Lai James J, Stayton Patrick S
Department of Bioengineering, University of Washington, Seattle, WA, 98195, USA.
Methods Mol Biol. 2015;1256:71-84. doi: 10.1007/978-1-4939-2172-0_5.
Optical detection technologies based on mobile devices can be utilized to enable many mHealth applications, including a reader for lateral-flow immunoassay (LFIA). However, an intrinsic challenge associated with LFIA for clinical diagnostics is the limitation in sensitivity. Therefore, rapid and simple specimen processing strategies can directly enable more sensitive LFIA by purifying and concentrating biomarkers. Here, a binary reagent system is presented for concentrating analytes from a larger volume specimen to improve the malaria LFIA's limit of detection (LOD). The biomarker enrichment process utilizes temperature-responsive gold-streptavidin conjugates, biotinylated antibodies, and temperature-responsive magnetic nanoparticles. The temperature-responsive gold colloids were synthesized by modifying the citrate-stabilized gold colloids with a diblock copolymer, containing a thermally responsive poly(N-isopropylacrylamide) (pNIPAAm) segment and a gold-binding block composed of NIPAAm-co-N,N-dimethylaminoethylacrylamide. The gold-streptavidin conjugates were synthesized by conjugating temperature-responsive gold colloids with streptavidin via covalent linkages using carbodiimide chemistry chemistry. The gold conjugates formed half-sandwiches, gold labeled biomarker, by complexing with biotinylated antibodies that were bound to Plasmodium falciparum histidine-rich protein 2 (PfHRP2), a malaria antigen. When a thermal stimulus was applied in conjunction with a magnetic field, the half-sandwiches and temperature-responsive magnetic nanoparticles that were both decorated with pNIPAAm formed large aggregates that were efficiently magnetically separated from human plasma. The binary reagent system was applied to a large volume (500 μL) specimen for concentrating biomarker 50-fold into a small volume and applied directly to an off-the-shelf malaria LFIA to improve the signal-to-noise ratio.
基于移动设备的光学检测技术可用于实现许多移动健康应用,包括一种用于侧向流动免疫分析(LFIA)的阅读器。然而,临床诊断中与LFIA相关的一个内在挑战是灵敏度的限制。因此,快速简单的样本处理策略可通过纯化和浓缩生物标志物直接实现更灵敏的LFIA。在此,提出了一种二元试剂系统,用于从更大体积的样本中浓缩分析物,以提高疟疾LFIA的检测限(LOD)。生物标志物富集过程利用了温度响应性金-链霉亲和素缀合物、生物素化抗体和温度响应性磁性纳米颗粒。通过用含有热响应性聚(N-异丙基丙烯酰胺)(pNIPAAm)链段和由NIPAAm-co-N,N-二甲基氨基乙基丙烯酰胺组成的金结合嵌段的二嵌段共聚物修饰柠檬酸盐稳定的金胶体,合成了温度响应性金胶体。通过使用碳二亚胺化学通过共价键将温度响应性金胶体与链霉亲和素缀合,合成了金-链霉亲和素缀合物。金缀合物通过与结合到疟原虫富含组氨酸蛋白2(PfHRP2)(一种疟疾抗原)的生物素化抗体络合,形成半三明治结构,即金标记的生物标志物。当结合磁场施加热刺激时,均用pNIPAAm修饰的半三明治和温度响应性磁性纳米颗粒形成大的聚集体,这些聚集体可从人血浆中有效地磁性分离出来。该二元试剂系统应用于大体积(500μL)样本,将生物标志物浓缩50倍至小体积,并直接应用于现成的疟疾LFIA,以提高信噪比。