Therapeutic nanoparticles for drug delivery in cancer

被引:2196
作者
Cho, Kwangjae [1 ]
Wang, Xu [1 ]
Nie, Shuming [2 ]
Chen, Zhuo [1 ]
Shin, Dong M. [1 ]
机构
[1] Emory Univ, Sch Med, Winship Canc Ctr, Dept Hematol & Oncol, Atlanta, GA 30322 USA
[2] Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
关键词
D O I
10.1158/1078-0432.CCR-07-1441
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer nanotherapeutics are rapidly progressing and are being implemented to solve several limitations of conventional drug delivery systems such as nonspecific biodistribution and targeting, lack of water solubility, poor oral bioavailability, and low therapeutic indices. To improve the biodistribution of cancer drugs, nanoparticles have been designed for optimal size and surface characteristics to increase their circulation time in the bloodstream. They are also able to carry their loaded active drugs to cancer cells by selectively using the unique pathophysiology of tumors, such as their enhanced permeability and retention effect and the tumor microenvironment. In addition to this passive targeting mechanism, active targeting strategies using ligands or antibodies directed against selected tumor targets amplify the specificity of these therapeutic nanoparticles. Drug resistance, another obstacle that impedes the efficacy of both molecularly targeted and conventional chemotherapeutic agents, might also be overcome, or at least reduced, using nanoparticles. Nanoparticles have the ability to accumulate in cells without being recognized by P-glycoprotein, one of the main mediators of multidrug resistance, resulting in the increased intracellular concentration of drugs. Multifunctional and multiplex nanoparticles are now being actively investigated and are on the horizon as the next generation of nanoparticles, facilitating personalized and tailored cancer treatment.
引用
收藏
页码:1310 / 1316
页数:7
相关论文
共 65 条
  • [1] Amphiphilic block copolymers for drug delivery
    Adams, ML
    Lavasanifar, A
    Kwon, GS
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 92 (07) : 1343 - 1355
  • [2] Ligand-targeted therapeutics in anticancer therapy
    Allen, TM
    [J]. NATURE REVIEWS CANCER, 2002, 2 (10) : 750 - 763
  • [3] Anthracycline antibiotics non-covalently incorporated into the block copolymer micelles: In vivo evaluation of anti-cancer activity
    Batrakova, EV
    Dorodnych, TY
    Klinskii, EY
    Kliushnenkova, EN
    Shemchukova, OB
    Goncharova, ON
    Arjakov, SA
    Alakhov, VY
    Kabanov, AV
    [J]. BRITISH JOURNAL OF CANCER, 1996, 74 (10) : 1545 - 1552
  • [4] Synthesis and in vivo antitumor activity of poly(L-glutamic acid) conjugates of 20(S)-camptothecin
    Bhatt, RL
    de Vries, P
    Tulinsky, J
    Bellamy, G
    Baker, B
    Singer, JW
    Klein, P
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (01) : 190 - 193
  • [5] Biomedical applications of functionalised carbon nanotubes
    Bianco, A
    Kostarelos, K
    Partidos, CD
    Prato, M
    [J]. CHEMICAL COMMUNICATIONS, 2005, (05) : 571 - 577
  • [6] Applications of carbon nanotubes in drug delivery
    Bianco, A
    Kostarelos, K
    Prato, M
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 2005, 9 (06) : 674 - 679
  • [7] Lectin-mediated drug targeting: history and applications
    Bies, C
    Lehr, CM
    Woodley, JF
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (04) : 425 - 435
  • [8] Angiogenesis in cancer and other diseases
    Carmeliet, P
    Jain, RK
    [J]. NATURE, 2000, 407 (6801) : 249 - 257
  • [9] CHO K, 2007, P AM ASSOC CANC RES, P48
  • [10] In vivo tumor targeting and radionuclide imaging with self-assembled nanoparticles: Mechanisms, key factors, and their implications
    Cho, Yong Woo
    Park, Soo Ah
    Han, Tae Hee
    Son, Dai Hyun
    Park, Ji Sun
    Oh, Seung Jun
    Moon, Dae Hyuk
    Cho, Kyung-Ja
    Ahn, Cheol-Hee
    Byun, Youngro
    Kim, In-San
    Kwon, Ick Chan
    Kim, Sang Yoon
    [J]. BIOMATERIALS, 2007, 28 (06) : 1236 - 1247