2010
DOI: 10.1016/j.bmc.2010.08.009
|View full text |Cite
|
Sign up to set email alerts
|

Intermolecular interaction and morphology investigation of drug loaded ABA-triblock copolymers with different hydrophilic/lipophilic ratios

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2012
2012
2016
2016

Publication Types

Select...
7

Relationship

3
4

Authors

Journals

citations
Cited by 9 publications
(3 citation statements)
references
References 16 publications
(14 reference statements)
0
3
0
Order By: Relevance
“…46 Also, the open nature of the dendritic architecture and an abundance of functional groups facilitate drug encapsulation into the branches of dendritic parts. 47 In comparison with our previous study, 48 it is concluded that an increase in the number of interactions between drug and the polyester play an important role to have appropriate drug loading. Moreover, according to another study of our research group, 35 the Brunauer−Emmet−Teller (BET) adsorption data revealed that the N 2 adsorption/desorption amount of dendritic structure is higher than that of linear structure.…”
Section: Resultsmentioning
confidence: 69%
“…46 Also, the open nature of the dendritic architecture and an abundance of functional groups facilitate drug encapsulation into the branches of dendritic parts. 47 In comparison with our previous study, 48 it is concluded that an increase in the number of interactions between drug and the polyester play an important role to have appropriate drug loading. Moreover, according to another study of our research group, 35 the Brunauer−Emmet−Teller (BET) adsorption data revealed that the N 2 adsorption/desorption amount of dendritic structure is higher than that of linear structure.…”
Section: Resultsmentioning
confidence: 69%
“…In comparison with previous study [55], it is clearly concluded that increase in the number of interactions between drug and the polyester play an important role to have appropriate drug loading. As a result, the presence of poly(amino-ester) block causes more interactions between the hydroxyl and ester groups of LPE and the functional groups of the polyester in the nanoparticle structure.…”
Section: Drug Loading and Encapsulation Efficiencymentioning
confidence: 78%
“…On the basis of these considerations and in continuum to our previous work [24], the main goal of this work was to develop new synthetic route for preparation of PLGA-PEG block copolymer in order to obtain stable nanomicelle with low CMC value. Here, amphiphilic block PLGA-PEG copolymer was strategically designed and synthesized by free radical copolymerization of functionalized macromers; acryloyl-terminated water-insoluble PLGA and acryloylterminated water-soluble PEG.…”
Section: Introductionmentioning
confidence: 98%