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Updated: Jan 3, 2026

Development of a Lateral Flow Immunochromatographic Strip for Rapid and Quantitative Detection of Small Molecule Compounds
Published on: November 13, 2021
Comparison of three sample addition methods in competitive and sandwich colloidal gold immunochromatographic assay
Yu Li1, Yaofeng Zhou1, Xirui Chen1
1State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang, 330047, PR China; School of Food Science and Technology, Nanchang University, Nanchang, 330047, PR China.
Insights
Sample addition methods minimally impact competitive immunochromatographic assays (ICAs) but significantly affect sandwich ICAs. This research provides crucial insights for optimizing ICA detection performance by selecting appropriate sample application techniques.
Area of Science:
- * Analytical Chemistry
- * Biosensors
- * Diagnostic Assays
Background:
- * Immunochromatographic assays (ICAs) are vital point-of-care diagnostic tools.
- * The influence of sample addition methods on ICA performance is understudied.
- * Gold nanoparticles (AuNPs) are effective visual labels for ICAs.
Purpose of the Study:
- * To investigate the impact of three sample addition methods (dry, wet, insert) on ICA analytical performance.
- * To compare these effects in both competitive and sandwich assay formats.
- * To provide guidance for selecting optimal sample addition methods in ICA development.
Main Methods:
- * Development of AuNP-based ICAs for competitive and sandwich assays.
- * Testing of dry, wet, and insert sample addition methods.
- * Analysis of assay performance using clenbuterol and human chorionic gonadotropin as analytes in buffer and serum matrices.
Main Results:
- * Competitive ICAs showed negligible differences in performance across methods in buffer.
- * The wet method impaired performance in pork samples for competitive ICAs.
- * Sandwich ICAs exhibited significantly different analytical performances based on sample addition method in buffer and serum.
- * The wet method altered linearity ranges in sandwich ICAs compared to dry and insert methods.
Conclusions:
- * Sample addition methods have a minor effect on competitive ICAs but a significant effect on sandwich ICAs.
- * Understanding these effects is crucial for interpreting and improving ICA detection results.
- * This study offers a reference for choosing appropriate sample addition methods in future ICA applications.
Abstract:
Immunochromatographic assays (ICAs) are mainstream point-of-care diagnostic tools in disease control, food safety, and environmental monitoring. However, the important issue pertaining to the influence of sample addition methods on the detection performance of ICAs has not been addressed, and related information is still lacking. Herein, we selected the well-accepted gold nanoparticles (AuNPs) as visual labels. AuNP-based ICA was then used to explore the effects of three sample addition methods (i.e., dry, wet, and insert) on the analytical performance of ICAs by using competitive and sandwich models. Under optimized conditions, the competitive ICA with clenbuterol as an analyte showed a negligible difference (p > 0.05) in the detection performance of the three methods in ideal phosphate buffered saline solution. However, the wet method demonstrated the worst performance in pork samples (p < 0.05). The sandwich ICA strip with human chorionic gonadotropin as an analyte revealed the significantly different analytical performances of the three approaches in phosphate buffer (PB) solution and spiked serum (p < 0.05). Two independent linear correlations were observed with the increase in target concentration. However, for the wet method in the PB solution and serum, the first linear correlation was at a relatively narrow target concentration range, and the second linear correlation was at a wider concentration range compared with those for the dry and insert methods. Our findings demonstrated that sample addition methods slightly influence competitive ICAs (p > 0.05) but remarkably affect sandwich ICAs (p < 0.05). We believe that this study can further explain the differences in detection results for the same target analyte in actual ICA detection. The results may serve as a reference in the rational selection of the appropriate sample addition method for succeeding ICA works.
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