Key result
THBA70 polymer coatings loaded with taxol or simvastatin produced dose-dependent inhibition of fibroblast proliferation and prevented thrombosis in vitro.
Why the study?
Does THBA70 polymer coating loaded with taxol or simvastatin inhibit cell proliferation and provide controlled drug release in vitro?
Does THBA70 polymer coating loaded with taxol or simvastatin inhibit cell proliferation and provide controlled drug release in vitro?
A novel THBA70 polymer coating for stents demonstrates controlled release of anti-proliferative drugs and dose-dependent inhibition of cell proliferation in vitro, highlighting its potential for drug-eluting stents.
Supports THBA70 stent coating development; leaves open in vivo efficacy and clinical translation.
Drug eluting coronary stents coated with a bioactive and biostable polymer system (THBA70), based on acrylate copolymers bearing a salicylic acid derivative as side substituent, were evaluated. The microstructural architecture of the copolymer THBA70 comprises a random copolymer of a methacrylate derivative from triflusal (4-trifluoromethyl salicylic acid) with 45 mol% of THEMA (2-methacryloyloxyethyl [2-(acetyloxy)-4-(trifluoromethyl)] benzoate), which makes the system anti-thrombogenic with good adhesion to the surface of metallic stents. The bioactive coating prevented thrombosis, an adverse effect associated with the implantation of drug-eluting stents. The in vitro drug delivery of drug-eluting stents under dynamic conditions indicated excellent controlled drug release. The THBA70 films loaded with relatively low concentrations of taxol or simvastatin in contact with fibroblasts produced inhibition of cell proliferation with a dose-dependent bioactivity.
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Rodrı́guez et al. (2012) studied this question. THBA70 polymer coating loaded with taxol or simvastatin was evaluated on Cell proliferation and thrombosis. THBA70 polymer coatings loaded with taxol or simvastatin produced dose-dependent inhibition of fibroblast proliferation and prevented thrombosis in vitro.
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