Development, validation and pharmacokinetic application of a simple and robust RP-HPLC method for quantitation of raloxifene in rat plasma

A simple and sensitive HPLC method has been developed and validated for the quantification of raloxifene in rat plasma. Liquid- liquid extraction procedure was employed for extracting raloxifene from rat plasma sample. Separation of raloxifene was achieved through a RP- C18 column with a mobile phas...

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Main Authors: Syed Jaffri, Syed Mahmood, Sengupta, Pinaki Ranjan, Mandal, Uttam Kumar, Chatterjee, Bappaditya D., Bakhtiar, M. Taher
Format: Article
Language:English
English
Published: Colegio de Farmaceuticos de la Provincia de Buenos Aires 2017
Subjects:
Online Access:http://irep.iium.edu.my/58589/
http://irep.iium.edu.my/58589/
http://irep.iium.edu.my/58589/1/Latin%20Journal%20LAJOP_36_9_1_35.pdf
http://irep.iium.edu.my/58589/7/58589_Development%2C%20validation_scopus.pdf
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spelling iium-585892018-04-18T03:19:14Z http://irep.iium.edu.my/58589/ Development, validation and pharmacokinetic application of a simple and robust RP-HPLC method for quantitation of raloxifene in rat plasma Syed Jaffri, Syed Mahmood Sengupta, Pinaki Ranjan Mandal, Uttam Kumar Chatterjee, Bappaditya D. Bakhtiar, M. Taher RM300 Drugs and their action A simple and sensitive HPLC method has been developed and validated for the quantification of raloxifene in rat plasma. Liquid- liquid extraction procedure was employed for extracting raloxifene from rat plasma sample. Separation of raloxifene was achieved through a RP- C18 column with a mobile phase consisted of phosphate buffer and acetonitrile (66:34 %, v/v). The method was validated for specificity, selectivity, sensitivity, linearity, accuracy, precision, recovery and stability parameters. A linear response (R2 value 0.9991) was found over the calibration range of 50 to 500 ng/mL. The accuracy for intra and inter day run varied between 86.73 to 102.30 % and 91.11 to 95.56%, respectively. The corresponding precision (% CV) were within 0.82 to 9.43% and 6.23 to 8.33%. The method was also found to be specific and stable. The applicability of the method was established through a single dose oral pharmacokinetic study of raloxifene in rat. Colegio de Farmaceuticos de la Provincia de Buenos Aires 2017-09 Article PeerReviewed application/pdf en http://irep.iium.edu.my/58589/1/Latin%20Journal%20LAJOP_36_9_1_35.pdf application/pdf en http://irep.iium.edu.my/58589/7/58589_Development%2C%20validation_scopus.pdf Syed Jaffri, Syed Mahmood and Sengupta, Pinaki Ranjan and Mandal, Uttam Kumar and Chatterjee, Bappaditya D. and Bakhtiar, M. Taher (2017) Development, validation and pharmacokinetic application of a simple and robust RP-HPLC method for quantitation of raloxifene in rat plasma. Latin American Journal of Pharmacy, 36 (9). pp. 1901-1907. ISSN 0326 2383 http://www.latamjpharm.org/
repository_type Digital Repository
institution_category Local University
institution International Islamic University Malaysia
building IIUM Repository
collection Online Access
language English
English
topic RM300 Drugs and their action
spellingShingle RM300 Drugs and their action
Syed Jaffri, Syed Mahmood
Sengupta, Pinaki Ranjan
Mandal, Uttam Kumar
Chatterjee, Bappaditya D.
Bakhtiar, M. Taher
Development, validation and pharmacokinetic application of a simple and robust RP-HPLC method for quantitation of raloxifene in rat plasma
description A simple and sensitive HPLC method has been developed and validated for the quantification of raloxifene in rat plasma. Liquid- liquid extraction procedure was employed for extracting raloxifene from rat plasma sample. Separation of raloxifene was achieved through a RP- C18 column with a mobile phase consisted of phosphate buffer and acetonitrile (66:34 %, v/v). The method was validated for specificity, selectivity, sensitivity, linearity, accuracy, precision, recovery and stability parameters. A linear response (R2 value 0.9991) was found over the calibration range of 50 to 500 ng/mL. The accuracy for intra and inter day run varied between 86.73 to 102.30 % and 91.11 to 95.56%, respectively. The corresponding precision (% CV) were within 0.82 to 9.43% and 6.23 to 8.33%. The method was also found to be specific and stable. The applicability of the method was established through a single dose oral pharmacokinetic study of raloxifene in rat.
format Article
author Syed Jaffri, Syed Mahmood
Sengupta, Pinaki Ranjan
Mandal, Uttam Kumar
Chatterjee, Bappaditya D.
Bakhtiar, M. Taher
author_facet Syed Jaffri, Syed Mahmood
Sengupta, Pinaki Ranjan
Mandal, Uttam Kumar
Chatterjee, Bappaditya D.
Bakhtiar, M. Taher
author_sort Syed Jaffri, Syed Mahmood
title Development, validation and pharmacokinetic application of a simple and robust RP-HPLC method for quantitation of raloxifene in rat plasma
title_short Development, validation and pharmacokinetic application of a simple and robust RP-HPLC method for quantitation of raloxifene in rat plasma
title_full Development, validation and pharmacokinetic application of a simple and robust RP-HPLC method for quantitation of raloxifene in rat plasma
title_fullStr Development, validation and pharmacokinetic application of a simple and robust RP-HPLC method for quantitation of raloxifene in rat plasma
title_full_unstemmed Development, validation and pharmacokinetic application of a simple and robust RP-HPLC method for quantitation of raloxifene in rat plasma
title_sort development, validation and pharmacokinetic application of a simple and robust rp-hplc method for quantitation of raloxifene in rat plasma
publisher Colegio de Farmaceuticos de la Provincia de Buenos Aires
publishDate 2017
url http://irep.iium.edu.my/58589/
http://irep.iium.edu.my/58589/
http://irep.iium.edu.my/58589/1/Latin%20Journal%20LAJOP_36_9_1_35.pdf
http://irep.iium.edu.my/58589/7/58589_Development%2C%20validation_scopus.pdf
first_indexed 2023-09-18T21:22:53Z
last_indexed 2023-09-18T21:22:53Z
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