DocumentCode
386434
Title
Incorporating dexamethasone release in hydrogel coated microdialysis probes
Author
Norton, Lon ; Wisniewski, Natalie ; Klima, Kathryn ; Reichert, W. Monty
Author_Institution
Dept. of Biomed. Eng., Duke Univ., Durham, NC, USA
Volume
1
fYear
2002
fDate
2002
Firstpage
508
Abstract
Microdialysis probes were used to study the influence of membrane modifications on glucose recovery. The microdialysis membranes were modified by adding a hydrogel coating. The coated probes were evaluated in vitro and in vivo for glucose permeability. It was found that percent glucose recovery was reduced by 25% in vitro using hydrogel coated probes compared to control probes. However, the glucose recoveries of the coated probes in vivo were more similar to that of control probe, with an average difference of 6%. From these results, it was concluded that the tissue resistance to glucose transport was much greater than the resistances of the hydrogel and biofouling. The hydrogel formulation was then changed to deliver a tissue modifying drug to reduce the tissue resistance. Dexamethasone was incorporated into the hydrogels to reduce inflammation. These hydrogels are capable of releasing drug up to 14 days. The dexamethasone hydrogels will be coated onto microdialysis probes in future in vivo studies to determine the effect of reduced inflammatory response on glucose recovery.
Keywords
drug delivery systems; gels; membranes; probes; 14 d; biofouling; coated probes; control probes; dexamethasone; dexamethasone release incorporation; glucose recovery; hydrogel; hydrogel coated microdialysis probes; hydrogel coating; hydrogel formulation; inflammation reduction; membrane modifications; microdialysis probes; reduced inflammatory response; tissue modifying drug; tissue resistance; Biomembranes; Biosensors; Coatings; Drugs; Immune system; In vitro; In vivo; Permeability; Probes; Sugar;
fLanguage
English
Publisher
ieee
Conference_Titel
Engineering in Medicine and Biology, 2002. 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society EMBS/BMES Conference, 2002. Proceedings of the Second Joint
ISSN
1094-687X
Print_ISBN
0-7803-7612-9
Type
conf
DOI
10.1109/IEMBS.2002.1136919
Filename
1136919
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