Cargando…

NIR triggered PLGA coated Au-TiO(2) core loaded CPT-11 nanoparticles for human papillary thyroid carcinoma therapy

MDR (multi-drug resistance) is one of the significant deterrents of effective chemotherapy for malignant growth. One of the powerful ways to deal with defeat of the MDR is to utilize inorganic nanoparticle-intervened tranquilize conveyance to build the medication aggregations in cancerous growth cel...

Descripción completa

Detalles Bibliográficos
Autores principales: Yu, Tianyu, Tong, Lingling, Ao, Yu, Zhang, Genmao, Liu, Yunpeng, Zhang, Hejia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216437/
https://www.ncbi.nlm.nih.gov/pubmed/32515668
http://dx.doi.org/10.1080/10717544.2020.1775723
_version_ 1783710418222448640
author Yu, Tianyu
Tong, Lingling
Ao, Yu
Zhang, Genmao
Liu, Yunpeng
Zhang, Hejia
author_facet Yu, Tianyu
Tong, Lingling
Ao, Yu
Zhang, Genmao
Liu, Yunpeng
Zhang, Hejia
author_sort Yu, Tianyu
collection PubMed
description MDR (multi-drug resistance) is one of the significant deterrents of effective chemotherapy for malignant growth. One of the powerful ways to deal with defeat of the MDR is to utilize inorganic nanoparticle-intervened tranquilize conveyance to build the medication aggregations in cancerous growth cells. In this work, we have developed the presentation that is accurately made of medication conveyance framework dependent on the TiO(2) nanoparticles stacked CPT-11 to defeat the thyroid malignancy cells. The synthesized nanoparticles are characterized by spectroscopy methods (UV–vis, XPS, SEM, TEM, and DLS). The TEM results suggested that the shape of PLGA-Au-TiO(2)@CPT-11 of nanoparticles is ∼250 nm. After successful synthesis, we have evaluated the MTT of PLGA-Au-TiO(2)@CPT-11 nanoparticles with and without NIR radiations. Further, the morphological changes were observed using various biochemical stainings, such as acridine orange and ethidium bromide (AO–EB) and nuclear staining through Hoechst-33258. Also, migration and cell invasion were examined. The results show that these PLGA-Au-TiO(2)@CPT-11 and PLGA-Au-TiO(2)@CPT-11 + NIR nanoparticles exhibited promising antimetastatic property and reduced the cell invasion activity in B-CPAP and FTC-133 thyroid cancer cell lines. Based on the above findings, these PLGA-Au-TiO(2)@CPT-11 and PLGA-Au-TiO(2)@CPT-11 + NIR nanoparticles can be used as a promising candidate for the malignant thyroid cells.
format Online
Article
Text
id pubmed-8216437
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-82164372021-07-06 NIR triggered PLGA coated Au-TiO(2) core loaded CPT-11 nanoparticles for human papillary thyroid carcinoma therapy Yu, Tianyu Tong, Lingling Ao, Yu Zhang, Genmao Liu, Yunpeng Zhang, Hejia Drug Deliv Original Article MDR (multi-drug resistance) is one of the significant deterrents of effective chemotherapy for malignant growth. One of the powerful ways to deal with defeat of the MDR is to utilize inorganic nanoparticle-intervened tranquilize conveyance to build the medication aggregations in cancerous growth cells. In this work, we have developed the presentation that is accurately made of medication conveyance framework dependent on the TiO(2) nanoparticles stacked CPT-11 to defeat the thyroid malignancy cells. The synthesized nanoparticles are characterized by spectroscopy methods (UV–vis, XPS, SEM, TEM, and DLS). The TEM results suggested that the shape of PLGA-Au-TiO(2)@CPT-11 of nanoparticles is ∼250 nm. After successful synthesis, we have evaluated the MTT of PLGA-Au-TiO(2)@CPT-11 nanoparticles with and without NIR radiations. Further, the morphological changes were observed using various biochemical stainings, such as acridine orange and ethidium bromide (AO–EB) and nuclear staining through Hoechst-33258. Also, migration and cell invasion were examined. The results show that these PLGA-Au-TiO(2)@CPT-11 and PLGA-Au-TiO(2)@CPT-11 + NIR nanoparticles exhibited promising antimetastatic property and reduced the cell invasion activity in B-CPAP and FTC-133 thyroid cancer cell lines. Based on the above findings, these PLGA-Au-TiO(2)@CPT-11 and PLGA-Au-TiO(2)@CPT-11 + NIR nanoparticles can be used as a promising candidate for the malignant thyroid cells. Taylor & Francis 2020-06-09 /pmc/articles/PMC8216437/ /pubmed/32515668 http://dx.doi.org/10.1080/10717544.2020.1775723 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yu, Tianyu
Tong, Lingling
Ao, Yu
Zhang, Genmao
Liu, Yunpeng
Zhang, Hejia
NIR triggered PLGA coated Au-TiO(2) core loaded CPT-11 nanoparticles for human papillary thyroid carcinoma therapy
title NIR triggered PLGA coated Au-TiO(2) core loaded CPT-11 nanoparticles for human papillary thyroid carcinoma therapy
title_full NIR triggered PLGA coated Au-TiO(2) core loaded CPT-11 nanoparticles for human papillary thyroid carcinoma therapy
title_fullStr NIR triggered PLGA coated Au-TiO(2) core loaded CPT-11 nanoparticles for human papillary thyroid carcinoma therapy
title_full_unstemmed NIR triggered PLGA coated Au-TiO(2) core loaded CPT-11 nanoparticles for human papillary thyroid carcinoma therapy
title_short NIR triggered PLGA coated Au-TiO(2) core loaded CPT-11 nanoparticles for human papillary thyroid carcinoma therapy
title_sort nir triggered plga coated au-tio(2) core loaded cpt-11 nanoparticles for human papillary thyroid carcinoma therapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216437/
https://www.ncbi.nlm.nih.gov/pubmed/32515668
http://dx.doi.org/10.1080/10717544.2020.1775723
work_keys_str_mv AT yutianyu nirtriggeredplgacoatedautio2coreloadedcpt11nanoparticlesforhumanpapillarythyroidcarcinomatherapy
AT tonglingling nirtriggeredplgacoatedautio2coreloadedcpt11nanoparticlesforhumanpapillarythyroidcarcinomatherapy
AT aoyu nirtriggeredplgacoatedautio2coreloadedcpt11nanoparticlesforhumanpapillarythyroidcarcinomatherapy
AT zhanggenmao nirtriggeredplgacoatedautio2coreloadedcpt11nanoparticlesforhumanpapillarythyroidcarcinomatherapy
AT liuyunpeng nirtriggeredplgacoatedautio2coreloadedcpt11nanoparticlesforhumanpapillarythyroidcarcinomatherapy
AT zhanghejia nirtriggeredplgacoatedautio2coreloadedcpt11nanoparticlesforhumanpapillarythyroidcarcinomatherapy