High Performance Liquid Chromatographic Method Development and Its Validation for Salbutamol

Muralidharan, Selvadurai and Kumar, Jayaraj (2012) High Performance Liquid Chromatographic Method Development and Its Validation for Salbutamol. British Journal of Pharmaceutical Research, 2 (4). pp. 228-237. ISSN 22312919

[thumbnail of Muralidharan-Kumar_2012BJPR1279.pdf] Text
Muralidharan-Kumar_2012BJPR1279.pdf - Published Version

Download (234kB)

Abstract

Aims: A simple and sensitive high performance liquid chromatographic (HPLC) method was developed for quantification of salbutamol in rat plasma. Terbutaline was used as an internal standard (IS).
Study Design: Validation study.
Methodology: The present method used solid phase extraction of salbutamol from rat plasma. Chromatographic separation achieved isocratically on reversed-phase c18 column (250 × 4.6 mm, 5μ) and the column effluent was monitored by uv detector at 276 nm. The mobile phase used was acetonitrile: 50mm ammonium acetate (ph 7.0), (80: 20 % v/v) at a flow rate of 1.0 ml/min.
Results and Discussion: This method was linear over the range of 50.0 – 1000.0 ng/ml with regression coefficient greater than 0.99.
Conclusion: The method was found to be precise, accurate and specific during the study. The simplicity of the method allows for application in laboratories that lack sophisticated analytical instruments such as LC–MS/MS or GC–MS/MS that are complicated, costly and time consuming rather than a simple HPLC–UV method. The method was successfully applied for pharmacokinetic study of salbutamol in rats.

Item Type: Article
Subjects: GO for STM > Medical Science
Depositing User: Unnamed user with email support@goforstm.com
Date Deposited: 29 Jun 2023 04:34
Last Modified: 20 Oct 2023 03:52
URI: http://archive.article4submit.com/id/eprint/1183

Actions (login required)

View Item
View Item