Co-processing of nateglinide with meglumine for enhanced dissolution rate: in vitro and in vivo evaluation
Author:
Affiliation:
1. Department of Pharmaceutical Technology, Pharmacy College, Delta University for Science and Technology, Gamasa, Egypt
2. Department of Pharmaceutical Technology, Faculty of Pharmacy, Tanta University, Tanta, Egypt
Publisher
Informa UK Limited
Subject
Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03639045.2020.1820035
Reference33 articles.
1. I. Technological approaches to improve the dissolution behavior of nateglinide, a lipophilic insoluble drug: Nanoparticles and co-mixing
2. Intestinal uptake of nateglinide by an intestinal fluorescein transporter
3. Niosomes for oral delivery of nateglinide:in situ–in vivocorrelation
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2. Avoiding pits on the energy landscape – alternative strategies for stabilizing nateglinide co-amorphous systems;CrystEngComm;2024
3. Improved Pharmaceutical Properties of Honokiol via Salification with Meglumine: an Exception to Oft-quoted ∆pKa Rule;Pharmaceutical Research;2022-07-14
4. Development of rebamipide-loaded spray-dried microsphere using distilled water and meglumine: physicochemical characterization and pharmacokinetics in rats;Pharmaceutical Development and Technology;2021-05-19
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