Hierarchical Targeting Strategy for Enhanced Tumor Tissue Accumulation/Retention and Cellular Internalization

被引:349
作者
Wang, Sheng [1 ,2 ,3 ,4 ]
Huang, Peng [1 ]
Chen, Xiaoyuan [4 ]
机构
[1] Shenzhen Univ, Guangdong Key Lab Biomed Measurements & Ultrasoun, Sch Biomed Engn, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Minist Educ, Key Lab Optoelect Devices & Syst, Shenzhen 518060, Peoples R China
[3] Shenzhen Univ, Coll Optoelect Engn, Shenzhen 518060, Peoples R China
[4] Natl Inst Biomed Imaging & Bioengn, Lab Mol Imaging & Nanomed, NIH, Bethesda, MD 20892 USA
基金
美国国家科学基金会;
关键词
hierarchical targeting; stimuli-responsive nanoplatforms; changeable particle sizes; switchable surface charges; activatable surface ligands; ANTICANCER DRUG-DELIVERY; MULTIFUNCTIONAL POLYMERIC MICELLE; MESOPOROUS SILICA NANOPARTICLES; SUPERPARAMAGNETIC IRON-OXIDE; GENERATING LIPOSOMAL SYSTEM; UP-CONVERSION NANOPARTICLES; PENETRATING PEPTIDE; GOLD NANOPARTICLES; CANCER-THERAPY; IN-VIVO;
D O I
10.1002/adma.201601498
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Targeted delivery of therapeutic agents is an important way to improve the therapeutic index and reduce side effects. To design nanoparticles for targeted delivery, both enhanced tumor tissue accumulation/retention and enhanced cellular internalization should be considered simultaneously. So far, there have been very few nanoparticles with immutable structures that can achieve this goal efficiently. Hierarchical targeting, a novel targeting strategy based on stimuli responsiveness, shows good potential to enhance both tumor tissue accumulation/retention and cellular internalization. Here, the recent design and development of hierarchical targeting nanoplatforms, based on changeable particle sizes, switchable surface charges and activatable surface ligands, will be introduced. In general, the targeting moieties in these nanoplatforms are not activated during blood circulation for efficient tumor tissue accumulation, but re-activated by certain internal or external stimuli in the tumor microenvironment for enhanced cellular internalization.
引用
收藏
页码:7340 / 7364
页数:25
相关论文
共 131 条
[1]   Lipid-Peptide Vesicle Nanoscale Hybrids for Triggered Drug Release by Mild Hyperthermia in Vitro and in Vivo [J].
Al-Ahmady, Zahraa S. ;
Al-Jamal, Wafa' T. ;
Bossche, Jeroen V. ;
Bui, Tam T. ;
Drake, Alex F. ;
Mason, A. James ;
Kostarelos, Kostas .
ACS NANO, 2012, 6 (10) :9335-9346
[2]   Synthesis, Characterization, and Application in HeLa Cells of an NIR Light Responsive Doxorubicin Delivery System Based on NaYF4:Yb,Tm@SiO2-PEG Nanoparticles [J].
Alonso-Cristobal, Paulino ;
Oton-Fernandez, Olalla ;
Mendez-Gonzalez, Diego ;
Fernando Diaz, J. ;
Lopez-Cabarcos, Enrique ;
Barasoain, Isabel ;
Rubio-Retama, Jorge .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (27) :14992-14999
[3]   pH (low) insertion peptide (pHLIP) inserts across a lipid bilayer as a helix and exits by a different path [J].
Andreev, Oleg A. ;
Karabadzhak, Alexander G. ;
Weerakkody, Dhammika ;
Andreev, Gregory O. ;
Engelman, Donald M. ;
Reshetnyak, Yana K. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (09) :4081-4086
[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]  
Ashley CE, 2011, NAT MATER, V10, P389, DOI [10.1038/NMAT2992, 10.1038/nmat2992]
[6]   Stimuli-Responsive Nanomaterials for Biomedical Applications [J].
Blum, Angela P. ;
Kammeyer, Jacquelin K. ;
Rush, Anthony M. ;
Callmann, Cassandra E. ;
Hahn, Michael E. ;
Gianneschi, Nathan C. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (06) :2140-2154
[7]   Enzyme-Activatable Cell-Penetrating Peptides through a Minimal Side Chain Modification [J].
Bode, Saskia A. ;
Hansen, Morten B. ;
Oerlemans, Roy A. J. F. ;
van Hest, Jan C. M. ;
Lowik, Dennis W. P. M. .
BIOCONJUGATE CHEMISTRY, 2015, 26 (05) :850-856
[8]   Hyperthermia-Mediated Local Drug Delivery by a Bubble-Generating Liposomal System for Tumor-Specific Chemotherapy [J].
Chen, Ko-Jie ;
Chaung, Er-Yuan ;
Wey, Shiaw-Pyng ;
Lin, Kun-Ju ;
Cheng, Felice ;
Lin, Chia-Chen ;
Liu, Hao-Li ;
Tseng, Hsiang-Wen ;
Liu, Chih-Peng ;
Wei, Ming-Cheng ;
Liu, Chun-Min ;
Sung, Hsing-Wen .
ACS NANO, 2014, 8 (05) :5105-5115
[9]   A Thermoresponsive Bubble-Generating Liposomal System for Triggering Localized Extracellular Drug Delivery [J].
Chen, Ko-Jie ;
Liang, Hsiang-Fa ;
Chen, Hsin-Lung ;
Wang, Yucai ;
Cheng, Po-Yuan ;
Liu, Hao-Li ;
Xia, Younan ;
Sung, Hsing-Wen .
ACS NANO, 2013, 7 (01) :438-446
[10]   An Imagable and Photothermal "Abraxane-Like" Nanodrug for Combination Cancer Therapy to Treat Subcutaneous and Metastatic Breast Tumors [J].
Chen, Qian ;
Liang, Chao ;
Wang, Chao ;
Liu, Zhuang .
ADVANCED MATERIALS, 2015, 27 (05) :903-910