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American Journal of PharmTech Research

Kotapati Nalini

Author Profile
Natco Pharma Limited, Natco Research Centre, B-13, Industrial Estate, Sanathnagar, Hyderabad-500018, Telangana, India.
2
Publications
2
Years Active
5
Collaborators
63
Citations

Publications by Kotapati Nalini

2 publications found • Active 2017-2020

2020

1 publication

Quantitative Method For The Determination Of Phenyl Hydrazine, A Potential Genotoxic Impurity Of Ondansetron Hydrochloride Using Tandem Mass Spectrometry

with Palnati Narmada 1* Kotapati Nalini, Gopal Vaidyanathan
10/1/2020

To estimate the level of Phenylhydrazine, a potential genotoxic impurity in Ondansetron Hydrochloride API, a new simple, sensitive and accurate method was developed using Liquid Chromatographic Mass Spectrometry (LC-MS/MS). The chromatographic separation was achieved on Inert Sustain Swift C18, 5µ (150 x 4.6) mm column with gradient programme and elution was monitored by mass spectrometer in Multiple Reaction Monitoring mode using electrospray ionization. The LOD and LOQ values found to be 5 ppm and 15 ppm for the impurity with respect to the test concentration 2 mg/ml. The method was linear (r2>0.99), precise (RSD<2%), accurate and well within acceptable ICH limits.

2017

1 publication

Simultaneous Quantitation of Two Potential Genotoxic Impurities In Imatinib by Liquid Chromatography Mass Spectrometry

with Palnati Narmada, Adibhatla Kali Satya Bhujanga Rao, Gopal Vaidyanathan, Sanasi Paul Douglas
2/1/2017

A new, simple, accurate and sensitive method was developed for the quantification of two potential genotoxic impurities 1-(2-methyl-5-nitro-phenyl)guanidine nitrate and  N-(2-methyl-5-nitro-phenyl)-4-(3-pyridyl)pyrimidin-2-amine at low level (2 ppm) in Imatinib using liquid chromatographic mass spectrometry. The chromatographic separation was achieved on Kromasil 100-3.5-C18 (150 x 2.1) mm column with gradient programme and elution was monitored by mass spectrometer in selective ion monitoring mode using electrospray ionization. The LOD and LOQ values found to be 0.2 ppm and 0.6 ppm for both the impurities with respect to the test concentration 5 mg/ml. The method was linear (r2>0.99), precise (RSD

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