Nanoparticle-based Drug Delivery Systems for Solid Brain Tumors

被引:6
作者
Feng, Bin [2 ,3 ]
Matsui, Hideki [2 ]
Tomizawa, Kazuhito [1 ]
机构
[1] Kumamoto Univ, Fac Life Sci, Dept Mol Physiol, Kumamoto 8608558, Japan
[2] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Physiol, Okayama 7008558, Japan
[3] Dalian Med Univ, Dept Biotechnol, Dalian 116044, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanoparticles; targeted drug delivery; blood-brain barrier; imaging; therapy; NEUTRON-CAPTURE THERAPY; STERICALLY STABILIZED LIPOSOMES; GENE-THERAPY; MAGNETIC NANOPARTICLES; IN-VITRO; SODIUM BOROCAPTATE; CANCER; RECEPTOR; CELLS; IMMUNOLIPOSOMES;
D O I
10.2174/157341311794480327
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The treatment of brain tumors including glioblastoma multiformes (GBMs) remains a challenge. The main option is still surgery to remove the bulk of the tumor and adjuvant treatments for the infiltrating parts. The blood brain barrier (BBB), however, restricts the access of chemotherapeutic agents to the tumor. The use of nanoparticle-based drug delivery systems (DDSs) has an increasing impact on disease diagnosis and therapy. By altering their size, composition, and surface chemistry, nanoparticles can be developed into a universal platform with multifunctional capabilities to meet the tunable requirements of different DDS. Thus, nanoparticles have the potential for targeted delivery of therapeutic cargo to brain tumors combined with simultaneous detection and imaging functions, providing a new strategy for effective therapy. The purpose of this article is to provide an updated review on the current progression and future possibilities of treating brain tumors with nanoparticles.
引用
收藏
页码:47 / 54
页数:8
相关论文
共 87 条
[1]   Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[2]   A NEW STRATEGY FOR ATTACHMENT OF ANTIBODIES TO STERICALLY STABILIZED LIPOSOMES RESULTING IN EFFICIENT TARGETING TO CANCER-CELLS [J].
ALLEN, TM ;
BRANDEIS, E ;
HANSEN, CB ;
KAO, GY ;
ZALIPSKY, S .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1995, 1237 (02) :99-108
[3]   Glioma stem cells promote radioresistance by preferential activation of the DNA damage response [J].
Bao, Shideng ;
Wu, Qiulian ;
McLendon, Roger E. ;
Hao, Yueling ;
Shi, Qing ;
Hjelmeland, Anita B. ;
Dewhirst, Mark W. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
NATURE, 2006, 444 (7120) :756-760
[4]   Boron neutron capture therapy of cancer: Current status and future prospects [J].
Barth, RF ;
Coderre, JA ;
Vicente, MGH ;
Blue, TE .
CLINICAL CANCER RESEARCH, 2005, 11 (11) :3987-4002
[5]  
Batist G, 2001, J CLIN ONCOL, V19, P3440
[6]   INFLUENCE OF POLYBUTYLCYANOACRYLATE NANOPARTICLES AND LIPOSOMES ON THE EFFICACY AND TOXICITY OF THE ANTICANCER DRUG MITOXANTRONE IN MURINE TUMOR-MODELS [J].
BECK, P ;
KREUTER, J ;
RESZKA, R ;
FICHTNER, I .
JOURNAL OF MICROENCAPSULATION, 1993, 10 (01) :101-114
[7]   Ligand liposomes and boron neutron capture therapy [J].
Carlsson, J ;
Kullberg, EB ;
Capala, J ;
Sjöberg, S ;
Edwards, K ;
Gedda, L .
JOURNAL OF NEURO-ONCOLOGY, 2003, 62 (01) :47-59
[8]   Nanotechnology Platforms in Diagnosis and Treatment of Primary Brain Tumors [J].
Caruso, Gerardo ;
Raudino, Giuseppe ;
Caffo, Mariella ;
Alafaci, Concetta ;
Granata, Francesca ;
Lucerna, Sebastiano ;
Salpietro, Francesco M. ;
Tomasello, Francesco .
RECENT PATENTS ON NANOTECHNOLOGY, 2010, 4 (02) :119-124
[9]   Role of thiamin (vitamin B-1) and transketolase in tumor cell proliferation [J].
Cascante, M ;
Centelles, JJ ;
Veech, RL ;
Lee, WNP ;
Boros, LG .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2000, 36 (02) :150-154
[10]  
Chen Y., 2004, Current Drug Delivery, V1, P361, DOI 10.2174/1567201043334542