Isolation and Characterisation of Nateglinide and its impurity in Bulk and Marketed Formulation by HPTLC Method
Author:
Affiliation:
1. P.E. Society’s Modern College of Pharmacy, Yamunanagar, Nigdi, Pune-411044 Maharashtra, India, 411044.
2. Maulana Azad University, Village Bujhawar, Tehsil Luni Jodhpur 342802.
Abstract
Publisher
A and V Publications
Subject
Pharmacology (medical),Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Reference19 articles.
1. Vashi D. Kumar S. Impurity Identification and Characterization of some Anti-Diabetic Drugs using various Analytical Methods. Asian J. Pharm. Res. 2019; 9(4):243-248.
2. Bakshi M. Singh S. Development of validated stability-indicating assay methods—critical review, J. Pharm. Biomed. Anal. 28 (2002) 1011–1040. DOI: 10.1016/s0731-7085(02)00047-x
3. Venkatesh S.Jyothi S.Chiluka R. Padmavathi Y. Development of UV- Spectrophotometric Method for the Simultaneous Estimation of Nateglinide and Piperine in Combined Tablet dosage form. Asian J. Pharm. Ana. 2020; 10(3):134-140.
4. Rana K. Sharma P. Development and Validation of a HPLC method for the Determination of Metformin hydrochloride, Nateglinide and Pioglitazone hydrochloride in Multicomponent Formulation. Asian J. Research Chem. 2021; 14(1):7-12.
5. Vasanthan K. Vijayageetha R. Arcot AS. Method Development and Validation of RP-HPLC Method for Estimation of Nateglinide in Bulk Drug and Pharmaceutical Formulation. Research J. Pharm. and Tech.3 (3): July-Sept. 2010; Page 804-806.
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1. In-Vitro Dissolution Study of Solid Dispersion Adsorbate of Nateglinide by Eco-Friendly Liquid Chromatography-Tandem Mass Spectrometric Method through Harmonized Approach of White Analytical Chemistry and Analytical Quality by Design;Chemistry Africa;2024-06-18
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