A review of stimuli-responsive nanocarriers for drug and gene delivery

被引:1861
作者
Ganta, Srinivas [1 ]
Devalapally, Harikrishna [1 ]
Shahiwala, Aliasgar [1 ]
Amiji, Mansoor [1 ]
机构
[1] Northeastern Univ, Sch Pharm, Dept Pharmaceut Sci, Boston, MA 02115 USA
关键词
nanotechnology; targeted delivery; stimuli-responsive nanocarriers; pH; temperature; redox potential;
D O I
10.1016/j.jconrel.2007.12.017
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanotechnology has shown tremendous promise in target-specific delivery of drugs and genes in the body. Although passive and active targeted-drug delivery has addressed a number of important issues, additional properties that can be included in nanocarrier systems to enhance the bioavailability of drugs at the disease site, and especially upon cellular internalization, are very important. A nanocarrier system incorporated with stimuli-responsive property (e.g., pH, temperature, or redox potential), for instance, would be amenable to address some of the systemic and intracellular delivery barriers. In this review, we discuss the role of stimuli-responsive nanocarrier systems for drug and gene delivery. The advancement in material science has led to design of a variety of materials, which are used for development of nanocarrier systems that can respond to biological stimuli. Temperature, pH, and hypoxia are examples of "triggers" at the diseased site that could be exploited with stimuli-responsive nanocarriers. With greater understanding of the difference between normal and pathological tissues and cells and parallel developments in material design, there is a highly promising role of stimuli-responsive nanocarriers for drug and gene delivery in the future. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:187 / 204
页数:18
相关论文
共 172 条
[1]   Combined radiofrequency ablation and adjuvant liposomal chemotherapy: Effect of chemotherapeutic agent, nanoparticle size, and circulation time [J].
Ahmed, M ;
Lukyanov, AN ;
Torchilin, V ;
Tournier, H ;
Schneider, AN ;
Goldberg, SN .
JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY, 2005, 16 (10) :1365-1371
[2]   Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[3]   EVIDENCE FOR SUPPRESSION OF SERUM-LH WITHOUT ELEVATION IN SERUM ESTRADIOL OR PROLACTIN WITH A BRAIN-ENHANCED REDOX DELIVERY SYSTEM FOR ESTRADIOL [J].
ANDERSON, WR ;
SIMPKINS, JW ;
BREWSTER, ME ;
BODOR, N .
LIFE SCIENCES, 1988, 42 (16) :1493-1502
[4]  
[Anonymous], DRUD DELIVERY SYST S
[5]   Magnetic nanoparticles for drug delivery [J].
Arruebo, Manuel ;
Fernandez-Pacheco, Rodrigo ;
Ibarra, M. Ricardo ;
Santamaria, Jesus .
NANO TODAY, 2007, 2 (03) :22-32
[6]   Thermosensitive pluronic micelles stabilized by shell cross-linking with gold nanoparticles [J].
Bae, Ki Hyun ;
Choi, Seung Ho ;
Park, Sung Young ;
Lee, Yuhan ;
Park, Tae Gwan .
LANGMUIR, 2006, 22 (14) :6380-6384
[7]  
Bae Y, 2005, MOL BIOSYST, V1, P242, DOI 10.1039/b500266d
[8]   Preparation and biological characterization of polymeric micelle drug carriers with intracellular pH-triggered drug release property: Tumor permeability, controlled subcellular drug distribution, and enhanced in vivo antitumor efficacy [J].
Bae, Y ;
Nishiyama, N ;
Fukushima, S ;
Koyama, H ;
Yasuhiro, M ;
Kataoka, K .
BIOCONJUGATE CHEMISTRY, 2005, 16 (01) :122-130
[9]   Lipoic acid-derived amphiphiles for redox-controlled DNA delivery [J].
Balakirev, M ;
Schoehn, G ;
Chroboczek, J .
CHEMISTRY & BIOLOGY, 2000, 7 (10) :813-819
[10]   SWELLING EQUILIBRIA FOR WEAKLY IONIZABLE, TEMPERATURE-SENSITIVE HYDROGELS [J].
BELTRAN, S ;
BAKER, JP ;
HOOPER, HH ;
BLANCH, HW ;
PRAUSNITZ, JM .
MACROMOLECULES, 1991, 24 (02) :549-551