Ellairaja Sundaram, Krithiga Narayanaswamy, Ponmariappan Sarkaraisamy, Vasantha Vairathevar Sivasamy
Department of Natural Products Chemistry, School of Chemistry, Madurai Kamaraj University , Madurai-625 021, Tamilnadu, India.
Department of Plant Biotechnology, School of Biotechnology, Madurai Kamaraj University , Madurai-625 021, Tamilnadu, India.
J Agric Food Chem. 2017 Mar 1;65(8):1802-1812. doi: 10.1021/acs.jafc.6b04790. Epub 2017 Feb 17.
A simple pyrimidine-based fluorescent probe (R)-4-(anthracen-9-yl)-6- (naphthalen-1-yl)-1,6-dihydropyrimidine-2-amine (ANDPA) was synthesized through the greener one pot reaction and characterized by IR, NMR, and ESI-Mass. Glucose stabilized silver nanoparticles (Glu-AgNPs) were also synthesized and characterized using UV, IR, XRD, SEM, and TEM. When ANDPA was tagged with Glu-AgNPs, the fluorescent intensity of ANDPA decreased drastically. When the monoclonal antibody (Ab) [immunoglobulin G (IgG)] of Pseudomonas aeruginosa (PA) was attached with ANDPA/Glu-AgNPs, the original intensity of the probe was recovered with minimal enhancement at 446 nm. On further attachment of PA with ANDPA/Glu-AgNPs/PA, the fluorescence intensity of the probe was enhanced obviously at 446 nm with red shift. This phenomenon was further supported by SEM and TEM. The linear range of detection is from 8 to 10 CFU/mL, and LOD is 1.5 CFU/mL. The immunosensor was successfully demonstrated to detect Pseudomonas aeruginosa in water, soil, and food products like milk, sugar cane, and orange juices.
通过更环保的一锅法反应合成了一种基于嘧啶的简单荧光探针(R)-4-(蒽-9-基)-6-(萘-1-基)-1,6-二氢嘧啶-2-胺(ANDPA),并通过红外光谱、核磁共振和电喷雾质谱对其进行了表征。还合成了葡萄糖稳定的银纳米颗粒(Glu-AgNPs),并使用紫外光谱、红外光谱、X射线衍射、扫描电子显微镜和透射电子显微镜对其进行了表征。当ANDPA与Glu-AgNPs结合时,ANDPA的荧光强度急剧下降。当铜绿假单胞菌(PA)的单克隆抗体(Ab)[免疫球蛋白G(IgG)]与ANDPA/Glu-AgNPs结合时,探针的原始强度得以恢复,在446 nm处有最小程度的增强。当PA进一步与ANDPA/Glu-AgNPs/PA结合时,探针的荧光强度在446 nm处明显增强且发生红移。扫描电子显微镜和透射电子显微镜进一步证实了这一现象。检测的线性范围为8至10 CFU/mL,检测限为1.5 CFU/mL。该免疫传感器已成功用于检测水、土壤以及牛奶、甘蔗和橙汁等食品中的铜绿假单胞菌。