Au-PLA nanocomposites for photothermally controlled drug delivery

被引:46
作者
Campardelli, Roberta [1 ]
Della Porta, Giovanna [1 ]
Gomez, Leyre [2 ]
Irusta, Silvia [2 ,3 ]
Reverchon, Ernesto [1 ]
Santamaria, Jesus [2 ,3 ]
机构
[1] Univ Salerno, Dept Ind Engn, Fisciano, SA, Italy
[2] Univ Zaragoza, INA, Dept Chem Engn, Zaragoza 50018, Spain
[3] CIBER Bioingn Biomat & Nanomed CIBER BBN, Zaragoza 50018, Spain
关键词
SUPERCRITICAL-FLUID EXTRACTION; HOLLOW GOLD NANOSPHERES; OPTICAL-PROPERTIES; LIGHT; NANOPARTICLES; RELEASE; EMULSIONS; PULSATILE; THERAPY; ENCAPSULATION;
D O I
10.1039/c3tb21099e
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Stimuli-responsive drug delivery systems were obtained by encapsulating near-infrared (NIR) sensitive hollow gold nanoshells (HGNs) together with the molecule to be released into biodegradable poly-lactic acid (PLA) sub-micron particles. The rapid heating of the PLA particles caused by NIR radiation enabled use of the PLA-HGN composites as a photo-triggered drug release system. Rhodamine was used as a test molecule to obtain release profiles under different irradiation conditions. HGNs (32 nm diameter, 4.5 nm shell thickness) were synthesized via galvanic replacement of cobalt nanoparticles, using poly(vinylpyrrolidone) (PVP) as a stabilizer. PLA-HGN sub-micron particles (with mean diameters around 200 nm) encapsulating rhodamine were obtained using the supercritical emulsion extraction (SEE) technique. A good gold dispersion and a loading efficiency around 50% in the polymeric matrix were obtained for different HGN loadings. The release rate could be tuned by controlling the intensity of NIR exposition. Rhodamine release was completed in less than 10 hours when applying intense NIR irradiation for a few minutes, whereas 12 days of release was necessary in its absence. The system also allowed rhodamine release in a pulsed pattern.
引用
收藏
页码:409 / 417
页数:9
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