-
1
-
-
0036828056
-
Excipient-drug interactions in parenteral formulations
-
DOI 10.1002/jps.10154
-
Akers MJ. (2002). Excipient-drug interactions in parenteral formulations. j Pharm Sci, 91:2283-2300. (Pubitemid 35231192)
-
(2002)
Journal of Pharmaceutical Sciences
, vol.91
, Issue.11
, pp. 2283-2300
-
-
Akers, M.J.1
-
2
-
-
0020567341
-
Binding of oestradiol, progesterone and prolactin in rat lung
-
Ben-Harari RR, Amit T, Youdim MB. (1983). Binding of oestradiol, progesterone and prolactin in rat lung. j Endocrinol, 97:301-310. (Pubitemid 13079816)
-
(1983)
Journal of Endocrinology
, vol.97
, Issue.2
, pp. 301-310
-
-
Ben Harari, R.R.1
Amit, T.2
Youdim, M.B.H.3
-
3
-
-
0033178415
-
Lab-scale production unit design for nanosuspensions of sparingly soluble cytotoxic drugs
-
Bernhard HL, Bohm Muller RH. (1999). Lab-scale production unit design for nanosuspensions of sparingly soluble cytotoxic drugs. Pharm Sci Tech Today, 2:336-339.
-
(1999)
Pharm Sci Tech Today
, vol.2
, pp. 336-339
-
-
Bernhard, H.L.1
Bohm Muller, R.H.2
-
4
-
-
4444379133
-
Nanoparticle and targeted systems for cancer therapy
-
DOI 10.1016/j.addr.2004.02.014, PII S0169409X04001450
-
Brannon-Peppas L, Blanchette JO. (2004). Nanoparticle and targeted systems for cancer therapy. Adv Drug Deliv Rev, 56:1649-1659. (Pubitemid 39177694)
-
(2004)
Advanced Drug Delivery Reviews
, vol.56
, Issue.11
, pp. 1649-1659
-
-
Brannon-Peppas, L.1
Blanchette, J.O.2
-
5
-
-
77953958625
-
The in vitro stability and in vivo pharmacokinetics of curcumin prepared as an aqueous nanoparticulate formulation
-
Chandana M, Sanjeeb K S. (2010). The in vitro stability and in vivo pharmacokinetics of curcumin prepared as an aqueous nanoparticulate formulation. Biomaterials, 31:6597-6611.
-
(2010)
Biomaterials
, vol.31
, pp. 6597-6611
-
-
Chandana, M.1
Sanjeeb, K.S.2
-
6
-
-
33746449598
-
Susceptibility of nanoparticle-encapsulated paclitaxel to P-glycoprotein-mediated drug efflux
-
DOI 10.1016/j.ijpharm.2006.03.045, PII S0378517306002869
-
Chavanpatil MD, Patil Y, Panyam J. (2006). Susceptibility of nanoparticle-encapsulated paclitaxel to P-glycoprotein-mediated drug efflux. Int j Pharm, 320:150-156. (Pubitemid 44128700)
-
(2006)
International Journal of Pharmaceutics
, vol.320
, Issue.1-2
, pp. 150-156
-
-
Chavanpatil, M.D.1
Patil, Y.2
Panyam, J.3
-
7
-
-
77955403169
-
Preparation and characterization of freeze-dried 2-methoxyestradiol nanoparticle powders
-
Du B, Li XT, Zhao Y, A YM, Zhang ZZ. (2010). Preparation and characterization of freeze-dried 2-methoxyestradiol nanoparticle powders. Pharmazie, 65:471-476.
-
(2010)
Pharmazie
, vol.65
, pp. 471-476
-
-
Du, B.1
Li, X.T.2
Zhao, Y.3
Ym, A.4
Zhang, Z.Z.5
-
8
-
-
84891665438
-
LC with fluorescence detection for the tissue pharmacokinetics of 2-methoxyestradiol solution and liposome after intravenous administrations to rats
-
Du B, Li Y, Li XT, A YM, Zhang ZZ. (2009). LC with fluorescence detection for the tissue pharmacokinetics of 2-methoxyestradiol solution and liposome after intravenous administrations to rats. Chromatographia, 70:1287-1290.
-
(2009)
Chromatographia
, vol.70
, pp. 1287-1290
-
-
Du, B.1
Li, Y.2
Li, X.T.3
Ym, A.4
Zhang, Z.Z.5
-
9
-
-
0033120537
-
Top ten considerations in the development of parenteral emulsions
-
DOI 10.1016/S1461-5347(99)00141-8, PII S1461534799001418
-
Floyd AG. (1999). Top ten considerations in the development of parenteral emulsions. Pharm Sci Technol Today, 4:134-143. (Pubitemid 29195746)
-
(1999)
Pharmaceutical Science and Technology Today
, vol.2
, Issue.4
, pp. 134-143
-
-
Floyd, A.G.1
-
10
-
-
58249109448
-
Formulation and pharmacokinetic evaluation of an asulacrine nanocrystalline suspension for intravenous delivery
-
Ganta S, Paxton JW, Baguley BC, Garg S. (2009). Formulation and pharmacokinetic evaluation of an asulacrine nanocrystalline suspension for intravenous delivery. Int j Pharm, 367:179-186.
-
(2009)
Int J Pharm
, vol.367
, pp. 179-186
-
-
Ganta, S.1
Paxton, J.W.2
Baguley, B.C.3
Garg, S.4
-
11
-
-
33645060731
-
HPLC determination of polydatin in rat biological matrices: Application to pharmacokinetic studies
-
Gao S, Fan G, Hong Z, Yin X, Yang S, Wu Y. (2006). HPLC determination of polydatin in rat biological matrices: application to pharmacokinetic studies. j Pharm Biomed Anal, 41:240-245.
-
(2006)
J Pharm Biomed Anal
, vol.41
, pp. 240-245
-
-
Gao, S.1
Fan, G.2
Hong, Z.3
Yin, X.4
Yang, S.5
Wu, Y.6
-
12
-
-
41349120910
-
Studies on pharmacokinetics and tissue distribution of oridonin nanosuspensions
-
Gao L, Zhang D, Chen M, Duan C, Dai W, Jia L et al. (2008). Studies on pharmacokinetics and tissue distribution of oridonin nanosuspensions. Int j Pharm, 355:321-327.
-
(2008)
Int J Pharm
, vol.355
, pp. 321-327
-
-
Gao, L.1
Zhang, D.2
Chen, M.3
Duan, C.4
Dai, W.5
Jia, L.6
-
13
-
-
67349239016
-
Preparation of hydrocortisone nanosuspension through a bottom-up nanoprecipitation technique using microfluidic reactors
-
Hany SM, Peter Y, Nicholas B. (2009). Preparation of hydrocortisone nanosuspension through a bottom-up nanoprecipitation technique using microfluidic reactors. Int J Pharm, 375:107-113.
-
(2009)
Int J Pharm
, vol.375
, pp. 107-113
-
-
Hany, S.M.1
Peter, Y.2
Nicholas, B.3
-
14
-
-
33750089277
-
Preparation and in vitro/in vivo evaluation of nano-sized crystals for dissolution rate enhancement of ucb-35440-3, a highly dosed poorly water-soluble weak base
-
DOI 10.1016/j.ejpb.2006.05.008, PII S0939641106001408
-
Hecq J, Deleers M, Fanara D, Vranckx H, Boulanger P, Le Lamer S et al. (2006). Preparation and in vitro/in vivo evaluation of nanosized crystals for dissolution rate enhancement of ucb-35440-3, a highly dosed poorly water-soluble weak base. Eur j Pharm Biopharm, 64:360-368. (Pubitemid 44585201)
-
(2006)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.64
, Issue.3
, pp. 360-368
-
-
Hecq, J.1
Deleers, M.2
Fanara, D.3
Vranckx, H.4
Boulanger, P.5
Le Lamer, S.6
Amighi, K.7
-
15
-
-
0024596954
-
The effect of particle size distribution on dissolution rate and oral absorption
-
DOI 10.1016/0378-5173(89)90069-0
-
Hintz RJ, Johnson KC. (1989). The effect of particle size distribution on dissolution rate and oral absorption. Int J Pharm, 51:9-17. (Pubitemid 19087827)
-
(1989)
International Journal of Pharmaceutics
, vol.51
, Issue.1
, pp. 9-17
-
-
Hintz, R.J.1
Johnson, K.C.2
-
16
-
-
53649089895
-
Multifunctional nanocarriers to overcome tumor drug resistance
-
Jabr-Milane LS, van Vlerken LE, Yadav S, Amiji MM. (2008). Multifunctional nanocarriers to overcome tumor drug resistance. Cancer Treat Rev, 34:592-602.
-
(2008)
Cancer Treat Rev
, vol.34
, pp. 592-602
-
-
Jabr-Milane, L.S.1
Van Vlerken, L.E.2
Yadav, S.3
Amiji, M.M.4
-
17
-
-
33750483598
-
Phase I safety, pharmacokinetic and pharmacodynamic studies of 2-methoxyestradiol alone or in combination with docetaxel in patients with locally recurrent or metastatic breast cancer
-
DOI 10.1007/s10637-006-9008-5
-
James J, Murry DJ, Treston AM, Storniolo AM, Sledge GW, Sidor C et al. (2007). Phase I safety, pharmacokinetic and pharmacodynamic studies of 2-methoxyestradiol alone or in combination with docetaxel in patients with locally recurrent or metastatic breast cancer. Invest New Drugs, 25:41-48. (Pubitemid 44657641)
-
(2007)
Investigational New Drugs
, vol.25
, Issue.1
, pp. 41-48
-
-
James, J.1
Murry, D.J.2
Treston, A.M.3
Storniolo, A.M.4
Sledge, G.W.5
Sidor, C.6
Miller, K.D.7
-
18
-
-
33846626309
-
In silico prediction of drug solubility in water-dioxane mixtures using the Jouyban-Acree model
-
DOI 10.1691/ph.2007.1.6057
-
Jouyban A. (2007). In silico prediction of drug solubility in waterdioxane mixtures using the Jouyban-Acree model. Pharmazie, 62:46-50. (Pubitemid 46173974)
-
(2007)
Pharmazie
, vol.62
, Issue.1
, pp. 46-50
-
-
Jouyban, A.1
-
19
-
-
34548049483
-
Nanosizing - Oral formulation development and biopharmaceutical evaluation
-
DOI 10.1016/j.addr.2007.05.003, PII S0169409X0700083X
-
Kesisoglou F, Panmai S, Wu Y. (2007). Nanosizing-oral formulation development and biopharmaceutical evaluation. Adv Drug Deliv Rev, 59:631-644. (Pubitemid 47285408)
-
(2007)
Advanced Drug Delivery Reviews
, vol.59
, Issue.7
, pp. 631-644
-
-
Kesisoglou, F.1
Panmai, S.2
Wu, Y.3
-
20
-
-
5344234787
-
The role of solid nanoparticle technology in the parenteral delivery of poorly water-soluble drugs
-
DOI 10.1016/j.ijpharm.2004.07.019, PII S0378517304004582
-
Kipp JE. (2004). The role of solid nanoparticle technology in the parenteral delivery of poorly water-soluble drugs. Int j Pharm, 284:109-122. (Pubitemid 39349144)
-
(2004)
International Journal of Pharmaceutics
, vol.284
, Issue.1-2
, pp. 109-122
-
-
Kipp, J.E.1
-
21
-
-
0026592483
-
Recognition of liposomes by cells: In vitro binding and endocytosis mediated by specific lipid headgroups and surface charge density
-
Kyung DL. (1992). Recognition of liposomes by cells: In vitro binding and endocytosis mediated by specific lipid headgroups and surface charge density. Biochimica et Biophys. Acta (BBA)-Biomembranes, 1103:185-197.
-
(1992)
Biochimica et Biophys. Acta (BBA)-Biomembranes
, vol.1103
, pp. 185-197
-
-
Kyung, D.L.1
-
22
-
-
0034614208
-
Microemulsion-based media as novel drug delivery systems
-
Lawrence MJ, Rees GD. (2000). Microemulsion-based media as novel drug delivery systems. Adv Drug Deliv Rev, 45:89-121.
-
(2000)
Adv Drug Deliv Rev
, vol.45
, pp. 89-121
-
-
Lawrence, M.J.1
Rees, G.D.2
-
24
-
-
0036742053
-
Poor aqueous solubility-an industry wide problem in drug discovery
-
Lipinski C A. (2002). Poor aqueous solubility-an industry wide problem in drug discovery. Am Pharm Rev, 5:82-85.
-
(2002)
Am Pharm Rev
, vol.5
, pp. 82-85
-
-
Lipinski, C.A.1
-
25
-
-
0029819323
-
Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization
-
DOI 10.1021/js950534b
-
Loftsson T, Brewster ME. (1996). Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization. j Pharm Sci, 85:1017-1025. (Pubitemid 26338912)
-
(1996)
Journal of Pharmaceutical Sciences
, vol.85
, Issue.10
, pp. 1017-1025
-
-
Loftsson, T.1
Brewster, M.E.2
-
26
-
-
68649106338
-
In vitro and in vivo antitumor activity of oridonin nanosuspension
-
Lou H, Zhang X, Gao L, Feng F, Wang J, Wei X et al. (2009). In vitro and in vivo antitumor activity of oridonin nanosuspension. Int j Pharm, 379:181-186.
-
(2009)
Int J Pharm
, vol.379
, pp. 181-186
-
-
Lou, H.1
Zhang, X.2
Gao, L.3
Feng, F.4
Wang, J.5
Wei, X.6
-
27
-
-
84863278598
-
New techniques and new dosage forms of drugs, 2nd ed
-
Lu B. (2005). New techniques and new dosage forms of drugs, 2nd ed., Bei Jing People's Medical Publishing House, 158-167
-
(2005)
Bei Jing: People's Medical Publishing House
, pp. 158-167
-
-
Lu, B.1
-
28
-
-
59649129751
-
In vivo investigation of tolerance and antitumor activity of cisplatin-loaded PLGA-mPEG nanoparticles
-
Mattheolabakis G, Taoufik E, Haralambous S, Roberts ML, Avgoustakis K. (2009). In vivo investigation of tolerance and antitumor activity of cisplatin-loaded PLGA-mPEG nanoparticles. Eur j Pharm Biopharm, 71:190-195.
-
(2009)
Eur J Pharm Biopharm
, vol.71
, pp. 190-195
-
-
Mattheolabakis, G.1
Taoufik, E.2
Haralambous, S.3
Roberts, M.L.4
Avgoustakis, K.5
-
30
-
-
0034996764
-
Long-circulating and target-specific nanoparticles: Theory to practice
-
Moghimi SM, Hunter AC, Murray JC. (2001). Long-circulating and target-specific nanoparticles: theory to practice. Pharmacol Rev, 53:283-318. (Pubitemid 32476118)
-
(2001)
Pharmacological Reviews
, vol.53
, Issue.2
, pp. 283-318
-
-
Moghimi, S.M.1
Hunter, A.C.2
Murray, J.C.3
-
31
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
-
Mosmann T. (1983). Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. j Immunol Methods, 65:55-63. (Pubitemid 14203433)
-
(1983)
Journal of Immunological Methods
, vol.65
, Issue.1-2
, pp. 55-63
-
-
Mosmann, T.1
-
33
-
-
0035937599
-
Nanosuspensions as particulate drug formulations in therapy: Rationale for development and what we can expect for the future
-
DOI 10.1016/S0169-409X(00)00118-6, PII S0169409X00001186
-
Müller RH, Jacobs C, Kayser O. (2001). Nanosuspensions as particulate drug formulations in therapy. Rationale for development and what we can expect for the future. Adv Drug Deliv Rev, 47:3-19. (Pubitemid 32209229)
-
(2001)
Advanced Drug Delivery Reviews
, vol.47
, Issue.1
, pp. 3-19
-
-
Muller, R.H.1
Jacobs, C.2
Kayser, O.3
-
34
-
-
4544275025
-
Challenges and solutions for the delivery of biotech drugs - A review of drug nanocrystal technology and lipid nanoparticles
-
DOI 10.1016/j.jbiotec.2004.06.007, PII S0168165604003128
-
Muller RH, Keck CM. (2004). Challenges and solutions for the delivery of biotech drugs-a review of drug nanocrystal technology and lipid nanoparticles. j Biotechnol, 113:151-170. (Pubitemid 39237077)
-
(2004)
Journal of Biotechnology
, vol.113
, Issue.1-3
, pp. 151-170
-
-
Muller, R.H.1
Keck, C.M.2
-
36
-
-
0029164807
-
Nanosuspensions for the i.v. administration of poorly soluble drugs-stability during sterilization and long-term storage
-
Washington DC
-
Müller RH, Peters K, Becker R, Kruss B. (1995). Nanosuspensions for the i.v. administration of poorly soluble drugs-stability during sterilization and long-term storage. 22nd International Symposium of Controlled Release of Bioactive Materials, Washington DC, 574-575.
-
(1995)
22nd International Symposium of Controlled Release of Bioactive Materials
, pp. 574-575
-
-
Müller, R.H.1
Peters, K.2
Becker, R.3
Kruss, B.4
-
37
-
-
0342897023
-
Nanosuspensions for the formulation of poorly soluble drugs. I. Preparation by a size-reduction technique
-
DOI 10.1016/S0378-5173(97)00311-6, PII S0378517397003116
-
Müller RH, Peters K. (1998). Nanosuspensions for the formulation of poorly soluble drugs: preparation by a size reduced technique. Int J Pharm, 160:229-237. (Pubitemid 28083096)
-
(1998)
International Journal of Pharmaceutics
, vol.160
, Issue.2
, pp. 229-237
-
-
Muller, R.H.1
Peters, K.2
-
38
-
-
0034614209
-
Places of emulsions in drug delivery
-
Nakano M. (2000). Places of emulsions in drug delivery. Adv Drug Deliv Rev, 45:1-4.
-
(2000)
Adv Drug Deliv Rev
, vol.45
, pp. 1-4
-
-
Nakano, M.1
-
39
-
-
0033015283
-
Novel injectable formulations of insoluble drugs
-
Pace SN, Pace GW, Parikh I, Mishra AK. (1999). Novel injectable formulations of insoluble drugs. Pharm Technol, 23:116-134. (Pubitemid 29135950)
-
(1999)
Pharmaceutical Technology
, vol.23
, Issue.3
, pp. 116-134
-
-
Pace, S.N.1
Pace, G.W.2
Parikh, I.3
Mishra, A.K.4
-
41
-
-
0033965872
-
Preparation of a clofazimine nanosuspension for intravenous use and evaluation of its therapeutic efficacy in murine Mycobacterium avium infection
-
Peters K, Leitzke S, Diederichs JE, Borner K, Hahn H, Müller RH et al. (2000). Preparation of a clofazimine nanosuspension for intravenous use and evaluation of its therapeutic efficacy in murine Mycobacterium avium infection. j Antimicrob Chemother, 45:77-83. (Pubitemid 30060237)
-
(2000)
Journal of Antimicrobial Chemotherapy
, vol.45
, Issue.1
, pp. 77-83
-
-
Peters, K.1
Leitzke, S.2
Diederichs, J.E.3
Borner, K.4
Hahn, H.5
Muller, R.H.6
Ehlers, S.7
-
42
-
-
4544383493
-
Nanosuspensions in drug delivery
-
DOI 10.1038/nrd1494
-
Rabinow BE. (2004). Nanosuspensions in drug delivery. Nat Rev Drug Discov, 3:785-796. (Pubitemid 39242830)
-
(2004)
Nature Reviews Drug Discovery
, vol.3
, Issue.9
, pp. 785-796
-
-
Rabinow, B.E.1
-
43
-
-
0010259723
-
NanopureTM pure drug nanoparticles for the formulation of porly soluble drugs
-
Radtke M. (2001). NanopureTM pure drug nanoparticles for the formulation of porly soluble drugs. New Drugs, 3:62-68.
-
(2001)
New Drugs
, vol.3
, pp. 62-68
-
-
Radtke, M.1
-
44
-
-
33751253462
-
Nanoparticles as potential oral delivery systems of proteins and vaccines: A mechanistic approach
-
DOI 10.1016/j.jconrel.2006.08.013, PII S0168365906004020
-
Rieux A, des Fievez V, Garinot M, Schneider YJ, Préat V. (2006). Nanoparticles as potential oral delivery systems of proteins and vaccines: amechanistic approach. J Control Release, 116:1-27. (Pubitemid 44792295)
-
(2006)
Journal of Controlled Release
, vol.116
, Issue.1
, pp. 1-27
-
-
Des Rieux, A.1
Fievez, V.2
Garinot, M.3
Schneider, Y.-J.4
Preat, V.5
-
45
-
-
38349094723
-
Effect of surface charge and density of distearylphosphatidylethanolamine-mPEG-2000 (DSPE-mPEG-2000) on the cytotoxicity of liposome-entrapped ricin: Effect of lysosomotropic agents
-
Shailendra SR, Prahlad CG. (2008). Effect of surface charge and density of distearylphosphatidylethanolamine-mPEG-2000 (DSPE-mPEG-2000) on the cytotoxicity of liposome-entrapped ricin: Effect of lysosomotropic agents. Int J Pharm, 350:79-94.
-
(2008)
Int J Pharm
, vol.350
, pp. 79-94
-
-
Shailendra, S.R.1
Prahlad, C.G.2
-
46
-
-
34447536520
-
When poor solubility becomes an issue: From early stage to proof of concept
-
DOI 10.1016/j.ejps.2007.05.110, PII S0928098707002345
-
Stegemann S, Leveiller F, Franchi D, de Jong H, Lindén H. (2007). When poor solubility becomes an issue: from early stage to proof of concept. Eur j Pharm Sci, 31:249-261. (Pubitemid 47079001)
-
(2007)
European Journal of Pharmaceutical Sciences
, vol.31
, Issue.5
, pp. 249-261
-
-
Stegemann, S.1
Leveiller, F.2
Franchi, D.3
De Jong, H.4
Linden, H.5
-
47
-
-
8244248457
-
Cyclodextrins: Their future in drug formulation and delivery
-
DOI 10.1023/A:1012136608249
-
Stella VJ, Rajewski RA. (1997). Cyclodextrins: their future in drug formulation and delivery. Pharm Res, 14:556-567. (Pubitemid 27220271)
-
(1997)
Pharmaceutical Research
, vol.14
, Issue.5
, pp. 556-567
-
-
Stella, V.J.1
Rajewski, R.A.2
-
48
-
-
25444531236
-
Solubility of crystalline nonelectrolyte solutes in organic solvents: Mathematical correlation of 4-chloro-3-nitrobenzoic acid and 2-chloro-5-nitrobenzoic acid solubilities with the Abraham solvation parameter model
-
DOI 10.1080/00319100500111293
-
Stovall DM, Givens C, Keown S, Hoover KR, Barnes R, Harris C, Lozano J, Nguyen M, Rodriguez E, Acree JWE, Abraham MH. (2005). Solubility of crystalline nonelectrolyte solutes in organic solvents: mathematical correlation of 4-chloro-3-nitrobenzoic acid and 2-chloro-5-nitrobenzoic acid solubilities with the abraham solvation parameter model. Phys Chem Liq, 43:351-360. (Pubitemid 41372317)
-
(2005)
Physics and Chemistry of Liquids
, vol.43
, Issue.4
, pp. 351-360
-
-
Stovall, D.M.1
Givens, C.2
Keown, S.3
Hoover, K.R.4
Barnes, R.5
Harris, C.6
Lozano, J.7
Nguyen, M.8
Rodriguez, E.9
Acree Jr., W.E.10
Abraham, M.H.11
-
49
-
-
79958811057
-
Nanonization of itraconazole by high pressure homogenization: Stabilizer optimization and effect of particle size on oral absorption
-
Sun W, Mao S, Shi Y, Li LC, Fang L. (2011). Nanonization of itraconazole by high pressure homogenization: stabilizer optimization and effect of particle size on oral absorption. j Pharm Sci, 100:3365-3373.
-
(2011)
J Pharm Sci
, vol.100
, pp. 3365-3373
-
-
Sun, W.1
Mao, S.2
Shi, Y.3
Li, L.C.4
Fang, L.5
-
50
-
-
52149103782
-
Current therapies and technological advances in aqueous aerosol drug delivery
-
Watts AB, McConville JT, Williams RO. (2008). Current therapies and technological advances in aqueous aerosol drug delivery. Drug Dev Ind Pharm, 34:913-922.
-
(2008)
Drug Dev Ind Pharm
, vol.34
, pp. 913-922
-
-
Watts, A.B.1
McConville, J.T.2
Williams, R.O.3
-
51
-
-
77749295726
-
Folate-mediated solid-liquid lipid nanoparticles for paclitaxel-coated poly(ethylene glycol)
-
Wu L, Tang C, Yin C. (2010). Folate-mediated solid-liquid lipid nanoparticles for paclitaxel-coated poly(ethylene glycol). Drug Dev Ind Pharm, 36:439-448.
-
(2010)
Drug Dev Ind Pharm
, vol.36
, pp. 439-448
-
-
Wu, L.1
Tang, C.2
Yin, C.3
-
52
-
-
77950858414
-
Effect of molecular weight on the oleoyl-chitosan nanoparticles as carriers for doxorubicin
-
Zhang J, Chen XG, Sun GZ, Huang L, Cheng XJ. (2010). Effect of molecular weight on the oleoyl-chitosan nanoparticles as carriers for doxorubicin. Colloids Surf b Biointerfaces, 77: 125-130.
-
(2010)
Colloids Surf B Biointerfaces
, vol.77
, pp. 125-130
-
-
Zhang, J.1
Chen, X.G.2
Sun, G.Z.3
Huang, L.4
Cheng, X.J.5
-
53
-
-
77956280563
-
2-Methoxyestradiol blocks cell-cycle progression at the G2/M phase and induces apoptosis in human acute T lymphoblastic leukemia CEM cells
-
Zhang X, Huang H, Xu Z, Zhan R. (2010). 2-Methoxyestradiol blocks cell-cycle progression at the G2/M phase and induces apoptosis in human acute T lymphoblastic leukemia CEM cells. Acta Biochim Biophys Sin (Shanghai), 42:615-622.
-
(2010)
Acta Biochim Biophys Sin (Shanghai
, vol.42
, pp. 615-622
-
-
Zhang, X.1
Huang, H.2
Xu, Z.3
Zhan, R.4
|