Results 251 to 260 of about 20,585 (286)
Dissolving microdroplet electroanalysis enables attomolar-level detection.
Nguyen JH, Rana A, Hatch SM, Dick JE.
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International Journal of Pharmaceutics, 2023
Dissolution testing is important in assessing the in vitro drug release performance for oral administration dosage forms. However, currently, a simple and efficient in vitro test to investigate critical factors that may impact the drug release and bioavailability at the development stage of a drug-loaded nanoemulsion (NE) is lacking.
Megumi Nishitani, Yukuyama +7 more
openaire +4 more sources
Dissolution testing is important in assessing the in vitro drug release performance for oral administration dosage forms. However, currently, a simple and efficient in vitro test to investigate critical factors that may impact the drug release and bioavailability at the development stage of a drug-loaded nanoemulsion (NE) is lacking.
Megumi Nishitani, Yukuyama +7 more
openaire +4 more sources
Characterization and dissolution–reprecipitation behavior of biphasic tricalcium phosphate powders
Journal of Alloys and Compounds, 2011Abstract α-tricalcium phosphate (α-TCP), biphasic α/β-tricalcium phosphate (α/β-TCP) with different two phase ratio and β-tricalcium phosphate (β-TCP) powders were prepared by calcining an amorphous calcium phosphate (ACP) precursor at a temperature ranging from 800 to 900 °C.
Chao Zou +6 more
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Dissolution of poorly water-soluble drugs in biphasic media using USP 4 and fiber optic system
Clinical Research and Regulatory Affairs, 2009A novel in-vitro dissolution system based on the principle of flow-through technique has been designed to evaluate the in-vitro release rate of poorly water-soluble compounds.
Saroj Vangani +8 more
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Journal of Drug Delivery Science and Technology, 2020
Abstract The formulation developments and the in vivo assessment of Biopharmaceutical Classification System (BCS) class II drugs are challenging due to their low solubility and high permeability in the human gastrointestinal (GI) tract. Since the pH change in the GI environment influences the drug dissolution of BCS class IIa and IIb drugs but not ...
Yasuhiro Tsume +5 more
openaire +3 more sources
Abstract The formulation developments and the in vivo assessment of Biopharmaceutical Classification System (BCS) class II drugs are challenging due to their low solubility and high permeability in the human gastrointestinal (GI) tract. Since the pH change in the GI environment influences the drug dissolution of BCS class IIa and IIb drugs but not ...
Yasuhiro Tsume +5 more
openaire +3 more sources
Journal of Controlled Release, 2017
The purpose of this study was to discriminate the release behavior from three differently formulated racecadotril (BCS II) granules and to establish an in vitro-in vivo correlation. Three granule formulations of the lipophilic drug were prepared with equivalent composition but prepared with different manufacturing processes (dry granulation, wet ...
Jia, Deng +5 more
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The purpose of this study was to discriminate the release behavior from three differently formulated racecadotril (BCS II) granules and to establish an in vitro-in vivo correlation. Three granule formulations of the lipophilic drug were prepared with equivalent composition but prepared with different manufacturing processes (dry granulation, wet ...
Jia, Deng +5 more
openaire +4 more sources
European Journal of Pharmaceutics and Biopharmaceutics, 2016
In a biphasic dissolution medium, the integration of the in vitro dissolution of a drug in an aqueous phase and its subsequent partitioning into an organic phase is hypothesized to simulate the in vivo drug absorption. Such a methodology is expected to improve the probability of achieving a successful in vitro-in vivo correlation.
Amal, Al Durdunji +2 more
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In a biphasic dissolution medium, the integration of the in vitro dissolution of a drug in an aqueous phase and its subsequent partitioning into an organic phase is hypothesized to simulate the in vivo drug absorption. Such a methodology is expected to improve the probability of achieving a successful in vitro-in vivo correlation.
Amal, Al Durdunji +2 more
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Dissolution Behavior of Submicron Biphasic Tricalcium Phosphate Powders
Key Engineering Materials, 2006Submicron α-tricalcium phosphate (α-TCP), β-tricalcium phosphate (β-TCP) and biphasic α/β-TCP powders were prepared by an amorphous calcium phosphate (ACP) precursor way. For the biphasic TCP powders, primary particle size was 300nm, α-TCP and β-TCP primary particles were homogeneously mixed in the submicron powders. When the TCP powders were soaked in
Rui Bing Wang +7 more
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Journal of Agricultural and Food Chemistry, 2023
In vitro dissolution methods correctly predicting in vivo bioavailability of compounds from complex mixtures are lacking. We therefore used data on the in vivo performance of bioavailability-improved curcumin formulations to implement an in vivo predictive dissolution method (BiPHa+).
Marvin Benedikt Brenner +4 more
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In vitro dissolution methods correctly predicting in vivo bioavailability of compounds from complex mixtures are lacking. We therefore used data on the in vivo performance of bioavailability-improved curcumin formulations to implement an in vivo predictive dissolution method (BiPHa+).
Marvin Benedikt Brenner +4 more
openaire +2 more sources

