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Design and testing of a centrifugal fluidic device for populating microarrays of spheroid cancer cell cultures
BACKGROUND: In current cancer spheroid culturing methods, the transfer and histological processing of specimens grown in 96-well plates is a time consuming process. A centrifugal fluidic device was developed and tested for rapid extraction of spheroids from a 96-well plate and subsequent deposition...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066855/ https://www.ncbi.nlm.nih.gov/pubmed/32190109 http://dx.doi.org/10.1186/s13036-020-0228-6 |
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author | Weisler, Warren Miller, Samuel Jernigan, Shaphan Buckner, Gregory Bryant, Matthew |
author_facet | Weisler, Warren Miller, Samuel Jernigan, Shaphan Buckner, Gregory Bryant, Matthew |
author_sort | Weisler, Warren |
collection | PubMed |
description | BACKGROUND: In current cancer spheroid culturing methods, the transfer and histological processing of specimens grown in 96-well plates is a time consuming process. A centrifugal fluidic device was developed and tested for rapid extraction of spheroids from a 96-well plate and subsequent deposition into a molded agar receiver block. The deposited spheroids must be compact enough to fit into a standard histology cassette while also maintaining a highly planar arrangement. This size and planarity enable histological processing and sectioning of spheroids in a single section. The device attaches directly to a 96-well plate and uses a standard centrifuge to facilitate spheroid transfer. The agar block is then separated from the device and processed. RESULTS: Testing of the device was conducted using six full 96-well plates of fixed Pa14C pancreatic cancer spheroids. On average, 80% of spheroids were successfully transferred into the agar receiver block. Additionally, the planarity of the deposited spheroids was evaluated using confocal laser scanning microscopy. This revealed that, on average, the optimal section plane bisected individual spheroids within 27% of their mean radius. This shows that spheroids are largely deposited in a planar fashion. For rare cases where spheroids had a normalized distance to the plane greater than 1, the section plane either misses or captures a small cross section of the spheroid volume. CONCLUSIONS: These results indicate that the proposed device is capable of a high capture success rate and high sample planarity, thus demonstrating the capabilities of the device to facilitate rapid histological evaluation of spheroids grown in standard 96-well plates. Planarity figures are likely to be improved by adjusting agar block handling prior to imaging to minimize deformation and better preserve the planarity of deposited spheroids. Additionally, investigation into media additives to reduce spheroid adhesion to 96-well plates would greatly increase the capture success rate of this device. |
format | Online Article Text |
id | pubmed-7066855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70668552020-03-18 Design and testing of a centrifugal fluidic device for populating microarrays of spheroid cancer cell cultures Weisler, Warren Miller, Samuel Jernigan, Shaphan Buckner, Gregory Bryant, Matthew J Biol Eng Research BACKGROUND: In current cancer spheroid culturing methods, the transfer and histological processing of specimens grown in 96-well plates is a time consuming process. A centrifugal fluidic device was developed and tested for rapid extraction of spheroids from a 96-well plate and subsequent deposition into a molded agar receiver block. The deposited spheroids must be compact enough to fit into a standard histology cassette while also maintaining a highly planar arrangement. This size and planarity enable histological processing and sectioning of spheroids in a single section. The device attaches directly to a 96-well plate and uses a standard centrifuge to facilitate spheroid transfer. The agar block is then separated from the device and processed. RESULTS: Testing of the device was conducted using six full 96-well plates of fixed Pa14C pancreatic cancer spheroids. On average, 80% of spheroids were successfully transferred into the agar receiver block. Additionally, the planarity of the deposited spheroids was evaluated using confocal laser scanning microscopy. This revealed that, on average, the optimal section plane bisected individual spheroids within 27% of their mean radius. This shows that spheroids are largely deposited in a planar fashion. For rare cases where spheroids had a normalized distance to the plane greater than 1, the section plane either misses or captures a small cross section of the spheroid volume. CONCLUSIONS: These results indicate that the proposed device is capable of a high capture success rate and high sample planarity, thus demonstrating the capabilities of the device to facilitate rapid histological evaluation of spheroids grown in standard 96-well plates. Planarity figures are likely to be improved by adjusting agar block handling prior to imaging to minimize deformation and better preserve the planarity of deposited spheroids. Additionally, investigation into media additives to reduce spheroid adhesion to 96-well plates would greatly increase the capture success rate of this device. BioMed Central 2020-03-12 /pmc/articles/PMC7066855/ /pubmed/32190109 http://dx.doi.org/10.1186/s13036-020-0228-6 Text en © The Author(s). 2020 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Weisler, Warren Miller, Samuel Jernigan, Shaphan Buckner, Gregory Bryant, Matthew Design and testing of a centrifugal fluidic device for populating microarrays of spheroid cancer cell cultures |
title | Design and testing of a centrifugal fluidic device for populating microarrays of spheroid cancer cell cultures |
title_full | Design and testing of a centrifugal fluidic device for populating microarrays of spheroid cancer cell cultures |
title_fullStr | Design and testing of a centrifugal fluidic device for populating microarrays of spheroid cancer cell cultures |
title_full_unstemmed | Design and testing of a centrifugal fluidic device for populating microarrays of spheroid cancer cell cultures |
title_short | Design and testing of a centrifugal fluidic device for populating microarrays of spheroid cancer cell cultures |
title_sort | design and testing of a centrifugal fluidic device for populating microarrays of spheroid cancer cell cultures |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066855/ https://www.ncbi.nlm.nih.gov/pubmed/32190109 http://dx.doi.org/10.1186/s13036-020-0228-6 |
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