使用 RGB 传感器的纸质设备定量检测全血中的肌酐。

IF 2.7 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Neha Gautam, Ranjana Verma, Priya Ranjan Muduli, Shantimoy Kar and Arnab Sarkar
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引用次数: 0

摘要

肌酐是肾功能的重要生物标志物,通常使用血液中的金标准贾菲反应来估算,这涉及到使用分光光度法测量,因此限制了其在护理点环境中的使用范围。在此,我们报告了一种利用基于纸的微流控装置对全血肌酐进行单步定量的方法。我们的平台使用集成了 LF1 膜的 Whatman 滤纸。血浆的片上分离是通过 LF1 膜实现的,而装置中的 Whatman 元件则包含用于贾菲反应的嵌入试剂。当分离出的血浆通过毛细管浸泡进入反应区时,两种不同等级纸张的组合可实现肌酐的单步定量。色度读数的量化使用的是 RGB 传感器而非智能手机,后者高度依赖于平台,与典型的护理点 (POC) 设备中的其他组件相比,成本相对较高。我们的传感器集成在一个 3D 盒子中,因此检测几乎不需要仪器,非常适合 POC 设置。我们设备的检测限(LOD)为 0.219 mg dL-1,属于生理值的较低范围。线性判定系数(R2)和中位数准确度分别为 0.978% 和 94.047%。在所开发的方案中,精确测量的相对标准偏差(RSD)保持在 5%以下。此外,我们还利用实验室环境中的 35 份临床样本与金标准测量结果进行了对比,验证了我们设备的性能。我们的 Bland-Altman 图以及 t 检验和卡方检验结果清楚地证实了我们设备在 95% 置信区间内的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Quantification of creatinine in whole blood by a paper-based device using an RGB sensor†

Quantification of creatinine in whole blood by a paper-based device using an RGB sensor†

Creatinine, an important biomarker for renal functions, is often conventionally estimated using the gold standard Jaffe reaction from blood, which involves the usage of a spectrophotometric measurement, thus restricting its utilization scope in point-of-care settings. Here, we report the development of a method for the single-step quantification of creatinine from whole blood using a paper-based microfluidic device. Our platform uses Whatman filter paper integrated with an LF1 membrane. The on-chip separation of blood plasma is achieved through the LF1 membrane, while the Whatman component of the device contains the embedded reagents for the Jaffe reaction. The combination of two different grades of paper enables a single-step quantification of creatinine as the separated blood plasma traverses to the reaction zone through capillary imbibition. Colorimetric readouts were quantified using an RGB sensor instead of a smartphone, which is highly platform dependent and incurs a relatively higher cost compared to the other components in typical point-of care (POC) devices. Our sensor was integrated within a 3D box, thereby making the detection virtually instrument free and perfectly suited for POC settings. The limit of detection (LOD) of our device was 0.219 mg dL−1, which falls within the lower range of physiological values. The coefficient of determination (R2) for the linearity and median accuracy were 0.978 and 94.047%, respectively. The relative standard deviation (RSD) for precision measurements remained below 5% for the developed protocol. Furthermore, we validated the performance of our device with 35 clinical samples in laboratory settings against the gold standard measurements. Our Bland–Altman plot as well as t-test and chi-square test results clearly confirmed the validity of our device within a 95% confidence interval.

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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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