首页> 美国卫生研究院文献>Springer Open Choice >Development and validation of a glass-silicon microdroplet-based system to measure sulfite concentrations in beverages
【2h】

Development and validation of a glass-silicon microdroplet-based system to measure sulfite concentrations in beverages

机译:开发和验证基于玻璃硅微滴的系统用于测量饮料中的亚硫酸盐浓度

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Sulfite is often added to beverages as an antioxidant and antimicrobial agent. In fermented beverages, sulfite is also naturally produced by yeast cells. However, sulfite causes adverse health effects in asthmatic patients and accurate measurement of the sulfite concentration is therefore very important. Current sulfite analysis methods are time- and reagent-consuming and often require costly equipment. Here, we present a system allowing sensitive, ultralow-volume sulfite measurements based on a reusable glass-silicon microdroplet platform on which microdroplet generation, addition of enzymes through chemical-induced emulsion destabilization and pillar-induced droplet merging, emulsion restabilization, droplet incubation, and fluorescence measurements are integrated. In a first step, we developed and verified a fluorescence-based enzymatic assay for sulfite by measuring its analytical performance (LOD, LOQ, the dynamic working range, and the influence of salts, colorant, and sugars) and comparing fluorescent microplate readouts of fermentation samples with standard colorimetric measurements using the 5,5′-dithiobis-(2-nitrobenzoic acid) assay of the standard Gallery Plus Beermaster analysis platform. Next, samples were analyzed on the microdroplet platform, which also showed good correlation with the standard colorimetric analysis. Although the presented platform does not allow stable reinjection of droplets due to the presence of a tight array of micropillars at the fluidics entrances to prevent channel clogging by dust, removing the pillars, and integrating miniaturized pumps and optics in a future design would allow to use this platform for high-throughput, automated, and portable screening of microbes, plant, or mammalian cells. >Graphical abstract
机译:亚硫酸盐通常作为抗氧化剂和抗菌剂添加到饮料中。在发酵饮料中,酵母细胞也自然产生亚硫酸盐。但是,亚硫酸盐会对哮喘患者产生不利的健康影响,因此准确测量亚硫酸盐的浓度非常重要。当前的亚硫酸盐分析方法既耗时又耗试剂,并且常常需要昂贵的设备。在这里,我们介绍了一个系统,该系统基于可重复使用的玻璃-硅微滴平台,可进行灵敏的超小体积亚硫酸盐测量,在该平台上可产生微滴,通过化学诱导的乳状液去稳定化酶添加酶和通过柱诱导的液滴合并,乳状液再稳定化,液滴温育,和荧光测量被集成。第一步,我们通过测量亚硫酸盐的分析性能(LOD,LOQ,动态工作范围以及盐,着色剂和糖的影响)并比较发酵中的荧光微孔板读数,开发并验证了基于荧光的亚硫酸盐酶促测定方法使用标准Gallery Plus Plus Beermaster分析平台的5,5'-二硫代双-(2-硝基苯甲酸)分析进行标准比色测量的样品。接下来,在微滴平台上分析样品,这也显示了与标准比色分析的良好相关性。尽管由于在流体入口处存在紧密的微柱阵列,以防止通道被灰尘堵塞,​​移走柱子并在将来的设计中集成小型化的泵和光学器件,因此所提出的平台不允许液滴的稳定再注入,但会在将来的设计中允许使用该平台用于高通量,自动化和便携式筛查微生物,植物或哺乳动物细胞。 <!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> >图形摘要<!- fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> <!-标题a7->ᅟ

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号