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首页> 外文期刊>Bulletin of Faculty of Pharmacy, Cairo University >Simultaneous determination of Carbazochrome and Troxerutin in their binary mixture by HPLC and HPTLC-Densitometric methods
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Simultaneous determination of Carbazochrome and Troxerutin in their binary mixture by HPLC and HPTLC-Densitometric methods

机译:HPLC和HPTLC-光密度法同时测定二元混合物中的咔唑铬和曲霉菌素

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Two accurate, precise and sensitive RP-HPLC and HPTLC-Densitometric methods have been developed for the determination of Carbazochrome and Troxerutin in their binary mixture without previous separation. Method (A) is RP-HPLC which depended on isocratic elution using C 18 column and mobile phase consisting of water containing (0.2% triethylamine (TEA), 1% tetrahydrofuran (THF)):methanol (65:35, by volume) at a flow rate of 1.5 mL min ?1 and the effluent was monitored at 350 nm. Good resolution was obtained with t R values of 2.069 and 5.174 min for Carbazochrome and Troxerutin, respectively. Method (B) is HPTLC-Densitometric method, using silica gel 60 F 254 HPTLC plates and methanol:chloroform:ammonia (40:60:7, by volume) as a developing system. The bands were scanned at 350 nm. The proposed methods have been validated as per ICH guidelines and their linearity was evident in the ranges of 0.25–10 and 5–50 μg mL ?1 for method (A) and 0.02–0.8 and 0.1–2 μg band ?1 for method (B) for Carbazochrome and Troxerutin, respectively. The developed methods have been applied for the determination of the above mentioned drugs in their pharmaceutical formulation where no interference from the excipients has been detected. Statistical comparison of the results obtained by the developed methods and those obtained by the reported HPLC methods showed no significant difference between them. The developed methods are sensitive, accurate and precise and can be easily used for quality control analysis of the studied drugs.
机译:已经开发了两种准确,精确和灵敏的RP-HPLC和HPTLC-光密度测定法,无需事先分离即可测定二元混合物中的咔唑铬和曲克芦丁。方法(A)是RP-HPLC,该方法取决于使用C 18柱的等度洗脱和流动相,流动相由水(体积比为0.2%三乙胺(TEA),1%四氢呋喃(THF)):甲醇(体积比为65:35)组成流速为1.5 mL min?1,并在350 nm处监测流出液。咔唑色素和曲克芦丁的t R值分别为2.069和5.174分钟,获得了良好的分离度。方法(B)是HPTLC-光密度法,使用硅胶60 F 254 HPTLC板和甲醇:氯仿:氨(体积比为40∶60∶7)作为显影系统。带在350nm处扫描。所提议的方法已经按照ICH指南进行了验证,方法(A)的线性范围在0.25–10和5–50μgmL?1范围内;方法(0.02)的范围在0.02–0.8和0.1–2μgmL?1范围内( B)分别为咔唑色素和Troxerutin。在未检测到赋形剂干扰的情况下,已开发的方法已用于测定其药物制剂中的上述药物。通过开发的方法获得的结果与通过报道的HPLC方法获得的结果的统计比较表明,它们之间没有显着差异。所开发的方法灵敏,准确,精确,可轻松用于所研究药物的质量控制分析。

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