Selection of In Vivo Relevant Dissolution Test Parameters for the Development of Cannabidiol Formulations with Enhanced Oral Bioavailability. [PDF]
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Oral delivery of stabilized lipid nanoparticles for nucleic acid therapeutics. [PDF]
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Mucin Mimics and Impacts the Function of Polymeric Inhibitors in Stabilizing Drug Supersaturation. [PDF]
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Quality by Design-Based Formulation Development of an Oral Semaglutide Tablet. [PDF]
Yoon JH, Kim DH, Kim JE.
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Exploring the impact of various zwitterionic surface modifications on the mucus diffusion and membrane permeability of lipid-based nanocarriers. [PDF]
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Bioavailability Enhancement and Polymorphic Stabilization of One BCS Class IV Metastable Drug Through Novel Formulation Approach. [PDF]
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The Advancement of In Vitro Lipolysis: Two-Step Flow-Through Method for the Evaluation of Lipid-Based Drug Delivery Systems. [PDF]
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Sources of dissolution variability into biorelevant media
International Journal of Pharmaceutics, 2022Identifying sources of dissolution variation is often challenging. Biorelevant dissolution media are compositionally complex, can require multiple steps to fabricate, and are utilized across differing laboratories. The objective was to determine the contributions of location, operator, media fabrication method, day, and tablet to total dissolution ...
Raqeeb, Jamil, James E, Polli
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The Use of Biorelevant Dissolution Media to Forecast the In Vivo Performance of a Drug [PDF]
Simulation of gastrointestinal conditions is essential to adequately predict the in vivo behavior of drug formulations. To reduce the size and number of human studies required to identify a drug product with appropriate performance in both the fed and fasted states, it is advantageous to be able to pre-screen formulations in vitro.
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Biorelevant dissolution media are aqueous solutions or suspensions whose composition and physicochemical characteristics closely resemble human fluids found along the different portions of the gastrointestinal tract, developed to study the solubility and/or dissolution profile of orally administered drugs in a more physiologically relevant manner.
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