研究目的
To synthesize fluorescent resveratrol nanogels via one-pot thiol-ene Michael addition polymerization for enhanced fluorescent emission and potential use in drug delivery and cell imaging applications.
研究成果
Fluorescent resveratrol nanogels were successfully synthesized with enhanced fluorescence intensity and stability in both water and organic solvents. The nanogels showed potential for use in cell imaging and as a trackable drug delivery system, with a quantum yield significantly higher than that of free resveratrol.
研究不足
The study focuses on the synthesis and initial characterization of resveratrol nanogels, with preliminary cell imaging results. Further studies are needed to explore the full potential of these nanogels in drug delivery and imaging applications, including in vivo studies and detailed pharmacokinetics.
1:Experimental Design and Method Selection:
The nanogels were synthesized via one-pot thiol-ene Michael addition polymerization of resveratrol triacrylate, 1,6-hexanedithiol, and methoxyl poly(ethylene glycol) acrylate under the catalysis of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).
2:0]undec-7-ene (DBU). Sample Selection and Data Sources:
2. Sample Selection and Data Sources: Trans-resveratrol was used as the starting material, and the nanogels were characterized using various techniques including NMR, FT-IR, TEM, SEM, DLS, UV-vis spectroscopy, and fluorescence spectroscopy.
3:List of Experimental Equipment and Materials:
Materials included trans-resveratrol, methoxyl poly(ethylene glycol), DBU, HDT, acryloyl chloride, and other reagents and solvents. Equipment included a Bruker NMR spectrometer, Bio-Rad Win-IR instrument, JEOL JEM-1011 transmission electron microscope, Wyatt QELS instrument, Zeiss Merlin field emission scanning electron microscope, Shimadzu UV-2401 PC spectrometer, and PTI quanta master fluorescence spectrometer.
4:Experimental Procedures and Operational Workflow:
The synthesis involved the preparation of resveratrol triacrylate, followed by copolymerization with mPEGA and HDT. The product was purified by dialysis and lyophilization. Characterization included size determination, stability tests, and fluorescence measurements.
5:Data Analysis Methods:
Data were analyzed using standard curve methods for UV-vis spectroscopy, Image J software for TEM images, and relative intensity calculations for fluorescence measurements.
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Bruker NMR spectrometer
300 MHz
Bruker
Recording proton nuclear magnetic resonance (1H NMR) spectra
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JEOL JEM-1011 transmission electron microscope
JEM-1011
JEOL
Transmission electron microscopy (TEM) measurements
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Zeiss Merlin field emission scanning electron microscope
Merlin
Zeiss
Scanning electron microscopy (SEM) measurements
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Shimadzu UV-2401 PC spectrometer
UV-2401 PC
Shimadzu
Recording UV–vis spectra
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Bio-Rad Win-IR instrument
Bio-Rad
Recording Fourier transform infrared (FT-IR) spectra
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Wyatt QELS instrument
DAWN EOS
Wyatt Technology
Dynamic laser scattering (DLS) measurements
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PTI quanta master fluorescence spectrometer
quanta master
PTI
Measuring photoluminescence (PL) spectra
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