Validated rp-hplc method for simultaneous estimation of cabotegravir and rilpivirine in tablet dosage form

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A validated rp-hplc method estimates cabotegravir and rilpivirine in tablets, confirming precision and accuracy.

The developed RP-HPLC method showed a relative standard deviation (RSD) below 2.0%, indicating high repeatability.
Chromatographic separation was achieved using a Waters Alliance e2695 system, ensuring reliable analytical performance.
The method validation followed ICH guidelines, proving it to be accurate and cost-effective for routine analysis.
Detection of analytes occurred at 269 nm, showcasing the method's suitability for quantitative determination.

PV et al. (2025) studied this question.

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