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Development and validation of a highly sensitive and robust LC-ESI-MS/MS method for simultaneous quantitation of simvastatin acid, amlodipine and valsartan in human plasma: application to a clinical pharmacokinetic study
Biomedical Chromatography
◽
10.1002/bmc.1161
◽
2009
◽
Vol 23
(6)
◽
pp. 615-622
◽
Cited By ~ 37
Author(s):
Addepalli V. Ramani
◽
Pinaki Sengupta
◽
Ramesh Mullangi
Keyword(s):
Human Plasma
◽
Clinical Pharmacokinetic
◽
Pharmacokinetic Study
◽
Esi Ms
◽
Simvastatin Acid
◽
Highly Sensitive
◽
Development And Validation
Download Full-text
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Simultaneous Quantification of Simvastatin and Simvastatin Acid in Human Plasma with a Highly Sensitive LC-ESI-MS/MS Method: Application to a Pharmacokinetic Study in Healthy Chinese Volunteers with a Fixed Dose of Simvastatin and Extended-Release Niacin Combination Tablet
Current Pharmaceutical Analysis
◽
10.2174/1573412911666150630182218
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Pharmacokinetic Study
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Extended Release
◽
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Combination Tablet
◽
Esi Ms
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Simultaneous Quantification
◽
Simvastatin Acid
◽
Highly Sensitive
◽
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Highly sensitive method for the determination of ropinirole with a lower limit of quantitation of 3.45 pg/mL in human plasma by LC-ESI-MS/MS: application to a clinical pharmacokinetic study
Biomedical Chromatography
◽
10.1002/bmc.1144
◽
2009
◽
Vol 23
(5)
◽
pp. 557-562
◽
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Clinical Pharmacokinetic
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Pharmacokinetic Study
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Esi Ms
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Highly Sensitive
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Limit Of Quantitation
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Sensitive Method
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Development and validation of a simple and sensitive LC-MS/MS method for the quantification of cefazolin in human plasma and its application to a clinical pharmacokinetic study
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Development and Validation of an LC–MS-MS Method for the Simultaneous Determination of Simvastatin, Simvastatin Acid and Ezetimibe in Human Plasma and Its Application to Pharmacokinetic Study in the Indian Population
Journal of Chromatographic Science
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10.1093/chromsci/bmw043
◽
2016
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Vol 54
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pp. 985-996
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Human Plasma
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Pharmacokinetic Study
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◽
Simvastatin Acid
◽
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Development and validation of a specific and sensitive LC–MS/MS method for determination of eslicarbazepine in human plasma and its clinical pharmacokinetic study
Journal of Chromatography B
◽
10.1016/j.jchromb.2019.02.027
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◽
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◽
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Development and validation of a rapid and sensitive UPLC–MS/MS method for quantification of kukoamine B in human plasma: Application to a clinical pharmacokinetic study
Journal of Pharmaceutical and Biomedical Analysis
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◽
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Development and Validation of an LC–ESI-MS Method for Quantitative Determination of Aripiprazole in Human Plasma and an Application to Pharmacokinetic Study
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Human Plasma
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Pharmacokinetic Study
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Development and validation of a HPLC method for simultaneous quantitation of gatifloxacin, sparfloxacin and moxifloxacin using levofloxacin as internal standard in human plasma: application to a clinical pharmacokinetic study
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Vol 22
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Development and validation of a highly sensitive LC-MS/MS method for quantitation of bivalirudin in human plasma: application to a human pharmacokinetic study
Biomedical Chromatography
◽
10.1002/bmc.2998
◽
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◽
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Highly Sensitive
◽
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◽
Development And Validation
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