Rapid biocompatibility analysis of materials via in vivo fluorescence imaging of mouse models.

BACKGROUND: Many materials are unsuitable for medical use because of poor biocompatibility. Recently, advances in the high throughput synthesis of biomaterials has significantly increased the number of potential biomaterials, however current biocompatibility analysis methods are slow and require his...

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Main Authors: Kaitlin M Bratlie, Tram T Dang, Stephen Lyle, Matthias Nahrendorf, Ralph Weissleder, Robert Langer, Daniel G Anderson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2850367?pdf=render
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spelling doaj-14189a502b854fedb05133e23f20547a2020-11-25T02:03:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-01-0154e1003210.1371/journal.pone.0010032Rapid biocompatibility analysis of materials via in vivo fluorescence imaging of mouse models.Kaitlin M BratlieTram T DangStephen LyleMatthias NahrendorfRalph WeisslederRobert LangerDaniel G AndersonBACKGROUND: Many materials are unsuitable for medical use because of poor biocompatibility. Recently, advances in the high throughput synthesis of biomaterials has significantly increased the number of potential biomaterials, however current biocompatibility analysis methods are slow and require histological analysis. METHODOLOGY/PRINCIPAL FINDINGS: Here we develop rapid, non-invasive methods for in vivo quantification of the inflammatory response to implanted biomaterials. Materials were placed subcutaneously in an array format and monitored for host responses as per ISO 10993-6: 2001. Host cell activity in response to these materials was imaged kinetically, in vivo using fluorescent whole animal imaging. Data captured using whole animal imaging displayed similar temporal trends in cellular recruitment of phagocytes to the biomaterials compared to histological analysis. CONCLUSIONS/SIGNIFICANCE: Histological analysis similarity validates this technique as a novel, rapid approach for screening biocompatibility of implanted materials. Through this technique there exists the possibility to rapidly screen large libraries of polymers in vivo.http://europepmc.org/articles/PMC2850367?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kaitlin M Bratlie
Tram T Dang
Stephen Lyle
Matthias Nahrendorf
Ralph Weissleder
Robert Langer
Daniel G Anderson
spellingShingle Kaitlin M Bratlie
Tram T Dang
Stephen Lyle
Matthias Nahrendorf
Ralph Weissleder
Robert Langer
Daniel G Anderson
Rapid biocompatibility analysis of materials via in vivo fluorescence imaging of mouse models.
PLoS ONE
author_facet Kaitlin M Bratlie
Tram T Dang
Stephen Lyle
Matthias Nahrendorf
Ralph Weissleder
Robert Langer
Daniel G Anderson
author_sort Kaitlin M Bratlie
title Rapid biocompatibility analysis of materials via in vivo fluorescence imaging of mouse models.
title_short Rapid biocompatibility analysis of materials via in vivo fluorescence imaging of mouse models.
title_full Rapid biocompatibility analysis of materials via in vivo fluorescence imaging of mouse models.
title_fullStr Rapid biocompatibility analysis of materials via in vivo fluorescence imaging of mouse models.
title_full_unstemmed Rapid biocompatibility analysis of materials via in vivo fluorescence imaging of mouse models.
title_sort rapid biocompatibility analysis of materials via in vivo fluorescence imaging of mouse models.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-01-01
description BACKGROUND: Many materials are unsuitable for medical use because of poor biocompatibility. Recently, advances in the high throughput synthesis of biomaterials has significantly increased the number of potential biomaterials, however current biocompatibility analysis methods are slow and require histological analysis. METHODOLOGY/PRINCIPAL FINDINGS: Here we develop rapid, non-invasive methods for in vivo quantification of the inflammatory response to implanted biomaterials. Materials were placed subcutaneously in an array format and monitored for host responses as per ISO 10993-6: 2001. Host cell activity in response to these materials was imaged kinetically, in vivo using fluorescent whole animal imaging. Data captured using whole animal imaging displayed similar temporal trends in cellular recruitment of phagocytes to the biomaterials compared to histological analysis. CONCLUSIONS/SIGNIFICANCE: Histological analysis similarity validates this technique as a novel, rapid approach for screening biocompatibility of implanted materials. Through this technique there exists the possibility to rapidly screen large libraries of polymers in vivo.
url http://europepmc.org/articles/PMC2850367?pdf=render
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