Microneedle Systems for Vaccine Delivery: the story so far

被引:28
作者
Hossain, Md Kamal [1 ]
Ahmed, Taksim [2 ]
Bhusal, Prabhat [3 ]
Subedi, Robhash Kusam [4 ]
Salahshoori, Iman [5 ]
Soltani, M. [6 ,7 ,8 ,9 ]
Hassanzadeganroudsari, Majid [1 ,5 ]
机构
[1] Victoria Univ, Inst Hlth & Sport, Melbourne, Vic, Australia
[2] Univ Toronto, Leslie Dan Fac Pharm, Toronto, ON, Canada
[3] Univ Otago, Sch Pharm, Dunedin, New Zealand
[4] Meera Biotech Pvt Ltd, Bhaktapur, Nepal
[5] Islamic Azad Univ, Sci & Res Branch, Tehran, Iran
[6] KN Toosi Univ Technol, Dept Mech Engn, Tehran, Iran
[7] Univ Waterloo, Fac Sci, Dept Elect & Comp Engn, Fac Engn,Sch Optometry & Vis Sci, Waterloo, ON, Canada
[8] Univ Waterloo, Ctr Biotechnol & Bioengn, Waterloo, ON, Canada
[9] KN Toosi Univ Technol, Multidisciplinary Int Complex, Adv Bioengn Initiat Ctr, Tehran, Iran
关键词
Skin; microneedle; fabrication; immunogenicity; vaccine;
D O I
10.1080/14760584.2020.1874928
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction Vaccine delivery via a microneedle (MN) system has been identified as a potential alternative to conventional vaccine delivery. MN can be self-administered, is pain-free and is capable of producing superior immunogenicity. Over the last few decades, significant research has been carried out in this area, and this review aims to provide a comprehensive picture on the progress of this delivery platform. Areas covered This review highlights the potential role of skin as a vaccine delivery route using a microneedle system, examines recent advancements in microneedle fabrication techniques, and provides an update on potential preclinical and clinical studies on vaccine delivery through microneedle systems against various infectious diseases. Articles for the review study were searched electronically in PubMed, Google, Google Scholar, and Science Direct using specific keywords to cover the scope of the article. The advanced search strategy was employed to identify the most relevant articles. Expert opinion A significant number of MN mediated vaccine candidates have shown promising results in preclinical and clinical trials. The recent emergence of cleanroom free, 3D or additive manufacturing of MN systems and stability, together with the dose-sparing capacity of the Nanopatch (R) system, have made this platform, commercially, highly lucrative.
引用
收藏
页码:1153 / 1166
页数:14
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