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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D.Sathis Kumar is working as an associate professor in Aditya Institute of Pharmaceutical Sciences and Research, AP, India. He have more than 90 publication in reputed journals. He has secured honors/awards from IBC, Cambridge, England. His biography was included in Marquis Who’s Who in the world.
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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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 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. 92 pp. Englisch. N° de réf. du vendeur 9783659630613
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Dinakaran Sathis KumarD.Sathis Kumar is working as an associate professor in Aditya Institute of Pharmaceutical Sciences and Research, AP, India. He have more than 90 publication in reputed journals. He has secured honors/awards from. N° de réf. du vendeur 5169653
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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -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 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.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 92 pp. Englisch. N° de réf. du vendeur 9783659630613
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - 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 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. N° de réf. du vendeur 9783659630613
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Taschenbuch. Etat : Neu. Method development of Amlodipine and Nevirapine by UVS and HPTLC | Sathis Kumar Dinakaran (u. a.) | Taschenbuch | 92 S. | Englisch | 2014 | LAP LAMBERT Academic Publishing | EAN 9783659630613 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. N° de réf. du vendeur 105002759
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