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基于金纳米颗粒为基底的表面增强拉曼光谱快速鉴别人肝癌细胞与正常肝细胞 被引量:1

Rapid identification of human hepatocellular carcinoma cells and normal liver cells by surface-enhanced Raman spectroscopy based on gold nanoparticles
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摘要 目的:采用金纳米颗粒为基底的表面增强拉曼光谱(surface-enhanced Raman spectroscopy,SERS)技术对人体正常细胞和不同种类肝癌细胞进行快速、准确地鉴别。方法:将肝癌细胞进行体外培养,金纳米颗粒作为基底加入培养基中进行孵育30 min,通过表面增强拉曼光谱测定人肝癌细胞。结果:基于金纳米颗粒为基底的表面增强拉曼光谱能够快速检测鉴别,呈现肝癌细胞的拉曼光谱,其中包括人肝癌细胞HepG2(RSD 1.20%)、人胆管细胞型肝癌细胞HCCC-9810(RSD 11.14%)、人肝母细胞瘤细胞HuH-6(RSD 9.50%)、人肝癌细胞SK-Hep(RSD 4.60%)、人正常肝细胞HL7702(RSD 4.50%)。并且用其他肿瘤细胞进行了对照,最后对SERS图谱进行峰归属。结论:金纳米颗粒为基底的表面增强拉曼光谱能够对人肝癌细胞进行快速鉴别。 Objective:To perform rapid and accurate identification of normal hepatocytes and different types of hepatocellular carcinoma cells using gold nanoparticle-based surface-enhanced Raman spectroscopy(SERS).Methods:Liver cancer cells were cultured in vitro and gold nanoparticles were added to the culture medium for 30 min.Accordingly,human hepatocellular carcinoma cells were determined using SERS.Results:The results revealed that gold nanoparticle-based SERS could rapidly detect and identify human hepatocellular carcinoma cells,including human hepatocellular carcinoma cells HepG2(RSD 1.20%),hepatic cholangiocarcinoma cells HCCC-9810(RSD 11.14%),human hepatoblastoma cells HuH-6(RSD 9.50%),human hepatocellular carcinoma cells SK-Hep(RSD 4.60%),and human normal hepatocytes HL7702(RSD 4.50%).These cell types were then compared with other tumour cells.Finally,peak assignments were performed on the SERS spectra.Conclusion:This investigation conclude that gold nanoparticle-based SERS is functionally capable of accurate and rapid identification of human hepatocellular carcinoma cells.
作者 周青 陆峰 ZHOU Qing;LU Feng(Naval Military Medical University,Shanghai 200433,China;Pharmaceutical Analysis Laboratory,School of Pharmacy,Naval Military Medical University,Shanghai 200433,China)
出处 《现代肿瘤医学》 CAS 北大核心 2023年第3期423-427,共5页 Journal of Modern Oncology
基金 国家自然科学基金面上项目(编号:82273894) 上海市军民融合发展专项(编号:2020-jmrh1-kj1102)。
关键词 肝癌细胞 表面增强拉曼散射 金纳米颗粒 肿瘤细胞 主成分分析 hepatocellular carcinoma cells surface-enhanced Raman spectroscopy gold nanoparticles tumor cells principal component analysis
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