scholarly journals Surface modification of polyvinyl chloride towards blood compatibility

1984 ◽  
Vol 6 (6) ◽  
pp. 1087-1091 ◽  
Author(s):  
Geetha Kurian ◽  
Chandra P Sharma
Author(s):  
Nan Huang ◽  
Ping Yang ◽  
Yong Xiang Leng ◽  
Jun Ying Chen ◽  
Jin Wang ◽  
...  

1989 ◽  
Vol 12 (6) ◽  
pp. 390-394 ◽  
Author(s):  
E. Brinkman ◽  
A. Poot ◽  
T. Beugeling ◽  
L. Van Der Does ◽  
A. Bantjes

Pellethane 2363 80A catheters were modified with poly(ethylene oxide) in order to improve their blood compatibility. Contact angle measurements showed that Pellethane 2363 80A surfaces had increased wettability after this modification. The results of in vitro blood compatibility tests showed that surface modification with poly(ethylene oxide) resulted in a five-fold reduction of platelet deposition. Activation of coagulation was not affected.


2019 ◽  
Vol 218 ◽  
pp. 167-172 ◽  
Author(s):  
Shuaijun Chen ◽  
Yingshuang Zhang ◽  
Chenchao Guo ◽  
Yiwei Zhong ◽  
Kangyu Wang ◽  
...  

2016 ◽  
Vol 6 (10) ◽  
pp. 780-787 ◽  
Author(s):  
Eugene Lih ◽  
So Yoon Chi ◽  
Tae Il Son ◽  
Yoon Ki Joung ◽  
Dong Keun Han

2008 ◽  
Vol 15 (06) ◽  
pp. 711-715 ◽  
Author(s):  
KEISUKE KUROSE ◽  
TETSUJI OKUDA ◽  
SATOSHI NAKAI ◽  
TSUNG-YUEH TSAI ◽  
WATARU NISHIJIMA ◽  
...  

The surface modification mechanism of polyvinyl chloride (PVC) by ozonation was investigated to study the selective hydrophilization of PVC surface among other plastics. Infrared analysis confirmed the increase of hydrophilic groups. XPS analysis revealed that the increase was due to the structural change in chlorine group in PVC to hydroxylic acid, ketone, and carboxylic groups by ozonation. This chemical reaction by ozone could occur only for polymers with chlorides in its structure and resulted in the selective hydrophilization of PVC among various polymers.


2018 ◽  
Vol 5 (6) ◽  
pp. 065401 ◽  
Author(s):  
Lingling Zhang ◽  
Xiaojuan Chen ◽  
Pingsheng Liu ◽  
Jing Wang ◽  
Haomiao Zhu ◽  
...  

1998 ◽  
Vol 4 (S2) ◽  
pp. 926-927
Author(s):  
S. Jo ◽  
T. Li ◽  
K. Park

Although significant advances have been made in the development of biocompatible materials, currently available biomaterials still present a number of problems for in vivo applications. One of the attempts to improve the biocompatibility, especially blood-compatibility, of biomaterials has been surface modification. Typically, poly(ethylene glycol) (PEG), albumin, heparin, and phospholipid molecules are grafted to the surface to prevent protein adsorption and cell adhesion. We have been modifying biomaterial surfaces by covalent grafting of PEG and albumin. The control and modified surfaces were examined using an atomic force microscope (AFM). In this study, we examined the surface topography changes by surface modification using PEO grafting to glass as a model system.Glass surfaces were modified with PEO using (N-triethoxysilylpropyl)-Omonomethoxy PEG urethane (PEG-Si), a PEG derivative containing a hydrophobic carbon chain and triethoxysilyl group at one end of the PEG chain. The presence of the hydrophobic carbon chain allowed self-assembly on the surface and triethoxysilyl resulted in covalent bonding to glass surfaces


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