Abstract
Background
Chemical hazard is one of the most prominent side effects that come out along with the benefits of pharmaceutical production. Chemicals usage and waste production are involved in each step of production and are found to be in high percentage at the stage of quality testing. Conventional quality testing (assay) involves the use of solvents and reagents that generates high flammable and non-flammable waste and also enhanced the per batch cost of the medicine, whereas green chemistry offers a benign environment for drug designing, manufacturing, and analysis.
Results
In the present study, a green FTIR method for assay of antiviral drugs entecavir is developed and validated as per ICH Q2_R1 guidelines. A calibration curve is plotted between absorbance and concentration, yielding excellent linearity with a correlation coefficient (
r
2
) value of 0.9991 in the concentration range of 0.25–0.75 mg.
Conclusion
The developed method was validated and was very specific, accurate (99.9–100%) at three levels of 80, 100, and 120% of test concentration and precise with < 1% RSD. The LOD of the method is 0.0674 mg and is able to quantify the active at the limit of 0.2042 mg. Four different drug brands available in the local market are assayed by the validated method, and %recoveries are found to be in the range of 99–101%.
Graphical abstract
Green Chemistry Approach: Method Development and Validation for Identification and Quantification of Entecavir using FT-IR in Bulk and Pharmaceutical Dosage Form