Synthesis and Characterization of SiO2/nGO/Fe3O4/SeQDs Nanoparticles as Potential Nanocarriers in Drug Delivery Systems

被引:1
|
作者
Fan, Chaochao [1 ,2 ]
Liu, Ye [3 ]
Gong, Qiuyu [4 ]
Zhou, Chunsheng [1 ,2 ]
Qiao, Chengfang [1 ,2 ]
机构
[1] Shangluo Univ, Coll Chem Engn & Modern Mat, Shaanxi Key Lab Comprehens Utilizat Tailings Resou, Shangluo 726000, Peoples R China
[2] Shangluo Univ, Shaanxi Engn Res Ctr Mineral Resources Clean & Eff, Shangluo 726000, Peoples R China
[3] Xian Technol Univ, Coll Freshman, Xian 710021, Peoples R China
[4] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Thorac Surg, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
MESOPOROUS SILICA NANOPARTICLES; TUMOR VASCULATURE; BREAST-CANCER; IN-VITRO; GRAPHENE; LIGHT; CHEMOTHERAPY; SELENIUM; FUNCTIONALIZATION; BIOCOMPATIBILITY;
D O I
10.1021/acs.langmuir.4c01376
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we constructed the branch-shaped SiO2/nano GO (nGO)/Fe3O4/selenium quantum dots (QDs) (SeQDs) nanoparticles (SGF/SeQDs) embodying magnetism, fluorescence, and microwave stimulus response properties to enhance the performance of releasing drugs. The SGF/SeQDs composite was characterized by technologies including powder X-ray diffraction, transmission electron microscopy, infrared spectroscopy, etc. In the nanoparticles, the branch-shaped SiO2 provides a large specific surface area, nGO as the dielectric loss-style material promotes microwave-absorbing performance, and the Fe3O4 serves as a magnetic targeting agent and microwave absorber. Integrating nGO and Fe3O4 could further strengthen the microwave absorption of the entire composite; selenium features both fluorescence and anticancer effects. The synthesized nanoparticles as carriers exhibited a branch-like mesoporous sphere of similar to 260 nm, a specific surface area of 258.57 m(2) g(-1), a saturation magnetization of 24.59 emu g(-1), and good microwave thermal conversion performance that the temperature was elevated from 25 to 70 degrees C under microwave irradiation. These physical characteristics, including large pore volume (5.30 nm), high specific surface area, and fibrous morphology, are in favor of loading drugs. Meanwhile, the cumulative etoposide (VP16) loading rate of the nanoparticles reached to 21 wt % after 360 min. The noncovalent interaction between the VP16 and SGF/SeQDs was mainly the hydrogen-bonding effect during the loading process. Furthermore, the drug release rates at 180 min were up to 81.46, 61.92, and 56.84 wt % at pH 4, 5, and 7, respectively. At 25, 37, and 50 degrees C, the rates of drug release reach 25.40, 56.84, and 65.32 wt %, respectively. After microwave stimulation at pH 7, the rate of releasing drug increased distinctly from 56.84 to 71.74 wt % compared to that of nonmicrowave irradiation. Cytotoxicity tests manifested that the carrier had good biocompatibility. Therefore, the nanoparticles are looking forward to paving one platform for further applications in biomedicine and drug delivery systems.
引用
收藏
页码:12792 / 12801
页数:10
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