2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy
OBJECTIVES/SPECIFIC AIMS: The specific objectives of this project are (1) identify, test, and validate the parameters for a simplified NLOM imaging probe that will provide specific research and point-of-care information on biofilm presence, therapeutic need and response of individual wounds to treat...
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description | OBJECTIVES/SPECIFIC AIMS: The specific objectives of this project are (1) identify, test, and validate the parameters for a simplified NLOM imaging probe that will provide specific research and point-of-care information on biofilm presence, therapeutic need and response of individual wounds to treatment. (2) Identify specific proteomic and metabolomic biomarkers of (i) wound susceptibility to infection, (ii) wound response to the most commonly used antibacterial measures in wounds, and (iii) establish criteria for more effective interventions. METHODS/STUDY POPULATION: First, optimal use parameters for NLOM including illumination, field of view, focal length, linear Versus concentric image acquisition, detection and filter wavelengths were identified. Parameters for evaluation included ease and speed of imaging, ability to map diagnostic criteria. Next, using the optimised NLOM imaging modality in bacterial biofilm isolates and subsequently a rabbit ear model of biofilm wound infection, proteomic and metabolomic biomarkers of susceptibility to infection were identified. The effects of 2 standard debridement and anti-infective treatments, polyvidone-iodine solution or cetrimide 15%+ chlorhexidine gluconate 1.5% were mapped in situ for up to 10 days using the NLOM probe. RESULTS/ANTICIPATED RESULTS: Using the novel custom NLOM probe, high resolution mapping of wound biofilm infection, as well as the underlying tissue was performed throughout the onset, development, treatment, and resolution of wound biofilm infection. Specific microbiological, microstructural, oxygenation, and pH parameters were mapped at defined surface and subsurface locations and time-points. Findings included the determination that some standard antimicrobial formulations provide a supportive environment for wound infection, and that micro-channels within the biofilm and their interface with the tissues serve as an important predictor and indicator of wound infection establishment, progression, and response. DISCUSSION/SIGNIFICANCE OF IMPACT: The novel multimodality in vivo NLOM imaging approach establishes an important tool for earlier and more specific diagnosis of wound infection risk, virulence, and invasiveness along with markers of successful treatment, and a simple clinical imaging tool for improving wound infection prevention and treatment. |
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(2) Identify specific proteomic and metabolomic biomarkers of (i) wound susceptibility to infection, (ii) wound response to the most commonly used antibacterial measures in wounds, and (iii) establish criteria for more effective interventions. METHODS/STUDY POPULATION: First, optimal use parameters for NLOM including illumination, field of view, focal length, linear Versus concentric image acquisition, detection and filter wavelengths were identified. Parameters for evaluation included ease and speed of imaging, ability to map diagnostic criteria. Next, using the optimised NLOM imaging modality in bacterial biofilm isolates and subsequently a rabbit ear model of biofilm wound infection, proteomic and metabolomic biomarkers of susceptibility to infection were identified. The effects of 2 standard debridement and anti-infective treatments, polyvidone-iodine solution or cetrimide 15%+ chlorhexidine gluconate 1.5% were mapped in situ for up to 10 days using the NLOM probe. RESULTS/ANTICIPATED RESULTS: Using the novel custom NLOM probe, high resolution mapping of wound biofilm infection, as well as the underlying tissue was performed throughout the onset, development, treatment, and resolution of wound biofilm infection. Specific microbiological, microstructural, oxygenation, and pH parameters were mapped at defined surface and subsurface locations and time-points. Findings included the determination that some standard antimicrobial formulations provide a supportive environment for wound infection, and that micro-channels within the biofilm and their interface with the tissues serve as an important predictor and indicator of wound infection establishment, progression, and response. DISCUSSION/SIGNIFICANCE OF IMPACT: The novel multimodality in vivo NLOM imaging approach establishes an important tool for earlier and more specific diagnosis of wound infection risk, virulence, and invasiveness along with markers of successful treatment, and a simple clinical imaging tool for improving wound infection prevention and treatment.</description><identifier>ISSN: 2059-8661</identifier><identifier>EISSN: 2059-8661</identifier><identifier>DOI: 10.1017/cts.2017.233</identifier><language>eng</language><publisher>Cambridge: Cambridge University Press</publisher><subject>Biofilms ; Biomarkers ; Chlorhexidine ; Infections ; Invasiveness ; Iodine ; Mechanistic Basic to Clinical ; Metabolomics ; Oxygenation ; Population studies ; Virulence ; Wound infection</subject><ispartof>Journal of clinical and translational science, 2017-09, Vol.1 (S1), p.65-65</ispartof><rights>The Association for Clinical and Translational Science 2018 This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>The Association for Clinical and Translational Science 2018 2018 The Association for Clinical and Translational Science</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799197/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799197/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Wilder-Smith, Petra</creatorcontrib><creatorcontrib>Ajdaharian, Janet</creatorcontrib><creatorcontrib>Golabgir Anbarani, Afarin</creatorcontrib><creatorcontrib>Ho, Jessica</creatorcontrib><creatorcontrib>Sahni, Karan</creatorcontrib><creatorcontrib>Mittal, Richa</creatorcontrib><creatorcontrib>Potma, Eric</creatorcontrib><title>2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy</title><title>Journal of clinical and translational science</title><description>OBJECTIVES/SPECIFIC AIMS: The specific objectives of this project are (1) identify, test, and validate the parameters for a simplified NLOM imaging probe that will provide specific research and point-of-care information on biofilm presence, therapeutic need and response of individual wounds to treatment. (2) Identify specific proteomic and metabolomic biomarkers of (i) wound susceptibility to infection, (ii) wound response to the most commonly used antibacterial measures in wounds, and (iii) establish criteria for more effective interventions. METHODS/STUDY POPULATION: First, optimal use parameters for NLOM including illumination, field of view, focal length, linear Versus concentric image acquisition, detection and filter wavelengths were identified. Parameters for evaluation included ease and speed of imaging, ability to map diagnostic criteria. Next, using the optimised NLOM imaging modality in bacterial biofilm isolates and subsequently a rabbit ear model of biofilm wound infection, proteomic and metabolomic biomarkers of susceptibility to infection were identified. The effects of 2 standard debridement and anti-infective treatments, polyvidone-iodine solution or cetrimide 15%+ chlorhexidine gluconate 1.5% were mapped in situ for up to 10 days using the NLOM probe. RESULTS/ANTICIPATED RESULTS: Using the novel custom NLOM probe, high resolution mapping of wound biofilm infection, as well as the underlying tissue was performed throughout the onset, development, treatment, and resolution of wound biofilm infection. Specific microbiological, microstructural, oxygenation, and pH parameters were mapped at defined surface and subsurface locations and time-points. Findings included the determination that some standard antimicrobial formulations provide a supportive environment for wound infection, and that micro-channels within the biofilm and their interface with the tissues serve as an important predictor and indicator of wound infection establishment, progression, and response. DISCUSSION/SIGNIFICANCE OF IMPACT: The novel multimodality in vivo NLOM imaging approach establishes an important tool for earlier and more specific diagnosis of wound infection risk, virulence, and invasiveness along with markers of successful treatment, and a simple clinical imaging tool for improving wound infection prevention and treatment.</description><subject>Biofilms</subject><subject>Biomarkers</subject><subject>Chlorhexidine</subject><subject>Infections</subject><subject>Invasiveness</subject><subject>Iodine</subject><subject>Mechanistic Basic to Clinical</subject><subject>Metabolomics</subject><subject>Oxygenation</subject><subject>Population studies</subject><subject>Virulence</subject><subject>Wound infection</subject><issn>2059-8661</issn><issn>2059-8661</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpVkMFKAzEQhoNUsNTefAOv7ppksjPJRZCiVih40XPIpoluaXdrsiv49m5pET3ND_PzzfAxdiV4KbigW9_nUo6hlABnbCp5ZQqNKCZ_8gWb57zhnAstEQGmbCIV0SU7j26bw_w0Z-zt8eF1sSxWL0_Pi_tV4YXkVAApT2sVuCEUCjSaoL0RNZKvouMEqg68CkCSCEgTylgp5yNKjCFGCTN2d-Tuh3oX1j60fXJbu0_NzqVv27nG_t-0zYd9774skjHC0Ai4PgFS9zmE3NtNN6R2_NlKDqgBQVZj6-bY8qnLOYX4e0Fwe3BlR1f24MqOruAHjRRY_g</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Wilder-Smith, Petra</creator><creator>Ajdaharian, Janet</creator><creator>Golabgir Anbarani, Afarin</creator><creator>Ho, Jessica</creator><creator>Sahni, Karan</creator><creator>Mittal, Richa</creator><creator>Potma, Eric</creator><general>Cambridge University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20170901</creationdate><title>2477</title><author>Wilder-Smith, Petra ; Ajdaharian, Janet ; Golabgir Anbarani, Afarin ; Ho, Jessica ; Sahni, Karan ; Mittal, Richa ; Potma, Eric</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1207-374c7d4e0976143869e8c91b67c5fa0734be05e37277378762f54acf626feff23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Biofilms</topic><topic>Biomarkers</topic><topic>Chlorhexidine</topic><topic>Infections</topic><topic>Invasiveness</topic><topic>Iodine</topic><topic>Mechanistic Basic to Clinical</topic><topic>Metabolomics</topic><topic>Oxygenation</topic><topic>Population studies</topic><topic>Virulence</topic><topic>Wound infection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilder-Smith, Petra</creatorcontrib><creatorcontrib>Ajdaharian, Janet</creatorcontrib><creatorcontrib>Golabgir Anbarani, Afarin</creatorcontrib><creatorcontrib>Ho, Jessica</creatorcontrib><creatorcontrib>Sahni, Karan</creatorcontrib><creatorcontrib>Mittal, Richa</creatorcontrib><creatorcontrib>Potma, Eric</creatorcontrib><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical and translational science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wilder-Smith, Petra</au><au>Ajdaharian, Janet</au><au>Golabgir Anbarani, Afarin</au><au>Ho, Jessica</au><au>Sahni, Karan</au><au>Mittal, Richa</au><au>Potma, Eric</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy</atitle><jtitle>Journal of clinical and translational science</jtitle><date>2017-09-01</date><risdate>2017</risdate><volume>1</volume><issue>S1</issue><spage>65</spage><epage>65</epage><pages>65-65</pages><issn>2059-8661</issn><eissn>2059-8661</eissn><abstract>OBJECTIVES/SPECIFIC AIMS: The specific objectives of this project are (1) identify, test, and validate the parameters for a simplified NLOM imaging probe that will provide specific research and point-of-care information on biofilm presence, therapeutic need and response of individual wounds to treatment. (2) Identify specific proteomic and metabolomic biomarkers of (i) wound susceptibility to infection, (ii) wound response to the most commonly used antibacterial measures in wounds, and (iii) establish criteria for more effective interventions. METHODS/STUDY POPULATION: First, optimal use parameters for NLOM including illumination, field of view, focal length, linear Versus concentric image acquisition, detection and filter wavelengths were identified. Parameters for evaluation included ease and speed of imaging, ability to map diagnostic criteria. Next, using the optimised NLOM imaging modality in bacterial biofilm isolates and subsequently a rabbit ear model of biofilm wound infection, proteomic and metabolomic biomarkers of susceptibility to infection were identified. The effects of 2 standard debridement and anti-infective treatments, polyvidone-iodine solution or cetrimide 15%+ chlorhexidine gluconate 1.5% were mapped in situ for up to 10 days using the NLOM probe. RESULTS/ANTICIPATED RESULTS: Using the novel custom NLOM probe, high resolution mapping of wound biofilm infection, as well as the underlying tissue was performed throughout the onset, development, treatment, and resolution of wound biofilm infection. Specific microbiological, microstructural, oxygenation, and pH parameters were mapped at defined surface and subsurface locations and time-points. Findings included the determination that some standard antimicrobial formulations provide a supportive environment for wound infection, and that micro-channels within the biofilm and their interface with the tissues serve as an important predictor and indicator of wound infection establishment, progression, and response. DISCUSSION/SIGNIFICANCE OF IMPACT: The novel multimodality in vivo NLOM imaging approach establishes an important tool for earlier and more specific diagnosis of wound infection risk, virulence, and invasiveness along with markers of successful treatment, and a simple clinical imaging tool for improving wound infection prevention and treatment.</abstract><cop>Cambridge</cop><pub>Cambridge University Press</pub><doi>10.1017/cts.2017.233</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biofilms Biomarkers Chlorhexidine Infections Invasiveness Iodine Mechanistic Basic to Clinical Metabolomics Oxygenation Population studies Virulence Wound infection |
title | 2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy |
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