Distribution of [3H]Dexamethasone in Rat Subcutaneous Tissue after Delivery from Osmotic Pumps
Abstract
Inflammation surrounding implantable glucose sensors may be controlled through local release of dexamethasone at the site of implantation. In the present study, we evaluated the distribution of dexamethasone in rat subcutaneous tissue during the first 2.5 days after local release. Osmotic pumps containing [3H]dexamethasone were implanted into the subcutaneous tissue of rats. Digital autoradiography was used to measure the distribution of the [3H]dexamethasone within the subcutaneous tissue at 6, 24, and 60 h after implantation. Measured concentration profiles, near the catheter tip through which the agent was released, were compared to mathematical models of drug diffusion and elimination. The results demonstrate that the majority of the [3H]dexamethasone delivered into the subcutaneous tissue was found within a 3 mm region surrounding the catheter tip. There was good agreement between the experimental data and the mathematical model. The diffusion coefficient for dexamethasone in subcutaneous tissue was found to be D = 4.11 +/- 1.77 x 10(-10) m2/s, and the elimination rate constant was found to be k = 3.65 +/- 2.24 x 10(-5) s(-1). The diffusion coefficient and elimination rate constants for dexamethasone in subcutaneous tissue have not been previously reported. The use of a mathematical model may be useful in predicting the effectiveness of local delivery of dexamethasone around implantable glucose sensors.
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Moussy et al. reported that locally administered [3H]dexamethasone travelled an average of only 2.70 mm from the delivery point after 24 h.
“Moussy et al. reported that [3H]DX travelled only an average of 2.70 mm from the point of delivery after 24 h when administered locally.180”
From Biocompatible Materials for Continuous Glucose Monitoring Devices (2013) · cites this paper as [180]
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Biocompatible Materials for Continuous Glucose Monitoring Devices
Nichols, S. P., Koh, A., Storm, W. L., Shin, J. H., & Schoenfisch, M. H. (2013) · Chemical Reviews · doi:10.1021/cr300387j · Cited by 347 · see citing works
Ward, W. K., Hansen, J. C., Massoud, R. G., Engle, J. M., Takeno, M. M., & Hauch, K. D. (2010) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.32651 · Cited by 26 · see citing works
- Authors
- Moussy, Y., Hersh, L., & Dungel, P.
- Affiliations
- University of South Florida (US)
- Corresponding author
- Moussy, Y.
- ORCID
- Dungel, P.
- Venue
- Biotechnology Progress
- Publisher
- Wiley
- Published
- 2006-06-02
- Volume
- 22
- Issue
- 3
- Pages
- 819-824
- ISSN
- 1520-6033 (ISSN-L)
- 8756-7938
- OpenAlex
- W1990085094
- Cited by
- 16
- References
- 0
- Citations by year
- 2019: 2 · 2018: 1 · 2017: 1 · 2013: 2 · 2012: 1
- FWCI
- 1.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biotechnology Progress (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Biomedical Imaging and Bioengineering (5 R01 EB01640-03, R01EB001640)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advancements in Transdermal Drug Delivery
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Keywords
- dexamethasone, subcutaneous tissue, osmotic pump, local drug delivery, implantable glucose sensor, drug diffusion, diffusion coefficient, elimination rate constant, tissue inflammation, autoradiography
- MeSH terms
- Animals, Autoradiography, Dexamethasone, Injections, Subcutaneous, Male, Models, Biological, Osmotic Pressure, Tritium, Infusion Pumps, Implantable, Drug Delivery Systems, Rats, Sprague-Dawley, Cell Culture Techniques, Subcutaneous Tissue, Rats
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