研究目的
To develop a targeted multifunctional bovine serum albumin (BSA)-functionalized CuFeS2/chlorin e6 (Ce6) nanohybrid for synergistic photothermal therapy (PTT) and photodynamic therapy (PDT) effects using a single laser.
研究成果
The Ce6:CuFeS2@BSA-FA nanohybrid demonstrated effective synergistic PTT/PDT effects under single laser irradiation, with low toxicity and high specificity towards folate receptor-overexpressing cells. This multifunctional nanoplatform holds promise for targeted cancer therapy.
研究不足
The study focuses on in vitro and in vivo preliminary evaluations. The depth of laser penetration for deep-seated tumors and the long-term biocompatibility of the nanohybrid in humans remain to be investigated.
1:Experimental Design and Method Selection:
The study involved the synthesis of CuFeS2 nanocrystals through a heating-up approach, followed by their transfer into an aqueous phase using BSA in an ultrasonic-assisted microemulsion method. The CuFeS2@BSA nanoparticles were then conjugated with folic acid (FA) and chlorin e6 (Ce6) to form the Ce6:CuFeS2@BSA-FA nanohybrid.
2:Sample Selection and Data Sources:
HeLa and HepG2 cells were used for in vitro studies, and zebrafish embryos were used for in vivo toxicity evaluation.
3:List of Experimental Equipment and Materials:
Chemicals included Copper (I) acetate, oleic acid, 2,2′-(ethylenedioxy)bis(ethylamine) (EDBA), DAPI, DCFH-DA, DMA, Sulfo-NHS, EDC, WST-1, 1-Dodecanethiol, 1-octadecene, FA, and BSA. Equipment included TEM, XRD, UV–visible absorption spectrometer, fluorescence spectrometer, DLS, FTIR spectrometer, confocal laser scanning microscope, CD spectrometer, and digital thermometer.
4:Experimental Procedures and Operational Workflow:
The synthesis of CuFeS2 NPs, their functionalization with BSA, conjugation with FA and Ce6, characterization, photothermal performance evaluation, singlet oxygen detection, cell viability tests, in vivo toxicity evaluation, cellular uptake studies, ROS generation evaluation, and PTT/PDT efficiency assessment were conducted.
5:Data Analysis Methods:
Data were analyzed using statistical techniques and software tools for fluorescence spectroscopy, absorbance measurements, and cell viability assays.
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X-ray diffractometer
Bruker D8
Bruker
Measurement of XRD patterns
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UV–visible absorption spectrometer
JASCO V-630
JASCO
Acquisition of UV–visible absorption spectra
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Fluorescence spectrometer
JASCO FP-6500
JASCO
Recording of fluorescence emission spectra
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Dynamic light scattering
Malvern Nano-ZS 90
Malvern
Measurement of hydrodynamic diameters
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Confocal laser scanning microscope
Leica TCS SP2
Leica
Visualization of fluorescence images of cells
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Circular dichroism spectrometer
J-715
Jasco
Recording of CD results
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Transmission electron microscopy
FEI Tecnai G2 F20
Philips
Characterization of nanoparticle morphology
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FTIR spectrometer
Nicolet 5700
Nicolet
Measurement of FTIR spectra
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