Kumar Anil, Solanki Pratima R
Nano-Bio Laboratory, Special Center for Nanoscience, Jawaharlal Nehru University, New Delhi 110067, India.
National Institute of Immunology, New Delhi 110067, India.
ACS Appl Bio Mater. 2025 Jun 16;8(6):4961-4972. doi: 10.1021/acsabm.5c00329. Epub 2025 Jun 2.
Hippuric acid (HA) is a well-known gut microbiota-derived metabolite involved in the development of various diseases such as chronic kidney disease, Chron's disease, and inflammatory bowel disease. HA being one of the most commonly found metabolites in gut microbiota is an important analyte considered for establishing an efficient, quick, sensitive, and reliable method for its detection in human samples. In this work, a molecularly imprinted polymer (MIP) technique has been focused on the electrochemical detection of HA using soft materials, as well as a bioinspired technique. Different characterization techniques have been used to validate the synthesis of MoSe NS, polypyrrole (PPY)@molybdenum diselenide (MoSe)-MIP, such as X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, atomic force microscopy, contact angle, Brunauer-Emmett-Teller method, and transmission electron microscopy. Also, density functional theory computational study has been used to establish the theoretical interaction between the pyrrole (monomer) and HA (target analyte), as well as explore the highest occupied molecular orbital and lowest unoccupied molecular orbital interactions followed by molecular electrostatic potential and Mulliken charges. The chitosan-polypyrrole@MoSe-MIP showed 14.92 μA log(ng/mL) cm sensitivity and a low limit of detection of 0.76 ng/mL in the presence of the analyte using the differential pulse voltammetry technique. The fabricated sensor was also deployed to assess the level of HA in the spiked urine sample, further showing the recovery of 93-108%. Also, the green profile score for the PPY-MIP-based sensor is assessed using the Analytical GREEness MIP (AGREEMIP) metric tool.
马尿酸(HA)是一种著名的肠道微生物群衍生代谢物,参与多种疾病的发展,如慢性肾病、克罗恩病和炎症性肠病。HA是肠道微生物群中最常见的代谢物之一,是建立一种高效、快速、灵敏且可靠的人体样本中HA检测方法时需要考虑的重要分析物。在这项工作中,分子印迹聚合物(MIP)技术聚焦于使用软材料以及一种仿生技术对HA进行电化学检测。已使用不同的表征技术来验证硒化钼纳米片(MoSe NS)、聚吡咯(PPY)@二硒化钼(MoSe)-MIP的合成,如X射线衍射、扫描电子显微镜、傅里叶变换红外光谱、原子力显微镜、接触角、布鲁诺尔-埃米特-泰勒法和透射电子显微镜。此外,密度泛函理论计算研究已用于建立吡咯(单体)与HA(目标分析物)之间的理论相互作用,以及探索最高占据分子轨道和最低未占据分子轨道相互作用,随后是分子静电势和穆利肯电荷。壳聚糖-聚吡咯@MoSe-MIP在使用差分脉冲伏安法技术时,在有分析物存在的情况下显示出14.92 μA log(ng/mL) cm的灵敏度和0.76 ng/mL的低检测限。所制备的传感器还被用于评估加标尿液样本中HA的水平,进一步显示回收率为93 - 108%。此外,使用分析绿色度MIP(AGREEMIP)度量工具评估了基于PPY-MIP的传感器的绿色度评分。