Design of esomeprazole solid dispersion for improved dissolution and bioavailability using the supercritical anti-solvent technique
YC Pyo, TN Nguyen, YS Lee, YE Choi… - Journal of Drug Delivery …, 2023 - Elsevier
Esomeprazole magnesium (ESM), a salt of esomeprazole (ESO), has low oral bioavailability
owing to its poor solubility. This study aimed to improve the solubility and bioavailability of …
owing to its poor solubility. This study aimed to improve the solubility and bioavailability of …
[HTML][HTML] Solid dispersion approach improving dissolution rate of stiripentol: a novel antiepileptic drug
S Afifi - Iranian Journal of Pharmaceutical Research: IJPR, 2015 - ncbi.nlm.nih.gov
Some drugs have low bioavailability due to their poor aqueous solubility and/or slow
dissolution rate in biological fluids. Stiripentol (STP) is a novel anticonvulsant drug that is …
dissolution rate in biological fluids. Stiripentol (STP) is a novel anticonvulsant drug that is …
Improvement in solubility and absorption of nifedipine using solid solution: Correlations between surface free energy and drug dissolution
S Tubtimsri, Y Weerapol - Polymers, 2021 - mdpi.com
Ternary solid solutions composed of nifedipine (NDP), amino methacrylate copolymer
(AMCP), and polysorbate (PS) 20, 60, or 65 were prepared using a solvent evaporation …
(AMCP), and polysorbate (PS) 20, 60, or 65 were prepared using a solvent evaporation …
[PDF][PDF] Enhancement of the solubility and dissolution rate of rebamipide by using solid dispersion technique (Part I)
MY Ismail, MM Ghareeb - Iraqi Journal of Pharmaceutical Sciences (P-ISSN …, 2018 - iasj.net
Solid dispersion is an attractive tool of pharmaceutical technology used to improve the
physical properties of drugs, among these properties is the solubility of the drugs …
physical properties of drugs, among these properties is the solubility of the drugs …
[PDF][PDF] Enhancement of solubility and dissolution profile of artesunate by employing solid dispersion approach: An in-vitro evaluation.
Current study was designed with an aim to improve the solubility and dissolution profile of
artesunate by preparing solid dispersions through solvent evaporation and freeze-drying …
artesunate by preparing solid dispersions through solvent evaporation and freeze-drying …
Characterization and In vitro Dissolution Assessment of Pitavastatin-polyvinyl Pyrrolidone and Kollicoat® IR Solid Dispersions Prepared by Solvent Evaporation and …
I Mikrani, KMR Prattay, MR Sarkar… - Bangladesh …, 2024 - banglajol.info
Pitavastatin (PTV) is a potent lipid lowering drug that acts on hepatocytes by blocking the 3-
hydroxy-3-methylglutaryl-CoA reductase enzyme. As a Biopharmaceutical Classification …
hydroxy-3-methylglutaryl-CoA reductase enzyme. As a Biopharmaceutical Classification …
[PDF][PDF] In vitro‐in vivo evaluation of fast‐dissolving tablets containing solid dispersion of oxcarbazepine
A Mohan, G Sangeetha - Int J Pharm Pharm Sci, 2016 - academia.edu
Objective: Investigation of in vitro/in vivo behaviour of fast-dissolving tablets containing solid
dispersions of oxcarbazepine is the focus of the present research work. Methods: The effect …
dispersions of oxcarbazepine is the focus of the present research work. Methods: The effect …
[PDF][PDF] Formulation and evaluation of verapamil solid dispersion tablets for solubility enhancement
R Arun Raj, AC Das, S Sreerekha… - Res. Rev. A J. Pharm …, 2016 - researchgate.net
This study was mainly designed to solve the drawbacks of conventional verapamil solid
dosage form, low bioavailability and limited clinical efficacy, by preparing solid dispersion …
dosage form, low bioavailability and limited clinical efficacy, by preparing solid dispersion …
ТЕХНОЛОГІЇ ОТРИМАННЯ ВИСОКОРОЗЧИННИХ ПОЛІМЕРНИХ КОМПОЗИЦІЙНИХ МАТЕРІАЛІВ З АКТИВНИМИ ФАРМАЦЕВТИЧНИМИ ІНГРЕДІЄНТАМИ
VM LISOVYI, VV LYZHNIUK, VG KOSTIUK… - Technologies and …, 2023 - jrnl.knutd.edu.ua
Практична значимість. Проведені дослідження доводять, що до перспективних методів
утворення твердих дисперсних систем, що дозволяють забезпечити значне …
утворення твердих дисперсних систем, що дозволяють забезпечити значне …
Synthesis of Drug Microparticle with Hydrophilic Carrier and Its Characterization
E Ozen, K Poturcu, T Hashemi, M Sozeri… - SETSCI-Conference …, 2024 - set-science.com
In the present study, a model drug, with its low permeable and low aqueous soluble
properties, was selected to produce microparticles using an anti-solvent precipitation …
properties, was selected to produce microparticles using an anti-solvent precipitation …