首页> 外文期刊>Journal of Liquid Chromatography & Related Technologies >IDENTIFICATION OF PRASUGREL (AN ANTIPLATELET DRUG) IMPURITIES BY LC-MS/MS, RAPID DETERMINATION OF PRASUGREL HYDROCHLORIDE-RELATED SUBSTANCES, AND DEGRADATION PRODUCTS IN ACTIVE PHARMACEUTICAL INGREDIENT AND PHARMACEUTICAL DOSAGE FORMS BY STABILITY INDICATING ULTRA-PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD
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IDENTIFICATION OF PRASUGREL (AN ANTIPLATELET DRUG) IMPURITIES BY LC-MS/MS, RAPID DETERMINATION OF PRASUGREL HYDROCHLORIDE-RELATED SUBSTANCES, AND DEGRADATION PRODUCTS IN ACTIVE PHARMACEUTICAL INGREDIENT AND PHARMACEUTICAL DOSAGE FORMS BY STABILITY INDICATING ULTRA-PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD

机译:LC-MS / MS鉴定普拉格雷(一种抗药性)杂质,快速测定盐酸普拉格雷的相关物质以及有效药物成分中的降解产物和通过化学比色法测定药物剂量形式的稳定性

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A simple, sensitive, and reproducible gradient reverse-phase ultra-performance liquid chromatographic (UPLC) method was developed for the quantitative determination of Prasugrel and all possible process-related impurities (positional isomers, degradants and byproducts) at the level of 0.5-2.0 µg mL−1. The main objective of this study is to control the impurities at crude and final stages of prasugrel hydrochloride. This method is applicable to drug substance and pharmaceutical dosage forms. Six potential impurities were formed during the process development, including the degradation products, and the desacetyl impurity existing in its keto and enol form was stabilized by using acidic pH. All these impurities were well separated primarily with a gradient HPLC method, based on their selectivity differences by using a polar embedded C8 column, monobasic potassium buffer, a basic organic modifier, and acetonitrile in the mobile phase. Initially, structures of all these impurities formed were identified by liquid chromatography equipped with mass spectrometer and further confirmed by spiking with the characterized impurities. The drug was subjected to International Conference on Harmonization (ICH) prescribed hydrolytic, oxidative, photolytic, and thermal stress conditions. The performance of the method was validated according to the present ICH guidelines.View full textDownload full textKeywordsforced degradation, identification by LC/MS/MS, Prasugrel hydrochloride, stability-indicating, UPLC, validationRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/10826076.2011.644052
机译:开发了一种简单,灵敏且可重现的梯度反相超高效液相色谱(UPLC)方法,用于定量测定普拉格雷和所有可能的过程相关杂质(位置异构体,降解物和副产物),含量为0.5-2.0微克mL â1。这项研究的主要目的是控制普拉格雷盐酸盐的粗制和最后阶段的杂质。该方法适用于原料药和药物剂型。在工艺开发过程中形成了六种潜在的杂质,包括降解产物,并通过使用酸性pH值稳定了以酮和烯醇形式存在的脱乙酰基杂质。通过使用极性嵌入式C8色谱柱,一元钾缓冲液,碱性有机改性剂和乙腈在流动相中的选择性差异,主要使用梯度HPLC方法将所有这些杂质很好地分离。首先,通过配备质谱仪的液相色谱法鉴定所有形成的所有杂质的结构,并通过加标有特征性杂质进一步确认。该药物经过国际协调会议(ICH)规定的水解,氧化,光解和热应激条件。该方法的性能已根据当前的ICH指南进行了验证。查看全文下载全文关键字强迫降解,通过LC / MS / MS鉴定,盐酸普拉格雷,稳定性指示,UPLC,验证相关的var addthis_config = {ui_cobrand:“ Taylor&Francis Online ”,services_compact:“ citeulike,网络振动,微博,technorati,美味,linkedin,facebook,stumbleupon,digg,google,更多”,发布号:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/10826076.2011.644052

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