-
1
-
-
0042168674
-
The application of the convective diffusion model and the film equilibrium model to surfactant-facilitated dissolution of gliclazide
-
Allaboun H, Alkhamis KA, AlMomani WY. (2003). The application of the convective diffusion model and the film equilibrium model to surfactant-facilitated dissolution of gliclazide. Eur J Pharm Sci 19:231-6.
-
(2003)
Eur J Pharm Sci
, vol.19
, pp. 231-236
-
-
Allaboun, H.1
Alkhamis, K.A.2
AlMomani, W.Y.3
-
2
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon GL, Lennernäs H, Shah VP, Crison JR. (1995). A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 12:413-20.
-
(1995)
Pharm Res
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernäs, H.2
Shah, V.P.3
Crison, J.R.4
-
3
-
-
33746444733
-
Implication of inclusion complexation of glimepiride in cyclodextrin-polymer systems on its dissolution, stability and therapeutic efficacy
-
Ammar HO, Salama HA, Ghorab M, Mahmouda AA. (2006). Implication of inclusion complexation of glimepiride in cyclodextrin-polymer systems on its dissolution, stability and therapeutic efficacy. Int J Pharm 320:53-7.
-
(2006)
Int J Pharm
, vol.320
, pp. 53-57
-
-
Ammar, H.O.1
Salama, H.A.2
Ghorab, M.3
Mahmouda, A.A.4
-
4
-
-
54949135704
-
Inclusion complexes of tadalafil with natural and chemically modified beta-cyclodextrins. I: Preparation and in-vitro evaluation
-
Badr-Eldin SM, Elkheshen SA, Ghorab MM. (2008). Inclusion complexes of tadalafil with natural and chemically modified beta-cyclodextrins. I: preparation and in-vitro evaluation. Eur J Pharm Biopharm 70:819-27.
-
(2008)
Eur J Pharm Biopharm
, vol.70
, pp. 819-827
-
-
Badr-Eldin, S.M.1
Elkheshen, S.A.2
Ghorab, M.M.3
-
5
-
-
3843128718
-
Surfactant-mediated dissolution: Contributions of solubility enhancement and relatively low micelle diffusivity
-
Balakrishnan A, Rege BD, Amidon GL, Polli JE. (2004). Surfactant-mediated dissolution: contributions of solubility enhancement and relatively low micelle diffusivity. J Pharm Sci 93:2064-75.
-
(2004)
J Pharm Sci
, vol.93
, pp. 2064-2075
-
-
Balakrishnan, A.1
Rege, B.D.2
Amidon, G.L.3
Polli, J.E.4
-
6
-
-
67449116319
-
Enhanced oral bioavailability of dexibuprofen by a novel solid Self-emulsifying drug delivery system (SEDDS)
-
Balakrishnan P, Lee BJ, Oh DH, et al. (2009). Enhanced oral bioavailability of dexibuprofen by a novel solid Self-emulsifying drug delivery system (SEDDS). Eur J Pharm Biopharm 72:539-45.
-
(2009)
Eur J Pharm Biopharm
, vol.72
, pp. 539-545
-
-
Balakrishnan, P.1
Lee, B.J.2
Oh, D.H.3
-
7
-
-
0035153857
-
Piroxicam concentrations in plasma and synovial fluid after a single dose of piroxicambeta-cyclodextrin
-
Bannwart B, Bertin P, Péhourcq F, et al. (2001). Piroxicam concentrations in plasma and synovial fluid after a single dose of piroxicambeta-cyclodextrin. Int J Clin Pharmacol Ther 39:33-6.
-
(2001)
Int J Clin Pharmacol Ther
, vol.39
, pp. 33-36
-
-
Bannwart, B.1
Bertin, P.2
Péhourcq, F.3
-
8
-
-
77949828159
-
Characterization of niosomes prepared with various nonionic surfactants for paclitaxel oral delivery
-
Bayindir ZS, Yuksel N. (2010). Characterization of niosomes prepared with various nonionic surfactants for paclitaxel oral delivery. J Pharm Sci 99:2049-60.
-
(2010)
J Pharm Sci
, vol.99
, pp. 2049-2060
-
-
Bayindir, Z.S.1
Yuksel, N.2
-
9
-
-
80054052328
-
Bioavailability enhancement strategies: Basics, formulation approaches and regulatory considerations
-
Beg S, Swain S, Rizwan Md, et al. (2011). Bioavailability enhancement strategies: basics, formulation approaches and regulatory considerations. Curr Drug Deliv 8:1-12.
-
(2011)
Curr Drug Deliv
, vol.8
, pp. 1-12
-
-
Beg, S.1
Swain, S.2
Rizwan, Md.3
-
10
-
-
77956217284
-
Alternative oral exemestane formulation: Improved dissolution and permeation
-
Burcin Y, Erem B, Imran V, Murat S. (2010). Alternative oral exemestane formulation: improved dissolution and permeation. Int J Pharm 398:137-45.
-
(2010)
Int J Pharm
, vol.398
, pp. 137-145
-
-
Burcin, Y.1
Erem, B.2
Imran, V.3
Murat, S.4
-
11
-
-
35248822616
-
The utility of cyclodextrins for enhancing oral bioavailability
-
Carrier RL, Miller LA, Ahmed I. (2007). The utility of cyclodextrins for enhancing oral bioavailability. J Control Release 123:78-99.
-
(2007)
J Control Release
, vol.123
, pp. 78-99
-
-
Carrier, R.L.1
Miller, L.A.2
Ahmed, I.3
-
12
-
-
84860992016
-
Pharmaceutical cocrystals: A novel approach for oral bioavailability enhancement of drugs
-
Chadha R, Saini A, Arora P, Bhandari S. (2012). Pharmaceutical cocrystals: a novel approach for oral bioavailability enhancement of drugs. Crit Rev Ther Drug Carrier Syst 29:183-218.
-
(2012)
Crit Rev Ther Drug Carrier Syst
, vol.29
, pp. 183-218
-
-
Chadha, R.1
Saini, A.2
Arora, P.3
Bhandari, S.4
-
13
-
-
67349092918
-
Assessment of solubilization characteristics of different surfactants for carvedilol phosphate as a function of pH
-
Chakraborty S, Shukla D, Jain A, et al. (2009). Assessment of solubilization characteristics of different surfactants for carvedilol phosphate as a function of pH. J Colloid Interface Sci 335:242-449.
-
(2009)
J Colloid Interface Sci
, vol.335
, pp. 242-449
-
-
Chakraborty, S.1
Shukla, D.2
Jain, A.3
-
14
-
-
33845576641
-
Design and evaluation of self-nanoemulsifying drug delivery systems (SNEDDS) for cefpodoxime proxetil
-
Date AA, Nagarsenker MS. (2007). Design and evaluation of self-nanoemulsifying drug delivery systems (SNEDDS) for cefpodoxime proxetil. Int J Pharm 329:166-72.
-
(2007)
Int J Pharm
, vol.329
, pp. 166-172
-
-
Date, A.A.1
Nagarsenker, M.S.2
-
15
-
-
74849101522
-
Modeling the influence of cyclodextrins on oral absorption of low solubility drugs: II. Experimental validation
-
Gamsiz ED, Miller L, Thombre AG, et al. (2010a). Modeling the influence of cyclodextrins on oral absorption of low solubility drugs: II. Experimental validation. Biotechnol Bioeng 105:421-30.
-
(2010)
Biotechnol Bioeng
, vol.105
, pp. 421-430
-
-
Gamsiz, E.D.1
Miller, L.2
Thombre, A.G.3
-
16
-
-
74849087408
-
Modeling the influence of cyclodextrins on oral absorption of low-solubility drugs: I. Model development
-
Gamsiz ED, Miller L, Thombre AG, et al. (2010b). Modeling the influence of cyclodextrins on oral absorption of low-solubility drugs: I. Model development. Biotechnol Bioeng 105:409-20.
-
(2010)
Biotechnol Bioeng
, vol.105
, pp. 409-420
-
-
Gamsiz, E.D.1
Miller, L.2
Thombre, A.G.3
-
17
-
-
78650900635
-
Drug salts and solubilization: Modeling the influence of cyclodextrins on oral absorption
-
Gamsiz ED, Thombre AG, Ahmed I, Carrier RL. (2011). Drug salts and solubilization: modeling the influence of cyclodextrins on oral absorption. Ann Biomed Eng 39:455-68.
-
(2011)
Ann Biomed Eng
, vol.39
, pp. 455-468
-
-
Gamsiz, E.D.1
Thombre, A.G.2
Ahmed, I.3
Carrier, R.L.4
-
18
-
-
77953342459
-
Preparation and in vitro evaluation of bilayer and floating bioadhesive tablets of rosiglitazone maleate
-
Girish SS, Devendra KJ, Dhananjay MM. (2007). Preparation and in vitro evaluation of bilayer and floating bioadhesive tablets of rosiglitazone maleate. Asian J Pharm Sci 2:161-9.
-
(2007)
Asian J Pharm Sci
, vol.2
, pp. 161-169
-
-
Girish, S.S.1
Devendra, K.J.2
Dhananjay, M.M.3
-
19
-
-
0028941436
-
Polymorphism in binary mixtures, as exemplified by nimodipine
-
Grunenberg A, Keil B, Henck JO. (1995). Polymorphism in binary mixtures, as exemplified by nimodipine. Int J Pharm 118:11-21.
-
(1995)
Int J Pharm
, vol.118
, pp. 11-21
-
-
Grunenberg, A.1
Keil, B.2
Henck, J.O.3
-
20
-
-
24944474831
-
Calcium silicate based microspheres of repaglinide for gastro retentive floating drug delivery: Preparation and in vitro characterization
-
Jain SK, Awasthi AM, Jain NK, Agrawal GP. (2005). Calcium silicate based microspheres of repaglinide for gastro retentive floating drug delivery: preparation and in vitro characterization. J Control Release 107:300-9.
-
(2005)
J Control Release
, vol.107
, pp. 300-309
-
-
Jain, S.K.1
Awasthi, A.M.2
Jain, N.K.3
Agrawal, G.P.4
-
21
-
-
84873049232
-
Development of a novel niosomal system for oral delivery of Ginkgo biloba extract
-
Jin Y, Wen J, Garg S, et al. (2013). Development of a novel niosomal system for oral delivery of Ginkgo biloba extract. Int J Nanomed 8: 421-30.
-
(2013)
Int J Nanomed
, vol.8
, pp. 421-430
-
-
Jin, Y.1
Wen, J.2
Garg, S.3
-
22
-
-
36248956708
-
Caffeine-loaded niosomes: Characterization and in vitro release studies
-
Khazaeli P, Pardakhty A, Shoorabi H. (2007). Caffeine-loaded niosomes: characterization and in vitro release studies. Drug Deliv 14:447-52.
-
(2007)
Drug Deliv
, vol.14
, pp. 447-452
-
-
Khazaeli, P.1
Pardakhty, A.2
Shoorabi, H.3
-
23
-
-
82855175094
-
Self-nanoemulsifying drug delivery system for Adefovir dipivoxil: Design, characterization, in vitro and ex vivo evaluation
-
Krutika K. Sawant, Shweta Guptha, Sandip Chavhan. (2011). Self-nanoemulsifying drug delivery system for Adefovir dipivoxil: design, characterization, in vitro and ex vivo evaluation. Colloids Surf A 392: 145-55.
-
(2011)
Colloids Surf A
, vol.392
, pp. 145-155
-
-
Sawant, K.K.1
Guptha, S.2
Chavhan, S.3
-
24
-
-
84872459102
-
Preparation and cyclodextrin assisted dissolution rate enhancement of itraconazolium dinitrate salt
-
Kumar N, Shishu, Bansal G, et al. (2013). Preparation and cyclodextrin assisted dissolution rate enhancement of itraconazolium dinitrate salt. Drug Dev Ind Pharm 39:342-51.
-
(2013)
Drug Dev Ind Pharm
, vol.39
, pp. 342-351
-
-
Kumar, N.1
Shishu2
Bansal, G.3
-
26
-
-
18044381309
-
Investigation of solubility and dissolution of a free base and two different salt forms as a function of pH
-
Li S, Wong S, Sethia S, et al. (2005). Investigation of solubility and dissolution of a free base and two different salt forms as a function of pH. Pharm Res:628-35.
-
(2005)
Pharm Res
, pp. 628-635
-
-
Li, S.1
Wong, S.2
Sethia, S.3
-
27
-
-
0343527392
-
Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards
-
Lobenberg R, Amidon GL. (2000). Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards. Eur J Pharm Biopharm 50:3-12.
-
(2000)
Eur J Pharm Biopharm
, vol.50
, pp. 3-12
-
-
Lobenberg, R.1
Amidon, G.L.2
-
28
-
-
84879104409
-
Improving oral bioavailability and pharmacokinetics of liposomal metformin by glycerolphosphate-chitosan microcomplexation
-
Manconi M, Nácher A, Merino V, et al. (2013). Improving oral bioavailability and pharmacokinetics of liposomal metformin by glycerolphosphate-chitosan microcomplexation. AAPS Pharm Sci Tech 14:485-96.
-
(2013)
AAPS Pharm Sci Tech
, vol.14
, pp. 485-496
-
-
Manconi, M.1
Nácher, A.2
Merino, V.3
-
29
-
-
0033855277
-
Improvement of solubility and oral bioavailability of rutin by complexation with 2-hydroxypropyl-beta-cyclodextrin
-
Miyake K, Arima H, Hirayama F, et al. (2000). Improvement of solubility and oral bioavailability of rutin by complexation with 2-hydroxypropyl-beta-cyclodextrin. Pharm Dev Technol 5: 399-407.
-
(2000)
Pharm Dev Technol
, vol.5
, pp. 399-407
-
-
Miyake, K.1
Arima, H.2
Hirayama, F.3
-
30
-
-
0036212425
-
Preparation and characterization of coenzyme QlO-Eudragit solid dispersion
-
Nazzal S, Guven N, Reddy IK, Khan MA. (2002a). Preparation and characterization of coenzyme QlO-Eudragit solid dispersion. Drug Dev Ind Pharm 28:49-57.
-
(2002)
Drug Dev Ind Pharm
, vol.28
, pp. 49-57
-
-
Nazzal, S.1
Guven, N.2
Reddy, I.K.3
Khan, M.A.4
-
31
-
-
0037139412
-
Preparation and in vitro characterization of a eutectic based semisolid self nanoemulsified drug delivery system (SNEDDS) of ubiquinone: Mechanism and progress of emulsion formation
-
Nazzal S, Smalyukh II, Lavrentovich OD, Khan MA. (2002b). Preparation and in vitro characterization of a eutectic based semisolid self nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation. Int J Pharm 235: 247-65.
-
(2002)
Int J Pharm
, vol.235
, pp. 247-265
-
-
Nazzal, S.1
Smalyukh, I.I.2
Lavrentovich, O.D.3
Khan, M.A.4
-
32
-
-
80054703087
-
Comparison of solid self-microemulsifying drug delivery system (solid SMEDDS) prepared with hydrophilic and hydrophobic solid carrier
-
Oh DH, Kang JH, Kim DW, et al. (2011). Comparison of solid self-microemulsifying drug delivery system (solid SMEDDS) prepared with hydrophilic and hydrophobic solid carrier. Int J Pharm 420: 412-8.
-
(2011)
Int J Pharm
, vol.420
, pp. 412-418
-
-
Oh, D.H.1
Kang, J.H.2
Kim, D.W.3
-
34
-
-
0033805858
-
Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems
-
Pouton CW. (2000). Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and 'self-microemulsifying' drug delivery systems. Eur J Pharm Sci 11:S93-8.
-
(2000)
Eur J Pharm Sci
, vol.11
, pp. S93-S98
-
-
Pouton, C.W.1
-
35
-
-
33751014029
-
Formulation of poorly water-soluble drugs for oral administration: Physicochemical and physiological issues and the lipid formulation classification system
-
Pouton CW. (2006). Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system. Eur J Pharm Sci 29: 278-87.
-
(2006)
Eur J Pharm Sci
, vol.29
, pp. 278-287
-
-
Pouton, C.W.1
-
36
-
-
80053574884
-
Pharmaceutical cocrystals: An overview
-
Qiao N, Li M, Schlindwein W, et al. (2011). Pharmaceutical cocrystals: an overview. Int J Pharm 419:1-11.
-
(2011)
Int J Pharm
, vol.419
, pp. 1-11
-
-
Qiao, N.1
Li, M.2
Schlindwein, W.3
-
37
-
-
85010080689
-
Pharmacokinetic and pharmacodynamic interaction of curcumin with glimepiride in normal and diabetic rats
-
Sandya RT, Sujatha S, Veeresham C. (2012). Pharmacokinetic and pharmacodynamic interaction of curcumin with glimepiride in normal and diabetic rats. Phcog Commn 2:14-21.
-
(2012)
Phcog Commn
, vol.2
, pp. 14-21
-
-
Sandya, R.T.1
Sujatha, S.2
Veeresham, C.3
-
38
-
-
34548032742
-
Salt formation to improve drug solubility
-
Serajuddin AT. (2007). Salt formation to improve drug solubility. Adv Drug Deliv Rev 59:603-16.
-
(2007)
Adv Drug Deliv Rev
, vol.59
, pp. 603-616
-
-
Serajuddin, A.T.1
-
39
-
-
0032885450
-
Solid dispersion of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs
-
Serajuddin TM. (1999). Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. J Pharm Sci 88:1058-66.
-
(1999)
J Pharm Sci
, vol.88
, pp. 1058-1066
-
-
Serajuddin, T.M.1
-
40
-
-
78049295075
-
Development and evaluation of self-microemulsifying liquid and pellet formulations of curcumin, and absorption studies in rats
-
Setthacheewakul S, Mahattanadul S, Phadoongsombut N, et al. (2010). Development and evaluation of self-microemulsifying liquid and pellet formulations of curcumin, and absorption studies in rats. Eur J Pharm Biopharm 76:475-85.
-
(2010)
Eur J Pharm Biopharm
, vol.76
, pp. 475-485
-
-
Setthacheewakul, S.1
Mahattanadul, S.2
Phadoongsombut, N.3
-
41
-
-
84886730364
-
Niosomes encapsulating paclitaxel for oral bioavailability enhancement: Preparation, characterization, pharmacokinetics and biodistribution
-
Epub ahead of print
-
Sezgin-Bayindir Z, Onay-Besikci A, Vural N, Yuksel N. (2013). Niosomes encapsulating paclitaxel for oral bioavailability enhancement: preparation, characterization, pharmacokinetics and biodistribution. J Microencapsul, [Epub ahead of print]. Pages 1-9.
-
(2013)
J Microencapsul
, pp. 1-9
-
-
Sezgin-Bayindir, Z.1
Onay-Besikci, A.2
Vural, N.3
Yuksel, N.4
-
42
-
-
43049170351
-
The role of cocrystals in pharmaceutical science
-
Shan N, Zaworotko MJ. (2008). The role of cocrystals in pharmaceutical science. Drug Discov Today 13:440-6.
-
(2008)
Drug Discov Today
, vol.13
, pp. 440-446
-
-
Shan, N.1
Zaworotko, M.J.2
-
43
-
-
80054981531
-
Solid self-nanoemulsifying drug delivery system (S-SNEDDS) containing phosphatidylcholine for enhanced bioavailability of highly lipophilic bioactive carotenoid lutein
-
Shanmugam S, Baskaran R, Balakrishnan P, et al. (2011). Solid self-nanoemulsifying drug delivery system (S-SNEDDS) containing phosphatidylcholine for enhanced bioavailability of highly lipophilic bioactive carotenoid lutein. Eur J Pharm Biopharm 79:250-7.
-
(2011)
Eur J Pharm Biopharm
, vol.79
, pp. 250-257
-
-
Shanmugam, S.1
Baskaran, R.2
Balakrishnan, P.3
-
44
-
-
82855175094
-
Self-nanoemulsifying drug delivery system for adefovir dipivoxil: Design, characterization, in vitro and ex vivo evaluation
-
Shweta G, Sandip C, Krutika KS. (2011). Self-nanoemulsifying drug delivery system for adefovir dipivoxil: design, characterization, in vitro and ex vivo evaluation. Colloid Surf A 392:145-55.
-
(2011)
Colloid Surf A
, vol.392
, pp. 145-155
-
-
Shweta, G.1
Sandip, C.2
Krutika, K.S.3
-
45
-
-
84866556997
-
Design and evaluation of hydrochlorthiazide gastroretentive floating drug delivery system
-
Srinivas M, Krishna S, Prabhakar RV. (2011). Design and evaluation of hydrochlorthiazide gastroretentive floating drug delivery system. Asian J Pharm Sci 6:208-17.
-
(2011)
Asian J Pharm Sci
, vol.6
, pp. 208-217
-
-
Srinivas, M.1
Krishna, S.2
Prabhakar, R.V.3
-
46
-
-
0024565173
-
Enhanced intestinal absorption of cyclosporine in rats through the reduction of emulsion droplet size
-
Tarr BD, Yalkowsky SH. (1989). Enhanced intestinal absorption of cyclosporine in rats through the reduction of emulsion droplet size. Pharm Res 6:40-3.
-
(1989)
Pharm Res
, vol.6
, pp. 40-43
-
-
Tarr, B.D.1
Yalkowsky, S.H.2
-
47
-
-
0034691643
-
Oral bioavailability and hypoglycaemic activity of tolbutamide/cyclodextrin inclusion complexes
-
Veiga F, Fernandes C, Teixeira F. (2000). Oral bioavailability and hypoglycaemic activity of tolbutamide/cyclodextrin inclusion complexes. Int J Pharm 202:165-71.
-
(2000)
Int J Pharm
, vol.202
, pp. 165-171
-
-
Veiga, F.1
Fernandes, C.2
Teixeira, F.3
-
49
-
-
0033752949
-
Comparative population pharmacokinetic-pharmacodynamic analysis for piroxicam-beta-cyclodextrin and piroxicam
-
Wang D, Miller R, Zheng J, Hu C. (2000). Comparative population pharmacokinetic-pharmacodynamic analysis for piroxicam-beta-cyclodextrin and piroxicam. J Clin Pharmacol 40:1257-66.
-
(2000)
J Clin Pharmacol
, vol.40
, pp. 1257-1266
-
-
Wang, D.1
Miller, R.2
Zheng, J.3
Hu, C.4
-
50
-
-
57449109685
-
Design and optimization of a new self-nanoemulsifying drug delivery system
-
Wang L, Dong J, Chen J, et al. (2009). Design and optimization of a new self-nanoemulsifying drug delivery system. J Colloid Interface Sci 330:443-8.
-
(2009)
J Colloid Interface Sci
, vol.330
, pp. 443-448
-
-
Wang, L.1
Dong, J.2
Chen, J.3
-
51
-
-
84887876064
-
Effect of liposomes on the absorption of water-soluble active pharmaceutical ingredients via oral administration
-
Yang Z, Lu A, Wong BC, et al. (2013). Effect of liposomes on the absorption of water-soluble active pharmaceutical ingredients via oral administration. Curr Pharm Des 19:6647-54.
-
(2013)
Curr Pharm Des
, vol.19
, pp. 6647-6654
-
-
Yang, Z.1
Lu, A.2
Wong, B.C.3
-
52
-
-
84877302171
-
Intestinal bile secretion promotes drug absorption from lipid colloidal phases via induction of supersaturation
-
Yeap YY, Trevaskis NL, Quach T, et al. (2013). Intestinal bile secretion promotes drug absorption from lipid colloidal phases via induction of supersaturation. Mol Pharm 10:1874-89.
-
(2013)
Mol Pharm
, vol.10
, pp. 1874-1889
-
-
Yeap, Y.Y.1
Trevaskis, N.L.2
Quach, T.3
|