Development and Validation of RP-UHPLC Method for Quantification of Gliclazide in Bulk and Pharmaceutical Dosage Form Using Quality-by-Design (QbD) Approach: A Shifting Paradigm-Reference-Cited by-同舟云学术

Development and Validation of RP-UHPLC Method for Quantification of Gliclazide in Bulk and Pharmaceutical Dosage Form Using Quality-by-Design (QbD) Approach: A Shifting Paradigm

Published:2022-06-22 Issue:8 Volume:85 Page:719-732
ISSN:0009-5893
Container-title:Chromatographia
language:en
Short-container-title:Chromatographia

Author:

Bordoloi Ripunjoy^ORCID,Ahmed Abdul Baquee,Baishya Himakshi

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Clinical Biochemistry,Biochemistry,Analytical Chemistry

Link

https://link.springer.com/content/pdf/10.1007/s10337-022-04175-7.pdf

Reference36 articles.

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3. Sandhu PS, Beg S, Katare OP, Singh B (2016) QbD-driven development and validation of a HPLC method for estimation of tamoxifen citrate with improved performance. J Chromatogr Sci 8:1–12. https://doi.org/10.1093/chromsci/bmw090

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5. Manwar JV, Vispute SS, Kumbhar DD, Manmode RS, Bakal RL, Jadhao RG, Jogdand SD (2016) Response surface based optimization of system variables for liquid chromatographic analysis of candesartan cilexetil. Integr Med Res. https://doi.org/10.1016/j.jtusci.2016.02.004