Design of a Porous and Stable Sodium Alginate–Silica Composite for Dual Fluorescent Detection of Fe3+ and 5-Fu in Colorectal Cancer Treatment

IF 3 4区 化学 Q2 CHEMISTRY, ANALYTICAL
Luminescence Pub Date : 2025-09-12 DOI:10.1002/bio.70315
Haohui Sun, Shuxin Qiu, Kangjia Luo, Rui Chen, Hao Liu, Feng Gao
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Abstract

In this study, a multifunctional fluorescent sensing platform was constructed via stepwise functional modification. The platform is based on a cobalt (II)-containing metal–organic framework (MOF) and was successively modified with donor–acceptor Stenhouse adducts (DASA), a natural product–derived compound 1, and 3-aminopropyltrimethoxysilane (APTMS), yielding the composite material 1-DASA-APTMS@CP1. This material was further employed for the loading and selective detection of the anticancer model drug 5-FU (1-DASA-ATPMS@CP1@5-Fu). Fluorescence sensing experiments revealed that 1-DASA-APTMS@CP1 exhibited excellent selectivity and sensitivity toward Fe3+ and 5-FU among a series of metal ions and antibiotics. The calculated Stern–Volmer quenching constants (Ksv) were 1.38 × 104 M−1 for Fe3+ and 1.77 × 104 M−1 for 5-FU, with corresponding detection limits of 6.04 and 4.71 μM, respectively. Furthermore, in vitro experiments using human colorectal cancer HCT116 cells confirmed the therapeutic potential of the platform. The 1-DASA-APTMS@CP1@5-Fu system significantly enhanced apoptosis induction, as demonstrated by CCK-8 assays, qPCR, and western blot analysis, which showed upregulation of the proapoptotic protein Bax. This study provides a novel strategy and experimental basis for colorectal cancer targeted drug delivery and fluorescence-guided cancer theranostics.

Abstract Image

Abstract Image

多孔稳定海藻酸钠-二氧化硅复合材料在结直肠癌治疗中的Fe3+和5-Fu双荧光检测设计
本研究通过逐步功能修饰构建多功能荧光传感平台。该平台基于含钴(II)的金属有机骨架(MOF),并先后用施恩-受体斯坦豪斯加合物(DASA)、天然产物衍生化合物1和3-氨基丙基三甲氧基硅烷(APTMS)进行修饰,得到复合材料1-DASA-APTMS@CP1。该材料进一步用于抗癌模型药物5-FU (1-DASA-ATPMS@CP1@5-Fu)的负载和选择性检测。荧光传感实验表明,1-DASA-APTMS@CP1在一系列金属离子和抗生素中对Fe3+和5-FU具有优异的选择性和敏感性。计算得到的Stern-Volmer猝灭常数(Ksv) Fe3+为1.38 × 104 M−1,5-FU为1.77 × 104 M−1,检出限分别为6.04和4.71 μM。此外,利用人类结直肠癌HCT116细胞进行的体外实验证实了该平台的治疗潜力。CCK-8检测、qPCR和western blot分析显示,1-DASA-APTMS@CP1@5-Fu系统显著增强了细胞凋亡诱导,显示促凋亡蛋白Bax上调。本研究为结直肠癌靶向给药和荧光引导肿瘤治疗提供了新的策略和实验依据。
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来源期刊
Luminescence
Luminescence 生物-生化与分子生物学
CiteScore
5.10
自引率
13.80%
发文量
248
审稿时长
3.5 months
期刊介绍: Luminescence provides a forum for the publication of original scientific papers, short communications, technical notes and reviews on fundamental and applied aspects of all forms of luminescence, including bioluminescence, chemiluminescence, electrochemiluminescence, sonoluminescence, triboluminescence, fluorescence, time-resolved fluorescence and phosphorescence. Luminescence publishes papers on assays and analytical methods, instrumentation, mechanistic and synthetic studies, basic biology and chemistry. Luminescence also publishes details of forthcoming meetings, information on new products, and book reviews. A special feature of the Journal is surveys of the recent literature on selected topics in luminescence.
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