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Study on antithrombogenicity of poly[beta-(acetylsalicylyloxy)ethyl methacrylate] relative to poly(hydroxyethyl methacrylate).

Abstract
The antithrombogenicity of a polymer made of aspirin bound to hydroxyethyl methacrylate (HEMA), abbreviated as ASA-polymer, was compared with that of poly(hydroxyethyl methacrylate) (PHEMA). Platelet from platelet rich plasma (PRP) incubated with ASA-polymer surface exhibited noticeable decreases in adhesion and aggregation as compared to platelets incubated with PHEMA. Low molecular weight components other than aspirin, which may be released from ASA-polymer during the incubation with PRP, or contact with ASA-polymer causing denaturation of platelets without morphological changes could be responsible for the decrease of adhesion and aggregation. Both PRP and PPP exposed to ASA-polymer-coated surfaces exhibited a much smaller partial thromboplastin time (PTT) than if exposed to PHEMA-coated surfaces; the PTT of ASA-polymer was similar to that of glass exposed plasma. With respect to the in vivo antithrombogenicity, the ASA-polymer surface led to thrombus formation. This may be due to the partial hydrolysis of the acetyl groups resulting in the formation of a negatively charged surface which in turn accelerates the coagulation cascade despite its inhibitory effects on platelet adhesion and aggregation. On the other hand, neointima formed around a thrombus layer on PHEMA-coated sutures after 14 days.
AuthorsH Sato, J Kojima, A Nakajima, T Morita, Y Noishiki, Z W Gu, F M Li, X D Feng
JournalJournal of biomaterials science. Polymer edition (J Biomater Sci Polym Ed) Vol. 2 Issue 1 Pg. 1-13 ( 1991) ISSN: 0920-5063 [Print] England
PMID1863573 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Delayed-Action Preparations
  • Fibrinolytic Agents
  • Platelet Aggregation Inhibitors
  • Polymethacrylic Acids
  • Polyhydroxyethyl Methacrylate
  • poly(beta-(acetylsalicylyloxy)ethylmethacrylate)
  • Aspirin
Topics
  • Animals
  • Aspirin (analogs & derivatives, pharmacology)
  • Blood Coagulation (drug effects)
  • Delayed-Action Preparations
  • Dogs
  • Fibrinolytic Agents
  • In Vitro Techniques
  • Molecular Structure
  • Platelet Adhesiveness (drug effects)
  • Platelet Aggregation Inhibitors
  • Polyhydroxyethyl Methacrylate (pharmacology)
  • Polymethacrylic Acids (pharmacology)

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