Eco Friendly and Economical Aqbd Analytical Method Development and Validation of Ramucirumab in Bulk and Injectable Dosage Form by Using RP-UPLC

An Easy, sensitive, specific, and precise RP-UPLC method for the pharmaceutical dose estimation of Bevacizumab in injectable dosage form. Chromatogram was run through ACQUITY UPLC HSS C18 Column, 130A, 1.7 um, 2.1 mm X 100 mm. Mobile phase containing 0.1% OPA: Acetonitrile taken in the ratio 60:40 was pumped through column at a flow rate of 0.3ml/min. Temperature was maintained at 30.7°C. Optimized wavelength selected was 215.0nm. Retention time of Bevacizumab was found to be 0.945 min. %RSD of the Bevacizumab were and found to be 0.8. %RSD of Method precision of Bevacizumab was found to be 0.2 %Recovery was obtained as 99.75% for Bevacizumab. LOD, LOQ values obtained from regression equation of Bevacizumab were 0.05, 0.16. Regression equation of Bevacizumab is y = 11549x + 1531.9. Retention times were decreased and that run time was decreased, so the method developed was simple and economical that can be adopted in regular Quality control test in Industries.

Authors

Publication Details

Journal
International Journal of Environmental Sciences
Published
2025-08-11
DOI
https://doi.org/10.64252/jth79v32
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
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article

Eco Friendly and Economical Aqbd Analytical Method Development and Validation of Ramucirumab in Bulk and Injectable Dosage Form by Using RP-UPLC

Subbavarapu Santhi Bhushan, C. Mallikarjuna Rao
International Journal of Environmental Sciences
Analytical Methods in Pharmaceuticals
article

Eco Friendly and Economical Aqbd Analytical Method Development and Validation of Ramucirumab in Bulk and Injectable Dosage Form by Using RP-UPLC

Subbavarapu Santhi Bhushan, C. Mallikarjuna Rao
article en

Abstract

An Easy, sensitive, specific, and precise RP-UPLC method for the pharmaceutical dose estimation of Bevacizumab in injectable dosage form. Chromatogram was run through ACQUITY UPLC HSS C18 Column, 130A, 1.7 um, 2.1 mm X 100 mm. Mobile phase containing 0.1% OPA: Acetonitrile taken in the ratio 60:40 was pumped through column at a flow rate of 0.3ml/min. Temperature was maintained at 30.7°C. Optimized wavelength selected was 215.0nm. Retention time of Bevacizumab was found to be 0.945 min. %RSD of the Bevacizumab were and found to be 0.8. %RSD of Method precision of Bevacizumab was found to be 0.2 %Recovery was obtained as 99.75% for Bevacizumab. LOD, LOQ values obtained from regression equation of Bevacizumab were 0.05, 0.16. Regression equation of Bevacizumab is y = 11549x + 1531.9. Retention times were decreased and that run time was decreased, so the method developed was simple and economical that can be adopted in regular Quality control test in Industries.

International Journal of Environmental Sciences
Openalex Percentile: Top 76%
Analytical Methods in Pharmaceuticals
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