石墨烯
材料科学
量子点
X射线光电子能谱
光谱学
量子产额
纳米技术
纳米材料
胶体金
纳米颗粒
复合数
生物相容性
光化学
荧光
化学工程
核化学
化学
复合材料
光学
工程类
物理
冶金
量子力学
作者
Beiguang Zhang,Jialin Wang,Ping Li,Yanfa Zhong,Fangzhi Li
出处
期刊:Science of Advanced Materials
[American Scientific Publishers]
日期:2020-09-01
卷期号:12 (9): 1312-1322
被引量:4
标识
DOI:10.1166/sam.2020.3829
摘要
Pancreatic cancer is a malignant tumor with high mutation rate of K-ras oncogene. Therefore, a material capable of detecting the expression of K-ras oncogene was prepared, and it was expected to realize the early diagnosis and treatment of cancer. Graphene quantum dots (GQDs), as a new carbon nanomaterial, has good optical stability and low toxicity biocompatibility. However, pure GQDs has the defect of low quantum yield, which limits its application in ultra-sensitive detection. To enhance quantum yield of GQDs, nitrogen atoms were introduced into GQDs to obtain nitrogen-doped GQDs (N-GQDs). Compared with the unalloyed GQDs, the electrochemical luminescence (ECL) efficiency of the doped N-GQDs was improved greatly. Through the analysis of its ECL mechanism, the deoxyribonucleic acid (DNA) was adopted as the connecting medium to adjust the distance between the GQDs and Aurum nanoparticles (AuNPs). Based on the energy transfer between GQDs and AuNPs, the change of ECL signal of GQDs was controlled. On the basis of this theory, N-GQDs@AuNPs-ssDNA composite was constructed, its morphology and chemical composition were characterized by various means, and its ECL properties were analyzed. Ultraviolet visible (UV-Vis) absorption spectroscopy, X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM) results showed that the graphene composite N-GQDs@AuNPs was successfully prepared. UV-Vis spectroscopy showed that the probe DNA was connected to AuNPs, which indicated that the production of N-GQDs@AuNPs-ssDNA was successfully realized. N-GQDs/AUNPs-ssDNA and target K-ras DNA were incubated at 37 C for 1 h to achieve DNA double-stranded hybridization. The results showed that the graphene composites prepared in this study could be used to quantitatively determine the target K-ras tumor markers.
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