PHYSICOCHEMICAL ASPECTS OF DRUG RELEASE .7. THE EFFECT OF SURFACTANT CONCENTRATION AND DRUG PARTICLE-SIZE ON SOLUBILITY AND DISSOLUTION RATE OF FELODIPINE, A SPARINGLY SOLUBLE DRUG

被引：35

作者：

ANDERBERG, EK ^{[1
]}

BISRAT, M ^{[1
]}

NYSTROM, C ^{[1
]}

机构：

[1] UNIV UPPSALA,DEPT PHARMACEUT,BOX 580,S-75123 UPPSALA,SWEDEN

来源：

INTERNATIONAL JOURNAL OF PHARMACEUTICS | 1988年 / 47卷 / 1-3期

关键词：

D O I：

10.1016/0378-5173(88)90216-5

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：67 / 77

页数：11

共 41 条

[11] THE RELATIONSHIP BETWEEN DRUG RELEASE RATE, PARTICLE-SIZE AND SWELLING OF SILICONE MATRICES
GOLOMB, G
FISHER, P
RAHAMIM, E
JOURNAL OF CONTROLLED RELEASE, 1990, 12 (02) : 121 - 132
[12] PHYSICOCHEMICAL ASPECTS OF DRUG RELEASE .12. THE EFFECT OF SOME CARRIER PARTICLE PROPERTIES AND LUBRICANT ADMIXTURE ON DRUG DISSOLUTION FROM TABLETED ORDERED MIXTURES
WESTERBERG, M
NYSTROM, C
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1991, 69 (02) : 129 - 141
[13] Effect of Drug Particle Size on Complexation, Physicochemical Properties and Dissolution of Cyclodextrin Inclusion Complexes
Ai, F.
Wang, J.
Li, Y.
Ma, Y.
INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2017, 79 (01) : 131 - 138
[14] INVITRO RELEASE CHARACTERISTICS OF A MEMBRANE-COATED PELLET FORMULATION - INFLUENCE OF DRUG SOLUBILITY AND PARTICLE-SIZE
RAGNARSSON, G
SANDBERG, A
JOHANSSON, MO
LINDSTEDT, B
SJOGREN, J
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1992, 79 (2-3) : 223 - 232
[15] PHYSICOCHEMICAL ASPECTS OF DRUG RELEASE .17. THE EFFECT OF DRUG SURFACE-AREA COVERAGE TO CARRIER MATERIALS ON DRUG DISSOLUTION FROM ORDERED MIXTURES
WESTERBERG, M
NYSTROM, C
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 90 (01) : 1 - 17
[16] DISSOLUTION OF SLIGHTLY SOLUBLE DRUGS .4. EFFECT OF PARTICLE-SIZE OF SULFONAMIDES ON INVITRO DISSOLUTION RATE AND INVIVO ABSORPTION RATE, AND THEIR RELATION TO SOLUBILITY
KANENIWA, N
WATARI, N
CHEMICAL & PHARMACEUTICAL BULLETIN, 1978, 26 (03) : 813 - 826
[17] Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug-polymer interactions
Karavas, Evangelos
Georgarakis, Emmanuel
Sigalas, Michael P.
Avgoustakis, Konstantinos
Bikiaris, Dimitrios
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2007, 66 (03) : 334 - 347
[18] Effect of grinding with hydroxypropyl cellulose on the dissolution and particle size of a poorly water-soluble drug
Yamada, T
Saito, N
Imai, T
Otagiri, M
CHEMICAL & PHARMACEUTICAL BULLETIN, 1999, 47 (09) : 1311 - 1313
[19] PHYSICOCHEMICAL ASPECTS OF DRUG RELEASE .13. THE EFFECT OF SODIUM DODECYL-SULFATE ADDITIONS ON THE STRUCTURE AND DISSOLUTION OF A DRUG IN SOLID DISPERSIONS
SJOKVIST, E
NYSTROM, C
ALDEN, M
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1991, 69 (01) : 53 - 62
[20] DISSOLUTION BEHAVIOR OF SOLID DRUGS .8. DETERMINATION OF PARTICLE-SIZE AND ITS DISTRIBUTION OF DRUG POWDER BY DISSOLUTION RATE MEASUREMENTS
SEKIGUCHI, K
IWATSURU, M
SHIROTANI, K
CHEMICAL & PHARMACEUTICAL BULLETIN, 1978, 26 (05) : 1598 - 1603

← 1 2 3 4 5 →