-
1
-
-
10444279209
-
Cyclodextrin-based pharmaceutics: Past, present and future
-
Davis ME, Brewster ME,. Cyclodextrin-based pharmaceutics: past, present and future. Nat Rev Drug Discov 2004; 12: 1023-1035.
-
(2004)
Nat Rev Drug Discov
, vol.12
, pp. 1023-1035
-
-
Davis, M.E.1
Brewster, M.E.2
-
2
-
-
78649654159
-
Pharmaceutical applications of cyclodextrins: Basic science and product development
-
Loftsson T, Brewster ME,. Pharmaceutical applications of cyclodextrins: basic science and product development. J Pharm Pharmacol 2010; 11: 1607-1621.
-
(2010)
J Pharm Pharmacol
, vol.11
, pp. 1607-1621
-
-
Loftsson, T.1
Brewster, M.E.2
-
3
-
-
44649133855
-
Rationalizing the selection of oral lipid based drug delivery systems by an in vitro dynamic lipolysis model for improved oral bioavailability of poorly water soluble drugs
-
Dahan A, Hoffman A,. Rationalizing the selection of oral lipid based drug delivery systems by an in vitro dynamic lipolysis model for improved oral bioavailability of poorly water soluble drugs. J Control Release 2008; 1: 1-10.
-
(2008)
J Control Release
, vol.1
, pp. 1-10
-
-
Dahan, A.1
Hoffman, A.2
-
4
-
-
35248822616
-
The utility of cyclodextrins for enhancing oral bioavailability
-
Carrier RL, et al. The utility of cyclodextrins for enhancing oral bioavailability. J Control Release 2007; 2: 78-99.
-
(2007)
J Control Release
, vol.2
, pp. 78-99
-
-
Carrier, R.L.1
-
5
-
-
0034988419
-
Comparative studies of the enhancing effects of cyclodextrins on the solubility and oral bioavailability of tacrolimus in rats
-
Hidetoshi A, et al. Comparative studies of the enhancing effects of cyclodextrins on the solubility and oral bioavailability of tacrolimus in rats. J Pharm Sci 2001; 6: 690-701.
-
(2001)
J Pharm Sci
, vol.6
, pp. 690-701
-
-
Hidetoshi, A.1
-
6
-
-
50249163680
-
Development and evaluation of novel itraconazole-loaded intravenous nanoparticles
-
Chen W, et al. Development and evaluation of novel itraconazole-loaded intravenous nanoparticles. Int J Pharm 2008; 1-2: 133-140.
-
(2008)
Int J Pharm
, vol.12
, pp. 133-140
-
-
Chen, W.1
-
7
-
-
0033106029
-
Mechanisms of drug release from cyclodextrin complexes
-
Valentino JS, et al. Mechanisms of drug release from cyclodextrin complexes. Adv Drug Del Rev 1999; 36: 3-16.
-
(1999)
Adv Drug Del Rev
, vol.36
, pp. 3-16
-
-
Valentino, J.S.1
-
8
-
-
33846498531
-
A mixed polymeric micellar formulation of itraconazole: Characteristics, toxicity and pharmacokinetics
-
Yi Y, et al. A mixed polymeric micellar formulation of itraconazole: characteristics, toxicity and pharmacokinetics. J Control Release 2007; 1: 59-67.
-
(2007)
J Control Release
, vol.1
, pp. 59-67
-
-
Yi, Y.1
-
9
-
-
0034691643
-
Oral bioavailability and hypoglycaemic activity of tolbutamide/ cyclodextrin inclusion complexes
-
Veiga F, et al. Oral bioavailability and hypoglycaemic activity of tolbutamide/cyclodextrin inclusion complexes. Int J Pharm 2000; 1-2: 165-171.
-
(2000)
Int J Pharm
, vol.12
, pp. 165-171
-
-
Veiga, F.1
-
10
-
-
27744575591
-
Cyclodextrins in drug delivery: An updated review
-
Rajeswari C, et al. Cyclodextrins in drug delivery: an updated review. AAPS PharmSciTech 2005; 2: E329-E357.
-
(2005)
AAPS PharmSciTech
, vol.2
-
-
Rajeswari, C.1
-
11
-
-
70349840419
-
Combined hydroxypropyl-beta-cyclodextrin and poly(anhydride) nanoparticles improve the oral permeability of paclitaxel
-
Agueros M, et al. Combined hydroxypropyl-beta-cyclodextrin and poly(anhydride) nanoparticles improve the oral permeability of paclitaxel. Eur J Pharm Sci 2009; 4: 405-413.
-
(2009)
Eur J Pharm Sci
, vol.4
, pp. 405-413
-
-
Agueros, M.1
-
12
-
-
77953360626
-
Increased oral bioavailability of paclitaxel by its encapsulation through complex formation with cyclodextrins in poly(anhydride) nanoparticles
-
Agüeros M, et al. Increased oral bioavailability of paclitaxel by its encapsulation through complex formation with cyclodextrins in poly(anhydride) nanoparticles. J Control Release 2010; 1: 2-8.
-
(2010)
J Control Release
, vol.1
, pp. 2-8
-
-
Agüeros, M.1
-
13
-
-
58149234269
-
Cyclodextrin as drug carrier molecule: A review
-
Arun R, et al. Cyclodextrin as drug carrier molecule: a review. Sci Pharm 2008; 4: 567-598.
-
(2008)
Sci Pharm
, vol.4
, pp. 567-598
-
-
Arun, R.1
-
14
-
-
80051674971
-
Pharmaceutical applications of cyclodextrins: Effects on drug permeation through biological membranes
-
Loftsson T, Brewster ME,. Pharmaceutical applications of cyclodextrins: effects on drug permeation through biological membranes. J Pharm Pharmacol 2011; 9: 1119-1135.
-
(2011)
J Pharm Pharmacol
, vol.9
, pp. 1119-1135
-
-
Loftsson, T.1
Brewster, M.E.2
-
15
-
-
60149100339
-
Micro- and macrorheology of mucus
-
Lai SK, et al. Micro- and macrorheology of mucus. Adv Drug Deliv Rev 2009; 2: 86-100.
-
(2009)
Adv Drug Deliv Rev
, vol.2
, pp. 86-100
-
-
Lai, S.K.1
-
16
-
-
60149111908
-
Mucus-penetrating nanoparticles for drug and gene delivery to mucosal tissues
-
Lai SK, et al. Mucus-penetrating nanoparticles for drug and gene delivery to mucosal tissues. Adv Drug Deliv Rev 2009; 2: 158-171.
-
(2009)
Adv Drug Deliv Rev
, vol.2
, pp. 158-171
-
-
Lai, S.K.1
-
17
-
-
79951896686
-
Cyclodextrin-based gene delivery systems
-
Ortiz Mellet C, et al. Cyclodextrin-based gene delivery systems. Chem Soc Rev 2011; 3: 1586-1608.
-
(2011)
Chem Soc Rev
, vol.3
, pp. 1586-1608
-
-
Ortiz Mellet, C.1
-
18
-
-
43449102775
-
Cyclodextrin-based supramolecular architectures: Syntheses, structures, and applications for drug and gene delivery
-
Li J, Loh XJ,. Cyclodextrin-based supramolecular architectures: syntheses, structures, and applications for drug and gene delivery. Adv Drug Deliv Rev 2008; 9: 1000-1017.
-
(2008)
Adv Drug Deliv Rev
, vol.9
, pp. 1000-1017
-
-
Li, J.1
Loh, X.J.2
-
19
-
-
33847105481
-
Integrity of liposomes in presence of cyclodextrins: Effect of liposome type and lipid composition
-
Hatzi P, et al. Integrity of liposomes in presence of cyclodextrins: effect of liposome type and lipid composition. Int J Pharm 2007; 1-2: 167-176.
-
(2007)
Int J Pharm
, vol.12
, pp. 167-176
-
-
Hatzi, P.1
-
20
-
-
69749121352
-
Development of a new topical system: Drug-in-cyclodextrin-in-deformable liposome
-
Gillet A, et al. Development of a new topical system: drug-in-cyclodextrin-in-deformable liposome. Int J Pharm 2009; 1-2: 174-180.
-
(2009)
Int J Pharm
, vol.12
, pp. 174-180
-
-
Gillet, A.1
-
21
-
-
79952268655
-
Biodegradable nanoparticles composed entirely of safe materials that rapidly penetrate human mucus
-
Yang M, et al. Biodegradable nanoparticles composed entirely of safe materials that rapidly penetrate human mucus. Angew Chem Int Ed 2011; 50: 2597-2600.
-
(2011)
Angew Chem Int Ed
, vol.50
, pp. 2597-2600
-
-
Yang, M.1
-
22
-
-
84862599039
-
Novel mucus-penetrating liposomes as a potential oral drug delivery system: Preparation, in vitro characterization, and enhanced cellular uptake
-
Li X, et al. Novel mucus-penetrating liposomes as a potential oral drug delivery system: preparation, in vitro characterization, and enhanced cellular uptake. Int J Nanomedicine 2011; 6: 3151-3162.
-
(2011)
Int J Nanomedicine
, vol.6
, pp. 3151-3162
-
-
Li, X.1
-
23
-
-
77954694522
-
Structure, dynamics, and energetics of siRNA-cationic vector complexation: A molecular dynamics study
-
Ouyang DF, et al. Structure, dynamics, and energetics of siRNA-cationic vector complexation: a molecular dynamics study. J Phys Chem B 2010; 28: 9220-9230.
-
(2010)
J Phys Chem B
, vol.28
, pp. 9220-9230
-
-
Ouyang, D.F.1
-
24
-
-
79958818504
-
Preparation, characterization, pharmacokinetics, and bioactivity of honokiol-in-hydroxypropyl-β-cyclodextrin-in-liposome
-
Wang X, et al. Preparation, characterization, pharmacokinetics, and bioactivity of honokiol-in-hydroxypropyl-β-cyclodextrin-in-liposome. J Pharm Sci 2011; 8: 3357-3364.
-
(2011)
J Pharm Sci
, vol.8
, pp. 3357-3364
-
-
Wang, X.1
-
25
-
-
33645020487
-
Betamethasone-in-cyclodextrin-in-liposome: The effect of cyclodextrins on encapsulation efficiency and release kinetics
-
Piel G, et al. Betamethasone-in-cyclodextrin-in-liposome: the effect of cyclodextrins on encapsulation efficiency and release kinetics. Int J Pharm 2006; 1-2: 75-82.
-
(2006)
Int J Pharm
, vol.12
, pp. 75-82
-
-
Piel, G.1
-
26
-
-
1042269559
-
Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine
-
Kostewicz ES, et al. Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine. J Pharm Pharmacol 2004; 1: 43-51.
-
(2004)
J Pharm Pharmacol
, vol.1
, pp. 43-51
-
-
Kostewicz, E.S.1
-
27
-
-
59649096972
-
Solubilisation of dipalmitoylphosphatidylcholine bilayers by sodium taurocholate: A model to study the stability of liposomes in the gastrointestinal tract and their mechanism of interaction with a model bile salt
-
Andrieux K, et al. Solubilisation of dipalmitoylphosphatidylcholine bilayers by sodium taurocholate: a model to study the stability of liposomes in the gastrointestinal tract and their mechanism of interaction with a model bile salt. Eur J Pharm Biopharm 2009; 2: 346-355.
-
(2009)
Eur J Pharm Biopharm
, vol.2
, pp. 346-355
-
-
Andrieux, K.1
-
28
-
-
48149088784
-
Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude mice
-
Lu JL, et al. Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude mice. Eur J Pharm Biopharm 2008; 3: 899-907.
-
(2008)
Eur J Pharm Biopharm
, vol.3
, pp. 899-907
-
-
Lu, J.L.1
-
29
-
-
62749095208
-
Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems
-
Cui J, et al. Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems. Int J Pharm 2009; 1-2: 148-155.
-
(2009)
Int J Pharm
, vol.12
, pp. 148-155
-
-
Cui, J.1
-
30
-
-
4344561085
-
Insertion and partition of sodium taurocholate into egg phosphatidylcholine vesicles
-
Karine A, et al. Insertion and partition of sodium taurocholate into egg phosphatidylcholine vesicles. Pharm Res 2004; 8: 1505-1516.
-
(2004)
Pharm Res
, vol.8
, pp. 1505-1516
-
-
Karine, A.1
-
31
-
-
0036278164
-
Tacrolimus is a class ?Low-solubility high-permeability drug: The effect of P-glycoprotein efflux on regional permeability of tacrolimus in rats
-
Shigeki T, et al. Tacrolimus is a class ?Low-solubility high-permeability drug: the effect of P-glycoprotein efflux on regional permeability of tacrolimus in rats. J Pharm Sci 2001; 91: 719-729.
-
(2001)
J Pharm Sci
, vol.91
, pp. 719-729
-
-
Shigeki, T.1
-
32
-
-
0038340961
-
The site-specific transport and metabolism of tacrolimus in rat small intestine
-
Tamura S, et al. The site-specific transport and metabolism of tacrolimus in rat small intestine. J Pharmacol Exp Ther 2003; 1: 310-316.
-
(2003)
J Pharmacol Exp Ther
, vol.1
, pp. 310-316
-
-
Tamura, S.1
-
33
-
-
49549091093
-
A novel nanocapsule delivery system to overcome intestinal degradation and drug transport limited absorption of P-glycoprotein substrate drugs
-
Nassar T, et al. A novel nanocapsule delivery system to overcome intestinal degradation and drug transport limited absorption of P-glycoprotein substrate drugs. Pharm Res 2008; 9: 2019-2029.
-
(2008)
Pharm Res
, vol.9
, pp. 2019-2029
-
-
Nassar, T.1
-
34
-
-
57049168640
-
Novel double coated nanocapsules for intestinal delivery and enhanced oral bioavailability of tacrolimus, a P-gp substrate drug
-
Nassar T, et al. Novel double coated nanocapsules for intestinal delivery and enhanced oral bioavailability of tacrolimus, a P-gp substrate drug. J Control Release 2009; 1: 77-84.
-
(2009)
J Control Release
, vol.1
, pp. 77-84
-
-
Nassar, T.1
-
35
-
-
60849130683
-
In vivo evaluation of safety and efficacy of self-assembled nanoparticles for oral insulin delivery
-
Sonaje K, et al. In vivo evaluation of safety and efficacy of self-assembled nanoparticles for oral insulin delivery. Biomaterials 2009; 12: 2329-2339.
-
(2009)
Biomaterials
, vol.12
, pp. 2329-2339
-
-
Sonaje, K.1
-
36
-
-
67349154874
-
Bioadhesive properties and biodistribution of cyclodextrin- poly(anhydride) nanoparticles
-
Agüeros M, et al. Bioadhesive properties and biodistribution of cyclodextrin-poly(anhydride) nanoparticles. Eur J Pharm Sci 2009; 3-4: 231-240.
-
(2009)
Eur J Pharm Sci
, vol.34
, pp. 231-240
-
-
Agüeros, M.1
-
37
-
-
79551528343
-
In vitro and in vivo evaluation of WGA-carbopol modified liposomes as carriers for oral peptide delivery
-
Makhlof A, et al. In vitro and in vivo evaluation of WGA-carbopol modified liposomes as carriers for oral peptide delivery. Eur J Pharm Biopharm 2011; 2: 216-224.
-
(2011)
Eur J Pharm Biopharm
, vol.2
, pp. 216-224
-
-
Makhlof, A.1
-
38
-
-
38349112036
-
Improved intestinal absorption of calcitonin by mucoadhesive delivery of novel pectin-liposome nanocomplexes
-
Thirawong N, et al. Improved intestinal absorption of calcitonin by mucoadhesive delivery of novel pectin-liposome nanocomplexes. J Control Release 2008; 3: 236-245.
-
(2008)
J Control Release
, vol.3
, pp. 236-245
-
-
Thirawong, N.1
-
39
-
-
0037035977
-
Computer-aided molecular modeling techniques for predicting the stability of drug-cyclodextrin inclusion complexes in aqueous solutions
-
Maria Teresa F, et al. Computer-aided molecular modeling techniques for predicting the stability of drug-cyclodextrin inclusion complexes in aqueous solutions. Chem Phys Lett 2002; 358: 383-390.
-
(2002)
Chem Phys Lett
, vol.358
, pp. 383-390
-
-
Maria Teresa, F.1
-
40
-
-
84862833264
-
Liposomes containing glycocholate as potential oral insulin delivery systems: Preparation, in vitro characterization, and improved protection against enzymatic degradation
-
Niu M, et al. Liposomes containing glycocholate as potential oral insulin delivery systems: preparation, in vitro characterization, and improved protection against enzymatic degradation. Int J Nanomedicine 2011; 6: 1155-1166.
-
(2011)
Int J Nanomedicine
, vol.6
, pp. 1155-1166
-
-
Niu, M.1
-
41
-
-
79151473262
-
Stability of liposomes containing bio-enhancers and tetraether lipids in simulated gastro-intestinal fluids
-
Parmentier J, et al. Stability of liposomes containing bio-enhancers and tetraether lipids in simulated gastro-intestinal fluids. Int J Pharm 2011; 1-2: 210-217.
-
(2011)
Int J Pharm
, vol.12
, pp. 210-217
-
-
Parmentier, J.1
-
42
-
-
80155182416
-
Enhanced oral bioavailability of cyclosporine A by liposomes containing a bile salt
-
Guan P, et al. Enhanced oral bioavailability of cyclosporine A by liposomes containing a bile salt. Int J Nanomedicine 2011; 6: 965-974.
-
(2011)
Int J Nanomedicine
, vol.6
, pp. 965-974
-
-
Guan, P.1
-
43
-
-
23844462026
-
Role of clathrin- and caveolae-mediated endocytosis in gene transfer mediated by lipo- and polyplexes
-
Rejman J, et al. Role of clathrin- and caveolae-mediated endocytosis in gene transfer mediated by lipo- and polyplexes. Mol Ther 2005; 3: 468-474.
-
(2005)
Mol Ther
, vol.3
, pp. 468-474
-
-
Rejman, J.1
-
44
-
-
79952268655
-
Biodegradable nanoparticles composed entirely of safe materials that rapidly penetrate human mucus
-
Yang M, et al. Biodegradable nanoparticles composed entirely of safe materials that rapidly penetrate human mucus. Angew Chem Int Ed Engl 2011; 11: 2597-2600.
-
(2011)
Angew Chem Int Ed Engl
, vol.11
, pp. 2597-2600
-
-
Yang, M.1
|