Doxorubicin-Loaded Melanin Particles for Enhanced Chemotherapy in Drug-Resistant Anaplastic Thyroid Cancer Cells
Anaplastic thyroid cancer (ATC) is highly aggressive and tends to develop drug resistance to standard chemotherapies. To overcome the drug resistance of ATC, we synthesized dopamine-melanin nanoparticles (MNPs) loaded with doxorubicin (Dox) molecules. The Dox-loaded MNPs (Dox-MNPs) developed exhibit...
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2018-01-01
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Series: | Journal of Nanomaterials |
Online Access: | http://dx.doi.org/10.1155/2018/2603712 |
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doaj-e82926064e524c918d846bd64ef2dced2020-11-24T21:15:19ZengHindawi LimitedJournal of Nanomaterials1687-41101687-41292018-01-01201810.1155/2018/26037122603712Doxorubicin-Loaded Melanin Particles for Enhanced Chemotherapy in Drug-Resistant Anaplastic Thyroid Cancer CellsKun Wang0Shouju Wang1Kun Chen2Yijing Zhao3Xingqun Ma4Lin Wang5Department of Endocrinology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing 211100, ChinaDepartment of Medical Imaging, Jinling Hospital, School of Medicine, Nanjing University, Nanjing 210000, ChinaDepartment of Endocrinology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing 211100, ChinaDepartment of Endocrinology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing 211100, ChinaDepartment of Oncology, The Affiliated Bayi Hospital of Nanjing University of Chinese Medicine, Nanjing 210002, ChinaDepartment of Oncology, The Affiliated Bayi Hospital of Nanjing University of Chinese Medicine, Nanjing 210002, ChinaAnaplastic thyroid cancer (ATC) is highly aggressive and tends to develop drug resistance to standard chemotherapies. To overcome the drug resistance of ATC, we synthesized dopamine-melanin nanoparticles (MNPs) loaded with doxorubicin (Dox) molecules. The Dox-loaded MNPs (Dox-MNPs) developed exhibited increased cellular uptake and enhanced therapeutic efficacy in drug-resistant ATC cell line HTh74R, compared with free Dox. The native MNPs were found to have excellent biocompatibility, which suggests that Dox-MNPs may have potential in the treatment of ATC.http://dx.doi.org/10.1155/2018/2603712 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kun Wang Shouju Wang Kun Chen Yijing Zhao Xingqun Ma Lin Wang |
spellingShingle |
Kun Wang Shouju Wang Kun Chen Yijing Zhao Xingqun Ma Lin Wang Doxorubicin-Loaded Melanin Particles for Enhanced Chemotherapy in Drug-Resistant Anaplastic Thyroid Cancer Cells Journal of Nanomaterials |
author_facet |
Kun Wang Shouju Wang Kun Chen Yijing Zhao Xingqun Ma Lin Wang |
author_sort |
Kun Wang |
title |
Doxorubicin-Loaded Melanin Particles for Enhanced Chemotherapy in Drug-Resistant Anaplastic Thyroid Cancer Cells |
title_short |
Doxorubicin-Loaded Melanin Particles for Enhanced Chemotherapy in Drug-Resistant Anaplastic Thyroid Cancer Cells |
title_full |
Doxorubicin-Loaded Melanin Particles for Enhanced Chemotherapy in Drug-Resistant Anaplastic Thyroid Cancer Cells |
title_fullStr |
Doxorubicin-Loaded Melanin Particles for Enhanced Chemotherapy in Drug-Resistant Anaplastic Thyroid Cancer Cells |
title_full_unstemmed |
Doxorubicin-Loaded Melanin Particles for Enhanced Chemotherapy in Drug-Resistant Anaplastic Thyroid Cancer Cells |
title_sort |
doxorubicin-loaded melanin particles for enhanced chemotherapy in drug-resistant anaplastic thyroid cancer cells |
publisher |
Hindawi Limited |
series |
Journal of Nanomaterials |
issn |
1687-4110 1687-4129 |
publishDate |
2018-01-01 |
description |
Anaplastic thyroid cancer (ATC) is highly aggressive and tends to develop drug resistance to standard chemotherapies. To overcome the drug resistance of ATC, we synthesized dopamine-melanin nanoparticles (MNPs) loaded with doxorubicin (Dox) molecules. The Dox-loaded MNPs (Dox-MNPs) developed exhibited increased cellular uptake and enhanced therapeutic efficacy in drug-resistant ATC cell line HTh74R, compared with free Dox. The native MNPs were found to have excellent biocompatibility, which suggests that Dox-MNPs may have potential in the treatment of ATC. |
url |
http://dx.doi.org/10.1155/2018/2603712 |
work_keys_str_mv |
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1716745780106100736 |