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一种新型便携式免疫装置,用于识别淋巴管内皮透明质酸受体-1生物标志物,该装置使用稳定在纤维素表面的GQD-AgNPrs导电墨水。

A novel portable immuno-device for the recognition of lymphatic vessel endothelial hyaluronan receptor-1 biomarker using GQD-AgNPrs conductive ink stabilized on the surface of cellulose.

作者信息

Mobed Ahmad, Kohansal Fereshteh, Dolati Sanam, Hasanzadeh Mohammad

机构信息

Pharmaceutical Analysis Research Center, Tabriz University of Medical Sciences Tabriz 51664 Iran

Aging Research Institute, Faculty of Medicine, Tabriz University of Medical Sciences Iran.

出版信息

RSC Adv. 2023 Oct 23;13(44):30925-30936. doi: 10.1039/d3ra06025j. eCollection 2023 Oct 18.

DOI:10.1039/d3ra06025j
PMID:37876653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10591117/
Abstract

Lymphatic vessel endothelium expresses various lymphatic marker molecules. LYVE-1, the lymphatic vessel endothelial hyaluronan (HA) receptor, a 322-residue protein belonging to the integral membrane glycoproteins which is found on lymph vessel wall and is completely absent from blood vessels. LYVE-1 is very effective in the passage of lymphocytes and tumor cells into the lymphatics. As regards cancer metastasis, studies indicate LYVE-1 to be involved in tumor cell adhesion. Researches show that, in neoplastic tissue, LYVE-1 is limited to the lymphovascular and could well be proper for studies of tumor lymphangiogenesis. So, the monitoring of LYVE-1 level in human biofluids has provided a valuable approach for research into tumor lymphangiogenesis. For the first time, an innovative paper-based electrochemical immune-platform was developed for recognition of LYVE-1. For this purpose, graphene quantum dots decorated silver nanoparticles nano-ink was synthesized and designed directly by writing pen-on paper technology on the surface of photographic paper. This nano-ink has a great surface area for biomarker immobilization. The prepared paper-based biosensor was so small and cheap and also has high stability and sensitivity. For the first time, biotinylated antibody of biomarker (LYVE-1) was immobilized on the surface of working electrode and utilized for the monitoring of specific antigen by simple immune-assay strategy. The designed biosensor showed two separated linear ranges in the range of 20-320 pg ml and 0.625-10 pg ml, with the acceptable limit of detection (LOD) of 0.312 pg ml. Additionally, engineered immunosensor revealed excellent selectivity that promises its use in complex biological samples and assistance for biomarker-related disease screening in clinical studies.

摘要

淋巴管内皮细胞表达多种淋巴标记分子。淋巴管内皮透明质酸(HA)受体LYVE-1是一种由322个氨基酸残基组成的蛋白质,属于整合膜糖蛋白,存在于淋巴管壁上,血管中则完全没有。LYVE-1在淋巴细胞和肿瘤细胞进入淋巴管的过程中非常有效。关于癌症转移,研究表明LYVE-1参与肿瘤细胞黏附。研究显示,在肿瘤组织中,LYVE-1局限于淋巴管,很适合用于肿瘤淋巴管生成的研究。因此,监测人体生物流体中LYVE-1的水平为肿瘤淋巴管生成的研究提供了一种有价值的方法。首次开发了一种创新的基于纸的电化学免疫平台用于识别LYVE-1。为此,合成了石墨烯量子点修饰的银纳米颗粒纳米墨水,并通过在相纸表面的笔写技术直接设计而成。这种纳米墨水具有很大的表面积用于生物标志物固定。制备的基于纸的生物传感器体积小、成本低,并且具有高稳定性和灵敏度。首次将生物标志物(LYVE-1)的生物素化抗体固定在工作电极表面,并通过简单的免疫分析策略用于监测特定抗原。所设计的生物传感器在20 - 320 pg/ml和0.625 - 10 pg/ml范围内显示出两个分离的线性范围,检测限(LOD)为0.312 pg/ml,可接受。此外,工程化免疫传感器显示出优异的选择性,有望用于复杂生物样品,并有助于临床研究中与生物标志物相关的疾病筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/b4053d68878c/d3ra06025j-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/484d18243944/d3ra06025j-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/1ec95ff09eee/d3ra06025j-s2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/5a9dccad395a/d3ra06025j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/dd9bfa26d448/d3ra06025j-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/efe94b7a15f9/d3ra06025j-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/b4053d68878c/d3ra06025j-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/484d18243944/d3ra06025j-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/1ec95ff09eee/d3ra06025j-s2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/5a9dccad395a/d3ra06025j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/dd9bfa26d448/d3ra06025j-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/efe94b7a15f9/d3ra06025j-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8611/10591117/b4053d68878c/d3ra06025j-f4.jpg

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