RP-HPLC Method Development and Validation for Simultaneous Estimation of Benidipine Hydrochloride, Telmisartan and Chlorthalidone in Tablet

JETIR March 2019, Volume 6, Issue 3

15 Pages Posted: 7 Apr 2020

See all articles by Bhoomi Patel

Bhoomi Patel

Saraswati Institute of Pharmaceutical Sciences

Ankit Chaudhary

Saraswati Institute of Pharmaceutical Sciences - Department of Quality Assurance

Sudhir Gami

Saraswati Institute of Pharmaceutical Sciences, Department of Quality Assurance

Date Written: March 13, 2019

Abstract

A simple, rapid, economical, precise and accurate RP-HPLC method for simultaneous estimation of Chlorthalidone, Telmisartan and Benidipine HCl in their Combined Dosage Form has been developed.

A reverse phase high performance liquid chromatographic method was developed for the simultaneous estimation of Chlorthalidone, Telmisartan and Benidipine HCl. in Their Combined Dosage Form has been developed. The separation was achieved by C18 (25 cm × 0.46 cm) Hypersil BDS column and Buffer (pH 3.0): Methanol (50:50 v/v) as mobile phase, at a flow rate of 1 ml/min. Detection was carried out at 230 nm. Retention time of Chlorthalidone, Benidipine HCl, and Telmisartan were found to be 4.887 min, 6.690 min and 8.813, respectively. The method has been validated for linearity, accuracy and precision. Linearity observed for Benidipine HCl 2-6 μg/ml, for Telmisartan 20-60 μg/ml and for Chlorthalidone 6.25-18.75 μg/ml. Developed method was found to be accurate, precise and rapid for simultaneous estimation of Chlorthalidone, Telmisartan and Benidipine HCl in their Combined Dosage Form.

Keywords: Benidipine HCl, Telmisartan, Chlorthalidone, Reverse Phase High Performance Liquid Chromatography Method, Infra-Red Spectroscopy Method, Validation

Suggested Citation

Patel, Bhoomi and Chaudhary, Ankit and Gami, Sudhir, RP-HPLC Method Development and Validation for Simultaneous Estimation of Benidipine Hydrochloride, Telmisartan and Chlorthalidone in Tablet (March 13, 2019). JETIR March 2019, Volume 6, Issue 3 , Available at SSRN: https://ssrn.com/abstract=3553661

Bhoomi Patel (Contact Author)

Saraswati Institute of Pharmaceutical Sciences ( email )

DHANAP
GHANDHINAGAR, GA 382355
India

Ankit Chaudhary

Saraswati Institute of Pharmaceutical Sciences - Department of Quality Assurance

India

Sudhir Gami

Saraswati Institute of Pharmaceutical Sciences, Department of Quality Assurance

India

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