内化
荧光
纳米颗粒
化学
纳米探针
生物物理学
共焦显微镜
荧光显微镜
光子上转换
PEG比率
活力测定
表面改性
共焦
纳米技术
细胞毒性
MTT法
钇
细胞
荧光寿命成像显微镜
癌细胞
聚乙二醇
显微镜
材料科学
药物输送
生物相容性
荧光光谱法
内吞作用
作者
Ester Butera,Regina Maria Chiechio,A Caponnetto,Carmen Ferrara,Cinzia Di Pietro,Paolo Musumeci,R. Reitano,Luca Lanzanò,F. Ruffino,Salvatore Petralia,Giovanni Arena,Carlotta Cosentino,Valérie Marchi,Annalinda Contino,Giuseppe Maccarrone
出处
期刊:ACS omega
[American Chemical Society]
日期:2026-03-04
卷期号:11 (10): 16936-16945
标识
DOI:10.1021/acsomega.6c00386
摘要
NPs) with a log-normal size distribution peaking at 43 nm were synthesized and coloaded with PEG and folic acid (FA) to achieve tumor cell targeting while maintaining good water dispersibility. Structural and optical analyses (TEM, FTIR, PL, upconversion) confirmed successful functionalization without significant alterations in the fluorescence signal. In colorectal cancer cells (HCT-116), MTT assays showed >80% viability for concentrations of NPs between 0.1 and 1 μg/mL, indicating low cytotoxicity. Confocal microscopy revealed fluorescence signals consistent with potential nanoparticle internalization, although contrast was limited by cellular autofluorescence. ICP-OES quantification supported greater internalization of PEG-FA nanoparticles compared to PEG nanoparticles, confirming the role of FA in enhancing internalization. Moreover, NIR excitation (980 nm) suppressed cellular autofluorescence, suggesting the potential of these nanoparticles for high-contrast bioimaging applications.
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