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首页> 外文期刊>Cell and tissue banking: An international journal of banking, engineering & transplantation of cells and tissues >Validation of the BacT/ALERT ~?3D automated culture system for the detection of microbial contamination of epithelial cell culture medium
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Validation of the BacT/ALERT ~?3D automated culture system for the detection of microbial contamination of epithelial cell culture medium

机译:BacT / ALERT〜?3D自动培养系统用于检测上皮细胞培养基中微生物污染的验证

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Living tissue engineering for regenerative therapy cannot withstand the usual pharmacopoeia methods of purification and terminal sterilization. Consequently, these products must be manufactured under aseptic conditions at microbiologically controlled environment facilities. This study was proposed to validate BacT/ALERT ~?3D automated culture system for microbiological control of epithelial cell culture medium (ECCM). Suspensions of the nine microorganisms recommended by the European Pharmacopoeia (Chap. 2.6.27: ''Microbiological control of cellular products''), plus one species from oral mucosa and two negative controls with no microorganisms were prepared in ECCM. They were inoculated in FA (anaerobic) and SN (aerobic) culture bottles (Biomérieux, Lyon, France) and incubated in a BacT/ALERT ~?3D automated culture system. For each species, five sets of bottles were inoculated for reproducibility testing: one sample was incubated at the French Health Products Agency laboratory (reference) and the four others at Cell and Tissue Bank of Lyon, France. The specificity of the positive culture bottles was verified by Gram staining and then subcultured to identify the microorganism grown. The BacT/ALERT ~?3D system detected all the inoculated microorganisms in less than 2 days except Propionibacterium acnes which was detected in 3 days. In conclusion, this study demonstrates that the BacT/ALERT ~?3D system can detect both aerobic and anaerobic bacterial and fungal contamination of an epithelial cell culture medium consistent with the European Pharmacopoeia chapter 2.6.27 recommendations. It showed the specificity, sensitivity, and precision of the BacT/ALERT ~?3D method, since all the microorganisms seeded were detected in both sites and the uncontaminated medium ECCM remained negative at 7 days.
机译:用于再生疗法的活体组织工程无法承受常规的药典方法进行纯化和最终灭菌。因此,这些产品必须在无菌条件下在微生物控制的环境设施中生产。本研究旨在验证BacT / ALERT〜3D自动培养系统对上皮细胞培养基(ECCM)的微生物控制。在ECCM中制备了欧洲药典推荐的9种微生物的悬浮液(第2.6.27章:“细胞产品的微生物控制”),以及口腔粘膜中的一种和两种不含微生物的阴性对照。将它们接种在FA(厌氧)和SN(需氧)培养瓶(法国,里昂,Biomérieux)中,并在BacT / ALERT〜?3D自动培养系统中孵育。对于每个物种,接种五组瓶子以进行再现性测试:其中一个样品在法国卫生产品局实验室(参考)中孵育,另外四个在法国里昂细胞和组织库中孵育。通过革兰氏染色验证阳性培养瓶的特异性,然后继代培养以鉴定生长的微生物。 BacT / ALERT〜?3D系统在不到2天的时间内检测到了所有接种的微生物,除了痤疮丙酸杆菌在3天内被检测到。总之,这项研究表明,BacT / ALERT〜?3D系统可以检测上皮细胞培养基中的好氧和厌氧细菌和真菌污染,符合《欧洲药典》第2.6.27章的建议。它显示了BacT / ALERT〜?3D方法的特异性,灵敏性和精密度,因为在这两个位置都检测到了所有接种的微生物,并且未污染的ECCM培养基在7天仍呈阴性。

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