Research Journal of Pharmacy and Technology
SCOPUS
  • Year: 2024
  • Volume: 17
  • Issue: 4

Development and validation of stability indicating RP-HPLC assay method for trospium chloride in tablet dosage form

  • Author:
  • Vikas D. Kedar*, Pritam N. Dube, Sachin N. Kapse, Yogita B. Thombare
  • Total Page Count: 4
  • Page Number: 1595 to 1598

Research Scholar Matoshri College of Pharmacy Ekalahare, Nashik, 422105, Maharashtra

*Corresponding Author E-mail: kedarvikas10@gmail.com

Online published on 10 June, 2024.

Abstract

A simple, rapid, accurate and sensitive method was developed for quantitative analysis of Trospium Chloride in tablet dosage form using Reverse Phase high performance liquid chromatography (RP-HPLC) with DAD detection. The chromatography separation was achieved Xterra RP18, (250 × 4.6mm, 5μParticle Size)), at column temperature 40°C±2, in the isocratic mobile phase mode using Acetonitrile (ACN): Buffer (65:35; v/v) at a flow rate of 1.0mL/min. The determination was performed using Buffer HPLC with DAD detector set at 215nm. Samples were prepared with diluent [Buffer: ACN (200:100; v/v)], and the volume injected was 50μL. The retention time for Trospium Chloride was 3.275 minute. The analytical curve was linear (r2 0.9993) over a wide concentration range (50.0-150.0 μg/mL). The presence of components of the tablet did not interfere in the results of the analysis. The method showed adequate precision with a relative standard deviation (RSD) less than 2%.

Keywords

Trospium Chloride, Assay, RP-HPLC, Method validation