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Sterilization of allograft bone: is 25 kGy the gold standard for gamma irradiation?同种异体骨的灭菌:25千戈瑞是伽马射线辐照的金标准吗?
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灭菌环糊精药物递送系统的热机械性能、抗生素释放及生物活性

Thermomechanical Properties, Antibiotic Release, and Bioactivity of a Sterilized Cyclodextrin Drug Delivery System.

作者信息

Halpern Jeffrey M, Gormley Catherine A, Keech Melissa, von Recum Horst A

机构信息

Case Western Reserve University, Department of Biomedical Engineering, 10900 Euclid Ave, Cleveland, OH 44118 USA ; Tel: +1 (216) 368-4969.

出版信息

J Mater Chem B. 2014 May 14;2(18):2764-2772. doi: 10.1039/C4TB00083H.

DOI:10.1039/C4TB00083H
PMID:24949201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4058863/
Abstract

Various local drug delivery devices and coatings are being developed as slow, sustained release mechanism for drugs, yet the polymers are typically not evaluated after commercial sterilization techniques. We examine the effect that commercial sterilization techniques have on the physical, mechanical, and drug delivery properties of polyurethane polymers. Specifically we tested cyclodextrin-hexamethyl diisocyanate crosslinked polymers before and after autoclave, ethylene oxide, and gamma radiation sterilization processes. We found that there is no significant change in the properties of polymers sterilized by ethylene oxide and gamma radiation compared to non-sterilized polymers. Polymers sterilized by autoclave showed increased tensile strength (p<0.0001) compared to non-sterilized polymers . In the release of drugs, which were loaded after the autoclave sterilization process, we observed a prolonged release (p<0.05) and a prolonged therapeutic effect (p<0.05) but less drug loading (p<0.0001) compared to non-sterilized polymers. The change in the release profile and tensile strength in polymers sterilized by autoclave was interpreted as being caused by additional crosslinking from residual, unreacted, or partially-reacted crosslinker contained within the polymer. Autoclaving therefore represents additional thermo-processing to modify rate and dose from polyurethanes and other materials.

摘要

各种局部给药装置和涂层正在被开发作为药物的缓慢、持续释放机制,然而聚合物通常在商业灭菌技术之后未被评估。我们研究了商业灭菌技术对聚氨酯聚合物的物理、机械和药物递送性能的影响。具体而言,我们测试了在高压灭菌、环氧乙烷和伽马射线灭菌过程之前和之后的环糊精 - 六亚甲基二异氰酸酯交联聚合物。我们发现,与未灭菌的聚合物相比,经环氧乙烷和伽马射线灭菌的聚合物的性能没有显著变化。与未灭菌的聚合物相比,经高压灭菌的聚合物显示出拉伸强度增加(p<0.0001)。在高压灭菌过程后加载药物的释放中,我们观察到与未灭菌的聚合物相比,释放延长(p<0.05)和治疗效果延长(p<0.05),但药物负载量较少(p<0.0001)。经高压灭菌的聚合物中释放曲线和拉伸强度的变化被解释为由聚合物中所含残留、未反应或部分反应的交联剂的额外交联引起。因此,高压灭菌代表了用于改变聚氨酯和其他材料的速率和剂量的额外热处理。