核酸
清脆的
核酸检测
注意事项
核酸定量
计算生物学
计算机科学
化学
纳米技术
生物
材料科学
生物化学
医学
基因
护理部
作者
Yohei Tanifuji,Guodong Tong,Yuki Hiruta,Daniel Citterio
出处
期刊:Analyst
[The Royal Society of Chemistry]
日期:2024-01-01
卷期号:149 (19): 4932-4939
摘要
Although CRISPR-based nucleic acid detection has great potential in point-of-care testing due to its simplicity, it has been rarely integrated into paper-based analytical devices (PADs), which are attractive platforms to simplify assays. This work introduces a CRISPR-assisted nucleic acid quantification approach integrated into a PAD with signal readout by a personal glucose meter (PGM). Retention of magnetic beads by filter paper and pre-deposition of all required reagents by freeze-drying stabilized with trehalose enabled the indirect quantification of human papilloma virus (HPV) DNA through a PGM readout without complicated user intervention and complex reagent handling. The calculated limit of detection was 57 pM, which is comparable with other amplification-free CRISPR-based assays detecting nucleic acids. The fully integrated device exhibited good storage stability for up to 4 weeks, suggesting its applicability toward practical point-of-care nucleic acid quantification.
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