2020
DOI: 10.1016/j.actbio.2020.01.036
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Cell membrane-camouflaged nanoparticles as drug carriers for cancer therapy

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Cited by 150 publications
(88 citation statements)
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“…This approach falls inside the development of biomimetic nanotechnologies based on the "camouflaging" methods. The biomimetic NPs not only retain the physicochemical features of the synthetic vehicles but also inherit the cell membranes' intrinsic functionalities [21,22]. As examples, erythrocytes (red blood cell (RBC) membrane-camouflaged nanocarriers (RBC-MCNs)) are used in studies for tunable paclitaxel (PTX) release kinetics from biocompatible isotactic and atactic polylactide (PLA) polymeric vesicles [23] and 5-fluorouracil (5-FU) delivery from by chitosan-coated poly(lactide-co-glycolic acid) nanoparticles [24].…”
Section: Polymeric Lipid and Hybrid Nanostructuresmentioning
confidence: 99%
“…This approach falls inside the development of biomimetic nanotechnologies based on the "camouflaging" methods. The biomimetic NPs not only retain the physicochemical features of the synthetic vehicles but also inherit the cell membranes' intrinsic functionalities [21,22]. As examples, erythrocytes (red blood cell (RBC) membrane-camouflaged nanocarriers (RBC-MCNs)) are used in studies for tunable paclitaxel (PTX) release kinetics from biocompatible isotactic and atactic polylactide (PLA) polymeric vesicles [23] and 5-fluorouracil (5-FU) delivery from by chitosan-coated poly(lactide-co-glycolic acid) nanoparticles [24].…”
Section: Polymeric Lipid and Hybrid Nanostructuresmentioning
confidence: 99%
“…Researchers intend to retain the unbelievable sensitivity and specificity in nature. Given the shortages of polymer materials, recently a novel biomimetic nanoplatform exploiting natural cell membrane as the cloaks of nanoparticles has emerged 2,6,21–23 . The membrane camouflaging technology was first proposed in 2011, in which researchers utilized erythrocytes as the source of membrane materials 22 .…”
Section: Introductionmentioning
confidence: 99%
“…Although many of the methods described in the literature lead to effective functionalization of nanomaterials surface, the issues with unspecific interactions may prevent successful utilization in some applications [30][31][32][33]. Due to specific requirements in the utilization of bio-functionalized UCNPs in dot blot assays, we focused to develop protocols allowing to obtain functionalized nanoparticles that lack nonspecific interactions with nitrocellulose and immobilon membranes.…”
Section: Introductionmentioning
confidence: 99%