Mesoporous silicate materials as substrates for molecular machines and drug delivery

被引:127
作者
Angelos, Sarah [1 ]
Liong, Monty [1 ]
Choi, Eunshil [1 ]
Zink, Jeffrey I. [1 ]
机构
[1] Univ Calif Los Angeles, Calif NanoSyst Inst, Dept Chem & Biochem, Los Angeles, CA 90095 USA
基金
美国国家科学基金会;
关键词
mesoporous silicates; functional materials; molecular machines; drug delivery;
D O I
10.1016/j.cej.2007.07.074
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Mesoporous silica thin films and nanoparticles prepared by surfactant-templated sol-gel techniques are versatile substrates that can be easily derivatized with active molecules to create functional materials. By exploiting the chemical and physical differences that exist in different regions of the mesostructure, active molecules can be deliberately placed using one-pot techniques, or they can be tethered to the exposed surfaces post-synthetically. ne methods available for functionalization have been used to design operational machines including nanoimpellers based on the dynamic photoisomerization of azobenzene, and nanovalves based on the switchable motion of supramolecular rotaxanes and pseudorotaxanes. The ability of nanoimpellers and nanovalves to control the release of molecules from the pores of mesoporous silica materials is demonstrated using luminescence spectroscopy. These machines can be designed to operate under a range of external stimuli, including light, electrical (redox) or chemical (pH, competitive binding) energy, making them useful systems for a variety of controlled release applications. Mesoporous silica nanoparticles not functionalized with molecular machines are capable of delivering water-insoluble anticancer drugs to cancer cells. Carefully designed nanoimpellers and nanovalves supported on mesoporous silica nanoparticles offer the ability to develop sophisticated drug delivery vehicles for a wide range of drug molecules. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:4 / 13
页数:10
相关论文
共 57 条
[1]  
Angelos S, 2007, J PHYS CHEM C, V111, P6589, DOI 10.1021/jp0707211
[2]  
Avnir D, 2006, J MATER CHEM, V16, P1013, DOI 10.1039/5512706h
[3]   Surface modification of silica nanoparticles to reduce aggregation and nonspecific binding [J].
Bagwe, RP ;
Hilliard, LR ;
Tan, WH .
LANGMUIR, 2006, 22 (09) :4357-4362
[4]   A NEW FAMILY OF MESOPOROUS MOLECULAR-SIEVES PREPARED WITH LIQUID-CRYSTAL TEMPLATES [J].
BECK, JS ;
VARTULI, JC ;
ROTH, WJ ;
LEONOWICZ, ME ;
KRESGE, CT ;
SCHMITT, KD ;
CHU, CTW ;
OLSON, DH ;
SHEPPARD, EW ;
MCCULLEN, SB ;
HIGGINS, JB ;
SCHLENKER, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10834-10843
[5]   BIOCHEMICALLY ACTIVE SOL-GEL GLASSES - THE TRAPPING OF ENZYMES [J].
BRAUN, S ;
RAPPOPORT, S ;
ZUSMAN, R ;
AVNIR, D ;
OTTOLENGHI, M .
MATERIALS LETTERS, 1990, 10 (1-2) :1-5
[6]  
Brinker C.J., 1990, SOL GEL SCI
[7]   Patterned hexagonal arrays of living cells in sol-gel silica films [J].
Chia, SY ;
Urano, J ;
Tamanoi, F ;
Dunn, B ;
Zink, JI .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (27) :6488-6489
[8]  
Chia SY, 2001, ANGEW CHEM INT EDIT, V40, P2447, DOI 10.1002/1521-3773(20010702)40:13<2447::AID-ANIE2447>3.0.CO
[9]  
2-P
[10]   Encapsulation of proteins in bulk and thin film sol-gel matrices [J].
Dave, BC ;
Miller, JM ;
Dunn, B ;
Valentine, JS ;
Zink, JI .
JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY, 1997, 8 (1-3) :629-634