2017
DOI: 10.1016/j.ijpharm.2017.09.005
|View full text |Cite
|
Sign up to set email alerts
|

Polymeric micelles: Basic research to clinical practice

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
107
0
2

Year Published

2018
2018
2023
2023

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 206 publications
(109 citation statements)
references
References 192 publications
0
107
0
2
Order By: Relevance
“…PEG is the hydrophilic portion and polyvinylcaprolactam-polyvinylacetate moieties are arranged in the hydrophobic core. The polymeric micelles have the possibility of incorporating functionality in both core and shell regions: the hydrophobic molecules in the core, less hydrophobic molecules in the core, but near the hydrophilic moiety [18].…”
Section: Introductionmentioning
confidence: 99%
“…PEG is the hydrophilic portion and polyvinylcaprolactam-polyvinylacetate moieties are arranged in the hydrophobic core. The polymeric micelles have the possibility of incorporating functionality in both core and shell regions: the hydrophobic molecules in the core, less hydrophobic molecules in the core, but near the hydrophilic moiety [18].…”
Section: Introductionmentioning
confidence: 99%
“…Micelles are studies for drug delivery system mostly composed of diblock, triblock copolymers or graft copolymers with hydrophilic or hydrophobic segments. Polymeric micelles have unique properties, such as low molecular weight, maximum encapsulation of drug, better stability, lower critical micelle concentration (CMC), and improved and higher drug accumulation at the tumour site for targeting [40]. This nanodrug delivery comprising of star-shaped CDDPloaded micelles was fabricated via the ring-opening polymerization method for passive targeting drug delivery system.…”
Section: Micellesmentioning
confidence: 99%
“…Recently, stimuli-responsive micelles have gained a widespread interest for their outstanding advantages [3]. More specifically, the micelles formed from amphiphilic copolymers can effectively encapsulate the hydrophobic drug in the hydrophobic inner core, and the hydrophilic outer shell can improve the compatibility of the system [4]. Due to the leaky vasculature in solid tumor tissues, the nanosized micelles can efficiently accumulate within tumor sites via the enhanced permeability and retention (EPR) effect [5].…”
Section: Introductionmentioning
confidence: 99%