研究目的
To develop a method for rapid identification and Raman imaging of living cancer cells using monodisperse Au@Ag core-shell nanoprobes with ultrasensitive SERS activity.
研究成果
The synthesized Au NBP@Ag NR-MBA-rBSA-FA nanoprobes exhibit high SERS activity, specificity, and targeting ability for living cancer cells, enabling rapid identification and Raman imaging. This approach has potential applications in cancer theranostics and biomedical detection, with excellent reproducibility and efficiency.
研究不足
The study is limited to specific cancer cell lines (MGC-803 and A549) and may not generalize to other cell types. The nanoprobes' performance in vivo or in clinical settings was not tested, and long-term stability in biological environments could be a concern. Optimization of parameters like laser power and exposure time might be needed for different applications.
1:Experimental Design and Method Selection:
The study involved synthesizing monodisperse Au NBP@Ag NR core-shell nanoparticles through a seed-mediated process, modifying them with 4-MBA, rBSA, and FA to create SERS-active nanoprobes. The design rationale was to combine the advantages of Au and Ag nanomaterials for high SERS enhancement, stability, and biocompatibility. Theoretical models include localized surface plasmon resonance (LSPR) for SERS enhancement.
2:Sample Selection and Data Sources:
Cancer cell lines MGC-803 and A549 were used, provided by the Cell Bank of Type Culture Collection of Chinese Academy. Cells were cultured in DMEM with fetal bovine serum and antibiotics.
3:List of Experimental Equipment and Materials:
Materials included HAuCl4·3H2O, CTAC, CTAB, AgNO3, AA, HCl, NaBH4, Na3Ct, BSA, FA, NHS, EDC·HCl, 4-MBA, ethanol, PBS, DMEM, fetal bovine serum, penicillin-streptomycin. Equipment included UV-vis spectrophotometer (Perkin-Elmer), TEM (Tecnai G2 SpiritBiotwin), HR-TEM, HAADF-STEM, SEM (JEOL JSM-7800F) with EDS, zeta potential analyzer (Omni), XPS (Axis Ultra spectrometer), XRD (Bruker D8 Advance), ICP-OES (Optima 2100DV), and Raman instrument (Renishaw inVia Reflex).
4:Experimental Procedures and Operational Workflow:
Steps included preparation of Au seeds and Au NBPs, growth of Ag shell to form Au NBP@Ag NRs, modification with 4-MBA, conjugation with rBSA-FA, characterization using various techniques, and application in cell culture for SERS detection and imaging. Cells were incubated with nanoprobes, rinsed, and analyzed with Raman spectroscopy.
5:Data Analysis Methods:
SERS spectra were analyzed for signal intensity, enhancement factor calculations, and statistical evaluation of reproducibility and specificity. Software tools for Raman data analysis were not specified.
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Scanning electron microscope
JEOL JSM-7800F
JEOL
Obtaining SEM and EDS images
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X-ray photoelectron spectrometer
Axis Ultra spectrometer
Kratos
Performing XPS analysis
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X-ray diffractometer
Bruker D8 Advance
Bruker
Performing XRD measurements
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Inductively coupled plasma optical emission spectrometer
Optima 2100DV
PerkinElmer
Determining concentration of nanoparticle solutions
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UV-vis spectrophotometer
Perkin-Elmer
Measuring UV-vis spectra of nanoparticles
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Transmission electron microscope
Tecnai G2 SpiritBiotwin
Obtaining TEM, HR-TEM, and HAADF-STEM images
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Zeta potential analyzer
Omni
Measuring zeta potentials of nanoparticles
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Raman instrument
Renishaw inVia Reflex
Renishaw
Recording SERS spectra and performing Raman imaging
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