TfR mAb-Cross-Linked Rituximab/MTX-PEG-PLL-PLGA Drug-Loaded Nanoparticles Enhance Anticancer Action in B Lymphocytes

Nanoparticles could enhance the drug targeted to the cancer cell by the enrichment of the drug levels, which leads to the improvement of the codelivery of both drugs for an antitumor effect. In the current study, we reported an efficient, local drug-loaded delivery strategy with a nanoparticle-loade...

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Main Authors: Ran Liu, Gang Zhao, Shujun Wang, Yan Gu, Qi Han, Baoan Chen
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Journal of Nanomaterials
Online Access:http://dx.doi.org/10.1155/2019/7265450
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spelling doaj-743a4c65483c406ebcad8ff947e34cde2020-11-25T02:06:40ZengHindawi LimitedJournal of Nanomaterials1687-41101687-41292019-01-01201910.1155/2019/72654507265450TfR mAb-Cross-Linked Rituximab/MTX-PEG-PLL-PLGA Drug-Loaded Nanoparticles Enhance Anticancer Action in B LymphocytesRan Liu0Gang Zhao1Shujun Wang2Yan Gu3Qi Han4Baoan Chen5Department of Hematology and Oncology, Zhongda Hospital Southeast University, Nanjing, Jiangsu Province 210009, ChinaDepartment of Hematology and Oncology, Zhongda Hospital Southeast University, Nanjing, Jiangsu Province 210009, ChinaDepartment of Blood Transfusion, Nanjing General Hospital of PLA, Nanjing, Jiangsu Province 210009, ChinaDepartment of Hematology and Oncology, Zhongda Hospital Southeast University, Nanjing, Jiangsu Province 210009, ChinaDepartment of Hematology and Oncology, Zhongda Hospital Southeast University, Nanjing, Jiangsu Province 210009, ChinaDepartment of Hematology and Oncology, Zhongda Hospital Southeast University, Nanjing, Jiangsu Province 210009, ChinaNanoparticles could enhance the drug targeted to the cancer cell by the enrichment of the drug levels, which leads to the improvement of the codelivery of both drugs for an antitumor effect. In the current study, we reported an efficient, local drug-loaded delivery strategy with a nanoparticle-loaded system. After the synthesis of Rituximab/MTX-PEG-PLL-PLGA, the transferrin receptor monoantibody (TfR mAb) was subsequently cross-linked to the nanoparticles. Compared to the traditional drug, the nanoparticle-loaded system can precisely and efficiently transport the Rituximab and Methotrexate (MTX) drug into SU-DHL-4 cells, a typical kind of B lymphocytes, which can significantly increase the cell apoptosis in the SU-DHL-4 cells. Thus, the multifunctional drug-loaded nanoparticles displayed the persistent stability and precise targeting properties, which enhanced the efficiency of anticancer efficiency in B lymphocytes.http://dx.doi.org/10.1155/2019/7265450
collection DOAJ
language English
format Article
sources DOAJ
author Ran Liu
Gang Zhao
Shujun Wang
Yan Gu
Qi Han
Baoan Chen
spellingShingle Ran Liu
Gang Zhao
Shujun Wang
Yan Gu
Qi Han
Baoan Chen
TfR mAb-Cross-Linked Rituximab/MTX-PEG-PLL-PLGA Drug-Loaded Nanoparticles Enhance Anticancer Action in B Lymphocytes
Journal of Nanomaterials
author_facet Ran Liu
Gang Zhao
Shujun Wang
Yan Gu
Qi Han
Baoan Chen
author_sort Ran Liu
title TfR mAb-Cross-Linked Rituximab/MTX-PEG-PLL-PLGA Drug-Loaded Nanoparticles Enhance Anticancer Action in B Lymphocytes
title_short TfR mAb-Cross-Linked Rituximab/MTX-PEG-PLL-PLGA Drug-Loaded Nanoparticles Enhance Anticancer Action in B Lymphocytes
title_full TfR mAb-Cross-Linked Rituximab/MTX-PEG-PLL-PLGA Drug-Loaded Nanoparticles Enhance Anticancer Action in B Lymphocytes
title_fullStr TfR mAb-Cross-Linked Rituximab/MTX-PEG-PLL-PLGA Drug-Loaded Nanoparticles Enhance Anticancer Action in B Lymphocytes
title_full_unstemmed TfR mAb-Cross-Linked Rituximab/MTX-PEG-PLL-PLGA Drug-Loaded Nanoparticles Enhance Anticancer Action in B Lymphocytes
title_sort tfr mab-cross-linked rituximab/mtx-peg-pll-plga drug-loaded nanoparticles enhance anticancer action in b lymphocytes
publisher Hindawi Limited
series Journal of Nanomaterials
issn 1687-4110
1687-4129
publishDate 2019-01-01
description Nanoparticles could enhance the drug targeted to the cancer cell by the enrichment of the drug levels, which leads to the improvement of the codelivery of both drugs for an antitumor effect. In the current study, we reported an efficient, local drug-loaded delivery strategy with a nanoparticle-loaded system. After the synthesis of Rituximab/MTX-PEG-PLL-PLGA, the transferrin receptor monoantibody (TfR mAb) was subsequently cross-linked to the nanoparticles. Compared to the traditional drug, the nanoparticle-loaded system can precisely and efficiently transport the Rituximab and Methotrexate (MTX) drug into SU-DHL-4 cells, a typical kind of B lymphocytes, which can significantly increase the cell apoptosis in the SU-DHL-4 cells. Thus, the multifunctional drug-loaded nanoparticles displayed the persistent stability and precise targeting properties, which enhanced the efficiency of anticancer efficiency in B lymphocytes.
url http://dx.doi.org/10.1155/2019/7265450
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