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Dr  Kancherla Prasad
Dr Kancherla Prasad
CSIR-Indian Institute of Integrative Medicine, Jammu
在 iiim.res.in 的电子邮件经过验证 - 首页
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引用次数
引用次数
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LC–MS/MS characterization of the forced degradation products of ezetemibe: Development and validation of a stability-indicating UPLC method
P Kancherla, V Velpuri, P Alegete, SS Albaseer, M Khagga, P Das
Journal of Taibah University for Science 10 (1), 148-160, 2016
82016
A fast and reliable LC-MS/MS method for simultaneous quantitation of fluoxetine and mirtazapine in human plasma
P Alegete, P Kancherla, SS Albaseer, S Boodida
Analytical Methods 6 (18), 7407-7414, 2014
72014
Identification, isolation, and synthesis of seven novel impurities of anti‐diabetic drug Repaglinide
P Kancherla, S Keesari, P Alegete, M Khagga, P Das
Drug Testing and Analysis 10 (1), 212-221, 2018
62018
Stability-Indicating RP-UPLC Method Development and Validation for the Process Related Impurities of Nebivolol and Structural Characterization of Its Forced Degradation …
P Kancherla, P Alegete, S Keesari, B Khagga, S Siddiraju, M Khagga, ...
Br J Pharm Res 14 (6), 1-13, 2016
62016
Development and validation of piribedil in tablet dosage form by HPLC: a QbD and OFAT approach
TSSJ Mohan, DP Varma, K Bhavyasri, K Prasad, K Mukkanti, HA Jogia
Asian Journal of Chemistry 29 (5), 1113, 2017
42017
A validated liquid chromatography–tandem mass spectrometric (LC-MS/MS) method for the estimation of fulvestrant in human plasma
P Alegete, P Kancherla, SS Albaseer, S Boodida
Oriental Journal of Chemistry 33 (3), 1146, 2017
42017
A simple alternative and improved HPLC method for the estimation of doravirine, lamivudine, and tenofovir disoproxil fumarate in solid oral dosage form
TK Kokkirala, P Kancherla, P Alegete, D Suryakala
Biomedical Chromatography 35 (8), e5121, 2021
32021
Bioanalytical Method Development and Validation for Quantitative Estimation of Valsartan by LC-MS/MS in Human Plasma.
K CHINTHALA, P KANCHERLA, P KUMAR
Asian Journal of Chemistry 29 (7), 2017
32017
Validation of HPLC-MS method in positive ion mode for estimation of phenytoin in human plasma using phenytoin D10 as internal standard
P Alegete, P Kancherla, S Keesari, SSR Yedlapalli, S Boodida
Asian Journal of Chemistry 29 (8), 1845-1852, 2017
32017
LC-MS/MS characterization of forced degradation products of repaglinide quality by design approach for stability-indicating LC method development and validation for degradation …
P Kancherla, K Srinivas, P Alegete, SS Albaseer
Analytical Chemistry Letters 10 (6), 740-757, 2020
12020
HPLC method for determining esomeprazole and its related substances in pharmaceutical formulations
TSSJ Mohan, DP Varma, K Bhavyasri, K Prasad, K Mukkanti, H AJogia
Asian Journal of Chemistry 29 (6), 1360-1364, 2017
12017
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