Suppr超能文献

冻干羊膜和骨移植辐射灭菌剂量的验证。

Validation of radiation sterilization dose for lyophilized amnion and bone grafts.

作者信息

Hilmy N, Febrida A, Basril A

机构信息

Batan Research Tissue Bank (BRTB), Centre for Research and Development of Isotopes and Radiation Technology, Batan, PO Box 7002, JKSKL Jakarta 12070, Indonesia.

出版信息

Cell Tissue Bank. 2000;1(2):143-8. doi: 10.1023/A:1010129720363.

Abstract

A limited number of grafts produced in one batch is the main constrain to validate radiation sterilization dose of amnion and bone grafts according to ISO standard. The validation experiments done were according to ISO 13409 with a slight modification in sampling method. The experiments were carried out three times by using 20 samples each, 10 for bio-burden enumeration and 10 for sterility test at verification dose. The average bio-burden with sample item portion (SIP) = 1 for amnion membranes were 98, 50 and 69 cfu respectively and 0 cfu for bone grafts. Verification dose experiments, were done at doses of 2.90 kGy for bone grafts and 5.13 kGy for amnion grafts and the results of sterility tests showed that amnion grafts got one positive and bone grafts got 0 positive. The results met the requirements of ISO 13409 so that the radiation sterilization dose, at sterility assurance level of 10(-6) was 25 kGy for both amnion and bone grafts. Viral contamination was excluded in this experiment.

摘要

根据ISO标准验证羊膜和骨移植物的辐射灭菌剂量时,一批生产的移植物数量有限是主要限制因素。所做的验证实验依据ISO 13409,在采样方法上稍有改动。实验进行了三次,每次使用20个样本,其中10个用于生物负荷计数,10个用于验证剂量下的无菌测试。羊膜样本项目部分(SIP)=1时的平均生物负荷分别为98、50和69 cfu,骨移植物的平均生物负荷为0 cfu。验证剂量实验中,骨移植物的剂量为2.90 kGy,羊膜移植物的剂量为5.13 kGy,无菌测试结果显示羊膜移植物有1个阳性,骨移植物有0个阳性。结果符合ISO 13409的要求,因此在无菌保证水平为10^(-6)时,羊膜和骨移植物的辐射灭菌剂量均为25 kGy。本实验排除了病毒污染。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验