Fluorescent carbon dot-gated multifunctional mesoporous silica nanocarriers for redox/enzyme dual-responsive targeted and controlled drug delivery and real-time bioimaging
Fluorescent carbon dot;
Mesoporous silica nanocarriers;
Redox/enzyme dual-responsive;
Targeted and controlled drug delivery;
Real-time bioimaging;
INTRACELLULAR DRUG;
FACILE SYNTHESIS;
NANOPARTICLES;
RELEASE;
DNA;
D O I:
10.1016/j.ejpb.2017.03.019
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
A distinctive and personalized nanocarrier is described here for controlled and targeted antitumor drug delivery and real-time bioimaging by combining a redox/enzyme dual-responsive disulfide-conjugated carbon dot with mesoporous silica nanoparticles (MSN-SS-CDHA). The carbon dot with controlling and targeting abilities was prepared through a polymerizing reaction by applying citric acid and HA as starting materials (named CDHA). The as-prepared MSN-SS-CDHA exhibited not only superior photostability and excellent biocompatibility, but also the ability to target A549 cells with overexpression of CD44 receptors. Upon loading the antitumor drug, doxorubicin (DOX), into the mesoporous channels of MSN nanoparticles, CDHA with a diameter size of 3 nm completely blocked the pore entrance of DOX-encapsulated MSN nanoparticles with a pore size of about 3 nm, thus preventing the premature leakage of DOX and increasing the antitumor activity until being triggered by specific stimuli in the tumor environment. The results of the cell imaging and cytotoxicity studies demonstrated that the redox/enzyme dual-responsive DOX-encapsulated MSN-SS-CDHA nanoparticles can selectively deliver and control the release of DOX into tumor cells. Ex vivo fluorescence images showed a much stronger fluorescence of MSN-SS-CDHA-DOX in the tumor site than in normal tissues, greatly facilitating the accumulation of DOX in the target tissue. However, its counterpart, MSN-SH-DOX exhibited no or much lower tumor cytotoxicity and drug accumulation in tumor tissue. In addition, MSN-SS-CD was also used as a control to investigate the ability of MSN-SS-CDHA to target A549 cells. The results obtained indicated that MSN-SS-CDHA possessed a higher cellular uptake through the CD44 receptor-mediated endocytosis compared with MSN-SS-CD in the A549 cells. Such specific redox/enzyme dual-responsive targeted nanocarriers are a useful strategy achieving selective controlled and targeted delivery of therapeutic reagents with realtime bioimaging, and may also facilitate the development of drug delivery systems for a number of clinical applications. (C) 2017 Elsevier B.V. All rights reserved.
机构:
Liaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, ChinaLiaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, China
Wu, Shu
Teng, Yi
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机构:
Liaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, ChinaLiaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, China
Teng, Yi
Qu, Zhengyang
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机构:
Liaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, ChinaLiaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, China
Qu, Zhengyang
Bai, Lu
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机构:
Liaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, ChinaLiaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, China
Bai, Lu
Yang, Wenxiao
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机构:
Liaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, ChinaLiaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, China
Yang, Wenxiao
Wu, Qiuhua
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机构:
Liaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, ChinaLiaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, China
Wu, Qiuhua
Zhang, Guolin
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机构:
Liaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, ChinaLiaoning Provincial Key Laboratory for Green Synthesis and Preparative Chemistry of Advanced Materials (Liaoning University), College of Chemistry, Liaoning University, Shenyang,110036, China
机构:
Nanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R ChinaNanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R China
Xu, Zhihui
Cai, Ling
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机构:
Nanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R ChinaNanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R China
Cai, Ling
Jiang, Huijun
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Nanjing Med Univ, Sch Pharm, Nanjing 211166, Jiangsu, Peoples R ChinaNanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R China
Jiang, Huijun
Wen, Yujie
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机构:
Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Nanjing 210023, Jiangsu, Peoples R China
Nanjing Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Life Sci, Nanjing 210023, Jiangsu, Peoples R ChinaNanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R China
Wen, Yujie
Peng, Luming
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h-index: 0
机构:
Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Nanjing 210023, Jiangsu, Peoples R China
Nanjing Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Life Sci, Nanjing 210023, Jiangsu, Peoples R ChinaNanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R China
Peng, Luming
Wu, Yuan
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机构:
Nanjing Med Univ, Jiangsu Canc Hosp, Jiangsu Inst Canc Res, Dept Med Oncol,Affiliated Canc Hosp, Nanjing 210009, Jiangsu, Peoples R ChinaNanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R China
Wu, Yuan
Chen, Jin
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机构:
Nanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R China
Nanjing Med Univ, Sch Publ Hlth, Key Lab Modern Toxicol, Minist Educ, Nanjing 211166, Jiangsu, Peoples R China
Nanjing Med Univ, Ctr Global Hlth, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R ChinaNanjing Med Univ, Sch Publ Hlth, Nanjing 211166, Jiangsu, Peoples R China