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首页> 外文期刊>Journal of separation science. >Development of a HPTLC method for in-process purity testing of pentoxifylline
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Development of a HPTLC method for in-process purity testing of pentoxifylline

机译:开发用于己酮可可碱的过程纯度测试的HPTLC方法

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摘要

A HPTLC method for the separation and identification of pentoxifylline and related substances, impurities of reaction partners, and side reaction products has been developed using different mobile and stationary phases. For quantitative assay of possible by-products as impurities, LiChrosphere (R) RP-18 F254s chromatoplates, acetone-chloroform-toluene-dioxane (221:11 v/v) as a mobile phase, and detection at 275 nm were employed. Linearity (r >= 0.997), recovery (86.5-115.5%), and determination limit (0.1-0.6%) were evaluated and found to be satisfactory. This method enables monitoring of the synthesis, as well as purity control of pentoxifylline-containing raw materials and pharmaceuticals.
机译:已开发出使用不同的流动相和固定相分离和鉴定己酮可可碱及相关物质,反应伙伴的杂质和副反应产物的HPTLC方法。为了定量分析可能的副产物杂质,使用LiChrosphere®RP-18 F254s色谱板,使用丙酮-氯仿-甲苯-二恶烷(221:11 v / v)作为流动相,并在275 nm处检测。评估线性(r> = 0.997),回收率(86.5-115.5%)和测定极限(0.1-0.6%),结果令人满意。该方法能够监测合成,并控制含有己酮可可碱的原料和药物的纯度。

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