Stimulus-responsive nanopreparations for tumor targeting

被引:193
作者
Zhu, Lin [1 ]
Torchilin, Vladimir P.
机构
[1] Northeastern Univ, Dept Pharmaceut Sci, Boston, MA 02115 USA
关键词
CELL-PENETRATING PEPTIDES; IRON-OXIDE NANOPARTICLES; DRUG-DELIVERY SYSTEMS; IN-VIVO; INTRACELLULAR DRUG; PHOTODYNAMIC THERAPY; PH; CANCER; GENE; DOXORUBICIN;
D O I
10.1039/c2ib20135f
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nanopreparations such as liposomes, micelles, polymeric and inorganic nanoparticles, and small molecule/nucleic acid/protein conjugates have demonstrated various advantages over "naked'' therapeutic molecules. These nanopreparations can be further engineered with functional moieties to improve their performance in terms of circulation longevity, targetability, enhanced intracellular penetration, carrier-mediated enhanced visualization, and stimuli-sensitivity. The idea of application of a stimulus-sensitive drug or imaging agent delivery system for tumor targeting is based on the significant abnormalities in the tumor microenvironment and its cells, such as an acidic pH, altered redox potential, up-regulated proteins and hyperthermia. These internal conditions as well as external stimuli, such as magnetic field, ultrasound and light, can be used to modify the behavior of the nanopreparations that control drug release, improve drug internalization, control the intracellular drug fate and even allow for certain physical interactions, resulting in an enhanced tumor targeting and antitumor effect. This article provides a critical view of current stimulus-sensitive drug delivery strategies and possible future directions in tumor targeting with primary focus on the combined use of stimulus-sensitivity with other strategies in the same nanopreparation, including multifunctional nanopreparations and theranostics.
引用
收藏
页码:96 / 107
页数:12
相关论文
共 91 条
  • [1] Systemic in vivo distribution of activatable cell penetrating peptides is superior to that of cell penetrating peptides
    Aguilera, Todd A.
    Olson, Emilia S.
    Timmers, Margaret M.
    Jiang, Tao
    Tsien, Roger Y.
    [J]. INTEGRATIVE BIOLOGY, 2009, 1 (5-6) : 371 - 381
  • [2] Stimuli responsive polymers for biomedical applications
    Alarcón, CDH
    Pennadam, S
    Alexander, C
    [J]. CHEMICAL SOCIETY REVIEWS, 2005, 34 (03) : 276 - 285
  • [3] Drug delivery systems: Entering the mainstream
    Allen, TM
    Cullis, PR
    [J]. SCIENCE, 2004, 303 (5665) : 1818 - 1822
  • [4] Protease-Sensitive, Polymer-Caged Liposomes: A Method for Making Highly Targeted Liposomes Using Triggered Release
    Basel, Matthew T.
    Shrestha, Tej B.
    Troyer, Deryl L.
    Bossmann, Stefan H.
    [J]. ACS NANO, 2011, 5 (03) : 2162 - 2175
  • [5] A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE
    BOUSSIF, O
    LEZOUALCH, F
    ZANTA, MA
    MERGNY, MD
    SCHERMAN, D
    DEMENEIX, B
    BEHR, JP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) : 7297 - 7301
  • [6] Angiogenesis in health and disease
    Carmeliet, P
    [J]. NATURE MEDICINE, 2003, 9 (06) : 653 - 660
  • [7] PEG-SS-PPS: Reduction-sensitive disulfide block copolymer vesicles for intracellular drug delivery
    Cerritelli, Simona
    Velluto, Diana
    Hubbell, Jeffrey A.
    [J]. BIOMACROMOLECULES, 2007, 8 (06) : 1966 - 1972
  • [8] pH and Reduction Dual-Sensitive Copolymeric Micelles for Intracellular Doxorubicin Delivery
    Chen, Jun
    Qiu, Xiaozhong
    Ouyang, Jun
    Kong, Jiming
    Zhong, Wen
    Xing, Malcolm M. Q.
    [J]. BIOMACROMOLECULES, 2011, 12 (10) : 3601 - 3611
  • [9] Glutathione-responsive nano-vehicles as a promising platform for targeted intracellular drug and gene delivery
    Cheng, Ru
    Feng, Fang
    Meng, Fenghua
    Deng, Chao
    Feijen, Jan
    Zhong, Zhiyuan
    [J]. JOURNAL OF CONTROLLED RELEASE, 2011, 152 (01) : 2 - 12
  • [10] Lipopolysaccharide upregulates uPA, MMP-2 and MMP-9 via ERK1/2 signaling in H9c2 cardiomyoblast cells
    Cheng, Yi-Chang
    Chen, Li-Mien
    Chang, Mu-Hsin
    Chen, Wei-Kung
    Tsai, Fuu-Jen
    Tsai, Chang-Hai
    Lai, Tung-Yuan
    Kuo, Wei-Wen
    Huang, Chih-Yang
    Liu, Chung-Jung
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2009, 325 (1-2) : 15 - 23