Analytical Method Development and Validation of Solifenacin in Pharmaceutical Dosage Forms by RP-HPLC-Reference-Cited by-同舟云学术

Analytical Method Development and Validation of Solifenacin in Pharmaceutical Dosage Forms by RP-HPLC

Published:2014-04-16 Issue: Volume:2014 Page:1-5
ISSN:2090-732X
Container-title:ISRN Analytical Chemistry
language:en
Short-container-title:ISRN Analytical Chemistry

Author:

Shaik Rihana Parveen¹²,Puttagunta Srinivasa Babu¹,Kothapalli Bannoth Chandrasekar²,Challa Bala Sekhara Reddy³

Affiliation:

1. Vignan Pharmacy College, Vadlamudi, Guntur, Andhra Pradesh 522213, India

2. Jawaharlal Nehru Technological University Anantapur, Andhra Pradesh 515002, India

3. Vaagdevi College of Pharmacy, Gurazala, Guntur, Andhra Pradesh 522415, India

Abstract

A new, accurate, precise, and robust HPLC method was developed and validated for the determination of solifenacin in tablet dosage form. The chromatographic separation was achieved on an Inertsil ODS 3V C18 (150 mm × 4.6 mm, 5 μm) stationary phase maintained at ambient temperature with a mobile phase combination of monobasic potassium phosphate (pH 3.5) containing 0.1% triethylamine and methanol (gradient mode) at a flow rate of 1.5 mL/min, and the detection was carried out by using UV detector at 220 nm. The performance of the method was validated according to the present ICH guidelines.

Publisher

Hindawi Limited

Subject

General Medicine

Link

http://downloads.hindawi.com/archive/2014/132020.pdf

Reference18 articles.

1. Clinical Pharmacokinetics and Pharmacodynamics of Solifenacin

2. Solifenacin succinate for the treatment of overactive bladder

3. Solifenacin Demonstrates High Absolute Bioavailability in Healthy Men

4. Pharmacokinetics and toxicity of antimuscarinic drugs for overactive bladder treatment in females

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