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- W2022269885 endingPage "449" @default.
- W2022269885 startingPage "419" @default.
- W2022269885 abstract "In order to achieve long circulation time and high drug accumulation in the tumor sites via the EPR effects, anticancer drugs have to be protected by non-fouling polymers such as poly(ethylene glycol) (PEG), poly(ethylene oxide) (PEO), dextran, and poly(acrylic acid) (PAA). However, the dense layer of stealth polymer also prohibits efficient uptake of anticancer drugs by target cancer cells. For cancer therapy, it is often more desirable to accomplish rapid cellular uptake after anticancer drugs arriving at the pathological site, which could on one hand maximize the therapeutic efficacy and on the other hand reduce probability of drug resistance in cells. In this review, special attention will be focused on the recent potential strategies that can enable drug-loaded polymeric nanoparticles to rapidly recognize cancer cells, leading to enhanced internalization." @default.
- W2022269885 created "2016-06-24" @default.
- W2022269885 creator A5056157813 @default.
- W2022269885 creator A5057964291 @default.
- W2022269885 date "1977-11-01" @default.
- W2022269885 modified "2023-09-23" @default.
- W2022269885 title "The permeability properties of the lysosomal membrane" @default.
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