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Synthesis of crosslinkable diblock terpolymers PDPA-b-P(NMS-co-OEG) and preparation of shell-crosslinked pH/redox-dual responsive micelles as smart nanomaterials.


ABSTRACT: Crosslinked polymer nanomaterials have attracted great attention due to their stability and highly controllable drug delivery; herein, a series of well-defined amphiphilic PDPA-b-P(NMS-co-OEG) diblock terpolymers (P1-P3) were designed and prepared via RAFT polymerization and were self-assembled into non-cross-linked (NCL) nanomicelles, which were further prepared into shell-cross-linked (SCL) micelles via cystamine-based in situ shell cross-linking. Using P3 as an optimized polymer, SCL-P3 micelles were prepared, which demonstrated remarkable pH/redox-dual responsive behaviour. For drug delivery, camptothecin (CPT)-loaded SCL-P3 micelles were prepared and showed much higher CPT-loading capability than their NCL-P3 counterparts. Notably, the SCL-P3 micelles showed good synergistic pH/redox-dual responsive CPT release properties, making them potential "smart" nanocarriers for drug delivery.

SUBMITTER: Sun J 

PROVIDER: S-EPMC9073896 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Synthesis of crosslinkable diblock terpolymers PDPA-<i>b</i>-P(NMS-<i>co</i>-OEG) and preparation of shell-crosslinked pH/redox-dual responsive micelles as smart nanomaterials.

Sun Jingjing J   Wang Zhao Z   Cao Amin A   Sheng Ruilong R  

RSC advances 20191029 59


Crosslinked polymer nanomaterials have attracted great attention due to their stability and highly controllable drug delivery; herein, a series of well-defined amphiphilic PDPA-<i>b</i>-P(NMS-<i>co</i>-OEG) diblock terpolymers (P1-P3) were designed and prepared <i>via</i> RAFT polymerization and were self-assembled into non-cross-linked (NCL) nanomicelles, which were further prepared into shell-cross-linked (SCL) micelles <i>via</i> cystamine-based <i>in situ</i> shell cross-linking. Using P3 as  ...[more]

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