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Sterilization of Drug-Loaded Composite Coatings for Implantable Glucose Biosensors

机译:用于可植入葡萄糖生物传感器的药物加载复合涂层的灭菌

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Background: An anti-inflammatory drug-loaded composite coating (dexamethasone-loaded poly (lactic-co-glycolic acid) [PLGA] microspheres/polyvinyl alcohol [PVA] hydrogel) was previously developed to counter the foreign body reaction to a fully implantable continuous glucose monitoring biosensor. The long-term sensor functionality was ensured in the presence of the drug-loaded composite coating thus facilitating better diabetes control and management. In order to advance such a drug-device combination product toward clinical testing, addressing sterilization remains a key step due to the heterogeneity of the product components. The main objective of this research was to investigate the effect of two terminal sterilization techniques: gamma radiation and ethylene oxide (EO) on the stability of the anti-inflammatory coatings as well as retention of the glucose sensing ability of the implantable sensor. Method: The composite coatings, their individual components, and the glucose-sensing elements of the biosensor were subjected to low-temperature gamma radiation and EO cycles. Detailed characterization was conducted on all components before and after sterilization. Results: Exposure to gamma radiation affected dexamethasone crystallinity and glucose response linearity of the sensing element, whereas physical aging of microspheres in composite coatings was observed poststerilization with EO. Despite these effects, dexamethasone drug release from coatings was not significantly affected by either technique. Conclusion: The research findings indicate that both sterilization techniques are feasible for the sterilization of the dexamethasone-loaded PLGA microspheres/PVA hydrogel composite coatings, while EO was preferred for the sterilization of the glucose-sensing element of the biosensor.
机译:背景:先前开发了一种抗炎药物加载的复合涂层(含有地塞塞酮加载的聚(乳酸 - 共乙醇酸)φ微球/聚乙烯醇[PVA]水凝胶),以对抗异物反应对完全植入的连续葡萄糖监测生物传感器。在载有药物加载的复合涂层存在下确保了长期传感器功能,从而促进了更好的糖尿病控制和管理。为了推进这种药物装置组合产品探讨临床测试,寻址灭菌仍然是由于产品组分的异质性仍然是一个关键步骤。本研究的主要目的是研究两个末端灭菌技术:γ辐射和环氧乙烷(EO)对抗炎涂层的稳定性以及植入传感器的葡萄糖感测能力的影响。方法:对生物传感器的复合涂层,各个组分和葡萄糖感测元件进行低温γ辐射和EO循环。在灭菌之前和之后的所有组分上进行了详细表征。结果:暴露于γ辐射影响传感元件的地塞米松结晶度和葡萄糖响应线性,而用EO观察到复合涂层中微球的物理老化。尽管有这些效果,从涂层中脱塞米松药物释放不受任何一种技术的显着影响。结论:研究结果表明,两种灭菌技术都可用于灭菌的地塞米松加载的PLGA微球/ PVA水凝胶复合涂层,而EO是优选的生物传感器的葡萄糖传感元件的灭菌。

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