A versatile modular preparation strategy for targeted drug delivery systems against multidrug-resistant cancer cells

被引:3
作者
Wang, Huanhuan [1 ]
Ning, Xiaoyue [1 ]
Wang, Xinnan [1 ]
Ding, Fei [2 ]
Wang, Yongjian [1 ]
机构
[1] Nankai Univ, Coll Life Sci, Key Lab Bioact Mat, Minist Educ, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Chem, Tianjin 300071, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
modular stacking; nano medicine; targeted drug delivery; mitochondrial targeting; multidrug resistance; PEGYLATED LIPOSOMAL DOXORUBICIN; TRANSLOCATOR PROTEIN; MICELLES; PH;
D O I
10.1088/1361-6528/ac317c
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanotechnology is widely used in targeted drug delivery, but different drug delivery systems need to 're-determine' different synthesis schemes, which greatly limits the further expansion of targeted nanomedicine applications. In this study, we propose a facile and versatile modular stacking strategy to fabricate targeted drug delivery systems to enable tailored designs for patient-specific therapeutic responses. The systems were constructed by a pH-sensitive prodrug module and a mitochondrial targeting module via self-assembly. Using this modular strategy, we successfully prepared two targeting nano-drug delivery systems, TPP-DOX and PK-DOX, where the mitochondrial targeting molecules were triphenylphosphonium (TPP) and 1-(2-Chlorophenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinolinecarboxamide (PK11195), respectively. Confocal laser microscopy and flow cytometry tests revealed that TPP-DOX and PK-DOX exhibited high mitochondria targeting capability and greatly improved the drug retention in drug-resistant cells. The antitumor activity tests showed that the IC50 values of TPP-DOX and PK-DOX in MCF-7/ADR cells were 2.5- and 8.2-fold lower than that of free DOX, respectively. These results indicated that PK was more effective than TPP. The studies on their therapeutic effects on human breast cancer resistant cells verified the feasibility of the modular approach, indicated that the two modular targeted drug delivery systems: (1) retain the drug toxicity and cell-killing effect of the prodrug module, (2) have precise targeting capabilities due to mitochondrial targeting module, (3) enhance drug uptake, reduce drug efflux and reverse the multidrug resistance effect to a certain extent. The results show that modular stacking is a practical, effective and versatile method for preparing targeting drugs with broad application prospects. This study provides an easy approach on preparing customizable targeted drug delivery systems to improve precision therapies.
引用
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页数:11
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共 36 条
[1]   The most prevalent side effects of pegylated liposomal doxorubicin monotherapy in women with metastatic breast cancer: a systematic review of clinical trials [J].
Ansari, L. ;
Shiehzadeh, F. ;
Taherzadeh, Z. ;
Nikoofal-Sahlabadi, S. ;
Momtazi-Borojeni, A. A. ;
Sahebkar, A. ;
Eslami, S. .
CANCER GENE THERAPY, 2017, 24 (05) :189-193
[2]   High-density doxorubicin-conjugated polymeric nanoparticles via ring-opening metathesis polymerization [J].
Bertin, PA ;
Smith, DD ;
Nguyen, ST .
CHEMICAL COMMUNICATIONS, 2005, (30) :3793-3795
[3]   Mitochondria as multifaceted regulators of cell death [J].
Bock, Florian J. ;
Tait, Stephen W. G. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2020, 21 (02) :85-100
[4]   Mitochondria-targeted drug delivery in cancers [J].
Cho, Hana ;
Cho, Yong-Yeon ;
Shim, Min Suk ;
Lee, Joo Young ;
Lee, Hye Suk ;
Kang, Han Chang .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2020, 1866 (08)
[5]   Rising horizon in circumventing multidrug resistance in chemotherapy with nanotechnology [J].
Choudhury, Hira ;
Pandey, Manisha ;
Yin, Tan Hui ;
Kaur, Taasjir ;
Jia, Gan Wei ;
Tan, S. Q. Lawrence ;
Weijie, How ;
Yang, Eric Koh Sze ;
Keat, Chin Guan ;
Bhattamishra, Subrat Kumar ;
Kesharwani, Prashant ;
Md, Shadab ;
Molugulu, Nagasekhara ;
Pichika, Mallikarjuna Rao ;
Gorain, Bapi .
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2019, 101 :596-613
[6]   Highly selective luminescent nanostructures for mitochondrial imaging and targeting [J].
Fanizza, E. ;
Iacobazzi, R. M. ;
Laquintana, V. ;
Valente, G. ;
Caliandro, G. ;
Striccoli, M. ;
Agostiano, A. ;
Cutrignelli, A. ;
Lopedota, A. ;
Curri, M. L. ;
Franco, M. ;
Depalo, N. ;
Denora, N. .
NANOSCALE, 2016, 8 (06) :3350-3361
[7]   Biodegradable Block Copolymer-Doxorubicin Conjugates via Different Linkages: Preparation, Characterization, and In Vitro Evaluation [J].
Hu, Xiuli ;
Liu, Shi ;
Huang, Yubin ;
Chen, Xuesi ;
Jing, Xiabin .
BIOMACROMOLECULES, 2010, 11 (08) :2094-2102
[8]   Structure of the Mitochondrial Translocator Protein in Complex with a Diagnostic Ligand [J].
Jaremko, Lukasz ;
Jaremko, Mariusz ;
Giller, Karin ;
Becker, Stefan ;
Zweckstetter, Markus .
SCIENCE, 2014, 343 (6177) :1363-1366
[9]   Recent Progress in Mitochondria-Targeted Drug and Drug-Free Agents for Cancer Therapy [J].
Jeena, M. T. ;
Kim, Sangpil ;
Jin, Seongeon ;
Ryu, Ja-Hyoung .
CANCERS, 2020, 12 (01)
[10]   Targeted delivery of anti-inflammatory cytokine by nanocarrier reduces atherosclerosis in Apo E-/- mice [J].
Kim, Manse ;
Sahu, Abhishek ;
Hwang, Youngmin ;
Kim, Gi Beom ;
Nam, Gi Hoon ;
Kim, In-San ;
Kwon, Ick Chan ;
Tae, Giyoong .
BIOMATERIALS, 2020, 226 (226)