Li Bo, Wang Ji, Yang Seung Yun, Zhou Chang, Wu Mei X
Wellman Center for Photomedicine, Massachusetts General Hospital, Department of Dermatology, Harvard Medical School, Boston, MA 02114, United States.
Division of Biomedical Engineering, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, United States.
Biomaterials. 2015 Aug;59:30-8. doi: 10.1016/j.biomaterials.2015.04.040. Epub 2015 May 15.
Surface modified microneedle (MN) arrays are being developed to capture circulating biomarkers from the skin, but inefficiency and unreliability of the current method limit its clinical applications. We describe here that illumination of a tiny area of the skin with hemoglobin-preferably absorbent laser increased the amount of circulating biomarkers in the upper dermis by more than 1000-fold. The hemoglobin-specific light altered the permeability of capillaries leading to extravasation of molecules but not blood cells beneath the skin involved. When specific probe-coated MN arrays were applied into the laser-treated skin, the biomarkers accumulated in the upper dermis were reliably, accurately, and sufficiently captured as early as 15 min of the assay. The maximal binding occurred in 1 h in a manner independent of penetration depth or a molecular mass of the biomarker. With anti-fluorescein isothiocyanate (FITC)-MNs, we were able to measure blood concentrations of FITC in mice receiving FITC intravenously. The sensitivity and accuracy were comparable to those attained by fluorescence spectrophotometer. Likewise, MNs containing influenza hemagglutinin (HA) could detect anti-HA antibody in mice or swine receiving influenza vaccines as effectively as standard immunoassays. The novel, minimally invasive approach holds great promise for measurement of multiple biomarkers by a single array for point-of-care diagnosis.
表面改性微针(MN)阵列正在被开发用于从皮肤中捕获循环生物标志物,但目前方法的低效性和不可靠性限制了其临床应用。我们在此描述,用血红蛋白特异性吸收激光照射皮肤的微小区域,可使真皮上层循环生物标志物的量增加1000倍以上。血红蛋白特异性光改变了毛细血管的通透性,导致分子渗出,但不涉及皮肤下方的血细胞。当将特定探针包被的MN阵列应用于激光处理过的皮肤时,早在检测开始15分钟时,真皮上层积累的生物标志物就能被可靠、准确且充分地捕获。最大结合在1小时内发生,其方式与生物标志物的穿透深度或分子量无关。使用抗异硫氰酸荧光素(FITC)-MNs,我们能够测量静脉注射FITC的小鼠血液中FITC的浓度。其灵敏度和准确性与荧光分光光度计相当。同样,含有流感血凝素(HA)的MNs能够像标准免疫测定一样有效地检测接种流感疫苗的小鼠或猪体内的抗HA抗体。这种新颖的微创方法对于通过单个阵列进行即时诊断测量多种生物标志物具有巨大的前景。