
-
4644310816
-
Improvement of lipophilicity and membrane transport of cefuroxime using in vitro models
-
Mrestani, Y.; Mrestani-Klaus, C.; Bretschneider, B.; Neubert, R.H.H., Improvement of lipophilicity and membrane transport of cefuroxime using in vitro models. Eur. J. Pharmaceut. Biopharmaceut., 2004, 58(3), 653-657.
-
(2004)
Eur. J. Pharmaceut. Biopharmaceut.
, vol.58
, Issue.3
, pp. 653-657
-
-
Mrestani, Y.1
Mrestani-Klaus, C.2
Bretschneider, B.3
Neubert, R.H.H.4
-
131
-
-
31144446867
-
Influence of absorption enhancers on the pharmacokinetic properties of non-oral betalactam-cefpirom using the rabbit (Chinchilla) in vivo model
-
Mrestani, Y.; Hartl, A.; Neubert, R.H.H., Influence of absorption enhancers on the pharmacokinetic properties of non-oral betalactam-cefpirom using the rabbit (Chinchilla) in vivo model. Int. J. Pharm., 2006, 309(1-2), 67-70.
-
(2006)
Int. J. Pharm.
, vol.309
, Issue.1-2
, pp. 67-70
-
-
Mrestani, Y.1
Hartl, A.2
Neubert, R.H.H.3
-
132
-
-
70349562924
-
Preparation and performance evaluation of saquinavir laden cationic submicron emulsions
-
Jain, V.; Prasad, V.; Jadhav, P.; Mishra, P.R., Preparation and performance evaluation of saquinavir laden cationic submicron emulsions. Drug Delivery, 2009, 16(1), 37-44.
-
(2009)
Drug Delivery
, vol.16
, Issue.1
, pp. 37-44
-
-
Jain, V.1
Prasad, V.2
Jadhav, P.3
Mishra, P.R.4
-
133
-
-
67349130543
-
Quasi-equilibrium analysis of the ion-pair mediated membrane transport of low-permeability drugs
-
Miller, J.M.; Dahan, A.; Gupta, D.; Varghese, S.; Amidon, G.L., Quasi-equilibrium analysis of the ion-pair mediated membrane transport of low-permeability drugs. J. Controlled Release, 2009, 137(1), 31-37.
-
(2009)
J. Controlled Release
, vol.137
, Issue.1
, pp. 31-37
-
-
Miller, J.M.1
Dahan, A.2
Gupta, D.3
Varghese, S.4
Amidon, G.L.5
-
134
-
-
32044453584
-
Optimization of suppository preparation containing sodium laurate and taurine that can safely improve rectal absorption of rebamipide
-
Miyake, M.; Minami, T.; Oka, Y.; Kamada, N.; Yamazaki, H.; Kato, Y.; Mukai, T.; Toguchi, H.; Odomi, M.; Ogawara, K.; Higaki, K.; Kimura, T., Optimization of suppository preparation containing sodium laurate and taurine that can safely improve rectal absorption of rebamipide. Biol. Pharm. Bull., 2006, 29(2), 330-335.
-
(2006)
Biol. Pharm. Bull.
, vol.29
, Issue.2
, pp. 330-335
-
-
Miyake, M.1
Minami, T.2
Oka, Y.3
Kamada, N.4
Yamazaki, H.5
Kato, Y.6
Mukai, T.7
Toguchi, H.8
Odomi, M.9
Ogawara, K.10
Higaki, K.11
Kimura, T.12
-
135
-
-
33749548071
-
Importance of bile acids for novel oral absorption system containing polyamines to improve intestinal absorption
-
Miyake, M.; Minami, T.; Toguchi, H.; Odomi, M.; Ogawara, K.-I.; Higaki, K.; Kimura, T., Importance of bile acids for novel oral absorption system containing polyamines to improve intestinal absorption. J. Controlled Release, 2006, 115(2), 130-133.
-
(2006)
J. Controlled Release
, vol.115
, Issue.2
, pp. 130-133
-
-
Miyake, M.1
Minami, T.2
Toguchi, H.3
Odomi, M.4
Ogawara, K.-I.5
Higaki, K.6
Kimura, T.7
-
136
-
-
58249123402
-
Novel oral absorption system containing polyamines and bile salts enhances drug transport via both transcellular and paracellular pathways across Caco-2 cell monolayers
-
Mukaizawa, F.; Taniguchi, K.; Miyake, M.; Ogawara, K.-i.; Odomi, M.; Higaki, K.; Kimura, T., Novel oral absorption system containing polyamines and bile salts enhances drug transport via both transcellular and paracellular pathways across Caco-2 cell monolayers. Int. J. Pharm., 2009, 367(1-2), 103-108.
-
(2009)
Int. J. Pharm.
, vol.367
, Issue.1-2
, pp. 103-108
-
-
Mukaizawa, F.1
Taniguchi, K.2
Miyake, M.3
Ogawara, K.-I.4
Odomi, M.5
Higaki, K.6
Kimura, T.7
-
137
-
-
38349134916
-
Dendrimers as drug carriers: Applications in different routes of drug administration
-
Cheng, Y.; Xu, Z.; Ma, M.; Xu, T., Dendrimers as drug carriers: Applications in different routes of drug administration. J. Pharm. Sci., 2008, 97(1), 123-143.
-
(2008)
J. Pharm. Sci.
, vol.97
, Issue.1
, pp. 123-143
-
-
Cheng, Y.1
Xu, Z.2
Ma, M.3
Xu, T.4
-
138
-
-
21744456395
-
Soluble polymer conjugates for drug delivery
-
Minko, T., Soluble polymer conjugates for drug delivery. Drug Discov. Today: Technol., 2005, 2, 15-20.
-
(2005)
Drug Discov. Today: Technol.
, vol.2
, pp. 15-20
-
-
Minko, T.1
-
139
-
-
42549116239
-
Novel drug nanocarriers combining hydrophilic cyclodextrins and chitosan
-
Trapani, A.; Garcia-Fuentes, M.; Alonso, M.J., Novel drug nanocarriers combining hydrophilic cyclodextrins and chitosan. Nanotechnology, 2008, 19(18).
-
(2008)
Nanotechnology
, vol.19
, Issue.18
-
-
Trapani, A.1
Garcia-Fuentes, M.2
Alonso, M.J.3
-
140
-
-
51049097152
-
The effect of dendrimers on the pharmacodynamic and pharmacokinetic behaviors of noncovalently or covalently attached drugs
-
Cheng, Y.; Xu, T., The effect of dendrimers on the pharmacodynamic and pharmacokinetic behaviors of noncovalently or covalently attached drugs. Eur. J. Med. Chem., 2008, 43(11), 2291-2297.
-
(2008)
Eur. J. Med. Chem.
, vol.43
, Issue.11
, pp. 2291-2297
-
-
Cheng, Y.1
Xu, T.2
-
141
-
-
12844258906
-
Dendrimers and dendritic polymers in drug delivery
-
Gillies, E.R.; Frechet, J.M.J., Dendrimers and dendritic polymers in drug delivery. Drug Discov. Today, 2005, 10(1), 35-43.
-
(2005)
Drug Discov. Today
, vol.10
, Issue.1
, pp. 35-43
-
-
Gillies, E.R.1
Frechet, J.M.J.2
-
142
-
-
60749099362
-
Dendrimers as versatile platform in drug delivery applications
-
Svenson, S., Dendrimers as versatile platform in drug delivery applications. Eur. J. Pharmaceut. Biopharmaceut., 2009, 71(3), 445-462.
-
(2009)
Eur. J. Pharmaceut. Biopharmaceut.
, vol.71
, Issue.3
, pp. 445-462
-
-
Svenson, S.1
-
143
-
-
0000478816
-
Hydraamphiphiles-novel linear dendritic block-copolymer surfactants
-
Chapman, T.M.; Hillyer, G.L.; Mahan, E.J.; Shaffer, K.A., Hydraamphiphiles-novel linear dendritic block-copolymer surfactants. J. Am. Chem. Soc., 1994, 116(24), 11195-11196.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, Issue.24
, pp. 11195-11196
-
-
Chapman, T.M.1
Hillyer, G.L.2
Mahan, E.J.3
Shaffer, K.A.4
-
144
-
-
68249138692
-
Partly-PEGylated Poly-L-lysine Dendrimers Have Reduced Plasma Stability and Circulation Times Compared With Fully PEGylated Dendrimers
-
Kaminskas, L.M.; Wu, Z.; Barlow, N.; Krippner, G.Y.; Boyd, B.J.; Porter, C.J.H., Partly-PEGylated Poly-L-lysine Dendrimers Have Reduced Plasma Stability and Circulation Times Compared With Fully PEGylated Dendrimers. J. Pharm. Sci., 2009, 98(10), 3871-3875.
-
(2009)
J. Pharm. Sci.
, vol.98
, Issue.10
, pp. 3871-3875
-
-
Kaminskas, L.M.1
Wu, Z.2
Barlow, N.3
Krippner, G.Y.4
Boyd, B.J.5
Porter, C.J.H.6
-
145
-
-
12244272432
-
Dendrisomes: Vesicular structures derived from a cationic lipidic dendron
-
Al-Jamal, K.T.; Sakthivel, T.; Florence, A.T., Dendrisomes: Vesicular structures derived from a cationic lipidic dendron. J. Pharm. Sci., 2005, 94(1), 102-113.
-
(2005)
J. Pharm. Sci.
, vol.94
, Issue.1
, pp. 102-113
-
-
Al-Jamal, K.T.1
Sakthivel, T.2
Florence, A.T.3
-
146
-
-
21744442224
-
Gastrointestinal absorption of heparin by lipidization or coadministration with penetration enhancers
-
Ross, B.P.; Toth, I., Gastrointestinal absorption of heparin by lipidization or coadministration with penetration enhancers. Curr. Drug Delivery, 2005, 2(3), 277-287.
-
(2005)
Curr. Drug Delivery
, vol.2
, Issue.3
, pp. 277-287
-
-
Ross, B.P.1
Toth, I.2
-
147
-
-
13444309866
-
Dendrimer-heparin complexation
-
Al-Jamal, K.T.; Sakthivel, T.; Florence, A.T., Dendrimer-heparin complexation. J. Pharm. Pharmacol., 2003, 55(Supplement).
-
(2003)
J. Pharm. Pharmacol.
, vol.55
, Issue.SUPPL.
-
-
Al-Jamal, K.T.1
Sakthivel, T.2
Florence, A.T.3
-
148
-
-
79953861695
-
A Study of PA DNA/Dendron Nanoparticles for Genetic Immunisation Against Anthrax
-
Ribeiro, S.J.; Rijpkema, S.G.; Durrani, Z.; Florence, A.T., A Study of PA DNA/Dendron Nanoparticles for Genetic Immunisation Against Anthrax. The Open Vaccine Journal, 2008, 1, 38-44.
-
(2008)
The Open Vaccine Journal
, vol.1
, pp. 38-44
-
-
Ribeiro, S.J.1
Rijpkema, S.G.2
Durrani, Z.3
Florence, A.T.4
-
149
-
-
0343315679
-
Structure-Activity Relationships in Aminoglycoside-Aminocyclitol Antibiotics
-
Marcel Dekker: New York
-
Nagabhushan, T.L.; Miller, G.H.; Weinstein, M.J., Structure-Activity Relationships in Aminoglycoside-Aminocyclitol Antibiotics. The Aminoglycosides: Microbiology, Clinical Use, and Toxicology; Marcel Dekker: New York, 3-27, 1982.
-
(1982)
The Aminoglycosides: Microbiology, Clinical Use, and Toxicology
, pp. 3-27
-
-
Nagabhushan, T.L.1
Miller, G.H.2
Weinstein, M.J.3
-
150
-
-
0033370077
-
Didanosine-An updated review of its use in HIV infection
-
Perry, C.M.; Noble, S., Didanosine-An updated review of its use in HIV infection. Drugs, 1999, 58(6), 1099-1135.
-
(1999)
Drugs
, vol.58
, Issue.6
, pp. 1099-1135
-
-
Perry, C.M.1
Noble, S.2
-
151
-
-
0035286778
-
Caco-2 monolayers in experimental and theoretical predictions of drug transport
-
Artursson, P.; Palm, K.; Luthman, K., Caco-2 monolayers in experimental and theoretical predictions of drug transport. Adv. Drug Delivery Rev., 2001, 46(1-3), 27-43.
-
(2001)
Adv. Drug Delivery Rev.
, vol.46
, Issue.1-3
, pp. 27-43
-
-
Artursson, P.1
Palm, K.2
Luthman, K.3
-
152
-
-
38749154735
-
Optimized LC-MS/MS quantification method for the detection of piperacillin and application to the development of charged liposaccharides as oral penetration enhancers
-
Violette, A.; Cortes, D.A.F.; Bergeon, J.A.; Falconer, R.A.; Toth, I., Optimized LC-MS/MS quantification method for the detection of piperacillin and application to the development of charged liposaccharides as oral penetration enhancers. Int. J. Pharm., 2008, 351(1-2), 152-157.
-
(2008)
Int. J. Pharm.
, vol.351
, Issue.1-2
, pp. 152-157
-
-
Violette, A.1
Cortes, D.A.F.2
Bergeon, J.A.3
Falconer, R.A.4
Toth, I.5
-
153
-
-
77951265379
-
In Vitro and In Vivo Evaluation of Positively Charged Liposaccharide Derivatives as Oral Absorption Enhancers for the Delivery of Anionic Drugs
-
Bergeon, J.A.; Ziora, Z.M.; Abdelrahim, A.S.; Pernevi, N.U.; Moss, A.R.; Toth, I., In Vitro and In Vivo Evaluation of Positively Charged Liposaccharide Derivatives as Oral Absorption Enhancers for the Delivery of Anionic Drugs. J. Pharm. Sci., 2010, 99(5), 2333-2342.
-
(2010)
J. Pharm. Sci.
, vol.99
, Issue.5
, pp. 2333-2342
-
-
Bergeon, J.A.1
Ziora, Z.M.2
Abdelrahim, A.S.3
Pernevi, N.U.4
Moss, A.R.5
Toth, I.6
-
154
-
-
0035157333
-
Effect of common excipients on Caco-2 transport of low-permeability drugs
-
Rege, B.D.; Yu, L.X.; Husain, A.S.; Polli, J.E., Effect of common excipients on Caco-2 transport of low-permeability drugs. J. Pharm. Sci., 2001, 90(11), 1776-1786.
-
(2001)
J. Pharm. Sci.
, vol.90
, Issue.11
, pp. 1776-1786
-
-
Rege, B.D.1
Yu, L.X.2
Husain, A.S.3
Polli, J.E.4
-
155
-
-
33748641168
-
Promoting absorption of drugs in humans using medium-chain fatty acid-based solid dosage forms: GIPET
-
Leonard, T.W.; Lynch, J.; McKenna, M.J.; Brayden, D.J., Promoting absorption of drugs in humans using medium-chain fatty acid-based solid dosage forms: GIPET. Expert Opin. Drug Deliv., 2006, 3(5), 685-692.
-
(2006)
Expert Opin. Drug Deliv.
, vol.3
, Issue.5
, pp. 685-692
-
-
Leonard, T.W.1
Lynch, J.2
McKenna, M.J.3
Brayden, D.J.4
-
156
-
-
67249086096
-
Dry Hybrid Lipid-Silica Microcapsules Engineered from Submicron Lipid Droplets and Nanoparticles as a Novel Delivery System for Poorly Soluble Drugs
-
Simovic, S.; Heard, P.; Hui, H.; Song, Y.; Peddie, F.; Davey, A.K.; Lewis, A.; Rades, T.; Prestidge, C.A., Dry Hybrid Lipid-Silica Microcapsules Engineered from Submicron Lipid Droplets and Nanoparticles as a Novel Delivery System for Poorly Soluble Drugs. Mol. Pharm., 2009, 6(3), 861-872.
-
(2009)
Mol. Pharm.
, vol.6
, Issue.3
, pp. 861-872
-
-
Simovic, S.1
Heard, P.2
Hui, H.3
Song, Y.4
Peddie, F.5
Davey, A.K.6
Lewis, A.7
Rades, T.8
Prestidge, C.A.9
-
157
-
-
79959565855
-
Modern Lipid-, Carbohydrate-, and Peptide-Based Delivery Systems for Peptide, Vaccine, and Gene Products
-
Simerska, P.; Moyle, P.M.; Toth, I., Modern Lipid-, Carbohydrate-, and Peptide-Based Delivery Systems for Peptide, Vaccine, and Gene Products. Med. Res. Rev., 2011, 31(4), 520-547.
-
(2011)
Med. Res. Rev.
, vol.31
, Issue.4
, pp. 520-547
-
-
Simerska, P.1
Moyle, P.M.2
Toth, I.3
-
158
-
-
84862684767
-
Perspective: Oral drug delivery research in Europe
-
Mrsny, R.J., Perspective: Oral drug delivery research in Europe. J. Control Release, 2012, http://dx.doi.org/10.1016/ j.jconrel.2012.01.017.
-
(2012)
J. Control Release
-
-
Mrsny, R.J.1
-
159
-
-
84867329999
-
Orally administered therapeutic peptide delivery:Enhanced absorption through the small intestine using permeation enhancers
-
doi: 10.1007/s10989-012-9299-7
-
Pillay, V.; Hibbins, A.R.; Choonara, Y.E.; du Toit, L.C.; Kumar, P.; Ndesendo, V.M.K., Orally administered therapeutic peptide delivery:enhanced absorption through the small intestine using permeation enhancers. Int. J. Pept. Res. Ther., 2012, doi: 10.1007/s10989-012-9299-7.
-
(2012)
Int. J. Pept. Res. Ther.
-
-
Pillay, V.1
Hibbins, A.R.2
Choonara, Y.E.3
du Toit, L.C.4
Kumar, P.5
Ndesendo, V.M.K.6
-
160
-
-
3042586026
-
Physical chemical considerations of lipid-based oral drug delivery-Solid lipid nanoparticles
-
Bummer, P.M., Physical chemical considerations of lipid-based oral drug delivery-Solid lipid nanoparticles. Critical Reviews in Therapeutic Drug Carrier Systems, 2004, 21(1), 1-19.
-
(2004)
Critical Reviews in Therapeutic Drug Carrier Systems
, vol.21
, Issue.1
, pp. 1-19
-
-
Bummer, P.M.1
-
161
-
-
84863445857
-
Enhancement of Intestinal Permeability Utilizing Solid Lipid Nanoparticles Increases γ-Tocotrienol Oral Bioavailability
-
Abuasal, B.S.; Lucas, C.; Peyton, B.; Alayoubi, A.; Nazzal, S.; Sylvester, P.W.; Kaddoumi, A., Enhancement of Intestinal Permeability Utilizing Solid Lipid Nanoparticles Increases γ-Tocotrienol Oral Bioavailability. Lipids, 2012, 47, 461-469.
-
(2012)
Lipids
, vol.47
, pp. 461-469
-
-
Abuasal, B.S.1
Lucas, C.2
Peyton, B.3
Alayoubi, A.4
Nazzal, S.5
Sylvester, P.W.6
Kaddoumi, A.7
-
162
-
-
3543106201
-
Influence of lipolysis and droplet size on tocotrienol absortion from self-emulsifying formulations
-
Yap, S.P.; Yuen, K.H., Influence of lipolysis and droplet size on tocotrienol absortion from self-emulsifying formulations. Int. J. Pharm., 2004, 281(1-2), 67-78.
-
(2004)
Int. J. Pharm.
, vol.281
, Issue.1-2
, pp. 67-78
-
-
Yap, S.P.1
Yuen, K.H.2
-
163
-
-
29244485443
-
A new self-emulsifying formulation of itraconazole with improved dissolution and oral absorption
-
Hong, J.Y.; Kim, J.K.; Song, Y.K.; Park, J.S.; Kim, C.K., A new self-emulsifying formulation of itraconazole with improved dissolution and oral absorption. J. Controlled Release, 2006, 110(2), 332-338.
-
(2006)
J. Controlled Release
, vol.110
, Issue.2
, pp. 332-338
-
-
Hong, J.Y.1
Kim, J.K.2
Song, Y.K.3
Park, J.S.4
Kim, C.K.5
-
164
-
-
84861469900
-
The in vitro and in vivo study on self-nanoemulsifying drug delivery system (SNEDDS) based on insulin-phospholipid complex
-
Zhang, Q.; He, N.; Zhang, L.; Zhu, F.; Chen, Q.; Qin, Y.; Zhang, Z.; Zhang, Q.; Wang, S.; He, Q., The in vitro and in vivo study on self-nanoemulsifying drug delivery system (SNEDDS) based on insulin-phospholipid complex. J. Biomed. Nanotechnol., 2012, 8, 90-97.
-
(2012)
J. Biomed. Nanotechnol.
, vol.8
, pp. 90-97
-
-
Zhang, Q.1
He, N.2
Zhang, L.3
Zhu, F.4
Chen, Q.5
Qin, Y.6
Zhang, Z.7
Zhang, Q.8
Wang, S.9
He, Q.10
-
165
-
-
84864323714
-
Influence of lipid composition and drug load on the In Vitro performance of selfnanoemulsifying drug delivery systems
-
Thomas, N.; Muellertz, A.; Graf, A.; Rades, T., Influence of lipid composition and drug load on the In Vitro performance of selfnanoemulsifying drug delivery systems. J. Pharm. Sci., 2012, 101, 1721-1731.
-
(2012)
J. Pharm. Sci.
, vol.101
, pp. 1721-1731
-
-
Thomas, N.1
Muellertz, A.2
Graf, A.3
Rades, T.4
-
166
-
-
84861529172
-
In vitro and in vivo performance of novel supersaturated self-nanoemulsifying drug delivery systems (super-SNEDDS)
-
Thomas, N.; Holm, R.; Mullertz, A.; Rades, T., In vitro and in vivo performance of novel supersaturated self-nanoemulsifying drug delivery systems (super-SNEDDS). J. Controlled Release, 2012, 160, 25-32.
-
(2012)
J. Controlled Release
, vol.160
, pp. 25-32
-
-
Thomas, N.1
Holm, R.2
Mullertz, A.3
Rades, T.4
-
167
-
-
75549087162
-
Nanosystem drug targeting: Facing up to complex realities
-
Ruenraroengsak, P.; Cook, J.M.; Florence, A.T., Nanosystem drug targeting: Facing up to complex realities. J. Controlled Release, 2010, 141(3), 265-276.
-
(2010)
J. Controlled Release
, vol.141
, Issue.3
, pp. 265-276
-
-
Ruenraroengsak, P.1
Cook, J.M.2
Florence, A.T.3
-
168
-
-
84869488700
-
"Targeting" nanoparticles: The constraints of physical laws and physical barriers
-
Florence, A.T., "Targeting" nanoparticles: The constraints of physical laws and physical barriers. J Control Release, 2012, http://dx.doi.org/10.1016/j.jconrel.2012.03.022.
-
(2012)
J Control Release
-
-
Florence, A.T.1
-
169
-
-
78650677036
-
Oral drug delivery in personalized medicine: Unmet needs and novel approaches
-
Wening, K.; Breitkreutz, J., Oral drug delivery in personalized medicine: Unmet needs and novel approaches. Int. J. Pharm., 2011, 404(1-2), 1-9.
-
(2011)
Int. J. Pharm.
, vol.404
, Issue.1-2
, pp. 1-9
-
-
Wening, K.1
Breitkreutz, J.2
-
170
-
-
79960181154
-
Personalised medicines: More tailored drugs, more tailored delivery
-
Florence, A.T.; Lee, V.H.L., Personalised medicines: More tailored drugs, more tailored delivery. Int. J. Pharm., 2011, 415(1-2), 29-33.
-
(2011)
Int. J. Pharm.
, vol.415
, Issue.1-2
, pp. 29-33
-
-
Florence, A.T.1
Lee, V.H.L.2
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