Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/169450
DC FieldValue
dc.titleRational Design of Nanocarriers for Intracellular Protein Delivery
dc.contributor.authorXiaofei Qin
dc.contributor.authorChangmin Yu
dc.contributor.authorJing Wei, Lin Li
dc.contributor.authorChengwu Zhang
dc.contributor.authorQiong Wu
dc.contributor.authorJinhua Liu
dc.contributor.authorShao Q. Yao
dc.contributor.authorWei Huang
dc.date.accessioned2020-06-05T07:00:29Z
dc.date.available2020-06-05T07:00:29Z
dc.date.issued2019-09-08
dc.identifier.citationXiaofei Qin, Changmin Yu, Jing Wei, Lin Li, Chengwu Zhang, Qiong Wu, Jinhua Liu, Shao Q. Yao, Wei Huang (2019-09-08). Rational Design of Nanocarriers for Intracellular Protein Delivery 31 (46) : 1902791. ScholarBank@NUS Repository.
dc.identifier.issn15214095
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/169450
dc.description.abstractAbstract Protein/antibody therapeutics have exhibited the advantages of high specificity and activity even at an extremely low concentration compared to small molecule drugs. However, they are accompanied by unfavorable physicochemical properties such as fragile tertiary structure, large molecular size, and poor penetration of the membrane, and thus the clinical use of protein drugs is hindered by inefficient delivery of proteins into the host cells. To overcome the challenges associated with protein therapeutics and enhance their biopharmaceutical applications, various protein‐loaded nanocarriers with desired functions, such as lipid nanocapsules, polymeric nanoparticles, inorganic nanoparticles, and peptides, are developed. In this review, the different strategies for intracellular delivery of proteins are comprehensively summarized. Their designed routes, mechanisms of action, and potential therapeutics in live cells or in vivo are discussed in detail. Furthermore, the perspective on the new generation of delivery systems toward the emerging area of protein‐based therapeutics is presented as well.
dc.description.urihttps://onlinelibrary.wiley.com/doi/abs/10.1002/adma.201902791
dc.language.isoen
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.volume31
dc.description.issue46
dc.description.page1902791
dc.published.statePublished
dc.grant.idSBP-P4, SBP-P8, GSK-EDB
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