Koch Institute for Integrative Cancer Research , Massachusetts Institute of Technology , Cambridge , Massachusetts 02139 , United States.
Department of Chemical Engineering , Massachusetts Institute of Technology , Cambridge , Massachusetts 02139 , United States.
ACS Nano. 2018 Oct 23;12(10):10272-10280. doi: 10.1021/acsnano.8b05373. Epub 2018 Oct 4.
The utility of layer-by-layer (LbL) coated microneedle (MN) skin patches for transdermal drug delivery has proven to be a promising approach, with advantages over hypodermal injection due to painless and easy self-administration. However, the long epidermal application time required for drug implantation by existing LbL MN strategies (15-90 min) can lead to potential medication noncompliance. Here, we developed a MN platform to shorten the application time in MN therapies based on a synthetic pH-induced charge-invertible polymer poly(2-(diisopropylamino) ethyl methacrylate- b-methacrylic acid) (PDM), requiring only 1 min skin insertion time to implant LbL films in vivo. Following MN-mediated delivery of 0.5 μg model antigen chicken ovalbumin (OVA) in the skin of mice, this system achieved sustained release over 3 days and led to an elevated immune response as demonstrated by significantly higher humoral immunity compared with OVA administration via conventional routes (subcutaneously and intramuscularly). Moreover, in an ex vivo experiment on human skin, we achieved efficient immune activation through MN-delivered LbL films, demonstrated by a rapid uptake of vaccine adjuvants by the antigen presenting cells. These features, rapid administration and the ability to elicit a robust immune response, can potentially enable a broad application of microneedle-based vaccination technologies.
层层(LbL)包被微针(MN)贴片在透皮药物输送方面的应用已被证明是一种很有前途的方法,与皮下注射相比具有无痛、易于自我给药的优势。然而,现有的 LbL MN 策略(15-90 分钟)用于药物植入所需的长表皮应用时间可能导致潜在的药物不依从。在这里,我们开发了一种 MN 平台,基于合成的 pH 诱导的电荷可逆聚合物聚(2-(二异丙基氨基)乙基甲基丙烯酸酯- b-甲基丙烯酸)(PDM),将 MN 疗法的应用时间缩短,只需 1 分钟的皮肤插入时间即可在体内植入 LbL 膜。在小鼠皮肤中经 MN 介导递送至 0.5 μg 模型抗原鸡卵清蛋白(OVA)后,该系统实现了长达 3 天的持续释放,并通过与通过常规途径(皮下和肌肉内)给药相比,显著提高了体液免疫反应,证明了其具有更高的免疫应答。此外,在人体皮肤的离体实验中,我们通过 MN 递送的 LbL 膜实现了有效的免疫激活,这可以通过抗原呈递细胞快速摄取疫苗佐剂来证明。这些特点,快速给药和引发强大免疫反应的能力,有可能使基于微针的疫苗接种技术得到广泛应用。