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首页> 外文期刊>International Journal of Pharmaceutics >A UV-Raman spectrometry method for quality control of anticancer preparations: Results after 18 months of implementation in hospital pharmacy
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A UV-Raman spectrometry method for quality control of anticancer preparations: Results after 18 months of implementation in hospital pharmacy

机译:用于抗癌制剂质量控制的紫外拉曼光谱法:在医院药房实施18个月后的结果

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摘要

In France, chemotherapy preparation units of hospital pharmacy compound cytotoxic infusion bags adapted to each patient. The narrow therapeutic index of these preparations led us to implement qualitative and quantitative control for patients' safety. To this aim, we calibrated an equipment combining UV-vis spectrometry and Raman spectroscopy (QC Prep+(R)) and monitored 14 different molecule-solvent combinations over a 18 months period. This rapid and specific method allowed the qualitative and quantitative analysis of 1 mL sample tests in less than 2 min. On 5742 anticancer preparations, we obtained accepted results with more than 99.4% solvent identification, 99.6% drug identification and only 1.52% of preparations not matching quantitative specifications (+/- 15% of theoretical concentration). This quantitative control enabled us to pinpoint some critical points of production for two of the most common preparations. We thus updated the procedures of reconstitution and preparation, increasing the quality of final product. UV-Raman spectrometry is thus an effective tool to control chemotherapy infusions and to improve good practices of preparation. (C) 2016 Elsevier B.V. All rights reserved.
机译:在法国,医院药房的化学疗法制备单位采用了适合每个患者的复合细胞毒性输液袋。这些制剂的狭窄治疗指数促使我们对患者的安全性进行定性和定量控制。为此,我们校准了将紫外可见光谱法和拉曼光谱法(QC Prep +(R))相结合的设备,并在18个月的时间内监测了14种不同的分子-溶剂组合。这种快速而特定的方法允许在不到2分钟的时间内对1 mL样品测试进行定性和定量分析。在5742种抗癌制剂上,我们获得了可接受的结果,其中溶剂鉴定率超过99.4%,药物鉴定率超过99.6%,只有1.52%的制剂与定量规格不符(理论浓度的+/- 15%)。这种定量控制使我们能够为两种最常用的制剂确定生产的关键点。因此,我们更新了重组和准备程序,提高了最终产品的质量。因此,紫外拉曼光谱法是控制化学疗法输注和改善准备的良好做法的有效工具。 (C)2016 Elsevier B.V.保留所有权利。

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