TABLETLERDEKİ AMLODİPİN BESİLAT'IN TRİNİTROBENZEN SÜLFONİK ASİT İLE SPEKTROFOTOMETRİK TAYİNİ

Amlodipin besilatın (AB) tayini için hızlı ve basit bir spektrofotometrik metod geliştirildi. Metod etken madde ile trinitrobenzensülfonik asitin renkli bir ürün oluşturmasına dayanmaktadır. Reaksiyon oda sıcaklığında alkali ortamda (pH 10) yürümektedir. Oluşan ürün kloroform fazına ekstre edildikten sonra 337 nm de absorbansı ölçülmektedir. Ekstraksiyonlu işlemde Beer kanunu 6.0-30.0 g.ml-1 AB aralığında geçerlidir. Metoddaki bütün değişkenler optimize edilmiş ve metodun uygulanabilirliği AB içeren tabletler analiz edilerek sınanmıştır. Sonuçların tekraredilebilirliği bağıl standart sapma olarak % 1.34 tür ve analiz edilen tabletlere ilave edilen saf AB için geri kazanım % 99.7 dir. Sonuçlar daha önce geliştirilen kloranil metoduyla istatistiksel olarak uyumludur.. Elde edilen veriler geliştirilen metodun tabletlerdeki AB nin analizinde kullanılabileceğini göstermektedir.

SPECTROPHOTOMETRIC DETERMINATION OF AMLODIPINE BESYLATE IN TABLETS WITH TRINITROBENZENE SULPHONIC ACID

A rapid and simple spectrophotometric method for the determination of amlodipine besylate was developed. The method was based on the formation of a colored derivative between the drug and trinitrobenzenesulphonic acid. The reaction proceeds at room temperature in alkaline media (pH 10). The product was extracted into chloroform and the absorbance was measured at 337 nm. The Beer law limits for the procedure with extraction step were between 6.0-30.0 g-ml-1AB. All variables in the method were optimized and the applicability of the method was examined by analyzing tablets containing AB. Reproducibility of the results was 1.34 % as relative standard deviation and the recovery for pure AB added to preanalyzed tablets was 99.7 %. The results were statistically in concordance with that of chloranil method, which was formerly developed. Data obtained shows that the developed method can be used for determination of AB in tablets.Reproducibility of the results was 1.34 % as relative standard deviation and the recovery for pure AB added to preanalyzed tablets was 99.7 %. The results were statistically in concordance with that of chloranil method, which was formerly developed. Data obtained shows that the developed method can be used for determination of AB in tablets.