首页> 美国卫生研究院文献>The Journal of Automatic Chemistry >Validation of an RPHPTLC-Densitometric Method Using Silica Gel 60 RP18WF254 for Simultaneous Determination of Nicotinamide in Selected Pharmaceutical Formulations
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Validation of an RPHPTLC-Densitometric Method Using Silica Gel 60 RP18WF254 for Simultaneous Determination of Nicotinamide in Selected Pharmaceutical Formulations

机译:验证使用硅胶60 RP18WF254进行RPHPTLC密度测定法同时测定选定药物制剂中的烟酰胺的有效性

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摘要

This research study describes the applicability of silica gel 60 RPW18F254 plates for the development and validation of new, simple, economic, accurate, and precise RPHPTLC-densitometric method suitable for the quantification of nicotinamide (as Vitamin PP) in three marketed preparations. The mobile phase used was methanol-water in volume composition 3 : 7. Detection wavelength was 200 nm. The proposed method was validated according to ICH guidelines and also based on Ferenczi-Fodor and Konieczka reports. Results were found to be linear over a range of 1.00 to 2.00 μg/spot. Limit of detection (LOD) and limit of quantification (LOQ) were 0.15 μg/spot and 0.45 μg/spot, respectively. The percent content of nicotinamide in the investigated preparations was found to be 99.2% (Product 1), 99.3% (Product 2), and 99.4% (Product 3). Developed method is accurate and precise (CV < 3%) and may be successfully applied for the quality control of pharmaceutical formulations containing nicotinamide in the presence of its derivatives, such as N,N-diethylnicotinamide, N-methylnicotinamide, and nicotinic acid.
机译:这项研究描述了硅胶60 RPW18F254板在开发和验证适用于定量三种市售制剂中烟酰胺(作为维生素PP)的新型,简单,经济,准确和精确的RPHPTLC光密度法的适用性。所用的流动相为甲醇-水,体积比为3:7,检测波长为200 nm。根据ICH指南以及Ferenczi-Fodor和Konieczka的报告对提出的方法进行了验证。发现结果在1.00至2.00μg/ s范围内呈线性。检测限(LOD)和定量限(LOQ)分别为0.15μg/ s和0.45μg/ s。发现所研究制剂中烟酰胺的百分比含量为99.2%(产品1),99.3%(产品2)和99.4%(产品3)。所开发的方法准确,精确(CV <3%),并且可以成功地用于含有烟酰胺的药物制剂的质量控制,该药物制剂包括N,N-二乙基烟酰胺,N-甲基烟酰胺和烟酸。

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