Zuo Yingchun, He Shiyu, Zhang Wenmeng, Wu Yanqing, Qiao Huijun, Zhou Xinguang, Yu Yanyan
Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, 209 Tongshan Road, Xuzhou, 221004, Jiangsu, PR China.
Shenzhen NTEK Testing Technology Co., Ltd., Shenzhen, 518000, Guangdong, PR China.
Biosens Bioelectron. 2025 Jul 25;288:117823. doi: 10.1016/j.bios.2025.117823.
Detection of biomarkers in interstitial fluid (ISF) by microneedles (MNs) has received extensive attentions as a non-invasive biosensing strategy. However, fewer work has focused on the long non-coding RNAs (lncRNAs) sensing, which are most likely present in ISF and engage in the occurrence and development of Alzheimer's disease (AD). In this work, taking adenocarcinoma transcript 1 (MALAT1) as the representative of lncRNAs, which is abnormally down-regulated in AD patients, a robust hydrogel MN array - based fluorescent patch was developed for MALAT1 by integrating a methacrylated gelatin (GelMA) hydrogel MN as the extraction tool with a strand displacement reaction (SDR) mediated fluorescent probe. Specifically, the MNs were prepared by the simple and feasible photo-crosslinking of GelMA, which displayed satisfactory swelling capability for extracting ISF and mechanical strength to penetrate the skin's cuticle layer. Subsequently, a triplex SDR amplification probe was constructed for MALAT1 sensing. By mixing with the prepolymer solution, the MNs patch loaded with the fluorescent probe was fabricated, which demonstrated excellent sensing performances in both PBS and agarose simulated skin, with lower limits of quantification (LLOQ) of 7.62 and 13.24 nM, respectively. The developed MN patch was proved highly suitable for distinguishing the down-regulated MALAT1 expressions in ISF of AD mice. This work represented the first example to correlate the changes in the levels of MALAT1 in ISF with AD pathology, providing a practical tool for the early non - invasive diagnosis of AD.
作为一种非侵入性生物传感策略,通过微针(MNs)检测间质液(ISF)中的生物标志物受到了广泛关注。然而,针对长链非编码RNA(lncRNAs)传感的研究较少,而lncRNAs很可能存在于ISF中,并参与阿尔茨海默病(AD)的发生和发展。在这项工作中,以在AD患者中异常下调的lncRNAs的代表——腺癌转录本1(MALAT1)为研究对象,通过将甲基丙烯酸化明胶(GelMA)水凝胶微针作为提取工具与链置换反应(SDR)介导的荧光探针相结合,开发了一种基于水凝胶微针阵列的稳健荧光贴片用于检测MALAT1。具体而言,通过简单可行的GelMA光交联制备微针,其在提取ISF方面表现出令人满意的溶胀能力以及穿透皮肤角质层的机械强度。随后,构建了用于检测MALAT1的三重SDR扩增探针。通过与预聚物溶液混合,制备了负载荧光探针的微针贴片,其在PBS和琼脂糖模拟皮肤中均表现出优异的传感性能,定量下限(LLOQ)分别为7.62和13.24 nM。所开发的微针贴片被证明非常适合区分AD小鼠ISF中下调的MALAT1表达。这项工作代表了将ISF中MALAT1水平变化与AD病理学相关联的首个实例,为AD的早期非侵入性诊断提供了一种实用工具。