The University of Queensland, Delivery of Drugs and Genes Group (D2G2), Australian Institute for Bioengineering and Nanotechnology, St. Lucia, Queensland 4072, Australia.
Small. 2010 Aug 16;6(16):1776-84. doi: 10.1002/smll.201000331.
The 'Nanopatch' (NP) comprises arrays of densely packed projections with a defined geometry and distribution designed to physically target vaccines directly to thousands of epidermal and dermal antigen presenting cells (APCs). These miniaturized arrays are two orders of magnitude smaller than standard needles-which deliver most vaccines-and are also much smaller than current microneedle arrays. The NP is dry-coated with antigen, adjuvant, and/or DNA payloads. After the NP was pressed onto mouse skin, a protein payload co-localized with 91.4 + or - 4.1 APC mm(-2) (or 2925 in total) representing 52% of the delivery sites within the NP contact area, agreeing well with a probability-based model used to guide the device design; it then substantially increases as the antigen diffuses in the skin to many more cells. APC co-localizing with protein payloads rapidly disappears from the application area, suggesting APC migration. The NP also delivers DNA payloads leading to cutaneous expression of encoded proteins within 24 h. The efficiency of NP immunization is demonstrated using an inactivated whole chikungunya virus vaccine and a DNA-delivered attenuated West Nile virus vaccine. The NP thus offers a needle-free, versatile, highly effective vaccine delivery system that is potentially inexpensive and simple to use.
“纳米贴”(NP)由密集排列的具有特定几何形状和分布的突起阵列组成,旨在将疫苗直接物理靶向传递到数千个表皮和真皮抗原呈递细胞(APC)。这些微型阵列比标准针——传递大多数疫苗——小两个数量级,也比当前的微针阵列小得多。NP 用抗原、佐剂和/或 DNA 有效载荷进行干涂。NP 被压在老鼠皮肤上后,一种蛋白质有效载荷与 91.4 ± 4.1 APC mm(-2)(或总共 2925 个)共定位,占 NP 接触区域内传递部位的 52%,这与用于指导设备设计的基于概率的模型非常吻合;然后,随着抗原在皮肤中的扩散,它会显著增加到更多的细胞。与蛋白质有效载荷共定位的 APC 迅速从应用区域消失,表明 APC 迁移。NP 还可以传递 DNA 有效载荷,导致编码蛋白在 24 小时内被皮肤表达。使用灭活的全基孔肯雅病毒疫苗和经 DNA 传递的减毒西尼罗河病毒疫苗证明了 NP 免疫的效率。因此,NP 提供了一种无针、多功能、高效的疫苗传递系统,具有潜在的低成本和简单易用的特点。