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10.1016/j.cocis.2021.101468

http://scihub22266oqcxt.onion/10.1016/j.cocis.2021.101468
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34093062!8164502!34093062
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suck abstract from ncbi


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pmid34093062      Curr+Opin+Colloid+Interface+Sci 2021 ; 55 (ä): 101468
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  • Opportunities for innovation: Building on the success of lipid nanoparticle vaccines #MMPMID34093062
  • Huang J; Yuen D; Mintern JD; Johnston APR
  • Curr Opin Colloid Interface Sci 2021[Oct]; 55 (ä): 101468 PMID34093062show ga
  • Lipid nanoparticle (LNP) formulations of messenger RNA (mRNA) have demonstrated high efficacy as vaccines against SARS-CoV-2. The success of these nanoformulations underscores the potential of LNPs as a delivery system for next-generation biological therapies. In this article, we highlight the key considerations necessary for engineering LNPs as a vaccine delivery system and explore areas for further optimisation. There remain opportunities to improve the protection of mRNA, optimise cytosolic delivery, target specific cells, minimise adverse side-effects and control the release of RNA from the particle. The modular nature of LNP formulations and the flexibility of mRNA as a payload provide many pathways to implement these strategies. Innovation in LNP vaccines is likely to accelerate with increased enthusiasm following recent successes; however, any advances will have implications for a broad range of therapeutic applications beyond vaccination such as gene therapy.
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