Distance-Based Paper Device for a Naked-Eye Albumin-to-Alkaline Phosphatase Ratio Assay

Journal article


Authors/Editors


Strategic Research Themes


Publication Details

Author listKamonchanok Phoonsawat, Kawin Khachornsakkul, Nalin Ratnarathorn, Charles S. Henry,
and Wijitar Dungchai

PublisherAmerican Chemical Society

Publication year2021

JournalACS Sensors (23793694)

Volume number6

Issue number8

Start page3047

End page3055

Number of pages9

ISSN23793694

eISSN2379-3694

URLhttps://pubs.acs.org/doi/10.1021/acssensors.1c01058

LanguagesEnglish-United States (EN-US)


View on publisher site


Abstract

The albumin-to-alkaline phosphatase ratio (AAPR)
has been a cancer prognostic indicator. This paper presents the
concept of a dual-color change distance-based paper device
(dPAD) for albumin (Alb) and alkaline phosphatase (ALP)
detection to evaluate this cancer prognostic index. Whereas Alb
interacts with the bromocresol green (BCG) indicator to form a
bluish-green complex, ALP hydrolyzes L-ascorbic acid-2-phosphate
(AAP) to produce ascorbic acid (AA), which reacts with KIO3 to
generate I2 and I−. I2/I− reacts with silver hexagonal nanoprisms
(purple color) in the presence of Cu2+, resulting in a color change
from purple to colorless. The distance of the color change from
yellow to the bluish-green and purple to colorless correlates to Alb
and ALP concentration, respectively. The angle index for the
AAPR is then defined by drawing a straight line that connects the
tops of the two changed band lengths in the detection area. The highest bluish-green color band length on the Alb region is the
midpoint, which is the position set of the protractor at 0°, and the angle is measured using a simple protractor. The results indicate
that an AAPR below 0.57 will have an angle greater than 40° and correlates with a risk factor for lung cancer. The naked-eye
detection limits for Alb and ALP were found to be 0.8 g/L and 5 U/L (n = 10), respectively. The practical application of the
developed dPAD was successfully demonstrated by Alb and ALP analysis in human serum and validated against standard methods.
The proposed method does not require incubation conditions for the ALP assay, which strongly reduces the overall analysis steps
and time. Moreover, our device provides a low-cost, simple, sensitive, selective, accurate, and precise determination of the AAPR.


Keywords

No matching items found.


Last updated on 2023-03-10 at 07:36