Synthetic Charge-Invertible Polymer for Rapid and Complete Implantation of Layer-by-Layer Microneedle Drug Films for Enhanced Transdermal Vaccination

被引:74
作者
He, Yanpu [1 ,2 ]
Hong, Celestine [1 ,2 ]
Li, Jiahe [1 ,2 ]
Howard, MayLin T. [1 ,2 ]
Li, Yingzhong [1 ,3 ]
Turvey, Michelle E. [4 ]
Uppu, Divakara S. S. M. [4 ]
Martin, John R. [1 ,2 ]
Zhang, Ketian [1 ,5 ]
Irvine, Darrell J. [1 ,3 ,5 ,6 ]
Hammond, Paula T. [1 ,2 ]
机构
[1] MIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] SMART, Infect Dis Interdisciplinary Res Grp, Singapore, Singapore
[5] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[6] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
关键词
polymer synthesis; layer-by-layer assembly; drug delivery; microneedle; vaccine; MESSENGER-RNA DELIVERY; SOD1; NANOZYME; PLASMID DNA; RELEASE; PROTEIN; RESPONSES; POTENT;
D O I
10.1021/acsnano.8b05373
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
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 mu g 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.
引用
收藏
页码:10272 / 10280
页数:9
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