研究目的
To assess the toxicity and biocompatibility of carbon quantum dots (CQDs) and their functionalized materials (N-doped CQDs and folic acid-modified CQDs) in vitro and in vivo for future biological applications.
研究成果
CQDs and their modified materials (NCQDs and FA-CQDs) exhibit low toxicity and good biocompatibility in vitro and in vivo at concentrations up to 15 mg/kg. FA-CQDs showed the lowest toxicity, making them suitable for biological applications such as cancer diagnosis, imaging, and drug delivery.
研究不足
The study focuses on short-term toxicity and biocompatibility; long-term effects and detailed mechanisms of toxicity were not explored. High concentrations (20 mg/kg) showed some toxic effects, indicating a need for careful dosage consideration.
1:Experimental Design and Method Selection:
Synthesis of CQDs, NCQDs, and FA-CQDs using hydrothermal treatment and amidation reaction. Characterization of materials using TEM, FT-IR, XPS, UV-vis absorption, and PL spectra.
2:Sample Selection and Data Sources:
L929, C6, and MDCK cells for in vitro studies; Balb/c nude mice for in vivo studies.
3:List of Experimental Equipment and Materials:
Transmission electron microscopy (TEM), FT-IR spectrometer, X-ray photoelectron spectroscopy (XPS), UV-vis spectrophotometer, photoluminescence (PL) spectrometer.
4:Experimental Procedures and Operational Workflow:
In vitro cytotoxicity assays (CCK-8 and LDH release tests), in vivo fluorescence bioimaging, blood biochemistry assays, and histological examination.
5:Data Analysis Methods:
Analysis of cell viability, LDH leakage, fluorescence intensity, blood biochemistry parameters, and histological changes.
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