研究目的
Developing a novel paper-based analytical device (PAD) coupled to LED-induced fluorescence (LIF) detection for the rapid, selective, and sensitive quantification of phenylalanine (Phe) in neonatal samples.
研究成果
The developed paper-based analytical device (fPAD) demonstrated high sensitivity, selectivity, and reproducibility for the neonatal screening of phenylketonuria (PKU). The incorporation of zinc oxide nanoparticles enhanced the device's performance, achieving a low detection limit of 0.125 μM. The method is simple, rapid, and cost-effective, making it suitable for routine diagnostic applications.
研究不足
The study did not explore the long-term stability of the device under various environmental conditions. Additionally, the interference from ascorbic acid at levels higher than the normal physiological range was noted, though no interference was observed at normal levels.
1:Experimental Design and Method Selection:
The study involved the development of a paper-based analytical device (PAD) modified with zinc oxide nanoparticles coated with chitosan (CH-ZnONPs) for the immobilization of enzymes Phenylalanine dehydrogenase (PheDH) and diaphorase. The device was designed for the quantification of phenylalanine (Phe) in neonatal samples using LED-induced fluorescence (LIF) detection.
2:Sample Selection and Data Sources:
Neonatal blood samples were used, with Phe extracted from blood spots collected on filter paper.
3:List of Experimental Equipment and Materials:
Instruments included a synchronized video microscope SVM340TM for fluorescent measurements, a Xerox Phaser printer for PAD fabrication, and a PDC-32G device for oxygen plasma treatment. Materials included Whatman N° 1 chromatographic paper, zinc oxide nanoparticles, chitosan, and enzymes PheDH and diaphorase.
4:Experimental Procedures and Operational Workflow:
The PADs were fabricated using wax printing and plasma oxidation. The enzymatic reaction involved the conversion of Phe and NAD+ to phenylpyruvate and NADH by PheDH, followed by the oxidation of NADH by diaphorase, reducing resazurin to resorufin, which was detected by LIF.
5:Data Analysis Methods:
Fluorescence intensity was measured to quantify Phe concentration, with data analyzed for linearity, detection limit, and precision.
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