Method development of Amlodipine and Nevirapine by UVS and HPTLC » książka
Method development of Amlodipine and Nevirapine by UVS and HPTLC
ISBN-13: 9783659630613 / Angielski / Miękka / 2014 / 92 str.
A simple, economical, and accurate absorption ratio method in UV Spectroscopy and HPTLC method were developed for the simultaneous estimation of Amlodipine besylate (AML) and Nevirapine (NEV) in bulk and tablet dosage form. In Spectroscopy, 0.1M HCl was used as a diluent to dissolve AML and NEV. The absorptions were observed at 252 nm (isobestic point) and 295 nm ( max of NEV), which were selected based on overlapping spectra of AML and NEV. The linearity range of the UV method was found to be 3-7 ug/ml at 252 nm for AML (r2=0.9995 0.0005) and 295 nm for NEV (r2=0.9985 0.0012). HPTLC method was developed with silica gel GF TLC Plate. Chloroform-Methanol-Glacial acetic acid (75.8:21.6:2.6) was used as a diluent. The spot after the chromatogram was identified in UV and Iodine chamber. The linearity range of HPTLC method was found to be 5-25 ug/ml for AML (r2=0.9994) and 295 nm for NEV (r2=0.999). Recovery study of UV and HPTLC methods were performed to confirm the accuracy of the methods. The methods were validated as per ICH guidelines. The methods were found to be simple, precise, accurate and rapid for the simultaneous determination of AML and NEV in bulk and tablet dosage form."
A simple, economical, and accurate absorption ratio method in UV Spectroscopy and HPTLC method were developed for the simultaneous estimation of Amlodipine besylate (AML) and Nevirapine (NEV) in bulk and tablet dosage form. In Spectroscopy, 0.1M HCl was used as a diluent to dissolve AML and NEV. The absorptions were observed at 252 nm (isobestic point) and 295 nm (λmax of NEV), which were selected based on overlapping spectra of AML and NEV. The linearity range of the UV method was found to be 3-7 µg/ml at 252 nm for AML (r2=0.9995±0.0005) and 295 nm for NEV (r2=0.9985±0.0012). HPTLC method was developed with silica gel GF TLC Plate. Chloroform-Methanol-Glacial acetic acid (75.8:21.6:2.6) was used as a diluent. The spot after the chromatogram was identified in UV and Iodine chamber. The linearity range of HPTLC method was found to be 5-25 µg/ml for AML (r2=0.9994) and 295 nm for NEV (r2=0.999). Recovery study of UV and HPTLC methods were performed to confirm the accuracy of the methods. The methods were validated as per ICH guidelines. The methods were found to be simple, precise, accurate and rapid for the simultaneous determination of AML and NEV in bulk and tablet dosage form.
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