TY - JOUR
T1 - Monoether-Tagged Biodegradable Polycarbonate Preventing Platelet Adhesion and Demonstrating Vascular Cell Adhesion
T2 - A Promising Material for Resorbable Vascular Grafts and Stents
AU - Fukushima, Kazuki
AU - Inoue, Yuto
AU - Haga, Yuta
AU - Ota, Takayuki
AU - Honda, Kota
AU - Sato, Chikako
AU - Tanaka, Masaru
N1 - Funding Information:
The authors acknowledge the Center of Innovation (COI), Frontier Center for Organic System Innovations, financially supported by the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan. K.F. thanks JSPS KAKENHI Grant Number 25870078 for financial support. M.T. acknowledges the Funding Program for Next-Generation World-Leading Researchers (NEXT Program) of MEXT.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/11/13
Y1 - 2017/11/13
N2 - We developed a biodegradable polycarbonate that demonstrates antithrombogenicity and vascular cell adhesion via organocatalytic ring-opening polymerization of a trimethylene carbonate (TMC) analogue bearing a methoxy group. The monoether-tagged polycarbonate demonstrates a platelet adhesion property that is 93 and 89% lower than those of poly(ethylene terephthalate) and polyTMC, respectively. In contrast, vascular cell adhesion properties of the polycarbonate are comparable to those controls, indicating a potential for selective cell adhesion properties. This difference in the cell adhesion property is well associated with surface hydration, which affects protein adsorption and denaturation. Fibrinogen is slightly denatured on the monoether-tagged polycarbonate, whereas fibronectin is highly activated to expose the RGD motif for favorable vascular cell adhesion. The surface hydration, mainly induced by the methoxy side chain, also contributes to slowing the enzymatic degradation. Consequently, the polycarbonate exhibits decent blood compatibility, vascular cell adhesion properties, and biodegradability, which is promising for applications in resorbable vascular grafts and stents.
AB - We developed a biodegradable polycarbonate that demonstrates antithrombogenicity and vascular cell adhesion via organocatalytic ring-opening polymerization of a trimethylene carbonate (TMC) analogue bearing a methoxy group. The monoether-tagged polycarbonate demonstrates a platelet adhesion property that is 93 and 89% lower than those of poly(ethylene terephthalate) and polyTMC, respectively. In contrast, vascular cell adhesion properties of the polycarbonate are comparable to those controls, indicating a potential for selective cell adhesion properties. This difference in the cell adhesion property is well associated with surface hydration, which affects protein adsorption and denaturation. Fibrinogen is slightly denatured on the monoether-tagged polycarbonate, whereas fibronectin is highly activated to expose the RGD motif for favorable vascular cell adhesion. The surface hydration, mainly induced by the methoxy side chain, also contributes to slowing the enzymatic degradation. Consequently, the polycarbonate exhibits decent blood compatibility, vascular cell adhesion properties, and biodegradability, which is promising for applications in resorbable vascular grafts and stents.
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U2 - 10.1021/acs.biomac.7b01210
DO - 10.1021/acs.biomac.7b01210
M3 - Article
C2 - 28972745
AN - SCOPUS:85034056482
SN - 1525-7797
VL - 18
SP - 3834
EP - 3843
JO - Biomacromolecules
JF - Biomacromolecules
IS - 11
ER -