Self-Assembled Smart Nanocarriers for Targeted Drug Delivery

被引:194
作者
Cui, Wei [1 ]
Li, Junbai [1 ]
Decher, Gero [2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Chem, Key Lab Colloid Interface & Chem Thermodynam, BNLMS, Beijing 100190, Peoples R China
[2] Univ Strasbourg, Fac Chim, 1 Rue Blaise Pascal, F-67008 Strasbourg, France
[3] Inst Charles Sadron, CNRS, 23 Rue Loess, F-67034 Strasbourg, France
关键词
molecular assembly; nanostructure; drug carriers; selective recognition; PEGYLATED LIPOSOMAL DOXORUBICIN; MESOPOROUS SILICA NANOPARTICLES; CANCER-TREATMENT; APOPTOSIS; CAPSULES; DESIGN; NANOARCHITECTONICS; MICROCAPSULES; THERAPEUTICS; ANGIOGENESIS;
D O I
10.1002/adma.201502479
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanostructured drug-carrier systems promise numerous benefits for drug delivery. They can be engineered to precisely control drug-release rates or to target specific sites within the body with a specific amount of therapeutic agent. However, to achieve the best therapeutic effects, the systems should be designed for carrying the optimum amount of a drug to the desired target where it should be released at the optimum rate for a specified time. Despite numerous attempts, fulfilling all of these requirements in a synergistic way remains a huge challenge. The trend in drug delivery is consequently directed toward integrated multifunctional carrier systems, providing selective recognition in combination with sustained or triggered release. Capsules as vesicular systems enable drugs to be confined for controlled release. Furthermore, carriers modified with recognition groups can enhance the capability of encapsulated drug efficacy. Here, recent advances are reviewed regarding designing and preparing assembled capsules with targeting ligands or size controllable for selective recognition in drug delivery.
引用
收藏
页码:1302 / 1311
页数:10
相关论文
共 93 条
[1]   Ligand-targeted therapeutics in anticancer therapy [J].
Allen, TM .
NATURE REVIEWS CANCER, 2002, 2 (10) :750-763
[2]  
Arias JL, 2011, MINI-REV MED CHEM, V11, P1
[3]   Novel Strategies to Improve the Anticancer Action of 5-Fluorouracil by Using Drug Delivery Systems [J].
Arias, Jose L. .
MOLECULES, 2008, 13 (10) :2340-2369
[4]   Layer-by-layer Nanoarchitectonics: Invention, Innovation, and Evolution [J].
Ariga, Katsuhiko ;
Yamauchi, Yusuke ;
Rydzek, Gaulthier ;
Ji, Qingmin ;
Yonamine, Yusuke ;
Wu, Kevin C. -W. ;
Hill, Jonathan P. .
CHEMISTRY LETTERS, 2014, 43 (01) :36-68
[5]   Enzyme nanoarchitectonics: organization and device application [J].
Ariga, Katsuhiko ;
Ji, Qingmin ;
Mori, Taizo ;
Naito, Masanobu ;
Yamauchi, Yusuke ;
Abe, Hideki ;
Hill, Jonathan P. .
CHEMICAL SOCIETY REVIEWS, 2013, 42 (15) :6322-6345
[6]   Forming nanomaterials as layered functional structures toward materials nanoarchitectonics [J].
Ariga, Katsuhiko ;
Ji, Qingmin ;
Hill, Jonathan P. ;
Bando, Yoshio ;
Aono, Masakazu .
NPG ASIA MATERIALS, 2012, 4 :e17-e17
[7]   Inorganic Nanoarchitectonics for Biological Applications [J].
Ariga, Katsuhiko ;
Ji, Qingmin ;
McShane, Michael J. ;
Lvov, Yuri M. ;
Vinu, Ajayan ;
Hill, Jonathan P. .
CHEMISTRY OF MATERIALS, 2012, 24 (05) :728-737
[8]   Layer-by-layer self-assembled shells for drug delivery [J].
Ariga, Katsuhiko ;
Lvov, Yuri M. ;
Kawakami, Kohsaku ;
Ji, Qingmin ;
Hill, Jonathan P. .
ADVANCED DRUG DELIVERY REVIEWS, 2011, 63 (09) :762-771
[9]   Layer-by-layer assembly for drug delivery and related applications [J].
Ariga, Katsuhiko ;
McShane, Mike ;
Lvov, Yuri M. ;
Ji, Qingmin ;
Hill, Jonathan P. .
EXPERT OPINION ON DRUG DELIVERY, 2011, 8 (05) :633-644
[10]   NEGATIVE STAINING OF PHOSPHOLIPIDS + THEIR STRUCTURAL MODIFICATION BY-SURFACE ACTIVE AGENTS AS OBSERVED IN ELECTRON MICROSCOPE [J].
BANGHAM, AD ;
HORNE, RW .
JOURNAL OF MOLECULAR BIOLOGY, 1964, 8 (05) :660-&