Hydrogel Microfilaments toward Intradermal Health Monitoring
Digital health promises a paradigm shift for medicine where biomarkers in individuals are continuously monitored to improve diagnosis and treatment of disease. To that end, a technology for minimally invasive quantification of endogenous analytes in bodily fluids will be required. Here, we describe...
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Published in | iScience Vol. 21; pp. 328 - 340 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
22.11.2019
Elsevier |
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Abstract | Digital health promises a paradigm shift for medicine where biomarkers in individuals are continuously monitored to improve diagnosis and treatment of disease. To that end, a technology for minimally invasive quantification of endogenous analytes in bodily fluids will be required. Here, we describe a strategy for designing and fabricating hydrogel microfilaments that can penetrate the skin while allowing for optical fluorescence sensing. The polyacrylamide formulation was selected to provide high elastic modulus in the dehydrated state and optical transparency in the hydrated state. The microfilaments can be covalently tethered to a fluorescent aptamer to enable functional sensing. The microfilament array can penetrate the skin with low pain and without breaking, contact the dermal interstitial fluid, and be easily removed from the skin. In the future, hydrogel microfilaments could be integrated with a wearable fluorometer to serve as a platform for continuous, minimally invasive monitoring of intradermal biomarkers.
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•Polyacrylamide hydrogel microfilaments were fabricated via replica molding•Microfilaments are stiff, when dehydrated, and optically transparent, when hydrated•Fluorescent aptamer can be tethered to hydrogel matrix for in situ analyte sensing•Microfilaments penetrate skin with low pain and contact interstitial fluid
Bioelectronics; Polymers; Biomedical Materials |
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AbstractList | Digital health promises a paradigm shift for medicine where biomarkers in individuals are continuously monitored to improve diagnosis and treatment of disease. To that end, a technology for minimally invasive quantification of endogenous analytes in bodily fluids will be required. Here, we describe a strategy for designing and fabricating hydrogel microfilaments that can penetrate the skin while allowing for optical fluorescence sensing. The polyacrylamide formulation was selected to provide high elastic modulus in the dehydrated state and optical transparency in the hydrated state. The microfilaments can be covalently tethered to a fluorescent aptamer to enable functional sensing. The microfilament array can penetrate the skin with low pain and without breaking, contact the dermal interstitial fluid, and be easily removed from the skin. In the future, hydrogel microfilaments could be integrated with a wearable fluorometer to serve as a platform for continuous, minimally invasive monitoring of intradermal biomarkers.
[Display omitted]
•Polyacrylamide hydrogel microfilaments were fabricated via replica molding•Microfilaments are stiff, when dehydrated, and optically transparent, when hydrated•Fluorescent aptamer can be tethered to hydrogel matrix for in situ analyte sensing•Microfilaments penetrate skin with low pain and contact interstitial fluid
Bioelectronics; Polymers; Biomedical Materials Digital health promises a paradigm shift for medicine where biomarkers in individuals are continuously monitored to improve diagnosis and treatment of disease. To that end, a technology for minimally invasive quantification of endogenous analytes in bodily fluids will be required. Here, we describe a strategy for designing and fabricating hydrogel microfilaments that can penetrate the skin while allowing for optical fluorescence sensing. The polyacrylamide formulation was selected to provide high elastic modulus in the dehydrated state and optical transparency in the hydrated state. The microfilaments can be covalently tethered to a fluorescent aptamer to enable functional sensing. The microfilament array can penetrate the skin with low pain and without breaking, contact the dermal interstitial fluid, and be easily removed from the skin. In the future, hydrogel microfilaments could be integrated with a wearable fluorometer to serve as a platform for continuous, minimally invasive monitoring of intradermal biomarkers. Digital health promises a paradigm shift for medicine where biomarkers in individuals are continuously monitored to improve diagnosis and treatment of disease. To that end, a technology for minimally invasive quantification of endogenous analytes in bodily fluids will be required. Here, we describe a strategy for designing and fabricating hydrogel microfilaments that can penetrate the skin while allowing for optical fluorescence sensing. The polyacrylamide formulation was selected to provide high elastic modulus in the dehydrated state and optical transparency in the hydrated state. The microfilaments can be covalently tethered to a fluorescent aptamer to enable functional sensing. The microfilament array can penetrate the skin with low pain and without breaking, contact the dermal interstitial fluid, and be easily removed from the skin. In the future, hydrogel microfilaments could be integrated with a wearable fluorometer to serve as a platform for continuous, minimally invasive monitoring of intradermal biomarkers. • Polyacrylamide hydrogel microfilaments were fabricated via replica molding • Microfilaments are stiff, when dehydrated, and optically transparent, when hydrated • Fluorescent aptamer can be tethered to hydrogel matrix for in situ analyte sensing • Microfilaments penetrate skin with low pain and contact interstitial fluid Bioelectronics; Polymers; Biomedical Materials Digital health promises a paradigm shift for medicine where biomarkers in individuals are continuously monitored to improve diagnosis and treatment of disease. To that end, a technology for minimally invasive quantification of endogenous analytes in bodily fluids will be required. Here, we describe a strategy for designing and fabricating hydrogel microfilaments that can penetrate the skin while allowing for optical fluorescence sensing. The polyacrylamide formulation was selected to provide high elastic modulus in the dehydrated state and optical transparency in the hydrated state. The microfilaments can be covalently tethered to a fluorescent aptamer to enable functional sensing. The microfilament array can penetrate the skin with low pain and without breaking, contact the dermal interstitial fluid, and be easily removed from the skin. In the future, hydrogel microfilaments could be integrated with a wearable fluorometer to serve as a platform for continuous, minimally invasive monitoring of intradermal biomarkers. : Bioelectronics; Polymers; Biomedical Materials Subject Areas: Bioelectronics, Polymers, Biomedical Materials |
Author | Colburn, David A.M. Guo, Vincent Tejavibulya, Nalin Yang, Kyung-Ae Sia, Samuel K. Chowdhury, Shilpika Stojanovic, Milan N. Marcogliese, Francis A. |
AuthorAffiliation | 2 Division of Experimental Therapeutics, Department of Medicine, Columbia University, New York, NY 10032, USA 1 Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, New York, NY 10027, USA |
AuthorAffiliation_xml | – name: 2 Division of Experimental Therapeutics, Department of Medicine, Columbia University, New York, NY 10032, USA – name: 1 Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, New York, NY 10027, USA |
Author_xml | – sequence: 1 givenname: Nalin surname: Tejavibulya fullname: Tejavibulya, Nalin organization: Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, New York, NY 10027, USA – sequence: 2 givenname: David A.M. surname: Colburn fullname: Colburn, David A.M. organization: Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, New York, NY 10027, USA – sequence: 3 givenname: Francis A. surname: Marcogliese fullname: Marcogliese, Francis A. organization: Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, New York, NY 10027, USA – sequence: 4 givenname: Kyung-Ae surname: Yang fullname: Yang, Kyung-Ae organization: Division of Experimental Therapeutics, Department of Medicine, Columbia University, New York, NY 10032, USA – sequence: 5 givenname: Vincent surname: Guo fullname: Guo, Vincent organization: Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, New York, NY 10027, USA – sequence: 6 givenname: Shilpika surname: Chowdhury fullname: Chowdhury, Shilpika organization: Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, New York, NY 10027, USA – sequence: 7 givenname: Milan N. surname: Stojanovic fullname: Stojanovic, Milan N. organization: Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, New York, NY 10027, USA – sequence: 8 givenname: Samuel K. orcidid: 0000-0003-0230-3542 surname: Sia fullname: Sia, Samuel K. email: ss2735@columbia.edu organization: Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace, 1210 Amsterdam Avenue, New York, NY 10027, USA |
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