METHOD DEVELOPMENT AND VALIDATION OF TRILACICLIB BY RP- HPLC METHOD

Authors

  • Syeda Heena M. Pharmacy Department of Quality Assurance, sultan ul uloom college of pharmacy, banjara hills, Mount hills, Hyderabad, 500034, Medchal Dist.

Keywords:

Trilaciclib, Method development, Validation, RP-HPLC

Abstract

Employing the RP-high- approach, an uncomplicated, clear, and reliable way of figuring out Trilaciclib was discovered. the circumstances applied are outlined below: Eluent used is 0.1% TFA and MeOh (55:45), Solid Adsorbent used is SunFire C18 Column, 5 μm, 4.6 mm X 150 cm], an ideal technique was used to finalize the parameters. The ambient tem of the S.p was set to 25 °C, as well as the threshold spectrum was 212 nm. a consistency investigates encompassing 7.5μg to 45μg took place and the R2 value was found to be 0.999. 2.042 records proved to be an Elutant rate. % variance was found to be 0.5%. The Repeatability exactitude RSD was calculated to be 0.6% .99.95% repossession was accomplished. % 99.47% assay was gathered. The equation for regression yielded sensitivity values of 0.03, 0.09. The equation for R2 is y = 210008x + 42435. The strategy that originated cost-effective, so it's appropriate for conventional inspections in industries. Both the rate of retention and the amount of time running were diminished.

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Published

2025-10-14

How to Cite

Syeda Heena. (2025). METHOD DEVELOPMENT AND VALIDATION OF TRILACICLIB BY RP- HPLC METHOD. World Journal of Pharmaceutical Sciences, 13(03). Retrieved from https://wjpsonline.com/index.php/wjps/article/view/1952

Issue

Section

Research Article