2009
DOI: 10.1007/s10853-009-3588-3
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Preparation and properties of a novel thermo-responsive poly(N-isopropylacrylamide) hydrogel containing glycyrrhetinic acid

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Cited by 16 publications
(14 citation statements)
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“…Then, GSE was dissolved in N, N-dimethylformamide (DMF) and added into EDA by dropping slowly to form glycyrrhetic acid amine derivatives (GA-NH 2 ). The GA-NH 2 solution of DMF reacted with acrylic acid in the presence of sulfo-NHS and EDC to synthesize glycyrrhetinic acid with vinyl monomer (AAc-GA) [10]. The chemical structure of AAc-GA is shown in Fig.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Then, GSE was dissolved in N, N-dimethylformamide (DMF) and added into EDA by dropping slowly to form glycyrrhetic acid amine derivatives (GA-NH 2 ). The GA-NH 2 solution of DMF reacted with acrylic acid in the presence of sulfo-NHS and EDC to synthesize glycyrrhetinic acid with vinyl monomer (AAc-GA) [10]. The chemical structure of AAc-GA is shown in Fig.…”
Section: Methodsmentioning
confidence: 99%
“…However, most of the studies about GA were focused on the hepatic targeted drug delivery system (HTDDS). Therefore, as reported in our previous literature [10], GA was introduced and PNIPAAm hydrogel containing glycyrrhetinic acid (poly(NIPAAmco-AAc-GA)) was prepared to improve the biocompatibility and the hepatic affinity of the traditional PNIPAAm hydrogel.…”
Section: Introductionmentioning
confidence: 99%
“…), which can be widely applied in biomedical and biotechnological fields such as controlled drug delivery and enzyme immobilization [4][5][6]. Among them, poly(N-isopropylacrylamide) (PNI-PAM) gained much attention because it undergo a phase transition from a hydrophilic, water-swollen state to a hydrophobic, globular state when heated above its volume phase transition temperature (VPTT) at 32°C in water [7][8][9][10][11]. However, it is difficult to guide the microgels in particular parts.…”
Section: Introductionmentioning
confidence: 99%
“…When cells are harvested using conventional cell detachment agents such as proteolytic trypsin, the cells may be irreparably damaged thus hindering consequent cell function [3][4][5][6][7][8]. In addition, cell junctions are cleaved thus rendering the cells useless for tissue regeneration purposes [7,9].…”
Section: Introductionmentioning
confidence: 99%
“…The major obstacle to using pNIPAm coatings for this desired outcome is that pNIPAm coatings tend to be poorly cell compatible, with cells resisting attaching to bare pNIPAm surfaces [9][10][11][12]. Efforts to overcome this lack of compatibility have involved the copolymerization of the NIPAm monomer with another suitably chosen monomer to attain a more biocompatible copolymer or by adding an over-layer of cell adhesion encouraging proteins to a pNIPAm coating [1,10,13].…”
Section: Introductionmentioning
confidence: 99%