[Raman spectroscopy applied to analytical quality control of injectable drugs: analytical evaluation and comparative economic versus HPLC and UV / visible-FTIR].

Journal de pharmacie de Belgique Pub Date : 2013-09-01
P Bourget, A Amin, F Vidal, C Merlette, P Troude, O Corriol
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Abstract

In France, central IV admixture of chemotherapy (CT) treatments at the hospital is now required by law. We have previously shown that the shaping of Therapeutic Objects (TOs) could profit from an Analytical Quality Assurance (AQA), closely linked to the batch release, for the three key parameters: identity, purity, and initial concentration of the compound of interest. In the course of recent and diversified works, we showed the technical superiority of non-intrusive Raman Spectroscopy (RS) vs. any other analytical option and, especially for both HPLC and vibrational method using a UV/visible-FTIR coupling. An interconnected qualitative and economic assessment strongly helps to enrich these relevant works. The study compares in operational situation, the performance of three analytical methods used for the AQC of TOs. We used: a) a set of evaluation criteria, b) the depreciation tables of the machinery, c) the cost of disposables, d) the weight of equipment and technical installations, e) the basic accounting unit (unit of work) and its composite costs (Euros), which vary according to the technical options, the weight of both human resources and disposables; finally, different combinations are described. So, the unit of work can take 12 different values between 1 and 5.5 Euros, and we provide various recommendations. A qualitative evaluation grid constantly places the SR technology as superior or equal to the 2 other techniques currently available. Our results demonstrated: a) the major interest of the non-intrusive AQC performed by RS, especially when it is not possible to analyze a TO with existing methods e.g. elastomeric portable pumps, and b) the high potential for this technique to be a strong contributor to the security of the medication circuit, and to fight the iatrogenic effects of drugs especially in the hospital. It also contributes to the protection of all actors in healthcare and of their working environment.

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[拉曼光谱在注射药物分析质量控制中的应用:与高效液相色谱和紫外/可见光-红外光谱的分析评价和比较经济学]。
在法国,法律现在要求医院进行中央静脉注射化疗(CT)治疗。我们之前已经表明,治疗对象(TOs)的成型可以从分析质量保证(AQA)中获益,与批释放密切相关,用于三个关键参数:感兴趣化合物的身份,纯度和初始浓度。在最近和多样化的工作过程中,我们展示了非侵入性拉曼光谱(RS)相对于任何其他分析选择的技术优势,特别是HPLC和使用UV/可见光- ftir耦合的振动方法。相互关联的定性和经济评估有力地有助于丰富这些相关工作。研究比较了三种分析方法在实际应用中的性能。我们使用了:a)一套评估标准,b)机械折旧表,c)一次性成本,d)设备和技术装置的重量,e)基本会计单位(工作单位)及其复合成本(欧元),根据技术选择,人力资源和一次性的重量而变化;最后,描述了不同的组合。因此,工作单位可以取1到5.5欧元之间的12个不同的值,我们提供各种建议。一个定性评估网格不断地将SR技术定位为优于或等于目前可用的其他两种技术。我们的研究结果表明:a) RS执行的非侵入式AQC的主要利益,特别是当无法使用现有方法(例如弹性便携式泵)分析to时;b)该技术具有很高的潜力,可以为药物电路的安全性做出强有力的贡献,并对抗药物的医源性影响,特别是在医院。它还有助于保护保健领域的所有行为者及其工作环境。
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