Progress in analytical techniques for remogliflozin etabonate, vildagliptin and metformin hydrochloride: a recently, approved fDC

P Joshi, R Kotadiya - Current Pharmaceutical Analysis, 2023 - benthamdirect.com
Background: Fixed-dose combinations (FDCs) are renowned formulations that contain two
or more drugs pooled in a single dosage form. Their recognition is justified due to several …

Analytical and Bioanalytical Methods for the Determination of Dipeptidyl Peptidase-4 Inhibitors in Various Matrices: A Comprehensive Review

S Hadawale, S Sharma - Current Diabetes Reviews, 2025 - benthamdirect.com
Background DPP-4 inhibitors, or gliptins, are new oral antidiabetic drugs for type 2 diabetes.
They help to regulate insulin and glucagon. These drugs have the advantage of a lower risk …

Chemometric-based AQbD and green chemistry approaches to chromatographic analysis of remogliflozin etabonate and vildagliptin

P Prajapati, H Ahir, B Prajapati… - Journal of AOAC …, 2023 - academic.oup.com
Background According to the green chemistry approach, during method development, the
usage of toxic and carcinogenic organic solvents should be avoided or minimized for the …

Identification, isolation and characterization of potential process-related impurity and its degradation product in vildagliptin

N Kumar, SR Devineni, G Singh, A Kadirappa… - … of pharmaceutical and …, 2016 - Elsevier
Vildagliptin is a member of a new class of oral anti-diabetic drug. One unknown impurity was
identified in the range of 0.01–0.06% in different laboratory batches of vildagliptin along with …

Voltammetric determination of vildagliptin in a pharmaceutical formulation

M Fadr, AN Amro, SB Aoun - Tropical Journal of Pharmaceutical Research, 2018 - ajol.info
Purpose: To determine vildagliptin concentration in a pharmaceutical formulation using
voltammetric analysis techniques, and optimize the parameters affecting the techniques …

[PDF][PDF] Stability indicating RP-HPLC method development and validation for the simultaneous determination of vildagliptin and metformin in pharmaceutical dosage …

R Jayaprakash, SK Natesan, K Lalitha - Int J Pharm Pharm Sci, 2017 - academia.edu
Objective: The present study was aimed to develop a rapid, accurate, linear, sensitive and
validate stability-indicating high performance liquid chromatographic [RP-HPLC] method for …

Voltammetric assay of vildagliptin drug as vildagliptin-Cu2+ complex and its biological applications

AM Hassanein, YI Moharram, SE Ebied… - Journal of Applied …, 2022 - Springer
A sensitive square-wave adsorptive cathodic stripping voltammetric method is reported for
determining the drug, vildagliptin (VILD), in bulk and commercial formulations with a mean …

Determination of Three Gliptins in Tablets by Reversed Phase Liquid Chromatography with an Application of Spiked Urine Samples

SC Andac, E Ozdemir, CA Andac - Pharmaceutical Chemistry Journal, 2023 - Springer
A fast and reliable reversed-phase high-performance liquid chromatography (HPLC) method
has been developed for the simultaneous determination of vildagliptin, sitagliptin and …

[PDF][PDF] Forced degradation studies of vildagliptin raw material alone and in the presence of excipients using HPLC-UV analysis.

E Al-Qudah, S Arar, K Sweidan - Journal of Excipients & …, 2020 - jefc.scholasticahq.com
The chemical stability of a drug formulation can change the potency and safety of the
finished medicinal product. A forced degradation study can be a good method to examine …

[PDF][PDF] Validated stability-indicating HPTLC method development for determination of vildagliptin as bulk drug and in tablet dosage form

SR Butle, PB Deshpande - Conference on Harmonisation …, 2015 - academia.edu
ABSTRACT A new simple, accurate, precise and selective stability-indicating high
performance thin layer chromatographic (HPTLC) method has been developed and …