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基于海藻酸盐的可持续传感器,用于检测人乳中的 。

Sustainable, Alginate-Based Sensor for Detection of in Human Breast Milk.

机构信息

Department of Bioengineering, Santa Clara University, Santa Clara, CA 95053, USA.

Department of Biology, Santa Clara University, Santa Clara, CA 95053, USA.

出版信息

Sensors (Basel). 2020 Feb 19;20(4):1145. doi: 10.3390/s20041145.

Abstract

There are no existing affordable diagnostics for sensitive, rapid, and on-site detection of pathogens in milk. To this end, an on-site colorimetric-based sustainable assay has been developed and optimized using an L (5) Taguchi design to obtain results in hours without PCR amplification. To determine the level of () contamination, after induction with 150 µL of breast milk, the B-Per bacterial protein extraction kit was added to a solution containing an alginate-based microcapsule assay. Within this 3 mm spherical novel sensor design, X-Gal (5-Bromo-4-Chloro-3-Indolyl β-d-Galactopyranoside) was entrapped at a concentration of 2 mg/mL. The outward diffusing X-Gal was cleaved by β-galactosidase from and dimerized in the solution to yield a blue color after incubation at 40 °C. Color intensity was correlated with the level of contamination using a categorical scale. After an 8 h incubation period, a continuous imaging scale based on intensity normalization was used to determine a binary lower limit of detection (LOD), which corresponded to 10 colony forming unit per mL (CFU/mL) and above. The cost of the overall assay was estimated to be $0.81 per sample, well under the $3 benchmark for state-of-the-art immune-based test kits for pathogen detection in biofluids. Considering the reported binary LOD cutoff of 10 CFU/mL and above, this proposed hydrogel-based assay is suited to meet global requirements for screening breast milk or milk for pathogenic organisms of 10 CFU/mL, with a percentage of false positives to be determined in future efforts.

摘要

目前尚无经济实惠的诊断方法能够在牛奶中实现对病原体的敏感、快速和现场检测。为此,本研究采用 L(5)田口设计对基于比色的现场可持续测定法进行了开发和优化,该方法无需 PCR 扩增即可在数小时内获得结果。为了确定污染水平,将含有基于藻酸盐的微胶囊测定法的溶液加入到含有 150 µL 母乳的溶液中,然后加入 B-Per 细菌蛋白提取试剂盒。在这个 3 毫米的球形新型传感器设计中,将 X-Gal(5-溴-4-氯-3-吲哚基-β-d-半乳糖吡喃糖苷)以 2 mg/mL 的浓度包埋。向外扩散的 X-Gal 被β-半乳糖苷酶从细菌中裂解,并在溶液中二聚化,在 40°C 孵育后产生蓝色。颜色强度与污染水平使用分类量表相关联。经过 8 小时孵育期后,使用基于强度归一化的连续成像量表来确定二进制检测下限(LOD),该下限对应于 10 个菌落形成单位每毫升(CFU/mL)及以上。总体测定法的成本估计为每个样品 0.81 美元,远低于用于生物体液中病原体检测的最先进免疫测试试剂盒的 3 美元基准。考虑到报告的二进制 LOD 截止值为 10 CFU/mL 及以上,这种基于水凝胶的测定法适合满足筛选母乳或牛奶中致病性生物 10 CFU/mL 的全球要求,未来的工作将确定假阳性率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db9e/7071128/d5bd902b77b3/sensors-20-01145-g001.jpg

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