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ABSTRACT Validation of High Performance Liquid Chromatography for Quantitative Analysis of Curcumin in Capsule Dosage Form Curcumin, the major yellow pigment of Curcuma sp. has several teresting biological activities, such as anticarcinogenecity, antiinflamatory tioxidant. Curcumin naturally occurs as major compound in curcumino bstance beside its derivatives, i.e. bisdemethoxycurcumin (BDC) methoxycurcumin (DC). Quantitative analysis of curcumin is difficult to carry out less prior to completely resolved curcumin from BDC and DC. A good resolution, producible, and accurate method for determination curcumin in pharmaceutical oduct (capsule formed) by HPLC has been carried out. Using C18 column and xture of acetonitrile: 1 % acetic acid glacial (45:55 v/v) as eluent; BDC, DC, an rcumin were retained with retention time of 10.79, 12.29, and 13.91 minutes, spectively. Curcumin was simultaneously separated from BDC or DC. The solution factor (Rs) between curcumin and DC was 1.73. Good linear relationship (r 0.9997, Vxo = 0.99 %) between peak area and concentrations was found at range of e curcumin concentration (23.5662.83) µg/ mL. Curcumin recoveries were (93.60- 8.17) % with the coefficient of variation (CV) 6.99 %. Curcumin content in each capsule sample was found to be (8.89 ± 0.06) mg. It showed that samples contained higher amount of curcumin than that claimed on its label, 5 mg. Keywords: Bisdemethoxycurcumin, Demethoxycurcumin,Curcumin,

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ABSTRACT. Validation of High Performance Liquid Chromatography for Quantitative. Analysis of Curcumin in Capsule Dosage Form. Curcumin, the major yellow pigment of Curcuma sp . has several - PowerPoint PPT Presentation

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ABSTRACT

Validation of High Performance Liquid Chromatography for QuantitativeAnalysis of Curcumin in Capsule Dosage Form

Curcumin, the major yellow pigment of Curcuma sp. has severalinteresting biological activities, such as anticarcinogenecity, antiinflamatory, andantioxidant. Curcumin naturally occurs as major compound in curcuminoidsubstance beside its derivatives, i.e. bisdemethoxycurcumin (BDC) anddemethoxycurcumin (DC). Quantitative analysis of curcumin is difficult to carry outunless prior to completely resolved curcumin from BDC and DC. A good resolution,reproducible, and accurate method for determination curcumin in pharmaceuticalproduct (capsule formed) by HPLC has been carried out. Using C18 column andmixture of acetonitrile: 1 % acetic acid glacial (45:55 v/v) as eluent; BDC, DC, andcurcumin were retained with retention time of 10.79, 12.29, and 13.91 minutes,respectively. Curcumin was simultaneously separated from BDC or DC. Theresolution factor (Rs) between curcumin and DC was 1.73. Good linear relationship (r= 0.9997, Vxo = 0.99 %) between peak area and concentrations was found at range ofthe curcumin concentration (23.5662.83) µg/ mL. Curcumin recoveries were (93.60-118.17) % with the coefficient of variation (CV) 6.99 %.

Curcumin content in each capsule sample was found to be (8.89 ± 0.06) mg. Itshowed that samples contained higher amount of curcumin than that claimed on itslabel, 5 mg.

Keywords: Bisdemethoxycurcumin, Demethoxycurcumin,Curcumin,