Results 11 to 20 of about 177,103 (312)
International Journal of Nanomedicine, 2012 Kwang-Ho Cha,1,3 Kyung-Jin Cho,3 Min-Soo Kim,4 Jeong-Soo Kim,3 Hee Jun Park,1,3 Junsung Park,1,3 Wonkyung Cho,1,3 Jeong-Sook Park,3 Sung-Joo Hwang1,21Yonsei Institute of Pharmaceutical Sciences, 2College of Pharmacy, Yonsei University, Incheon, Republic ...
Cha KH +8 more
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On methods of expressing dissolution rate data
Journal of Pharmacy and Pharmacology, 1978 Abstract The value of the Weibull, logarithmic-logistic, and logarithmic-normal plots in expressing dissolution rate data is considered for the combinations of zero and first-order release with sink and non-sink conditions, and for actual dissolution rate data of diazepam from tablets in a medium of pH 2.
J A, Goldsmith, N, Randall, S D, Ross
openaire +3 more sources
Preparation and characterization of fenofibrate-loaded zeolitic imidazolate frameworks and their evaluation in dissolution enhancement of the formulation [PDF]
شیمی کاربردی روز, 2021 The purpose of this study was to develop zeolitic imidazolate frameworks (ZIFs) incorporated with poorly water-soluble drug fenofibrate (FEN), belonging to Biopharmaceutical Classification System (BCS) class II, to improve drug dissolution, intended to ...
Aziz maleki +5 more
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Foods, 2021 Casein phosphopeptide (CPP) has been widely used as micronutrient supplementation for certain populations. However, its solubility performance is far from satisfying.
Jian Zhu +5 more
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Pharmaceutics, 2019 The aims of this study were to investigate how the release of tadalafil is influenced by two grades of polyvinylpyrrolidone (Kollidon® 12 PF and Kollidon® VA 64) and various methods of preparing solid dispersions (solvent evaporation, spray ...
Tereza Školáková +5 more
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ENHANCEMENT OF DISSOLUTION AND THE ANTIINFLAMMATORY EFFECT OF NIMESULIDE, USING LIQUISOLID COMPACT FOR ORAL APPLICATION [PDF]
Bulletin of Pharmaceutical Sciences. Assiut University, 2011 Nimesulide is a poorly soluble drug, the rate of its oral absorption is often controlled bythe dissolution rate in the gastrointestinal tract. There are several techniques to enhance thedissolution of poorly soluble drugs.
H. El-Saghir, M. Hassan
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Liquisolid technique for dissolution rate enhancement of a high dose water-insoluble drug (carbamazepine) [PDF]
, 2007 Different liquisolid formulations of carbamazepine were accomplished by dissolving the drug in the non-toxic hydrophilic liquids, and adsorbing the solution onto the surface of silica.
Yousef Javadzadeh +8 more
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Intrinsic dissolution simulation of highly and poorly soluble drugs for BCS solubility classification [PDF]
, 2017 Intrinsic dissolution testing allows characterizing drug substances through its dissolution rate when exposed to a specified surface area in a specific dissolution media, This can be used to determine if a drug substance is highly or poorly soluble.
Raimar Löbenberg +13 more
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Moving and Union Dissolution [PDF]
, 2008 This paper examines the effect of migration and residential mobility on union dissolution among married and cohabiting couples. Moving is a stressful life event, and a large, multidisciplinary litera-ture has shown that family migration often benefits ...
Cooke, T. +11 more
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Pharmaceutics, 2021 The effectiveness of oral drug administration is related to the solubility of a drug in the gastrointestinal tract and its ability to penetrate the biological membranes. As most new drugs are poorly soluble in water, there is a need to develop novel drug
Adrianna Dadej +8 more
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