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Microbiopsy engineered for minimally invasive and suture-free sub-millimetre skin sampling
We describe the development of a sub-millimetre skin punch biopsy device for minimally invasive and suture-free skin sampling for molecular diagnosis and research. Conventional skin punch biopsies range from 2-4 mm in diameter. Local anaesthesia is required and sutures are usually used to close the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907159/ https://www.ncbi.nlm.nih.gov/pubmed/24627782 http://dx.doi.org/10.12688/f1000research.2-120.v2 |
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author | Lin, Lynlee L Prow, Tarl W Raphael, Anthony P Harrold III, Robert L Primiero, Clare A Ansaldo, Alexander B Soyer, H Peter |
author_facet | Lin, Lynlee L Prow, Tarl W Raphael, Anthony P Harrold III, Robert L Primiero, Clare A Ansaldo, Alexander B Soyer, H Peter |
author_sort | Lin, Lynlee L |
collection | PubMed |
description | We describe the development of a sub-millimetre skin punch biopsy device for minimally invasive and suture-free skin sampling for molecular diagnosis and research. Conventional skin punch biopsies range from 2-4 mm in diameter. Local anaesthesia is required and sutures are usually used to close the wound. Our microbiopsy is 0.50 mm wide and 0.20 mm thick. The microbiopsy device is fabricated from three stacked medical grade stainless steel plates tapered to a point and contains a chamber within the centre plate to collect the skin sample. We observed that the application of this device resulted in a 0.21 ± 0.04 mm wide puncture site in volunteer skin using reflectance confocal microscopy. Histological sections from microbiopsied skin revealed 0.22 ± 0.12 mm wide and 0.26 ± 0.09 mm deep puncture sites. Longitudinal observation in microbiopsied volunteers showed that the wound closed within 1 day and was not visible after 7 days. Reflectance confocal microscope images from these same sites showed the formation of a tiny crust that resolved by 3 weeks and was completely undetectable by the naked eye. The design parameters of the device were optimised for molecular analysis using sampled DNA mass as the primary end point in volunteer studies. Finally, total RNA was characterized. The optimised device extracted 5.9 ± 3.4 ng DNA and 9.0 ± 10.1 ng RNA. We foresee that minimally invasive molecular sampling will play an increasingly significant role in diagnostic dermatology and skin research. |
format | Online Article Text |
id | pubmed-3907159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-39071592014-03-12 Microbiopsy engineered for minimally invasive and suture-free sub-millimetre skin sampling Lin, Lynlee L Prow, Tarl W Raphael, Anthony P Harrold III, Robert L Primiero, Clare A Ansaldo, Alexander B Soyer, H Peter F1000Res Method Article We describe the development of a sub-millimetre skin punch biopsy device for minimally invasive and suture-free skin sampling for molecular diagnosis and research. Conventional skin punch biopsies range from 2-4 mm in diameter. Local anaesthesia is required and sutures are usually used to close the wound. Our microbiopsy is 0.50 mm wide and 0.20 mm thick. The microbiopsy device is fabricated from three stacked medical grade stainless steel plates tapered to a point and contains a chamber within the centre plate to collect the skin sample. We observed that the application of this device resulted in a 0.21 ± 0.04 mm wide puncture site in volunteer skin using reflectance confocal microscopy. Histological sections from microbiopsied skin revealed 0.22 ± 0.12 mm wide and 0.26 ± 0.09 mm deep puncture sites. Longitudinal observation in microbiopsied volunteers showed that the wound closed within 1 day and was not visible after 7 days. Reflectance confocal microscope images from these same sites showed the formation of a tiny crust that resolved by 3 weeks and was completely undetectable by the naked eye. The design parameters of the device were optimised for molecular analysis using sampled DNA mass as the primary end point in volunteer studies. Finally, total RNA was characterized. The optimised device extracted 5.9 ± 3.4 ng DNA and 9.0 ± 10.1 ng RNA. We foresee that minimally invasive molecular sampling will play an increasingly significant role in diagnostic dermatology and skin research. F1000Research 2013-07-31 /pmc/articles/PMC3907159/ /pubmed/24627782 http://dx.doi.org/10.12688/f1000research.2-120.v2 Text en Copyright: © 2013 Lin LL et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/publicdomain/zero/1.0/ Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication). |
spellingShingle | Method Article Lin, Lynlee L Prow, Tarl W Raphael, Anthony P Harrold III, Robert L Primiero, Clare A Ansaldo, Alexander B Soyer, H Peter Microbiopsy engineered for minimally invasive and suture-free sub-millimetre skin sampling |
title | Microbiopsy engineered for minimally invasive and suture-free sub-millimetre skin sampling |
title_full | Microbiopsy engineered for minimally invasive and suture-free sub-millimetre skin sampling |
title_fullStr | Microbiopsy engineered for minimally invasive and suture-free sub-millimetre skin sampling |
title_full_unstemmed | Microbiopsy engineered for minimally invasive and suture-free sub-millimetre skin sampling |
title_short | Microbiopsy engineered for minimally invasive and suture-free sub-millimetre skin sampling |
title_sort | microbiopsy engineered for minimally invasive and suture-free sub-millimetre skin sampling |
topic | Method Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907159/ https://www.ncbi.nlm.nih.gov/pubmed/24627782 http://dx.doi.org/10.12688/f1000research.2-120.v2 |
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