Clinical Significance. Biomaterials are widely used for devices that are implanted (e.g., catheters, defibrillators, stents, and sensors) and are being considered for tissue engineering applications to provide tissue restructuring after disease or injury. For all biomaterials, biocompatibility must involve not only an ability to integrate into the host, but also to function. Macrophage cells provide the chemical cues that act in synergy with the tissue that surrounds the implant to integrate it with the host. Despite many years of in vitro cell culture studies to assess the macrophage response to materials and in vivo histopathological experiments, a true theory of biocompatibility does not exist. Absolute confirmation of the in vivo signaling molecules involved has remained elusive due to lack of bioanalytical tools capable of addressing this complex chemical analysis problem. Achieving rapid progress in tissue bioengineering will require an in vivo understanding of the signaling chemicals involved at different temporal stages after biomaterial implantation. Experimental Approach. The proposed work has three specific aims.
Aim 1 focuses on creating novel microdialysis sampling strategies for in vivo measurements of the foreign body response chemistry. Particular analyte targets include cytokines, eicosanoids, and matrix metalloproteinases.
Aim 2 will use methods previously created in conjunction with Aim 1 to test the in vivo bioagent agent release to implanted biomaterials. Finally, Aim 3 will focus on understanding how different prophylactic approaches such as cytokine, drug, or growth factor release affects the underlying macrophage cellular signaling chemistry. Lay Public Health Statement. Implantation of effective devices or engineered tissue provides promise for improvement of quality of life under many circumstances. However, these devices often have incompatibility with the host and sometimes need to be removed. The frequency of the explantation process would be significantly reduced by a more quantitative approach to in vivo measurement of the responsible chemical signals associated with the foreign body response. Additional benefits may arise for the fields that require an intimate understanding and need to control a wound healing response such as plastic surgery. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB001441-06
Application #
7483744
Study Section
Enabling Bioanalytical and Biophysical Technologies Study Section (EBT)
Program Officer
Lee, Albert
Project Start
2003-07-11
Project End
2009-05-31
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
6
Fiscal Year
2008
Total Cost
$257,520
Indirect Cost
Name
Rensselaer Polytechnic Institute
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
002430742
City
Troy
State
NY
Country
United States
Zip Code
12180
Stenken, Julie A; Poschenrieder, Andreas J (2015) Bioanalytical chemistry of cytokines--a review. Anal Chim Acta 853:95-115
Paul, David W; Stenken, Julie A (2015) A review of flux considerations for in vivo neurochemical measurements. Analyst 140:3709-30
Sides, Cynthia R; Stenken, Julie A (2014) Microdialysis sampling techniques applied to studies of the foreign body reaction. Eur J Pharm Sci 57:74-86
von Grote, Erika C; Venkatakrishnan, Venkat; Duo, Jia et al. (2011) Long-term subcutaneous microdialysis sampling and qRT-PCR of MCP-1, IL-6 and IL-10 in freely-moving rats. Mol Biosyst 7:150-61
Wisniewski, Natalie A; Klueh, Uli; Stenken, Julie (2011) Interstitial fluid physiology as it relates to glucose monitoring technologies: symposium introduction. J Diabetes Sci Technol 5:579-82
Duo, Jia; Stenken, Julie A (2011) In vitro and in vivo affinity microdialysis sampling of cytokines using heparin-immobilized microspheres. Anal Bioanal Chem 399:783-93
Herbaugh, Anthony W; Stenken, Julie A (2011) Antibody-enhanced microdialysis collection of CCL2 from rat brain. J Neurosci Methods 202:124-7
Duo, Jia; Stenken, Julie A (2011) Heparin-immobilized microspheres for the capture of cytokines. Anal Bioanal Chem 399:773-82
Mou, Xiaodun; Lennartz, Michelle R; Loegering, Daniel J et al. (2011) Modulation of the foreign body reaction for implants in the subcutaneous space: microdialysis probes as localized drug delivery/sampling devices. J Diabetes Sci Technol 5:619-31
Stenken, Julie A; Church, Martin K; Gill, Carolyn A et al. (2010) How minimally invasive is microdialysis sampling? A cautionary note for cytokine collection in human skin and other clinical studies. AAPS J 12:73-8

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