Cancer Nanotheranostics: Improving Imaging and Therapy by Targeted Delivery Across Biological Barriers

被引:432
作者
Kievit, Forrest M. [1 ]
Zhang, Miqin [1 ]
机构
[1] Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA
关键词
MESENCHYMAL STEM-CELLS; IRON-OXIDE NANOPARTICLES; CONVECTION-ENHANCED DELIVERY; METAL-ORGANIC FRAMEWORKS; BLOOD-BRAIN-BARRIER; IN-VIVO TRACKING; PEGYLATED LIPOSOMAL DOXORUBICIN; OVERCOME MULTIDRUG-RESISTANCE; MULTIMODAL CONTRAST AGENTS; COATED GOLD NANOPARTICLES;
D O I
10.1002/adma.201102313
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cancer nanotheranostics aims to combine imaging and therapy of cancer through use of nanotechnology. The ability to engineer nanomaterials to interact with cancer cells at the molecular level can significantly improve the effectiveness and specificity of therapy to cancers that are currently difficult to treat. In particular, metastatic cancers, drug-resistant cancers, and cancer stem cells impose the greatest therapeutic challenge for targeted therapy. Targeted therapy can be achieved with appropriately designed drug delivery vehicles such as nanoparticles, adult stem cells, or T cells in immunotherapy. In this article, we first review the different types of nanotheranostic particles and their use in imaging, followed by the biological barriers they must bypass to reach the target cancer cells, including the blood, liver, kidneys, spleen, and particularly the blood-brain barrier. We then review how nanotheranostics can be used to improve targeted delivery and treatment of cancer cells. Finally, we discuss development of nanoparticles to overcome current limitations in cancer therapy.
引用
收藏
页码:H217 / H247
页数:31
相关论文
共 404 条
[1]   Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[2]   Neural stem cells display extensive tropism for pathology in adult brain: Evidence from intracranial gliomas [J].
Aboody, KS ;
Brown, A ;
Rainov, NG ;
Bower, KA ;
Liu, SX ;
Yang, W ;
Small, JE ;
Herrlinger, U ;
Ourednik, V ;
Black, PM ;
Breakefield, XO ;
Snyder, EY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) :12846-12851
[3]   Systemic in vivo distribution of activatable cell penetrating peptides is superior to that of cell penetrating peptides [J].
Aguilera, Todd A. ;
Olson, Emilia S. ;
Timmers, Margaret M. ;
Jiang, Tao ;
Tsien, Roger Y. .
INTEGRATIVE BIOLOGY, 2009, 1 (5-6) :371-381
[4]   Pushing the Sensitivity Envelope of Lanthanide-Based Magnetic Resonance Imaging (MRI) Contrast Agents for Molecular Imaging Applications [J].
Aime, Silvio ;
Castelli, Daniela Delli ;
Crich, Simonetta Geninatti ;
Gianolio, Eliana ;
Terreno, Enzo .
ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (07) :822-831
[5]  
Akers WJ, 2010, NANOMEDICINE-UK, V5, P715, DOI [10.2217/nnm.10.38, 10.2217/NNM.10.38]
[6]   Development and brain delivery of chitosan-PEG nanoparticles functionalized with the monoclonal antibody OX26 [J].
Aktas, Y ;
Yemisci, M ;
Andrieux, K ;
Gürsoy, RN ;
Alonso, MJ ;
Fernandez-Megia, E ;
Novoa-Carballal, R ;
Quiñoá, E ;
Riguera, R ;
Sargon, MF ;
Çelik, HH ;
Demir, AS ;
Hincal, AA ;
Dalkara, T ;
Çapan, Y ;
Couvreur, P .
BIOCONJUGATE CHEMISTRY, 2005, 16 (06) :1503-1511
[7]   Convection-enhanced delivery of nanocarriers for the treatment of brain tumors [J].
Allard, Emilie ;
Passirani, Catherine ;
Benoit, Jean-Pierre .
BIOMATERIALS, 2009, 30 (12) :2302-2318
[8]   Use of genetically engineered bone marrow-derived mesenchymal stem cells for glioma gene therapy [J].
Amano, Shinji ;
Li, Shaoyi ;
Gu, Chunyu ;
Gao, Yun ;
Koizumi, Shinichiro ;
Yamamoto, Seiji ;
Terakawa, Susumu ;
Namba, Hiroki .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2009, 35 (06) :1265-1270
[9]  
[Anonymous], ACC CHEM RES
[10]  
[Anonymous], CAUS DEATH 2008 SUMM