Non-invasive monitoring of pharmacodynamics during the skin wound healing process using multimodal optical microscopy

Objective Impaired diabetic wound healing is one of the serious complications associated with diabetes. In patients with diabetes, this impairment is characterized by several physiological abnormalities such as metabolic changes, reduced collagen production, and diminished angiogenesis. We designed...

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Main Authors: David Adams, Jose Rico-Jimenez, Jang Hyuk Lee, Aneesh Alex, Salma Musaad, Eric Chaney, Ronit Barkalifa, Eric Olson, Marina Marjanovic, Zane Arp, Stephen A Boppart, Darold R Spillman Jr
Format: Article
Language:English
Published: BMJ Publishing Group 2020-04-01
Series:BMJ Open Diabetes Research & Care
Online Access:https://drc.bmj.com/content/8/1/e000974.full
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spelling doaj-c8746c5681c149ba88036e26357201c02021-06-10T10:04:18ZengBMJ Publishing GroupBMJ Open Diabetes Research & Care2052-48972020-04-018110.1136/bmjdrc-2019-000974Non-invasive monitoring of pharmacodynamics during the skin wound healing process using multimodal optical microscopyDavid Adams0Jose Rico-Jimenez1Jang Hyuk Lee2Aneesh Alex3Salma Musaad4Eric Chaney5Ronit Barkalifa6Eric Olson7Marina Marjanovic8Zane Arp9Stephen A Boppart10Darold R Spillman Jr11Eli Lilly and Company, Indianapolis, Indiana, USABeckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USABeckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USAGlaxoSmithKline, Philadelphia, Pennsylvania, USAInterdisciplinary Health Sciences Institute, University of Illinois at Urbana-Champaign, Urbana, Illinois, USABeckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USABeckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USAGlaxoSmithKline, Philadelphia, Pennsylvania, USABeckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USAGlaxoSmithKline, Philadelphia, Pennsylvania, USABeckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USABeckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USAObjective Impaired diabetic wound healing is one of the serious complications associated with diabetes. In patients with diabetes, this impairment is characterized by several physiological abnormalities such as metabolic changes, reduced collagen production, and diminished angiogenesis. We designed and developed a multimodal optical imaging system that can longitudinally monitor formation of new blood vessels, metabolic changes, and collagen deposition in a non-invasive, label-free manner.Research design and methods The closure of a skin wound in (db/db) mice, which presents delayed wound healing pathologically similar to conditions in human type 2 diabetes mellitus, was non-invasively followed using the custom-built multimodal microscope. In this microscope, optical coherence tomography angiography was used for studying neovascularization, fluorescence lifetime imaging microscopy for nicotinamide adenine dinucleotide (phosphate) (NAD(P)H) assessment, fluorescence intensity changes of NAD(P)H and flavin adenine dinucleotide (FAD) cofactors for evaluating metabolic changes, and second harmonic generation microscopy for analyzing collagen deposition and organization. The animals were separated into four groups: control, placebo, low concentration (LC), and high concentration (HC) treatment. Images of the wound and surrounding areas were acquired at different time points during a 28-day period.Results Various physiological changes measured using the optical imaging modalities at different phases of wound healing were compared. A statistically significant improvement in the functional relationship between angiogenesis, metabolism, and structural integrity was observed in the HC group.Conclusions This study demonstrated the capability of multimodal optical imaging to non-invasively monitor various physiological aspects of the wound healing process, and thus become a promising tool in the development of better diagnostic, treatment, and monitoring strategies for diabetic wound care.https://drc.bmj.com/content/8/1/e000974.full
collection DOAJ
language English
format Article
sources DOAJ
author David Adams
Jose Rico-Jimenez
Jang Hyuk Lee
Aneesh Alex
Salma Musaad
Eric Chaney
Ronit Barkalifa
Eric Olson
Marina Marjanovic
Zane Arp
Stephen A Boppart
Darold R Spillman Jr
spellingShingle David Adams
Jose Rico-Jimenez
Jang Hyuk Lee
Aneesh Alex
Salma Musaad
Eric Chaney
Ronit Barkalifa
Eric Olson
Marina Marjanovic
Zane Arp
Stephen A Boppart
Darold R Spillman Jr
Non-invasive monitoring of pharmacodynamics during the skin wound healing process using multimodal optical microscopy
BMJ Open Diabetes Research & Care
author_facet David Adams
Jose Rico-Jimenez
Jang Hyuk Lee
Aneesh Alex
Salma Musaad
Eric Chaney
Ronit Barkalifa
Eric Olson
Marina Marjanovic
Zane Arp
Stephen A Boppart
Darold R Spillman Jr
author_sort David Adams
title Non-invasive monitoring of pharmacodynamics during the skin wound healing process using multimodal optical microscopy
title_short Non-invasive monitoring of pharmacodynamics during the skin wound healing process using multimodal optical microscopy
title_full Non-invasive monitoring of pharmacodynamics during the skin wound healing process using multimodal optical microscopy
title_fullStr Non-invasive monitoring of pharmacodynamics during the skin wound healing process using multimodal optical microscopy
title_full_unstemmed Non-invasive monitoring of pharmacodynamics during the skin wound healing process using multimodal optical microscopy
title_sort non-invasive monitoring of pharmacodynamics during the skin wound healing process using multimodal optical microscopy
publisher BMJ Publishing Group
series BMJ Open Diabetes Research & Care
issn 2052-4897
publishDate 2020-04-01
description Objective Impaired diabetic wound healing is one of the serious complications associated with diabetes. In patients with diabetes, this impairment is characterized by several physiological abnormalities such as metabolic changes, reduced collagen production, and diminished angiogenesis. We designed and developed a multimodal optical imaging system that can longitudinally monitor formation of new blood vessels, metabolic changes, and collagen deposition in a non-invasive, label-free manner.Research design and methods The closure of a skin wound in (db/db) mice, which presents delayed wound healing pathologically similar to conditions in human type 2 diabetes mellitus, was non-invasively followed using the custom-built multimodal microscope. In this microscope, optical coherence tomography angiography was used for studying neovascularization, fluorescence lifetime imaging microscopy for nicotinamide adenine dinucleotide (phosphate) (NAD(P)H) assessment, fluorescence intensity changes of NAD(P)H and flavin adenine dinucleotide (FAD) cofactors for evaluating metabolic changes, and second harmonic generation microscopy for analyzing collagen deposition and organization. The animals were separated into four groups: control, placebo, low concentration (LC), and high concentration (HC) treatment. Images of the wound and surrounding areas were acquired at different time points during a 28-day period.Results Various physiological changes measured using the optical imaging modalities at different phases of wound healing were compared. A statistically significant improvement in the functional relationship between angiogenesis, metabolism, and structural integrity was observed in the HC group.Conclusions This study demonstrated the capability of multimodal optical imaging to non-invasively monitor various physiological aspects of the wound healing process, and thus become a promising tool in the development of better diagnostic, treatment, and monitoring strategies for diabetic wound care.
url https://drc.bmj.com/content/8/1/e000974.full
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