2007
DOI: 10.1002/term.45
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Cholic acid functionalized star poly(DL-lactide) for promoting cell adhesion and proliferation

Abstract: Cholic acid functionalized star poly(DL-lactide) was synthesized through the ring-opening polymerization of DL-lactide initiated by cholic acid. The properties and cell behaviour of the cholic acid functionalized star poly(DL-lactide) were investigated as compared with linear poly(DL-lactide)s with different molecular weights and a star poly(DL-lactide) initiated by glycerol. In comparison to linear poly(DL-lactide)s, the cholic acid functionalized star poly(DL-lactide) had better wettability and slightly high… Show more

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Cited by 26 publications
(26 citation statements)
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“…Because of the PLA arms with different reactive terminal groups and the specificity of CA, the CA-modified PDLLA may provide greater cell affinity and, hence, advantages for applications in drug-release microspheres and tissue engineering. 12,13 The novel direct copolycondensation method is simple and effective. More importantly, this research on the synthesis and characterization of PDLLA modified by CA via direct melt copolycondensation provides a good example of the synthesis of an asymmetrical star-shaped PLA material, especially starting from an asymmetrical core with different reactive groups, which is advantageous for the simple and practical syntheses of more biodegradable PLA materials and their more extensive applications in biomedicine.…”
Section: Discussionmentioning
confidence: 99%
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“…Because of the PLA arms with different reactive terminal groups and the specificity of CA, the CA-modified PDLLA may provide greater cell affinity and, hence, advantages for applications in drug-release microspheres and tissue engineering. 12,13 The novel direct copolycondensation method is simple and effective. More importantly, this research on the synthesis and characterization of PDLLA modified by CA via direct melt copolycondensation provides a good example of the synthesis of an asymmetrical star-shaped PLA material, especially starting from an asymmetrical core with different reactive groups, which is advantageous for the simple and practical syntheses of more biodegradable PLA materials and their more extensive applications in biomedicine.…”
Section: Discussionmentioning
confidence: 99%
“…At the same time, the biodegradable material poly(D,L-lactide-cholate) had a special affinity to cells; the use of PDLLA modified by CA as drug-delivery material was advantageous for the improvement of the medicinal effect. 12,13 Therefore, the direct synthesis of poly(D,L-lactidecholate) is practically valuable.…”
Section: Gpc Characterization Of Poly(dl-lactide-cholate)mentioning
confidence: 99%
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“…According to our previous studies, CA‐(DLL) n has an accelerated degradation rate because of its branched structure compared to conventional linear poly( DL ‐lactide) (PDLLA), and the degradation of CA‐(DLL) n is dominated by surface erosion mechanism when its molecular weight is not very high 17. Moreover, compared to PDLLA, CA‐(DLL) n has a better performance in promoting cell attachment and growth 19. For comparison, we also investigated the film‐mediated transfection using conventional linear PDLLA as the matrix.…”
Section: Resultsmentioning
confidence: 99%
“…A series of star-shaped polymers were prepared with cholic acid as the core and DL-lactide, ε-caprolactone or other carbonates as branches through ring-opening polymerization by the group of Zhuo (Figure 8, A-D). These polymers can be useful in applications such as drug release [38][39][40][41][42] and gene delivery [43] , and can serve as scaffolds to promote cell attachment and growth [44,45] . When thermo-sensitive groups were attached onto position 24 of cholic acid, ringopening polymerization yielded thermo-sensitive drug carriers [46] .…”
Section: Bile Acids As the Core Of Star-shaped Polymersmentioning
confidence: 99%