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用于检测食品基质中[具体物质未给出]的光学免疫传感器。

Optical Immunosensor for the Detection of in Food Matrixes.

作者信息

Servarayan Karthika Lakshmi, Krishnamoorthy Govindan, Sundaram Ellairaja, Karuppusamy Masiyappan, Murugan Marudhamuthu, Piraman Shakkthivel, Vasantha Vairathevar Sivasamy

机构信息

Department of Natural Products Chemistry, School of Chemistry, Madurai Kamaraj University, Madurai 625021, Tamil Nadu, India.

Translational Research Platform for Veterinary Biologicals, Central University Laboratory, TANUVAS, Chennai 600051, Tamil Nadu, India.

出版信息

ACS Omega. 2023 Apr 24;8(18):15979-15989. doi: 10.1021/acsomega.2c07848. eCollection 2023 May 9.

Abstract

In this paper, simple imine-based organic fluorophore 4-amino-3-(anthracene-9 yl methyleneamino) phenyl (phenyl) methanone (APM) has been synthesized via a greener approach and the same was used to construct a fluorescent immunoassay for the detection of (LM). A monoclonal antibody of LM was tagged with APM via the conjugation of the amine group in APM and the acid group of anti-LM through EDC/NHS coupling. The designed immunoassay was optimized for the specific detection of LM in the presence of other interfering pathogens based on the aggregation-induced emission mechanism and the formation of aggregates and their morphology was confirmed with the help of scanning electron microscopy. Density functional theory studies were done to further support the sensing mechanism-based changes in the energy level distribution. All photophysical parameters were measured by using fluorescence spectroscopy techniques. Specific and competitive recognition of LM was done in the presence of other relevant pathogens. The immunoassay shows a linear appreciable range from 1.6 × 10-2.7024 × 10 cfu/mL using the standard plate count method. The LOD has been calculated from the linear equation and the value is found as 3.2 cfu/mL, and this is the lowest LOD value reported for the detection of LM so far. The practical applications of the immunoassay were demonstrated in various food samples, and their accuracy obtained was highly comparable with the standard existing ELISA method.

摘要

在本文中,通过一种更环保的方法合成了基于简单亚胺的有机荧光团4-氨基-3-(蒽-9-基亚甲基氨基)苯基(苯基)甲酮(APM),并将其用于构建一种荧光免疫分析法以检测单核细胞增生李斯特菌(LM)。通过APM中的胺基与抗LM的酸基经EDC/NHS偶联反应,将LM的单克隆抗体用APM进行标记。基于聚集诱导发光机制,对所设计的免疫分析法进行优化,以在存在其他干扰病原体的情况下特异性检测LM,并借助扫描电子显微镜确认聚集体的形成及其形态。进行密度泛函理论研究以进一步支持基于传感机制的能级分布变化。所有光物理参数均使用荧光光谱技术进行测量。在存在其他相关病原体的情况下对LM进行特异性和竞争性识别。使用标准平板计数法,该免疫分析法的线性范围为1.6×10⁻².⁷⁰²⁴×10⁻³cfu/mL。根据线性方程计算出检测限,其值为3.2 cfu/mL,这是迄今为止报道的检测LM的最低检测限值。该免疫分析法的实际应用在各种食品样品中得到了验证,其获得的准确性与现有的标准ELISA方法高度可比。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e684/10173425/b5d63d893930/ao2c07848_0007.jpg

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