Authors :
Ramya Kumari Kadagandla; Ranjith Kumar Kadagandla; Dr. Baswaraju Macha; ChandraPrakash Bayya; Swetha Malyala; Saritha Devi
Volume/Issue :
Volume 11 - 2026, Issue 8 - August
Google Scholar :
https://tinyurl.com/2s7yeskc
DOI :
https://doi.org/10.38124/ijisrt/26aug1079
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working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and
ResearchGate.
Abstract :
metformin
hydrochloride, ramipril, atorvastatin, and glimepiride were 100, 0.5, 2.0, and 0.2 µg/mL, respectively, while the
corresponding limits of detection were 10 µg/mL, 20 ng/mL, 50 ng/mL, and 200 ng/mL. The proposed method was found to
be rapid, sensitive, and suitable for the simultaneous determination of all four drugs. Therefore, it can be applied to the
routine quality-control analysis of metformin hydrochloride, ramipril, atorvastatin, and glimepiride in bulk materials and
combined pharmaceutical formulations.
Keywords :
Metformin Hydrochloride; Ramipril; Atorvastatin; Glimepiride; Simultaneous Estimation; RP-HPLC; Method Validation.
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metformin
hydrochloride, ramipril, atorvastatin, and glimepiride were 100, 0.5, 2.0, and 0.2 µg/mL, respectively, while the
corresponding limits of detection were 10 µg/mL, 20 ng/mL, 50 ng/mL, and 200 ng/mL. The proposed method was found to
be rapid, sensitive, and suitable for the simultaneous determination of all four drugs. Therefore, it can be applied to the
routine quality-control analysis of metformin hydrochloride, ramipril, atorvastatin, and glimepiride in bulk materials and
combined pharmaceutical formulations.
Keywords :
Metformin Hydrochloride; Ramipril; Atorvastatin; Glimepiride; Simultaneous Estimation; RP-HPLC; Method Validation.