Simultaneous RP-HPLC Quantification of Praziquantel and Abamectin in Formulations: Method Development and Validation

Authors

  • Alikepalli Sujatha Malineni Lakshmaiah College of Pharmacy Author
  • Karavadi Thejomoorthy Malineni Lakshmaiah College of Pharmacy Author
  • Saibabu Chennupalli Malineni Lakshmaiah College of Pharmacy Author
  • Dr K Nithiyananthan Adikavi Nannaya University image/svg+xml Author

Keywords:

RP-HPLC, Praziquantel, Abamectin, Tablet, Validation

Abstract

A validated RP-HPLC method was developed for simultaneous estimation of Praziquantel (PZ) and Abamectin (AB). Chromatographic separation was achieved using Methanol: Tetrahydrofuran: 0.1% Orthophosphoric acid in the ratio 85:05:10 (V/V/V), providing optimum peak shape and low baseline noise on an Inertsil ODS-C18 column (250 × 4.6 mm, 5μ), detected at 272 nm. Total analysis time was 10 minutes with a flow rate of 1 mL/min. Standard curves showed correlation coefficients r2r^2r2 ≥ 0.999 over concentrations 5–35 µg/mL for both drugs. The method was successfully applied for drug analysis in bulk and formulations. 

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Published

2025-09-30

How to Cite

Simultaneous RP-HPLC Quantification of Praziquantel and Abamectin in Formulations: Method Development and Validation. (2025). Global Journal of Innovative Research in Multidisciplinary Areas (3049-4168), 1(7), 31-41. https://gjirma.com/index.php/home/article/view/15

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