Chemically modified polystyrene containing pendant vinyl groups: a photosensitive polymer exhibiting chemical amplification

Polymer ◽  
1983 ◽  
Vol 24 (1) ◽  
pp. 114-116 ◽  
Author(s):  
M.Jean Farrall ◽  
Michele Alexis ◽  
Mark Trecarten
2008 ◽  
Vol 44 (5) ◽  
pp. 1501-1511 ◽  
Author(s):  
Jamil R. Memon ◽  
Saima Q. Memon ◽  
M.I. Bhanger ◽  
M.Y. Khuhawar ◽  
Geoffrey C. Allen ◽  
...  

2015 ◽  
Vol 51 (52) ◽  
pp. 10377-10380 ◽  
Author(s):  
Tomàs Guinovart ◽  
Pascal Blondeau ◽  
Francisco J. Andrade

Novel membrane-free chemically modified polystyrene microspheres for the optical detection of sulphate in aqueous media are introduced.


1989 ◽  
Vol 61 (01) ◽  
pp. 131-136 ◽  
Author(s):  
Richard A Harvey ◽  
Hugh C Kim ◽  
Jonathan Pincus ◽  
Stanley Z Trooskin ◽  
Josiah N Wilcox ◽  
...  

SummaryTissue plasminogen activator labeled with radioactive iodine (125I-tPA) was immobilized on vascular prostheses chemically modified with a thin coating of water-insoluble surfactant, tridodecylmethylammonium chloride (TDM AC). Surfactant- treated Dacron, polytetrafluoroethylene (PTFE), silastic, polyethylene and polyurethane bound appreciable amounts of 125I- tPA (5-30 μg 125I-tPA/cm2). Upon exposure to human plasma, the amount of 125I-tPA bound to the surface shows an initial drop during the first hour of incubation, followed by a slower, roughly exponential release with a t½ of appoximately 75 hours. Prostheses containing bound tPA show fibrinolytic activity as measured both by lysis of clots formed in vitro, and by hydrolysis of a synthetic polypeptide substrate. Prior to incubation in plasma, tPA bound to a polymer surface has an enzymic activity similar, if not identical to that of the native enzyme in buffered solution. However, exposure to plasma causes a decrease in the fibrinolytic activity of both bound tPA and enzyme released from the surface of the polymer. These data demonstrate that surfactant-treated prostheses can bind tPA, and that these chemically modified devices can act as a slow-release drug delivery system with the potential for reducing prosthesis-induced thromboembolism.


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