File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Biodegradable Microrobots for DNA Vaccine Delivery

TitleBiodegradable Microrobots for DNA Vaccine Delivery
Authors
Issue Date18-May-2023
PublisherWiley-VCH Verlag
Citation
Advanced Healthcare Materials, 2023 How to Cite?
Abstract

The delivery of nucleic acid vaccine to stimulate host immune responses against Coronavirus disease 2019 shows promise. However, nucleic acid vaccines have drawbacks, including rapid clearance and poor cellular uptake, that limit their therapeutic potential. Microrobots can be engineered to sustain vaccine release and further control the interactions with immune cells that are vital for robust vaccination. Here, the 3D fabrication of biocompatible and biodegradable microrobots via the two-photon polymerization of gelatin methacryloyl (GelMA) and their proof-of-concept application for DNA vaccine delivery is reported. Programmed degradation and drug release by varying the local exposure dose in 3D laser lithography and further functionalized the GelMA microspheres with polyethyleneimine for DNA vaccine delivery to dendritic cell and primary cells is demonstrated. In mice, the DNA vaccine delivered by functionalized microspheres elicited fast, enhanced, and durable antigen expression, which may lead to prolonged protection. Furthermore, we demonstrated the maneuverability of microrobots by fabricating GelMA microspheres on magnetic skeletons. In conclusion, GelMA microrobots may provide an efficient vaccination strategy by controlling the expression duration of DNA vaccines.


Persistent Identifierhttp://hdl.handle.net/10722/328232
ISSN
2021 Impact Factor: 11.092
2020 SCImago Journal Rankings: 2.288

 

DC FieldValueLanguage
dc.contributor.authorChen, Shuxun-
dc.contributor.authorTan, Zhiwu-
dc.contributor.authorLiao, Pan-
dc.contributor.authorLi, Yanfang-
dc.contributor.authorQu, Yun-
dc.contributor.authorZhang, Qi-
dc.contributor.authorYang, Mingxuan-
dc.contributor.authorChan, Kannie Wai Yan-
dc.contributor.authorZhang, Li-
dc.contributor.authorMan, Kwan-
dc.contributor.authorChen, Zhiwei-
dc.contributor.authorSun, Dong -
dc.date.accessioned2023-06-28T04:39:49Z-
dc.date.available2023-06-28T04:39:49Z-
dc.date.issued2023-05-18-
dc.identifier.citationAdvanced Healthcare Materials, 2023-
dc.identifier.issn2192-2640-
dc.identifier.urihttp://hdl.handle.net/10722/328232-
dc.description.abstract<p> <span>The delivery of nucleic acid vaccine to stimulate host immune responses against Coronavirus disease 2019 shows promise. However, nucleic acid vaccines have drawbacks, including rapid clearance and poor cellular uptake, that limit their therapeutic potential. Microrobots can be engineered to sustain vaccine release and further control the interactions with immune cells that are vital for robust vaccination. Here, the 3D fabrication of biocompatible and biodegradable microrobots via the two-photon polymerization of gelatin methacryloyl (GelMA) and their proof-of-concept application for DNA vaccine delivery is reported. Programmed degradation and drug release by varying the local exposure dose in 3D laser lithography and further functionalized the GelMA microspheres with polyethyleneimine for DNA vaccine delivery to dendritic cell and primary cells is demonstrated. In mice, the DNA vaccine delivered by functionalized microspheres elicited fast, enhanced, and durable antigen expression, which may lead to prolonged protection. Furthermore, we demonstrated the maneuverability of microrobots by fabricating GelMA microspheres on magnetic skeletons. In conclusion, GelMA microrobots may provide an efficient vaccination strategy by controlling the expression duration of DNA vaccines.</span> <br></p>-
dc.languageeng-
dc.publisherWiley-VCH Verlag-
dc.relation.ispartofAdvanced Healthcare Materials-
dc.titleBiodegradable Microrobots for DNA Vaccine Delivery-
dc.typeArticle-
dc.identifier.doi10.1002/adhm.202202921-
dc.identifier.eissn2192-2659-
dc.identifier.issnl2192-2640-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats