登革热
量油尺
生物标志物
寨卡病毒
检测点注意事项
表面增强拉曼光谱
免疫分析
注意事项
病毒学
金标准(测试)
医学
生物
免疫学
拉曼光谱
抗体
病理
内科学
病毒
拉曼散射
物理
光学
尿
生物化学
作者
Maria Sánchez-Purrà,Marc Carré-Camps,Helena de Puig,Irene Bosch,Lee Gehrke,Kimberly Hamad‐Schifferli
标识
DOI:10.1021/acsinfecdis.7b00110
摘要
Zika and dengue are mosquito-borne diseases that present similar nonspecific symptoms but possess dramatically different outcomes. The first line of defense in epidemic outbreaks are rapid point-of-care diagnostics. Because many outbreaks occur in areas that are resource poor, assays that are easy to use, inexpensive, and require no power have become invaluable in patient treatment, quarantining, and surveillance. Paper-based sandwich immunoassays such as lateral flow assays (LFAs) are attractive as point-of-care solutions as they have the potential for wider deployability than lab-based assays such as PCR. However, their low sensitivity imposes limitations on their ability to detect low biomarker levels and early diagnosis. Here, we exploit the high sensitivity of surface-enhanced Raman spectroscopy (SERS) in a multiplexed assay that can distinguish between Zika and dengue nonstructural protein 1 (NS1) biomarkers. SERS-encoded gold nanostars were conjugated to specific antibodies for both diseases and used in a dipstick immunoassay, which exhibited 15-fold and 7-fold lower detection limits for Zika NS1 and dengue NS1, respectively. This platform combines the simplicity of a LFA with the high sensitivity of SERS and could not only improve Zika diagnosis but also detect diseases sooner after infection when biomarker levels are low.
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