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首页> 外文期刊>Journal of Liquid Chromatography & Related Technologies >A VALIDATED STABILITY INDICATING UPLC METHOD FOR SIMULTANEOUS DETERMINATION OF ASSAY, RELATED SUBSTANCES, AND DEGRADATION PRODUCTS OF PALIPERIDONE PALMITATE ACTIVE PHARMACEUTICAL INGREDIENT AND ITS PHARMACEUTICAL INJECTION FORMS
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A VALIDATED STABILITY INDICATING UPLC METHOD FOR SIMULTANEOUS DETERMINATION OF ASSAY, RELATED SUBSTANCES, AND DEGRADATION PRODUCTS OF PALIPERIDONE PALMITATE ACTIVE PHARMACEUTICAL INGREDIENT AND ITS PHARMACEUTICAL INJECTION FORMS

机译:验证稳定性的UPLC方法,同时测定帕利哌酮棕榈酸酯活性药物成分及其药物注射剂的含量,相关物质和降解产物

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A simple, sensitive, and reproducible ultra-performance liquid chromatography (UPLC) coupled with a photodiode array detector method was developed for the quantitative determination of Paliperidone palmitate in API and pharmaceutical injectable forms. The method is applicable to the quantification of related substances and assay of Paliperidone palmitate. Chromatographic separation was achieved on Acquity UPLC BEH (50 mm, 2.1 mm, and 1.7 µm) C-18 column, and the impurities are eluted with a gradient program of runtime about 10.0 min. The eluted compounds were monitored at 238 nm, the flow rate was 0.5 mL/min, and the column oven temperature was maintained at 35°C. The resolution of Paliperidone palmitate and eight (potential, bi-products and degradation) impurities was greater than 2.0 for all pairs of components. The high correlation coefficient (r2  0.999) values indicated clear correlations between the investigated compound concentrations and their peak areas within the test ranges. The repeatability and intermediate precision, expressed by RSD, were less than 10.0%. The accuracy and validity of the method were further ascertained by performing recovery studies via a spike method. The accuracy of the method expressed as relative error was satisfactory. The drug was subjected to the 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 for specificity, limit of detection, limit of quantification, linearity, accuracy, precision, ruggedness, and robustness.View full textDownload full textKeywordsforced degradation, method development, paliperidone palmitate, 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/10.1080/10826076.2011.601503
机译:开发了一种简单,灵敏,可重现的超高效液相色谱(UPLC)和光电二极管阵列检测器方法,用于定量测定API和药物注射形式的帕潘立酮棕榈酸酯。该方法适用于相关物质的定量和棕榈酸帕潘立酮的测定。在Acquity UPLC BEH(50 mm,2.1 mm和1.7 µm)C-18色谱柱上实现色谱分离,并使用约10.0 min的运行时梯度程序洗脱了杂质。洗脱的化合物在238 nm处进行监测,流速为0.5 mL / min,并且柱箱温度保持在35°C。对于所有成对组分,帕潘立酮棕榈酸酯和八种(潜在的,副产物和降解的)杂质的分离度均大于2.0。高的相关系数(r2> 0.999)值表明调查的化合物浓度与其在测试范围内的峰面积之间的明确相关性。用RSD表示的重复性和中间精度均小于10.0%。该方法的准确性和有效性通过使用穗状细胞方法进行回收率研究进一步确定。用相对误差表示的方法的准确性令人满意。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目前的ICH指南进行了验证,包括特异性,检测限,定量限,线性,准确性,精密度,坚固性和鲁棒性。 ,UPLC,validationRelated var addthis_config = {ui_cobrand:“泰勒和弗朗西斯在线”,servicescompact:“ citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,更多”,发布日期:“ ra-4dff56cd6bb1830b” };添加到候选列表链接永久链接http://dx.doi.org/10.1080/10826076.2011.601503

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