TY - JOUR
T1 - Studies on a new radiopaque polymeric biomaterial
AU - Benzina, A.
AU - Kruft, M.A.B.
AU - Bär, F.W.H.M.
AU - Veen, van der, F.H.
AU - Bastiaansen, C.W.M.
AU - Heijnen, V.
AU - Reutelingsperger, C.P.M.
AU - Koole, L.H.
PY - 1994
Y1 - 1994
N2 - A new radiopaque polymeric biomaterial has been synthesized. The material, which actually represents an entire family of analogous radiopaque materials, is composed of 2-(p-iodobenzoyl)ethyl methacrylate (21 mol%), Me methacrylate (MMA, 60 mol%), and 2-hydroxyethyl methacrylate (HEMA, 19 mol%). The terpolymer was synthesized in a radical polymn. reaction physiochem. characterization techniques (gel permeation chromatog., 500 MHz 1H NMR in deuterated DMSO (d6-DMSO) sol., DSC, dynamic water contact angle measurements), as well as to an in vitro thrombogenicity assay. Furthermore, SEM was used to study interactions of the material with blood platelets. The most important findings are: (a) the material is a genuine polymer with excellent X-ray visibility, even in the form of thin (0.4 mm) drawn fibers. This was established under realistic conditions. (B) the material exhibits low in vitro thrombogenicity, i.e. comparable to polyvinyl chloride, which is known as a passive material. These observations lead us to the suggestion that this type of radiopaque polymer holds promise with respect to application as a construction material for a new type of endovascular stent. This could be relevant in particular to stents to be used in conjuction with percutaneous transluminal coronary angioplasty (PTCA), also known as Dottering. Currently there is a clear trend away from metallic stents towards all-polymeric stents, since the latter have superior biocompatibility. Biocompatibility of the stent material is of vital importance with respect to the long-term performance of the stent, i.e. its ability to prevent the phenomenon of restenosis. Note that both stent material- vessel wall and stent material- blood interactions are crucial. Application of a radiopaque polymer as described therein should enable us to construct a new stent type with improved biocompatibility with respect to the metallic counterpart, combined with excellent X-ray visibility. [on SciFinder (R)]
AB - A new radiopaque polymeric biomaterial has been synthesized. The material, which actually represents an entire family of analogous radiopaque materials, is composed of 2-(p-iodobenzoyl)ethyl methacrylate (21 mol%), Me methacrylate (MMA, 60 mol%), and 2-hydroxyethyl methacrylate (HEMA, 19 mol%). The terpolymer was synthesized in a radical polymn. reaction physiochem. characterization techniques (gel permeation chromatog., 500 MHz 1H NMR in deuterated DMSO (d6-DMSO) sol., DSC, dynamic water contact angle measurements), as well as to an in vitro thrombogenicity assay. Furthermore, SEM was used to study interactions of the material with blood platelets. The most important findings are: (a) the material is a genuine polymer with excellent X-ray visibility, even in the form of thin (0.4 mm) drawn fibers. This was established under realistic conditions. (B) the material exhibits low in vitro thrombogenicity, i.e. comparable to polyvinyl chloride, which is known as a passive material. These observations lead us to the suggestion that this type of radiopaque polymer holds promise with respect to application as a construction material for a new type of endovascular stent. This could be relevant in particular to stents to be used in conjuction with percutaneous transluminal coronary angioplasty (PTCA), also known as Dottering. Currently there is a clear trend away from metallic stents towards all-polymeric stents, since the latter have superior biocompatibility. Biocompatibility of the stent material is of vital importance with respect to the long-term performance of the stent, i.e. its ability to prevent the phenomenon of restenosis. Note that both stent material- vessel wall and stent material- blood interactions are crucial. Application of a radiopaque polymer as described therein should enable us to construct a new stent type with improved biocompatibility with respect to the metallic counterpart, combined with excellent X-ray visibility. [on SciFinder (R)]
U2 - 10.1016/0142-9612(94)90232-1
DO - 10.1016/0142-9612(94)90232-1
M3 - Article
SN - 0142-9612
VL - 15
SP - 1122
EP - 1128
JO - Biomaterials
JF - Biomaterials
IS - 14
ER -