Department of Biomedical Engineering, University of Connecticut, Storrs, CT, USA.
Department of Pathobiology and Veterinary Science, University of Connecticut, Storrs, CT, USA.
Nat Biomed Eng. 2021 Sep;5(9):998-1007. doi: 10.1038/s41551-020-00650-4. Epub 2020 Nov 23.
Repeated bolus injections are associated with higher costs and poor compliance and can hinder the implementation of global immunization campaigns. Here, we report the development and preclinical testing of patches of transdermal core-shell microneedles-which were fabricated by the micromoulding and alignment of vaccine cores and shells made from poly(lactic-co-glycolic acid) with varying degradability kinetics-for the preprogrammed burst release of vaccine payloads over a period of a few days to more than a month from a single administration. In rats, microneedles loaded with a clinically available vaccine (Prevnar-13) against the bacterium Streptococcus pneumoniae induced immune responses that were similar to immune responses observed after multiple subcutaneous bolus injections, and led to immune protection against a lethal bacterial dose. Microneedle patches delivering preprogrammed doses may offer an alternative strategy to prophylactic and therapeutic protocols that require multiple injections.
重复的推注与更高的成本和较差的顺应性有关,并且可能会阻碍全球免疫运动的实施。在这里,我们报告了经皮核心-壳型微针贴片的开发和临床前测试,该贴片是通过微成型和排列由聚(乳酸-共-乙醇酸)制成的疫苗核心和外壳制成的,这些核心和外壳具有不同的降解动力学,可在数天至一个月以上的时间内从单次给药中预编程释放疫苗有效负载。在大鼠中,负载有临床可用疫苗(肺炎球菌 13 价结合疫苗)的微针引发的免疫反应与多次皮下推注后观察到的免疫反应相似,并导致对致死细菌剂量的免疫保护。预编程剂量的微针贴片可能为需要多次注射的预防性和治疗性方案提供替代策略。