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卡拉胶和 l-赖氨酸合成的富胺碳点作为检测叶酸和治疗药物肿瘤靶向递送的双重探针。

Amine-Rich Carbon Dots Synthesized from Kappa-Carrageenan and l-Lysine as a Dual Probe for Detection of Folic Acid and Tumor-Targeted Delivery of Therapeutics.

机构信息

Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam 781039, India.

Centre for Nanotechnology, Indian Institute of Technology Guwahati, Guwahati, Assam 781039, India.

出版信息

ACS Appl Bio Mater. 2024 Sep 16;7(9):6034-6043. doi: 10.1021/acsabm.4c00678. Epub 2024 Aug 23.

DOI:10.1021/acsabm.4c00678
PMID:39180146
Abstract

Strategically designed, heteroatom-rich surface functionalized blue fluorescent carbon dots (CDs) were synthesized for high-throughput detection of folic acid (vitamin B9). The highly stable CDs could particularly detect vitamin B9 in the presence of 35 analytes, even up to 40 nM of the vitamin. The versatile CDs were found to have a high affinity for folic acid in wastewater, folic acid tablets, and food samples enriched with folic acid. The hemocompatibility of the CDs was also studied by using a hemolysis assay, confirming the CDs to be nontoxic to human blood samples up to 400 μg/mL. The CDs were then covalently conjugated to biotin, which possesses receptors that are overexpressed in tumor cells. The MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide dye) assay and confocal bioimaging studies proved the biotin-modified CDs (CDBT) were remarkably nontoxic in healthy cell lines (HEK-293) and highly target-specific toward tumor cells (HeLa), including triple-negative breast cancer cells (MDA-MB-231). The cytotoxicity assay of 5-fluorouracil encapsulated CDs (CDBTFu) showed the IC value to be 81 μM in HeLa cells and 185 μM in MDA-MB-231 cells, respectively, and significantly higher in HEK-293 cells (over 300 μM), owing to high specificity toward tumor cells.

摘要

我们设计并合成了富杂原子的表面功能化蓝色荧光碳点(CDs),用于高通量检测叶酸(维生素 B9)。这些高度稳定的 CDs 可以在存在 35 种分析物的情况下,特别是在高达 40 nM 的维生素 B9 存在下检测到维生素 B9。研究发现,这些多功能的 CDs 对废水中、叶酸片中以及富含叶酸的食物样本中的叶酸具有高亲和力。我们还通过溶血试验研究了 CDs 的血液相容性,证实了 CDs 在高达 400 μg/mL 的浓度下对人体血液样本是无毒的。然后,我们将 CDs 共价偶联到生物素上,生物素具有在肿瘤细胞中过表达的受体。MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐)测定法和共聚焦生物成像研究证明,修饰后的生物素化 CDs(CDBT)在健康细胞系(HEK-293)中表现出显著的非毒性,并且对肿瘤细胞(HeLa),包括三阴性乳腺癌细胞(MDA-MB-231)具有高度的靶向特异性。封装了 5-氟尿嘧啶的 CDs(CDBTFu)的细胞毒性测定表明,在 HeLa 细胞中的 IC 值为 81 μM,在 MDA-MB-231 细胞中的 IC 值为 185 μM,而在 HEK-293 细胞中的 IC 值分别为 300 μM 以上,这是因为其对肿瘤细胞具有高度的特异性。

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