用络合材料去除抗癌药物对细菌生长的抑制作用

Maïté Sangnier, Guillaume Bouguéon, A. Berroneau, V. Dubois, S. Crauste-Manciet
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引用次数: 1

摘要

摘要针对医院药房批量生产细胞毒性药物,需要进行无菌检验的情况,目的是验证快速微生物学方法(RMM)的使用,并制定适当的中和方法,以抑制细菌生长。选择3种用于批量生产的抗癌药物(5氟尿嘧啶、伊立替康和奥沙利铂),在BacT/ALERT®系统上评估其潜在的微生物生长抑制作用。在细胞毒药物中,采用快速微生物学方法,只有5FU对微生物生长有抑制作用。为了抵消这种影响,我们的目的是使用中和剂络合药物,即。活性炭或离子交换树脂。5FU的微生物杀菌浓度很低(1.10-4 mg/mL),说明在无菌试验前绝对需要中和全药。采用高效液相色谱法对中和剂后溶液中残留的5FU浓度进行了验证。当先前稀释为5mg /mL时,只有活性炭能够完全捕获5FU。相反,在研究条件下,无论稀释程度如何,树脂都不能完全捕获5FU。活性炭处理后的BacT/ALERT®系统上的微生物生长成功证实为金黄色葡萄球菌。根据这一验证结果,然后制定了一种方法,以便能够对生产的批次进行常规无菌检查,并对五种微生物物种(如:金黄色葡萄球菌、铜绿假单胞菌、枯草芽孢杆菌、白色念珠菌、巴西曲霉)。我们的工作为考虑用快速微生物学方法进行无菌检测提供了新的见解,即使对微生物生长有抑制作用的药物也是如此。
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Removal of bacterial growth inhibition of anticancer drugs by using complexation materials
Abstract In the context of batch production of cytotoxic drugs in hospital pharmacies with the need of sterility testing, the objective was to validate the use of Rapid Microbiological Method (RMM), and to develop adequate neutralization method in case of inhibition of bacterial growth. The potential microbiological growth inhibitory effect of three anticancer drugs (5 fluorouracil, irinotecan and oxaliplatin) selected for batch production was assessed on BacT/ALERT® system. Among cytotoxic drugs, only 5FU exhibited inhibitory effect on microbiological growth using rapid microbiological method. To counteract this effect our purpose was to use neutralizing agents complexing the drug i. e. activated carbon or ion exchange resins. The microbiological bactericidal concentration of 5FU was very low (1.10–4 mg/mL) indicating the absolute need to neutralize the whole drug before sterility test. The complexation was validated by High Performance Liquid Chromatography control of the residual 5FU concentration in solution after the use of neutralizing agents. Only activated carbon was able to fully capture 5FU when previously diluted at 5 mg/mL. Conversely, the resins, in the condition of the study, were not able to fully capture 5FU whatever the dilution. The microbiological growth on BacT/ALERT® system after active carbon treatment was successfully confirmed with Staphylococcus aureus. Based on this validation results a method was then developed to routinely be able to perform sterility test of the batches produced and was confirmed on five microbiological species (i. e. S. aureus, Pseudomonas aeruginosa, Bacillus subtilis, Candida albicans, Aspergillus brasiliensis). Our work gives a new insight for considering sterility testing by rapid microbiological method even for drugs exhibiting inhibitory effect on microbiological growth.
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