共 50 条
pH-Responsive drug release and NIR-triggered singlet oxygen generation based on a multifunctional core-shell-shell structure
被引:27
|作者:
Han, Renlu
[1
]
Yi, Haopeng
[1
]
Shi, Junhui
[1
]
Liu, Zongjun
[2
]
Wang, Hao
[1
]
Hou, Yafei
[1
]
Wang, You
[1
]
机构:
[1] Harbin Inst Technol, Sch Mat Sci & Engn, Harbin 150001, Peoples R China
[2] Harbin Inst Technol, Sch Chem Engn & Technol, Harbin 150001, Peoples R China
基金:
中国国家自然科学基金;
关键词:
MESOPOROUS SILICA NANOPARTICLES;
NEAR-INFRARED LIGHT;
IN-VIVO;
PHOTODYNAMIC THERAPY;
GUEST MOLECULES;
DELIVERY;
CANCER;
NANOCOMPOSITES;
NANOCAPSULES;
NANORODS;
D O I:
10.1039/c6cp05308d
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
A multifunctional platform with pH-responsive drug release and near-infrared (NIR) light-triggered photodynamic therapy (PDT) was designed and prepared using the novel core-shell-shell structure. The multifunctional platform consists of an upconversion nanoparticle (UCNP) emission core, a photosensitizer methylene blue (MB) embedded dense silica sandwich shell, and a polyethyleneimine conjugated folic acid (PEI-FA) gated mesoporous silica (MS) outmost shell with doxorubicin hydrochloride (DOX) loaded inside. The simulated drug release experiments revealed that DOX will release from the nanoparticles because of the distortion in the PEI-FA layer under acidic conditions. Moreover, under 980 nm NIR irradiation, a 660 nm red light emission was excited, activating MB to generate a singlet oxygen (O-1(2)), which acts as the PDT drug. The multifunctional platform integrated pH-responsive drug release and UCNP-based PDT drug together show promising potential in nanomedicine for future chemotherapy and NIR-triggered PDT.
引用
收藏
页码:25497 / 25503
页数:7
相关论文