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• W3165718103 endingPage "2002020" @default.
• W3165718103 startingPage "2002020" @default.
• W3165718103 abstract "Biomimetic strategies are useful for designing potent vaccines. Decorating a nanoparticulate adjuvant with cell membrane fragments as the antigen-presenting source exemplifies, such as a promising strategy. For translation, a standardizable, consistent, and scalable approach for coating nanoadjuvant with the cell membrane is important. Here a turbulent mixing and self-assembly method called flash nanocomplexation (FNC) for producing cell membrane-coated nanovaccines in a scalable manner is demonstrated. The broad applicability of this FNC technique compared with bulk-sonication by using ten different core materials and multiple cell membrane types is shown. FNC-produced biomimetic nanoparticles have promising colloidal stability and narrow particle polydispersity, indicating an equal or more homogeneous coating compared to the bulk-sonication method. The potency of a nanovaccine comprised of B16-F10 cancer cell membrane decorating mesoporous silica nanoparticles loaded with the adjuvant CpG is then demonstrated. The FNC-fabricated nanovaccines when combined with anti-CTLA-4 show potency in lymph node targeting, DC antigen presentation, and T cell immune activation, leading to prophylactic and therapeutic efficacy in a melanoma mouse model. This study advances the design of a biomimetic nanovaccine enabled by a robust and versatile nanomanufacturing technique." @default.
• W3165718103 created "2021-06-07" @default.
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• W3165718103 date "2021-05-01" @default.
• W3165718103 modified "2023-10-13" @default.
• W3165718103 title "A Versatile and Robust Platform for the Scalable Manufacture of Biomimetic Nanovaccines" @default.
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• W3165718103 doi "https://doi.org/10.1002/advs.202002020" @default.
• W3165718103 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8336609" @default.
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• W3165718103 hasPublicationYear "2021" @default.
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