研究目的
To construct functional Ce6-AuNR@SiO2-d-CPP for treating breast cancer by photothermal/photodynamic therapy and to verify its efficacy in vitro and in vivo.
研究成果
Ce6-AuNR@SiO2-d-CPP effectively treats breast cancer through combined PTT and PDT, inducing cytotoxicity and apoptosis via multiple pathways. It offers a promising alternative to conventional therapies, with robust efficacy in preclinical models.
研究不足
The study is limited to in vitro and animal models (nude mice), and clinical applicability in humans is not addressed. Potential toxicity and long-term effects of the nanoconstruct are not fully explored. The mechanism of d-CPP-mediated uptake is not completely elucidated.
1:Experimental Design and Method Selection:
The study designed a nanoconstruct using gold nanorods coated with mesoporous silica, pegylated, modified with d-CPP, and loaded with Ce6 for combined PTT and PDT. Methods included synthesis, characterization, cellular uptake studies, cytotoxicity assays, apoptosis mechanism analysis, and in vivo efficacy testing in nude mice.
2:Sample Selection and Data Sources:
Human breast cancer MCF-7 cells were used, obtained from National Infrastructure of Cell Line Resources. In vivo studies used female Nu/Nu nude mice with MCF-7 xenografts.
3:List of Experimental Equipment and Materials:
Equipment included UV-Vis-NIR spectrophotometer (UV-1800PC, Mapada Instruments), Malvern Zetasizer, transmission electron microscope (JEM1400PLUS, JEOL), fluorescence microscope (IX-81, Olympus), fluorescence spectrophotometer (Cary Eclipse, Agilent), multimode reader (FlexStation 3, Molecular Devices), Operetta high-content screening system (PerkinElmer). Materials included chloroauric acid, CTAB, NaBH4, AgNO3, AA, TEOS, APTES, maleimide-PEG2000-NHS, mPEG2000-NHS, d-CPP, RPMI-1640 medium, FBS, and various chemicals from specified suppliers.
4:Experimental Procedures and Operational Workflow:
Synthesis of AuNRs by seed-mediated growth, coating with SiO2, pegylation, d-CPP modification, Ce6 loading. Characterization included extinction spectra, zeta potential, size, entrapment efficiency. Cellular uptake studies with inhibitors, cytotoxicity assays under dark, PTT, PDT, and combined conditions, apoptosis mechanism studies, and in vivo treatment with laser irradiation.
5:Data Analysis Methods:
Statistical analysis using one-way ANOVA with Bonferroni correction for multiple comparisons. Data presented as mean ± SD.
独家科研数据包,助您复现前沿成果,加速创新突破
获取完整内容-
Fluorescence Microscope
IX-81
Olympus
Imaging live/dead staining and apoptosis in cells.
-
Fluorescence Spectrophotometer
Cary Eclipse
Agilent
Recording fluorescence intensity for singlet oxygen measurement.
-
High-content Screening System
Operetta
PerkinElmer
Recording fluorescence intensity for apoptotic enzyme activities.
-
Transmission Electron Microscope
JEM1400PLUS
JEOL
Observing the form of nanoparticles and cellular uptake.
-
UV-Vis-NIR Spectrophotometer
UV-1800PC
Mapada Instruments
Recording absorbance spectra of AuNRs in the wavelength range of 300–1000 nm.
-
Zetasizer
Malvern Instruments
Measuring zeta potential and hydrodynamic diameter of nanoparticles.
-
Multimode Reader
FlexStation 3
Molecular Devices
Measuring ROS levels and mitochondrial membrane potential.
-
Laser
Changchun New Industries Optoelectronics Technology Co., Ltd.
Irradiation at 808 nm and 650 nm for PTT and PDT.
-
登录查看剩余6件设备及参数对照表
查看全部