Wang Gaobo, Zhang Yuyue, Kwong Hoi Kwan, Zheng Mengjia, Wu Jianpeng, Cui Chenyu, Chan Kannie W Y, Xu Chenjie, Chen Ting-Hsuan
Department of Biomedical Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon Tong, Hong Kong SAR, 999077, China.
Hong Kong Centre for Cerebro-Cardiovascular Health Engineering, Rm 1115-1119, Building 19W, 19 Science Park West Avenue, Hong Kong SAR, 999077, China.
Adv Sci (Weinh). 2024 Apr;11(16):e2306188. doi: 10.1002/advs.202306188. Epub 2024 Feb 28.
Malignant melanoma (MM) is the most aggressive form of skin cancer. The delay in treatment will induce metastasis, resulting in a poor prognosis and even death. Here, a two-step strategy for on-site diagnosis of MM is developed based on the extraction and direct visual quantification of S100A1, a biomarker for melanoma. First, a swellable microneedle is utilized to extract S100A1 in skin interstitial fluid (ISF) with minimal invasion. After elution, antibody-conjugated magnetic microparticles (MMPs) and polystyrene microparticles (PMPs) are introduced. A high expression level of S100A1 gives rise to a robust binding between MMPs and PMPs and reduces the number of free PMPs. By loading the reacted solution into the device with a microfluidic particle dam, the quantity of free PMPs after magnetic separation is displayed with their accumulation length inversely proportional to S100A1 levels. A limit of detection of 18.7 ng mL for S100A1 is achieved. The animal experiment indicates that ISF-based S100A1 quantification using the proposed strategy exhibits a significantly higher sensitivity compared with conventional serum-based detection. In addition, the result is highly comparable with the gold standard enzyme-linked immunosorbent assay based on Lin's concordance correlation coefficient, suggesting the high practicality for routine monitoring of melanoma.
恶性黑色素瘤(MM)是最具侵袭性的皮肤癌形式。治疗延迟会导致转移,从而预后不良甚至死亡。在此,基于黑色素瘤生物标志物S100A1的提取和直接视觉定量,开发了一种用于MM现场诊断的两步策略。首先,使用可膨胀微针以最小的侵入性提取皮肤间质液(ISF)中的S100A1。洗脱后,引入抗体偶联的磁性微粒(MMPs)和聚苯乙烯微粒(PMPs)。S100A1的高表达水平导致MMPs和PMPs之间的强结合,并减少游离PMPs的数量。通过将反应后的溶液加载到带有微流体颗粒坝的装置中,磁性分离后游离PMPs的数量通过其积累长度显示,该长度与S100A1水平成反比。实现了S100A1的检测限为18.7 ng/mL。动物实验表明,与传统的基于血清的检测相比,使用所提出的策略基于ISF的S100A1定量具有显著更高的灵敏度。此外,基于林氏一致性相关系数,该结果与金标准酶联免疫吸附测定法具有高度可比性,表明该方法在黑色素瘤常规监测中具有很高的实用性。