Chinese Journal of Chromatography ›› 2025, Vol. 43 ›› Issue (5): 413-423.DOI: 10.3724/SP.J.1123.2024.11004
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WANG Haiyan1, XIE Peijuan1, QIAO Xiaoqiang1,*(
), ZHANG Liyuan2,*(
)
Received:2024-11-04
Online:2025-05-08
Published:2025-05-07
Supported by:CLC Number:
WANG Haiyan, XIE Peijuan, QIAO Xiaoqiang, ZHANG Liyuan. Typical strategy and research progress of efficient isolation methods of exosomes based on affinity interaction[J]. Chinese Journal of Chromatography, 2025, 43(5): 413-423.
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URL: https://www.chrom-china.com/EN/10.3724/SP.J.1123.2024.11004
Fig. 4 (a) Exosome isolation mechanism of TiO2-BSA-SPM[25]; (b) exosome adhesion on MB@CP via high-affinity choline phosphate-phosphatidylcholine (CP-PC) interactions[27]; (c) exosome enrichment in plasma using Fe3O4@SiO2@Eu2O3 nanomaterials[28]
Fig. 5 (a)Applications of SiO2@BSA@Fe-TA6 for exosome isolation and downstream analysis [29]; (b) an exosome detection platform based on the phospholipids-molecularly imprinted polymers-nanozyme-linked immunosorbent assay-surface-enhanced Raman scattering (PS-MIPs-NELISA-SERS)[31]; (c) an exosome isolation and detection platform based on g-C3N4 nanosheets (BCNNS)[32]
| Approach | Capture efficiency/% | Advantages | Insufficiencies | Applications | Ref. |
|---|---|---|---|---|---|
| Tim4@ILI-01 | 85.2 | high capture efficiency; easy nondestructive release; good biological activities of the captured exosomes | potentially exosome loss due to multiple mechanical centrifugation steps | sera of healthy persons and lung adenocarcinoma patients | [ |
| Fe3O4@SiO2- ILI-0l@Tim4 | 90.3 | high-efficiency and high-throughput exosome capture and release; simple and quick sample handling | increased economic cost due to the employment of Tim4 | high-throughput exosomal PD-L1 screening for accurately predicting anti-PD-1 response | [ |
| pH-HGN | 90.2 | highly efficient homogeneous capture and rapid recovery of intact exosomes | biological interference of enriched exosome in clinical treatment due to the conjugation of anti-CD63 antibody | differentiating lung-cancer patients from healthy persons | [ |
| SiO2@BSA@ Fe-TA6 | 85.4 | label-free, universal, low-cost, and easy to scale-up exosome capture | difficulty in exosome elution | lung-cancer diagnosis and typing | [ |
Table 1 Comparison of exosome-enrichment methods developed by our group, based on affinity-interaction
| Approach | Capture efficiency/% | Advantages | Insufficiencies | Applications | Ref. |
|---|---|---|---|---|---|
| Tim4@ILI-01 | 85.2 | high capture efficiency; easy nondestructive release; good biological activities of the captured exosomes | potentially exosome loss due to multiple mechanical centrifugation steps | sera of healthy persons and lung adenocarcinoma patients | [ |
| Fe3O4@SiO2- ILI-0l@Tim4 | 90.3 | high-efficiency and high-throughput exosome capture and release; simple and quick sample handling | increased economic cost due to the employment of Tim4 | high-throughput exosomal PD-L1 screening for accurately predicting anti-PD-1 response | [ |
| pH-HGN | 90.2 | highly efficient homogeneous capture and rapid recovery of intact exosomes | biological interference of enriched exosome in clinical treatment due to the conjugation of anti-CD63 antibody | differentiating lung-cancer patients from healthy persons | [ |
| SiO2@BSA@ Fe-TA6 | 85.4 | label-free, universal, low-cost, and easy to scale-up exosome capture | difficulty in exosome elution | lung-cancer diagnosis and typing | [ |
Fig. 6 (a) Exosome-isolation process by a microfluidic chip and a perylene tetracarboxylic acid diimide derivative (PTCDI)-aptamer fluorescence signal transduction strategy for detecting exosomes[36]; (b) schematic depicting salivary exosome proteomic analysis and the high-throughput array detection of asthma biomarkers[37]; (c) scheme depicting exosome capture by a supporting lipid membrane (SLM)[38]; (d) exosome isolation and purification procedure using serpentine channels[39]
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