Chinese Journal of Chromatography ›› 2025, Vol. 43 ›› Issue (11): 1187-1199.DOI: 10.3724/SP.J.1123.2025.04011
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LIU Xintong, SHI Jia, SHI Meng*(
)
Received:2025-04-28
Online:2025-11-08
Published:2025-11-07
Supported by:CLC Number:
LIU Xintong, SHI Jia, SHI Meng. Research progress on paper-based microfluidic chips in pathogen detection[J]. Chinese Journal of Chromatography, 2025, 43(11): 1187-1199.
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URL: https://www.chrom-china.com/EN/10.3724/SP.J.1123.2025.04011
| Type | Structure | Analysis methods | Features |
|---|---|---|---|
| 2D | type 1: lateral flow assay strip,a fluid analysis platform based on porous membranes/paper substrates type 2: single-layer planar structure with linearly arranged functional regions | relies on specific antigen-antibody binding or biochemical reactions, with detection achieved through marker signals, immunoanalysis (e.g., immunochromatography) | limited space and limited multi-target detection capability |
| 3D | three-dimensional channel network formed by folding/bending 2D structures or bonding multi-layer paper substrates | immunoanalysis, biochemical analysis (e.g., enzymatic reactions, multi-step separation-detection integration) | sample space allows for multi-step operations and is also suitable for multi-target analysis |
Table 1 Comparison of paper-based structures
| Type | Structure | Analysis methods | Features |
|---|---|---|---|
| 2D | type 1: lateral flow assay strip,a fluid analysis platform based on porous membranes/paper substrates type 2: single-layer planar structure with linearly arranged functional regions | relies on specific antigen-antibody binding or biochemical reactions, with detection achieved through marker signals, immunoanalysis (e.g., immunochromatography) | limited space and limited multi-target detection capability |
| 3D | three-dimensional channel network formed by folding/bending 2D structures or bonding multi-layer paper substrates | immunoanalysis, biochemical analysis (e.g., enzymatic reactions, multi-step separation-detection integration) | sample space allows for multi-step operations and is also suitable for multi-target analysis |
Fig. 1 Procedure for identifying viable bacterial cells of the target species, E. coli.[36] APTEs: 3-aminopropyltriethoxysilane; CPRG: chlorophenol red-β-D-galactopyranoside; μPAD: paper-based microfluidic devices
| Technology | Advantages | Disadvantages | Refs. |
|---|---|---|---|
| Wax printing | easy to manufacture and simple to operate | low-resolution, solid ink printer discontinued | [ |
| Photolithography | rapid fabrication of μPAD with good precision | highly specialized, expensive equipment | [ |
| Inkjet printing | The product is easy to operate, has a high resolution, and is cost-effective | low precision | [ |
| Laser cutting | quick one-step production | expensive and highly specialized equipment | [ |
| Laser printing | high precision | difficult pattern drawing, expensive instruments | [ |
| Heat transfer printing | fast production, high-resolution, and durable µPAD | high production costs and complex assembly of carbon ribbons | [ |
Table 2 Manufacturing process for μPAD
| Technology | Advantages | Disadvantages | Refs. |
|---|---|---|---|
| Wax printing | easy to manufacture and simple to operate | low-resolution, solid ink printer discontinued | [ |
| Photolithography | rapid fabrication of μPAD with good precision | highly specialized, expensive equipment | [ |
| Inkjet printing | The product is easy to operate, has a high resolution, and is cost-effective | low precision | [ |
| Laser cutting | quick one-step production | expensive and highly specialized equipment | [ |
| Laser printing | high precision | difficult pattern drawing, expensive instruments | [ |
| Heat transfer printing | fast production, high-resolution, and durable µPAD | high production costs and complex assembly of carbon ribbons | [ |
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