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American Journal of PharmTech Research

Adibhatla Kali Satya Bhujanga Rao

Author Profile
Natco Pharma Limited, Natco Research Centre, B-13, Industrial Estate, Sanathnagar, Hyderabad-500018, Telangana, India.
2
Publications
2
Years Active
6
Collaborators
82
Citations

Publications by Adibhatla Kali Satya Bhujanga Rao

2 publications found • Active 2013-2017

2017

1 publication

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

with Kotapati Nalini, Palnati Narmada, 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

2013

1 publication

LC–MS–MS Determination of Zolmitriptan In Human Plasma

with Palnati Narmada, Gannamani Nalini, Kasisomayajula Venkata Jogi
6/1/2013

A specific and sensitive liquid chromatography-electrospray ionization tandem mass spectrometry method was developed for the determination of zolmitriptan in human plasma. Zolmitriptan and the internal standard (IS) rizatriptan were extracted by liquid–liquid extraction and were separated on a sunfire C18 column (100 x 2.1mm and 3.5µm) with isocratic elution of mobile phase consisting of 10mM ammonium formate containing 0.1% formic acid and acetonitrile. Electrospray ionization in multiple reaction monitoring mode was used to monitor the parent and the daughter ions of the analyte and the internal standard. The response is linear over a range of 0.5 to 100.0 ng/ml concentration with a correlation coefficient (r2) greater than 0.99 and an extraction efficiency of about 95%. The validated method can be applied to pharmacokinetic, toxicokinetic and bioequivalence studies.

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