Development and validation of RP-HPLC method for quantification of repaglinide in mPEG-PCL polymeric nanoparticles: QbD-driven optimization, force degradation study, and assessment of in vitro release mathematic modeling-Reference-Cited by-同舟云学术

Development and validation of RP-HPLC method for quantification of repaglinide in mPEG-PCL polymeric nanoparticles: QbD-driven optimization, force degradation study, and assessment of in vitro release mathematic modeling

Published:2021-09 Issue: Volume:168 Page:106491
ISSN:0026-265X
Container-title:Microchemical Journal
language:en
Short-container-title:Microchemical Journal

Author:

Wadhwa Geetika,Krishna Kowthavarapu Venkata,Dubey Sunil Kumar,Taliyan Rajeev

Funder

Indian Council of Medical Research

Publisher

Elsevier BV

Subject

Spectroscopy,Analytical Chemistry

Reference29 articles.

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2. Characteristics of repaglinide and its mechanism of action on insulin secretion in patients with newly diagnosed type-2 diabetes mellitus;Wang;Med. (United States).,2018

3. Repaglinide pharmacokinetics in healthy young adult and elderly subjects;Hatorp;Clin. Ther.,1999

4. Repaglinide: A review of its therapeutic use in type 2 diabetes mellitus;Culy;Drugs.,2001

5. Stability-indicating assay of repaglinide in bulk and optimized nanoemulsion by validated high performance thin layer chromatography technique;Akhtar;J. Pharm. Bioallied Sci.,2013

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