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Development of supercritical fluid (carbon dioxide) based ultra performance convergence chromatographic stability indicating assay method for the determination of clofarabine in injection

机译:基于超临界流体(二氧化碳)的超高性能收敛色谱稳定性指示法测定注射用氯法拉滨的研制

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摘要

The present study reports the development and validation of a stability indicating assay method for clofarabine in injection on a UPC2a?¢ (ultra performance convergence chromatography) instrument, which utilizes the unrealized potential of supercritical fluid chromatography. The use of UPC2a?¢ provides a single viable technique that is a sustainable, reduced cost, and green technology that lowers the use of organic solvents. Based on this advantage, we explored a simple and robust method in order to increase sample throughput and productivity to quantify clofarabine in the presence of its potential impurities and other degradants. The separation was achieved on a BEH-2-ethyl pyridine (BEH 2EP) column (100 mm ?— 3.0 mm I.D. with an average pore diameter of 1.7 ??m) by using methanol as a co-solvent and carbon dioxide as a mobile phase in the ratio of 30:70. The detection is carried out at a wavelength of 254 nm. We are able to achieve the separation of clofarabine from its potential impurities and other degradants in less than 6 minutes with a low amount of solvent consumption. The new method is validated in accordance with the ICH-guidelines and exhibited good intra- and inter-day precision, accuracy and linearity (r2 a‰¥ 0.999) over a range of 50% to 150% of target concentration.
机译:本研究报告了在UPC2a?3(超高性能收敛色谱)仪器上注射氯法拉滨的稳定性指示测定方法的开发和验证,该方法利用了超临界流体色谱的潜在潜力。使用UPC2a™可以提供一种可行的技术,这种技术是可持续的,降低了成本,并且是绿色技术,可以减少有机溶剂的使用。基于这一优势,我们探索了一种简单而可靠的方法,以提高样品的通量和生产率,从而在存在潜在杂质和其他降解物的情况下对氯法拉滨进行定量。通过使用甲醇作为助溶剂和二氧化碳作为移动溶剂,在BEH-2-乙基吡啶(BEH 2EP)色谱柱(100 mmβ-3.0 mm内径,平均孔径为1.7μm)上实现分离。相的比例为30:70。该检测在254nm的波长下进行。我们能够在不到6分钟的时间内以较低的溶剂消耗量将氯法拉滨与潜在的杂质和其他降解物分离。该新方法已按照ICH指南进行了验证,并且在目标浓度的50%至150%范围内显示出良好的日内和日间精度,准确度和线性(r2 a ¥¥ 0.999)。

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