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1.
Journal of Biomedical Engineering ; (6): 90-94, 2011.
Article in Chinese | WPRIM | ID: wpr-306615

ABSTRACT

Based on non-enzymatic protein glycated reaction, the sodium periodate-oxidated low molecular weight heparin-antithrombin covalent complex (SPLMWATH) was produced. By using polyethyleneimine-glutaraldehyde bonding technique, polyvinyl chloride (PVC) tubings were coated with SPLMWATH, heparin and low molecular weight heparin (LMWH). Spectrophotometry and dynamic clotting time experiment were used to determine the synthetic ratio of SPLMWATH, graft density, coating leaching ratio and to evaluate the antithrombogenicity of different coating on the PVC tubings. The results showed that the synthetic ratio of SPLMWATH was approximately 55%, and compared with heparin coating and LMWH coating, the graft density of SPLMWATH coating on the PVC tubing was smaller, but its coating stability and antithrombogenicity were significantly better than that of heparin coating and LMWH coating on the PVC tubings.


Subject(s)
Humans , Anticoagulants , Pharmacology , Coated Materials, Biocompatible , Pharmacology , Extracorporeal Circulation , Heparin, Low-Molecular-Weight , Chemistry , Pharmacology , Polyvinyl Chloride , Chemistry , Surface Properties
2.
Journal of Biomedical Engineering ; (6): 739-741, 2005.
Article in Chinese | WPRIM | ID: wpr-238352

ABSTRACT

In this study, heparin ionically coated polyvinyl chloride (PVC) material was prepared by heparin-benzalkonium chloride complex (Group A), heparin-benzalkonium bromide complex (Group B) and heparin-polyethyleneimine compound (Group C). Cytotoxicity evaluation was conducted by direct cell contact evaluation and MTT colorimetry method. The results showed Group A and Group B caused L-929 cells to die out while Group C showed good compatibility with cells. The OD levels of Group A and B were lower than that of the Group C in MTT test. Method A and method B of heparin coating had remarkable cytotoxicity, while method C had little cytotoxicity and could be further studied for clinical use.


Subject(s)
Animals , Mice , Cells, Cultured , Coated Materials, Biocompatible , Toxicity , Fibroblasts , Cell Biology , Heparin , Toxicity , Materials Testing , Polyvinyl Chloride , Toxicity
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