A NOVEL RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR THE QUANTIFICATION OF A POTENTIAL ANTI-DIABETIC DRUG METFORMIN HYDROCHLORIDE IN TABLET DOSAGE FORM [PDF]
Objective: This study was conducted to develop a simple, economical, linear, rapid method for the assay studies of Metformin HCl by RP-HPLC method and to carry out the method validation.
HIREMATH, JAYASHREE A., KUMAR, HARISH
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Investigation of an Active Film Coating of Teneligliptin to Prepare Fixed- Dose Combination for the Treatment of Diabetes [PDF]
In this study, the aqueous film coating process and slugging technique was successfully employed to manufacture two different drug delivery systems exhibiting immediate and delayed release of THH and MTH, respectively.
Sangavi, T
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Optimization of green LC-MS method for rosuvastatin and teneligliptin using AQbD chemometric approach [PDF]
Background: Rosuvastatin combined with Teneligliptin formulation is commonly used in the treatment of Diabetic dyslipidaemia. However, only a few analytical methods have been published for the examination of this drug in a synthetic mixture or in a ...
Hemnath Elango, S R Aswathy
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Verificação de desempenho de metodologia para determinação de íon nitrato em amostras de água potável [PDF]
Contaminated water is one of the main public health risks. One way to assess its quality is by quantifying nitrate through ultraviolet (UV) spectrophotometry. In this work, the performance of the UV spectrophotometric method for nitrate ion determination
Andrade, Marcelo Farias de +5 more
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Analytical Method Development and Validation for the Estimation of Teneligliptin in Oral Solid Dosage Form by Revesre Phase Chromatographic Technique Using UHPLC [PDF]
AIM AND OBJECTIVE:Teneligliptin is a pharmaceutical drug for the treatment of type 2 diabetes mellitus. It belongs to the class of anti-diabetic drugs known as dipeptidyl peptidase-4 inhibitors or "gliptins". Teneligliptin HBr hydrate is a novel, potent,
Ganesh Prabhu, K
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Background Diabetes mellitus affects millions globally, necessitating effective management strategies. Glenmark Pharmaceutical Limited introduced a fixed-dose combination of teneligliptin and dapagliflozin in 2022 to address this need.
Thummar Kashyap +3 more
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REGULATORY REQUIREMENTS AND REGISTRATION PROCESS FOR DRUG APPROVAL OF FIXED DOSE COMBINATIONS (FDC S ) IN INDIA: A REVIEW [PDF]
The article reveals the data required for fixed-dose combinations (FDCs) in Indian market occupies a higher pedestal when the efficacy of a finished product is under question. Although these have advantages that make them appear a good therapy option, In
&, Ankit Saxena
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Simultaneous Estimation of Dapagliflozin and Teneligliptin by Analytical Method Development Using HPLC [PDF]
Analytical methods need to be validated or revalidated prior to their introduction into routine analyses. Chromatography is an analytical techniques based on the separation of molecules due to differences in their structure and/or composition. In general,
Sunil Gaikwad, Laxmikant B. Borse, Kamlesh Dandagvhal, Dinesh Rautmale
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Stability Indicating Method Development and Validation of Teneligliptin and Pioglitazone using UHPLC in Pure and Pharmaceutical Formulation. [PDF]
Introduction: Teneligliptin and Pioglitazone in pharmaceutical combined form can use to treat and control the type 2 diabetes mellitus. Objective: The objective is to develop a novel, easy, fast, accurate UHPLC method and validate it as per the ICH ...
Sameer Narayan Godase, Mahesh Hari Kolhe, Shubham Balasaheb Mhaske, Kavita Vitthalrao Dhamak, Rohit Jaysing Bhor
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A novel HPLC method for the simultaneous determination of empagliflozin and dapagliflozin: Development, validation, robustness testing and greenness assessment [PDF]
Empagliflozin (EMPA) and Dapagliflozin (DAPA) are mainly recommended for the treatment of type 2 diabetes mellitus and heart failure. Based on the principles of green analytical chemistry, a simple, rapid and robust HPLC method was developed for the ...
Dotsikas Yannis +2 more
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