Dual targeted magnetic photosensitive liposomes for photothermal/photodynamic tumor therapy

被引:27
|
作者
Anilkumar, T. S. [1 ]
Lu, Yu-Jen [2 ]
Chen, Huai-An [1 ]
Hsu, Hao-Lung [1 ]
Jose, Gils [1 ]
Chen, Jyh-Ping [1 ,3 ,4 ,5 ,6 ,7 ]
机构
[1] Chang Gung Univ, Dept Chem & Mat Engn, Taoyuan 33302, Taiwan
[2] Chang Gung Mem Hosp, Dept Neurosurg, Taoyuan 33305, Taiwan
[3] Chang Gung Mem Hosp, Dept Plast & Reconstruct Surg, Taoyuan 33305, Taiwan
[4] Chang Gung Mem Hosp, Craniofacial Res Ctr, Taoyuan 33305, Taiwan
[5] Chang Gung Univ Sci & Technol, Coll Human Ecol, Res Ctr Chinese Herbal Med, Taoyuan 33302, Taiwan
[6] Chang Gung Univ Sci & Technol, Coll Human Ecol, Res Ctr Food & Cosmet Safety, Taoyuan 33302, Taiwan
[7] Ming Chi Univ Technol, Dept Mat Engn, New Taipei 24301, Taiwan
关键词
Magnetic liposomes; Magnetic nanoparticles; Indocyanine green; Photothermal therapy; IRON-OXIDE NANOPARTICLES; PHOTODYNAMIC THERAPY; PHOTOTHERMAL THERAPY; INDOCYANINE GREEN; DRUG-DELIVERY; IN-VITRO; CANCER; STABILITY; REMOVAL;
D O I
10.1016/j.jmmm.2018.10.020
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this work, we prepared a nano-vehicle for dual targeted (magnetic and ligand) and dual mode (photothermal/photodynamic) cancer therapy. For this purpose, magnetic photosensitive liposomes (MPLs) from 1,2-distearoylsn-glycero-3-phosphocholine, dimethyldioctadecyl ammonium bromide (DDAB) and cholesterol were prepared using solvent evaporation/hydration technique to encapsulate the photosensitizer indocyanine green (ICG) and citric acid-coated MNPs (CMNPs). Hyaluronic acid-polyethylene glycol (HA-PEG) was coated to the MPLs by self-assembly of HA-PEG on liposome surface through ionic interactions between negatively charged HA and positively charged lipid DDAB to fabricate HA-PEG-MPLs with similar to 220 nm particle size. The HA-PEG-MPLs aqueous solution showed highly efficient photothermal effects as the solution temperature reaches 45 degrees C in 3 min after exposure to near infrared (NIR) 808 nm laser at 2 W/cm(2). The in vitro cell culture experiments after treating human glioblastoma cells (U-87MG) with HA-PEG-MPLs confirmed enhanced cytotoxicity after 4 min exposure to NIR laser. A xenograft tumor model from subcutaneously implanted U87MG cells in nude mice demonstrated accumulation of HA-PEG-MPLs at tumor sites. By combination with successive NIR laser treatment, tumor growth could be prevented and the tumor volume at the end of treatment was 12.7% that of the control. Excellent and consistent anti-tumor efficacy with laser+ HA-PEG-MPLs treatment was also demonstrated from the survival rates of animals, in vivo bioluminescence imaging and histology of tumor sections.
引用
收藏
页码:241 / 252
页数:12
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