Bernard Lise, Cueff Régis, Bourdeaux Daniel, Breysse Colette, Sautou Valérie
CHU Clermont-Ferrand, Pôle Pharmacie, rue Montalembert, 63003, Clermont-Ferrand, France,
Anal Bioanal Chem. 2015 Feb;407(6):1651-9. doi: 10.1007/s00216-014-8426-z. Epub 2015 Jan 11.
Medical devices (MDs) for infusion and enteral and parenteral nutrition are essentially made of plasticized polyvinyl chloride (PVC). The first step in assessing patient exposure to these plasticizers, as well as ensuring that the MDs are free from di(2-ethylhexyl) phthalate (DEHP), consists of identifying and quantifying the plasticizers present and, consequently, determining which ones are likely to migrate into the patient's body. We compared three different extraction methods using 0.1 g of plasticized PVC: Soxhlet extraction in diethyl ether and ethyl acetate, polymer dissolution, and room temperature extraction in different solvents. It was found that simple room temperature chloroform extraction under optimized conditions (30 min, 50 mL) gave the best separation of plasticizers from the PVC matrix, with extraction yields ranging from 92 to 100% for all plasticizers. This result was confirmed by supplemented Fourier transform infrared spectroscopy-attenuated total reflection (FTIR-ATR) and gravimetric analyses. The technique was used on eight marketed medical devices and showed that they contained different amounts of plasticizers, ranging from 25 to 36% of the PVC weight. These yields, associated with the individual physicochemical properties of each plasticizer, highlight the need for further migration studies.
用于输液以及肠内和肠外营养的医疗设备(MDs)主要由增塑聚氯乙烯(PVC)制成。评估患者对这些增塑剂的接触情况以及确保医疗设备不含邻苯二甲酸二(2-乙基己基)酯(DEHP)的第一步,包括识别和量化存在的增塑剂,并据此确定哪些增塑剂可能迁移到患者体内。我们使用0.1 g增塑PVC比较了三种不同的提取方法:在乙醚和乙酸乙酯中进行索氏提取、聚合物溶解以及在不同溶剂中进行室温提取。结果发现,在优化条件(30分钟,50毫升)下进行简单的室温氯仿提取能使增塑剂从PVC基质中得到最佳分离,所有增塑剂的提取产率在92%至100%之间。补充傅里叶变换红外光谱 - 衰减全反射(FTIR - ATR)和重量分析证实了这一结果。该技术应用于八种市售医疗设备,结果表明它们含有不同量的增塑剂,占PVC重量的25%至36%。这些产率以及每种增塑剂的个体物理化学性质凸显了进一步进行迁移研究的必要性。