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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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Autores principales: Wilder-Smith, Petra, Ajdaharian, Janet, Golabgir Anbarani, Afarin, Ho, Jessica, Sahni, Karan, Mittal, Richa, Potma, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799197/
http://dx.doi.org/10.1017/cts.2017.233
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author Wilder-Smith, Petra
Ajdaharian, Janet
Golabgir Anbarani, Afarin
Ho, Jessica
Sahni, Karan
Mittal, Richa
Potma, Eric
author_facet Wilder-Smith, Petra
Ajdaharian, Janet
Golabgir Anbarani, Afarin
Ho, Jessica
Sahni, Karan
Mittal, Richa
Potma, Eric
author_sort Wilder-Smith, Petra
collection PubMed
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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spelling pubmed-67991972019-10-28 2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy Wilder-Smith, Petra Ajdaharian, Janet Golabgir Anbarani, Afarin Ho, Jessica Sahni, Karan Mittal, Richa Potma, Eric J Clin Transl Sci Mechanistic Basic to Clinical 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. Cambridge University Press 2018-05-10 /pmc/articles/PMC6799197/ http://dx.doi.org/10.1017/cts.2017.233 Text en © The Association for Clinical and Translational Science 2018 http://creativecommons.org/licenses/by/4.0/ 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.
spellingShingle Mechanistic Basic to Clinical
Wilder-Smith, Petra
Ajdaharian, Janet
Golabgir Anbarani, Afarin
Ho, Jessica
Sahni, Karan
Mittal, Richa
Potma, Eric
2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy
title 2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy
title_full 2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy
title_fullStr 2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy
title_full_unstemmed 2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy
title_short 2477: Biofilms in wounds: Detection, individualizing treatment and monitoring response to therapy
title_sort 2477: biofilms in wounds: detection, individualizing treatment and monitoring response to therapy
topic Mechanistic Basic to Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799197/
http://dx.doi.org/10.1017/cts.2017.233
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