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用于表面介导药物递送的层层薄膜下的合成剥离聚合物。

Synthetic Lift-off Polymer beneath Layer-by-Layer Films for Surface-Mediated Drug Delivery.

作者信息

He Yanpu, Li Jiahe, Turvey Michelle E, Funkenbusch MayLin T, Hong Celestine, Uppu Divakara Ssm, He Hongkun, Irvine Darrell J, Hammond Paula T

机构信息

Infectious Diseases Interdisciplinary Research Group, Singapore-MIT Alliance for Research and Technology (SMART), Singapore, Singapore.

Howard Hughes Medical Institute, Chevy Chase, Maryland 20815, United States.

出版信息

ACS Macro Lett. 2017 Nov 21;6(11):1320-1324. doi: 10.1021/acsmacrolett.7b00584. Epub 2017 Nov 9.

Abstract

A broad range of biomaterials coatings and thin film drug delivery systems require a strategy for the immobilization, retention, and release of coatings from surfaces such as patches, inserts, and microneedles under physiological conditions. Here we report a polymer designed to provide a dynamic surface, one that first functions as a platform for electrostatic thin film assembly and releases the film once in an in vivo environment. Atom transfer radical polymerization (ATRP) was used to synthesize this polymer poly(-nitrobenzyl-methacrylate--hydroxyethyl-methacrylate--poly(ethylene-glycol)-methacrylate) (PNHP), embedded beneath multilayered polyelectrolyte films. Such a base layer is designed to photochemically pattern negative charge onto a solid substrate, assist deposition of smooth layer-by-layer (LbL) polyelectrolyte in mildly acidic buffers and rapidly dissolve at physiological pH, thus lifting off the LbL films. To explore potential uses in the biomedical field, a lysozyme (Lys)/poly(acrylic acid) (PAA) multilayer film was developed on PNHP-coated silicon wafers to construct prototype antimicrobial shunts. Film thickness was shown to grow exponentially with increasing deposition cycles, and effective drug loading and in vitro release was confirmed by the dose-dependent inhibition of growth. The efficacy of this approach is further demonstrated in LbL-coated microscale needle arrays ultimately of interest for vaccine applications. Using PNHP as a photoresist, LbL films were confined to the tips of the microneedles, which circumvented drug waste at the patch base. Subsequent confocal images confirmed rapid LbL film implantation of PNHP at microneedle penetration sites on mouse skin. Furthermore, in human skin biopsies, we achieved efficient immune activation demonstrated by a rapid uptake of vaccine adjuvant from microneedle-delivered PNHP LbL film in up to 37% of antigen-presenting cells (APC), providing an unprecedented LbL microneedle platform for human vaccination.

摘要

广泛的生物材料涂层和薄膜药物递送系统需要一种策略,用于在生理条件下将涂层固定、保留并从诸如贴片、植入物和微针等表面释放。在此,我们报告一种设计用于提供动态表面的聚合物,该聚合物首先作为静电薄膜组装的平台,一旦进入体内环境就会释放薄膜。原子转移自由基聚合(ATRP)用于合成这种聚合物聚(甲基丙烯酸 - 对硝基苄酯 - 甲基丙烯酸 - 羟乙酯 - 聚(乙二醇)甲基丙烯酸酯)(PNHP),其嵌入多层聚电解质薄膜之下。这样的基层旨在通过光化学作用在固体基质上形成负电荷图案,在轻度酸性缓冲液中协助光滑的逐层(LbL)聚电解质沉积,并在生理pH值下迅速溶解,从而使LbL薄膜脱落。为了探索在生物医学领域的潜在用途,在涂有PNHP的硅片上制备了溶菌酶(Lys)/聚丙烯酸(PAA)多层膜,以构建原型抗菌分流器。结果表明,膜厚度随沉积循环次数的增加呈指数增长,并且通过剂量依赖性的生长抑制证实了有效的药物负载和体外释放。这种方法的有效性在最终用于疫苗应用的LbL涂层微尺度针阵列中得到进一步证明。使用PNHP作为光刻胶,LbL薄膜被限制在微针尖端,这避免了贴片底部的药物浪费。随后的共聚焦图像证实了PNHP的LbL薄膜在小鼠皮肤微针穿透部位的快速植入。此外,在人体皮肤活检中,我们实现了高效的免疫激活,高达37%的抗原呈递细胞(APC)从微针递送的PNHP LbL薄膜中快速摄取疫苗佐剂,为人类疫苗接种提供了一个前所未有的LbL微针平台。

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