2015
DOI: 10.1016/j.colsurfb.2015.06.057
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of multi-functional nanocapsules via interfacial AGET ATRP in miniemulsion for tumor micro-environment responsive drug delivery

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
18
0

Year Published

2017
2017
2020
2020

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 24 publications
(18 citation statements)
references
References 33 publications
0
18
0
Order By: Relevance
“…Subsequently, the monomer was added along with cross-linker and initiator and started to form polymeric shell via free radical polymerization. Then the pre-synthesized amphiphilic copolymer was removed by hydrolysis to provide hollow inner structure [102][103][104]. For example, pH sensitive polymeric nanocapsules were formulated by using RAFT/emulsion polymerization.…”
Section: B Emulsion-coacervation Methodsmentioning
confidence: 99%
“…Subsequently, the monomer was added along with cross-linker and initiator and started to form polymeric shell via free radical polymerization. Then the pre-synthesized amphiphilic copolymer was removed by hydrolysis to provide hollow inner structure [102][103][104]. For example, pH sensitive polymeric nanocapsules were formulated by using RAFT/emulsion polymerization.…”
Section: B Emulsion-coacervation Methodsmentioning
confidence: 99%
“…To investigate the drug loading properties of crosslinked micelles, DOX was used as a model drug molecule because the p K a of DOX is 8.25 and it is a positively charged cation in neutral and acidic environments . It can be loaded into the electronegative crosslinked micelles by electrostatic interaction at neutral pH …”
Section: Resultsmentioning
confidence: 99%
“…On the other hand, crosslinker can also be utilized to introduce stimuli‐responsivity to the resulting CPNCs. For instance, Tian et al synthesized pH and reduction dual‐responsive PEG‐ block ‐poly(acrylic acid)‐based CPNCs in which pH‐sensitivity was from polymeric structures and reduction responsivity was from the disulfide‐functionalized crosslinker, N , N ‐bis(acryloyl) cystamine (Tian et al, 2015). Drug release from these CPNCs became fast at pH 5.0 relative to pH 7.4, and could be critically triggered with the presence of glutathione (GSH) as the reducing agent to cleave the disulfide‐based crosslinkages of the CPNCs.…”
Section: Therapeutic Applications Of Cpncsmentioning
confidence: 99%