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Electrospun Polylactic Acid (PLLA) Microtube Array Membrane (MTAM)—An Advanced Substrate for Anticancer Drug Screening
The advent of personalized cancer treatment resulted in the shift from the administration of cytotoxic drugs with broad activity spectrum to a targeted tumor-specific therapy. Aligned to this development, the focus of this study revolved around the application of our novel and patented microtube arr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416630/ https://www.ncbi.nlm.nih.gov/pubmed/30769818 http://dx.doi.org/10.3390/ma12040569 |
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author | Tseng, Chia-Hsuan Huang, Wan-Ting Chew, Chee Ho Lai, Jun-Kai Tu, Shih-Hsin Wei, Po-Li Lee, Kang-Yun Lai, Gi-Ming Chen, Chien-Chung |
author_facet | Tseng, Chia-Hsuan Huang, Wan-Ting Chew, Chee Ho Lai, Jun-Kai Tu, Shih-Hsin Wei, Po-Li Lee, Kang-Yun Lai, Gi-Ming Chen, Chien-Chung |
author_sort | Tseng, Chia-Hsuan |
collection | PubMed |
description | The advent of personalized cancer treatment resulted in the shift from the administration of cytotoxic drugs with broad activity spectrum to a targeted tumor-specific therapy. Aligned to this development, the focus of this study revolved around the application of our novel and patented microtube array membrane (MTAM) in the US National Cancer Institute (NCI) developed an HFA (hollow fiber assay) assay; hereinafter known as MTAM/HFA. Electrospun poly-L-lactic acid (PLLA) MTAM was sterilized and loaded with cell lines/patient derived tumor cells (PDTC) and subcutaneously implanted into the backs of BALB/C mice. Anticancer drugs were administered at the respective time points and the respective MTAMs were retrieved and the viability tumor cells within were quantified with the MTT assay. Results revealed that the MTAMs were excellent culture substrate for various cancer cell lines and PDTCs (patient derived tumor cells). Compared to traditional HFA systems that utilize traditional hollow fibers, MTAM/HFA revealed superior drug sensitivity for a wide range of anticancer drug classes. Additionally, the duration for each test was <14 days; all this while capable of producing similar trend outcome to the current gold-standard xenograft models. These benefits were observed in both the in vitro and in vivo stages, making it a highly practical phenotypic-based solution that could potentially be applied in personalized medicine. |
format | Online Article Text |
id | pubmed-6416630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64166302019-03-29 Electrospun Polylactic Acid (PLLA) Microtube Array Membrane (MTAM)—An Advanced Substrate for Anticancer Drug Screening Tseng, Chia-Hsuan Huang, Wan-Ting Chew, Chee Ho Lai, Jun-Kai Tu, Shih-Hsin Wei, Po-Li Lee, Kang-Yun Lai, Gi-Ming Chen, Chien-Chung Materials (Basel) Article The advent of personalized cancer treatment resulted in the shift from the administration of cytotoxic drugs with broad activity spectrum to a targeted tumor-specific therapy. Aligned to this development, the focus of this study revolved around the application of our novel and patented microtube array membrane (MTAM) in the US National Cancer Institute (NCI) developed an HFA (hollow fiber assay) assay; hereinafter known as MTAM/HFA. Electrospun poly-L-lactic acid (PLLA) MTAM was sterilized and loaded with cell lines/patient derived tumor cells (PDTC) and subcutaneously implanted into the backs of BALB/C mice. Anticancer drugs were administered at the respective time points and the respective MTAMs were retrieved and the viability tumor cells within were quantified with the MTT assay. Results revealed that the MTAMs were excellent culture substrate for various cancer cell lines and PDTCs (patient derived tumor cells). Compared to traditional HFA systems that utilize traditional hollow fibers, MTAM/HFA revealed superior drug sensitivity for a wide range of anticancer drug classes. Additionally, the duration for each test was <14 days; all this while capable of producing similar trend outcome to the current gold-standard xenograft models. These benefits were observed in both the in vitro and in vivo stages, making it a highly practical phenotypic-based solution that could potentially be applied in personalized medicine. MDPI 2019-02-14 /pmc/articles/PMC6416630/ /pubmed/30769818 http://dx.doi.org/10.3390/ma12040569 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tseng, Chia-Hsuan Huang, Wan-Ting Chew, Chee Ho Lai, Jun-Kai Tu, Shih-Hsin Wei, Po-Li Lee, Kang-Yun Lai, Gi-Ming Chen, Chien-Chung Electrospun Polylactic Acid (PLLA) Microtube Array Membrane (MTAM)—An Advanced Substrate for Anticancer Drug Screening |
title | Electrospun Polylactic Acid (PLLA) Microtube Array Membrane (MTAM)—An Advanced Substrate for Anticancer Drug Screening |
title_full | Electrospun Polylactic Acid (PLLA) Microtube Array Membrane (MTAM)—An Advanced Substrate for Anticancer Drug Screening |
title_fullStr | Electrospun Polylactic Acid (PLLA) Microtube Array Membrane (MTAM)—An Advanced Substrate for Anticancer Drug Screening |
title_full_unstemmed | Electrospun Polylactic Acid (PLLA) Microtube Array Membrane (MTAM)—An Advanced Substrate for Anticancer Drug Screening |
title_short | Electrospun Polylactic Acid (PLLA) Microtube Array Membrane (MTAM)—An Advanced Substrate for Anticancer Drug Screening |
title_sort | electrospun polylactic acid (plla) microtube array membrane (mtam)—an advanced substrate for anticancer drug screening |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416630/ https://www.ncbi.nlm.nih.gov/pubmed/30769818 http://dx.doi.org/10.3390/ma12040569 |
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