Development of valsartan-loaded gelatin microcapsule without crystal change using hydroxypropylmethylcellulose as a stabilizer
Author:
Publisher
Informa UK Limited
Subject
Pharmaceutical Science,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/10717541003717031
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1. Physicochemical aspects of drug release. VII. The effect of surfactant concentration and drug particle size on solubility and dissolution rate of felodipine, a sparingly soluble drug
2. Improvement of Solubility and Stability of Valsartan by Hydroxypropyl-\boldbeta-Cyclodextrin
3. Effect of pH on Diclofenac Release from Eudragit RS100® Microparticles. A Kinetic Study by DSC
4. In situ gelling and mucoadhesive liquid suppository containing acetaminophen: enhanced bioavailability
5. Development and In Vitro Evaluation of Pantoprazole-Loaded Microspheres
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1. Current Trends in Gelatin-Based Drug Delivery Systems;Pharmaceutics;2023-05-15
2. Characterization of nimodipine amorphous nanopowder prepared by quenching cooling combined with wet milling and spray drying;International Journal of Pharmaceutics;2022-11
3. Enhancement of Valsartan Dissolution Rate by the Increased Porosity of Pellets Using Supercritical CO2: Optimization via Central Composite Design;Journal of Pharmaceutical Innovation;2022-09-30
4. Central composite design optimization for a controlled valsartan release from polycaprolactone microspheres;Journal of Applied Polymer Science;2021-09-02
5. Role of Hydrogen Bonds in Formation of Co-amorphous Valsartan/Nicotinamide Compositions of High Solubility and Durability with Anti-hypertension and Anti-COVID-19 Potential;Molecular Pharmaceutics;2021-04-01
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