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通过测定基质金属蛋白酶-9辅助乳腺癌诊断和分类的电化学免疫平台。

Electrochemical immunoplatform to assist in the diagnosis and classification of breast cancer through the determination of matrix-metalloproteinase-9.

作者信息

Arévalo Beatriz, Ben Hassine Amira, Valverde Alejandro, Serafín Verónica, Montero-Calle Ana, Raouafi Noureddine, Camps Jordi, Arenas Meritxell, Barderas Rodrigo, Yáñez-Sedeño Paloma, Campuzano Susana, Pingarrón José M

机构信息

Analytical Chemistry Dept., Faculty of Chemistry, Complutense University of Madrid, E-28040, Madrid, Spain.

University of Tunis El Manar, Tunis Faculty of Science, Sensors and Biosensors Group, Laboratory of Analytical Chemistry and Electrochemistry, 2092, Tunis El Manar, Tunisia.

出版信息

Talanta. 2021 Apr 1;225:122054. doi: 10.1016/j.talanta.2020.122054. Epub 2020 Dec 27.

Abstract

Matrix metalloproteinase 9 (MMP-9) is a zinc-dependent endopeptidase that promotes angiogenesis, tumor growth, metastasis and cell invasion through the degradation of extracellular matrix. This work reports a magnetic microbeads (MBs)-based sandwich immunoassay for the amperometric determination of MMP-9 at screen-printed carbon electrodes (SPCEs). The suitable capture antibody (cAb) is immobilized onto carboxylic MBs to selectively capture the antigen which is sandwiched with a biotinylated detector antibody (biotin-dAb) further conjugated with a commercial streptavidin-horseradish peroxidase (Strep-HRP) polymer. This immunoplatform provides great analytical characteristics in terms of selectivity and sensitivity, achieving a LOD value of 2.4 pg mL for standards in buffered solutions. Although this value is similar to those reported for some other approaches described so far, the method described here is simpler involving a single 30 min incubation step which makes it ideal for automation or implementation in POC devices. Moreover, the method was assayed for the accurate determination of endogenous MMP-9 in both cancer cell lysates and serum samples of patients diagnosed with different subtypes of breast cancer (BC) after a simple dilution. The results obtained show that the disposable and affordable immunoplatform developed is able not only to discriminate BC patients from healthy individuals but also to do it for the worst outcome triple negative (TNBC) subtype.

摘要

基质金属蛋白酶9(MMP - 9)是一种锌依赖性内肽酶,它通过降解细胞外基质促进血管生成、肿瘤生长、转移和细胞侵袭。本研究报道了一种基于磁性微珠(MBs)的夹心免疫分析法,用于在丝网印刷碳电极(SPCEs)上安培法测定MMP - 9。将合适的捕获抗体(cAb)固定在羧基化MBs上,以选择性捕获抗原,该抗原与生物素化的检测抗体(生物素 - dAb)夹心,生物素 - dAb进一步与商业链霉亲和素 - 辣根过氧化物酶(Strep - HRP)聚合物偶联。这种免疫分析平台在选择性和灵敏度方面具有出色的分析特性,在缓冲溶液中对标准品的检测限为2.4 pg/mL。尽管该值与目前报道的其他一些方法相似,但本文所述方法更简单,仅涉及一个30分钟的孵育步骤,这使其非常适合自动化或在即时检测(POC)设备中应用。此外,在简单稀释后,该方法用于准确测定诊断为不同亚型乳腺癌(BC)的患者癌细胞裂解物和血清样本中的内源性MMP - 9。所得结果表明,所开发的一次性且价格低廉的免疫分析平台不仅能够区分BC患者和健康个体,还能够区分预后最差的三阴性(TNBC)亚型。

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