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HERO ID
4394500
Reference Type
Journal Article
Title
Effects of poly(ethylene glycol) doping on the behavior of pyrene, rhodamine 6G, and acrylodan-labeled bovine serum albumin sequestered within tetramethylorthosilane-derived sol-gel-processed composites
Author(s)
Baker, GA; Jordan, JD; Bright, FV
Year
1998
Is Peer Reviewed?
Yes
Journal
Journal of Sol-Gel Science and Technology
ISSN:
0928-0707
EISSN:
1573-4846
Publisher
Springer Netherlands
Location
DORDRECHT
Volume
11
Issue
1
Page Numbers
43-54
Language
English
DOI
10.1023/A:1008680714826
Web of Science Id
WOS:000072873100006
Abstract
We investigate the effects of controlled poly(ethylene glycol) (PEG) doping on the behavior of pyrene, rhodamine 6G (R6G), and acrylodan-labeled bovine serum albumin (BSA-Ac) sequestered within tetramethyiorthosilicate (TMOS)-derived sol-gel-processed materials. To probe the dipolarity of the local environment within the composite we performed static fluorescence measurements on pyrene as the composites aged. We found that small levels of PEG loading effected significant enhancements in the local dipolarity surrounding the average pyrene molecule. Time-resolved fluorescence anisotropy measurements were used to follow the rotational reorientation dynamics of R6G as the composites aged. As the PEG loading increased, the R6G reorientational mobility increased. Nitrogen adsorption techniques were used to quantify the effects of PEG doping level on the surface area and final xerogel pore features. A large reduction in surface area was observed with PEG doping, but no detectable change in pore size was noted. The effects of PEG doping on a biomolecule were probed by following the time-resolved fluorescence anisotropy decay of BSA-Ac. These results showed that PEG doping resulted in increased biomolecule dynamics relative to that found for a neat, undoped TMOS-derived composites. Together these results show that PEG doping can be used to tune the sol-gel-processed composite dipolarity, alter the mobility of dopants sequestered within the composite, control analyte acessibility to the sensing chemistry, and modulate the internal dynamics within a biodopant.
Keywords
time-resolved fluorescence; sol-gel glass doping; dopant dynamics; polymer co-doping; poly ethylene glycol
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