Harvard-Massachusetts Institute of Technology Division of Health Sciences and Technology, Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA 02139.
Proc Natl Acad Sci U S A. 2014 Mar 11;111(10):3671-6. doi: 10.1073/pnas.1314651111. Epub 2014 Feb 24.
With noncommunicable diseases (NCDs) now constituting the majority of global mortality, there is a growing need for low-cost, noninvasive methods to diagnose and treat this class of diseases, especially in resource-limited settings. Molecular biomarkers combined with low-cost point-of-care assays constitute a potential solution for diagnosing NCDs, but the dearth of naturally occurring, predictive markers limits this approach. Here, we describe the design of exogenous agents that serve as synthetic biomarkers for NCDs by producing urinary signals that can be quantified by a companion paper test. These synthetic biomarkers are composed of nanoparticles conjugated to ligand-encoded reporters via protease-sensitive peptide substrates. Upon delivery, the nanoparticles passively target diseased sites, such as solid tumors or blood clots, where up-regulated proteases cleave the peptide substrates and release reporters that are cleared into urine. The reporters are engineered for detection by sandwich immunoassays, and we demonstrate their quantification directly from unmodified urine; furthermore, capture antibody specificity allows the probes to be multiplexed in vivo and quantified simultaneously by ELISA or paper lateral flow assay (LFA). We tailor synthetic biomarkers specific to colorectal cancer, a representative solid tumor, and thrombosis, a common cardiovascular disorder, and demonstrate urinary detection of these diseases in mouse models by paper diagnostic. Together, the LFA and injectable synthetic biomarkers, which could be tailored for multiple diseases, form a generalized diagnostic platform for NCDs that can be applied in almost any setting without expensive equipment or trained medical personnel.
随着非传染性疾病(NCDs)现在构成了全球死亡的主要原因,对于低成本、非侵入性的方法来诊断和治疗这类疾病的需求日益增长,尤其是在资源有限的环境中。分子生物标志物与低成本即时检测分析结合起来,为诊断 NCDs 提供了一种潜在的解决方案,但由于缺乏天然存在的、可预测的标志物,这种方法受到限制。在这里,我们描述了设计外源性试剂的方法,这些试剂可以作为 NCD 的合成生物标志物,通过产生可由配套测试论文定量的尿液信号。这些合成生物标志物由与配体编码的报告分子偶联的纳米颗粒组成,通过蛋白酶敏感的肽底物。在递送后,纳米颗粒被动靶向疾病部位,如实体瘤或血栓,在这些部位,上调的蛋白酶会切割肽底物并释放出可被清除到尿液中的报告分子。报告分子被设计用于夹心免疫测定法进行检测,我们直接从未修饰的尿液中对其进行了定量;此外,捕获抗体的特异性允许在体内同时进行多重分析,并通过 ELISA 或纸质侧向流动测定(LFA)进行定量。我们针对代表性实体瘤结直肠癌和常见心血管疾病血栓形成定制了合成生物标志物,并通过纸质诊断在小鼠模型中证明了这些疾病的尿液检测。总的来说,LFA 和可注射的合成生物标志物可以针对多种疾病进行定制,为 NCD 形成了一种通用的诊断平台,可以在几乎任何环境中应用,而无需昂贵的设备或训练有素的医务人员。