pHe-Induced Charge-Reversible NIR Fluorescence Nanoprobe for Tumor-Specific Imaging

被引:24
作者
Dong, Chunhong [1 ]
Liu, Zhongyun [3 ]
Zhang, Lei [1 ,2 ]
Guo, Weisheng [1 ]
Li, Xue [1 ]
Liu, Junqing [1 ]
Wang, Hanjie [1 ,4 ]
Chang, Jin [1 ,4 ]
机构
[1] Tianjin Univ, Sch Life Sci, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Environm Sci & Engn, Tianjin 300072, Peoples R China
[3] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Yantai 264003, Shandong, Peoples R China
[4] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
QDs nanoprobe; tumor extracellular pH; pH-sensitive; charge reversion; tumor specific imaging; QUANTUM DOTS; DRUG-DELIVERY; HIGHLY LUMINESCENT; SURFACE-CHARGE; IN-VIVO; NANOPARTICLES; MICROENVIRONMENT; NANOCARRIERS; INTERNALIZATION; THERAPY;
D O I
10.1021/am509011y
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Inspired by the specificity of acid tumor microenvironment, we constructed a flexible charge-reversible near-infrared (NIR) fluorescence nanoprobe in response to tumor extracellular pH (pHe) for effective tumor-specific imaging. The nanoprobe consists of an NIR-emitted CuInS2/ZnS quantum dot (CIS/ZS QDs) core and a tailored lauric acid and 2,3-dimethylmaleic anhydride modified e-polylysine (epsilon-PL-g-LA/DMA) shell, which provides not only a dense protective layer for the QDs but also the ability of pHe-induced positive charge-mediated endocytosis into tumor cells. The results showed that the QDs@epsilon-PL-g-LA/DMA nanoprobe with a uniform size of 40 nm had high chemical stability at pH 7.4 and excellent optical properties. Especially, it swiftly reversed its surface charge to positive in 20 min when exposed to pHe due to the cleavage of the beta-carboxyl amide bond of epsilon-PL-g-LA/DMA. Moreover, the cell uptake of the pHe-sensitive QDs nanoprobe exposed at pH 6.8 into HeLa cells is much more significant than that at pH 7.4, which further verified the availability of the electrostatic adsorptive endocytosis facilitated targeting ability. The pHe-induced targeting imparted the QDs nanoprobe a broad targeting ability in a variety of solid tumors. Furthermore, as an effective alternative mechanism for tumor targeting, responsive charge reversion is also universally applicable to other cancer theranostics agent.
引用
收藏
页码:7566 / 7575
页数:10
相关论文
共 50 条
[1]   Smart drug delivery systems: from fundamentals to the clinic [J].
Alvarez-Lorenzo, Carmen ;
Concheiro, Angel .
CHEMICAL COMMUNICATIONS, 2014, 50 (58) :7743-7765
[2]   Recent advances in stealth coating of nanoparticle drug delivery systems [J].
Amoozgar, Zohreh ;
Yeo, Yoon .
WILEY INTERDISCIPLINARY REVIEWS-NANOMEDICINE AND NANOBIOTECHNOLOGY, 2012, 4 (02) :219-233
[3]   Modulating Pharmacokinetics, Tumor Uptake and Biodistribution by Engineered Nanoparticles [J].
Arvizo, Rochelle R. ;
Miranda, Oscar R. ;
Moyano, Daniel F. ;
Walden, Chad A. ;
Giri, Karuna ;
Bhattacharya, Resham ;
Robertson, J. David ;
Rotello, Vincent M. ;
Reid, Joel M. ;
Mukherjee, Priyabrata .
PLOS ONE, 2011, 6 (09)
[4]   Effect of Nanoparticle Surface Charge at the Plasma Membrane and Beyond [J].
Arvizo, Rochelle R. ;
Miranda, Oscar R. ;
Thompson, Michael A. ;
Pabelick, Christina M. ;
Bhattacharya, Resham ;
Robertson, J. David ;
Rotello, Vincent M. ;
Prakash, Y. S. ;
Mukherjee, Priyabrata .
NANO LETTERS, 2010, 10 (07) :2543-2548
[5]   Zwitterionic Biocompatible Quantum Dots for Wide pH Stability and Weak Nonspecific Binding to Cells [J].
Breus, Vladimir V. ;
Heyes, Colin D. ;
Tron, Kyrylo ;
Nienhaus, G. Ulrich .
ACS NANO, 2009, 3 (09) :2573-2580
[6]   The role of disturbed pH dynamics and the Na+/H+ exchanger in metastasis [J].
Cardone, RA ;
Casavola, V ;
Reshkin, SJ .
NATURE REVIEWS CANCER, 2005, 5 (10) :786-795
[7]   Multifunctional Nanoparticles: Cost Versus Benefit of Adding Targeting and Imaging Capabilities [J].
Cheng, Zhiliang ;
Al Zaki, Ajlan ;
Hui, James Z. ;
Muzykantov, Vladimir R. ;
Tsourkas, Andrew .
SCIENCE, 2012, 338 (6109) :903-910
[8]   Understanding the Role of Surface Charges in Cellular Adsorption versus Internalization by Selectively Removing Gold Nanoparticles on the Cell Surface with a I2/KI Etchant [J].
Cho, Eun Chul ;
Xie, Jingwei ;
Wurm, Patricia A. ;
Xia, Younan .
NANO LETTERS, 2009, 9 (03) :1080-1084
[9]  
Cho Y. W., 2007, PHARM SCI ENCY, V14, P1
[10]  
Choi HS, 2010, NAT NANOTECHNOL, V5, P42, DOI [10.1038/NNANO.2009.314, 10.1038/nnano.2009.314]