Hedgehog-inspired magnetic nanoparticles for effectively capturing and detecting exosomes
Source abstract
Abstract
Abstract Exosomes, as one type of extracellular vesicle derived from multiple cells, have much potential as cancer biomarkers in clinical applications, but their enrichment and detection remain a huge challenge. Herein, inspired by the burr-like structure of the hedgehog, we present a new nanoparticle with a nanoneedle-assembled shell and a magnetic core for the effective capture and detection of exosomes. The unique nanoneedle structures endowed the magnetic nanoparticles with a large surface area for antibody modification so that the nanoparticles could serve as a platform for efficient exosome capture. In addition, the controllable movement of exosome-combined nanoparticles, which is due to the magnetic iron oxide cores, provides tremendous convenience for separating exosomes. The practical value of these nanoparticles in exosome analyses of serum from healthy patients and patients with liver cancer has also been demonstrated. Thus, we believe that bioinspired hierarchical nanoparticles are promising for biomedical and clinical applications.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Extracellular vesicles in disease · MicroRNA in disease regulation · Gold and Silver Nanoparticles Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (41)
Show source-provided references
1. Liebler, D. C. et al. Reassessment of exosome composition. Cell 177, 428–445 (2019).10.1016/j.cell.2019.02.029 ↗
2. Jeppesen, D. K. et al. Application of exosomes as liquid biopsy in clinical diagnosis. Signal. Transduct. Tar. 5, 1–14 (2020).10.1038/s41392-019-0089-y ↗
3. Kalluri, R. & LeBleu, V. S. The biology, function, and biomedical applications of exosomes. Science 367, 6478 (2020).10.1126/science.aau6977 ↗
4. Chen, G. et al. Exosomal PD-L1 contributes to immunosuppression and is associated with anti-PD-1 response. Nature 560, 382–386 (2018).10.1038/s41586-018-0392-8 ↗
5. Yu, Y., Wang, Qiao, Wang, C. & Shang, L. Living materials for regenerative medicine. Eng. Regen. 2, 96–104 (2021).
6. Wang, J. et al. Chemically edited exosomes with dual ligand purified by microfluidic device for active targeted drug delivery to tumor cells. ACS Appl. Mater. Interfaces 9, 27441–27452 (2017).10.1021/acsami.7b06464 ↗
7. Wang, H., Lu, Z. & Zhao, X. Tumorigenesis, diagnosis, and therapeutic potential of exosomes in liver cancer. J. Hematol. Oncol. 12, 1–21 (2019).10.1186/s13045-019-0806-6 ↗
8. Di, H. et al. Nanozyme-assisted sensitive profiling of exosomal proteins for rapid cancer diagnosis. Theranostics 10, 9303 (2020).10.7150/thno.46568 ↗
9. Wang, W., Luo, J. & Wang, S. Recent progress in isolation and detection of extracellular vesicles for cancer diagnostics. Adv. Health Mater. 7, 1800484 (2018).10.1002/adhm.201800484 ↗
10. Kim, S. M. et al. Cancer-derived exosomes as a delivery platform of CRISPR/Cas9 confer cancer cell tropism-dependent targeting. J. Control. Release 26, 8–16 (2017).10.1016/j.jconrel.2017.09.013 ↗
11. Zhao, S., Yu, X., Qian, Y., Chen, W. & Shen, J. Multifunctional magnetic iron oxide nanoparticles: An advanced platform for cancer theranostics. Theranostics 10, 6278 (2020).10.7150/thno.42564 ↗
12. Hu, J. et al. Cell membrane-inspired polymeric vesicles for combined photothermal and photodynamic prostate cancer therapy. ACS Appl. Mater. Interfaces 12, 42511–42520 (2020).10.1021/acsami.0c11636 ↗
13. Li, J., Cantu, C. P., Wang, Z. & Zhang, Y. S. Improving bioprinted volumetric tumor microenvironments in vitro. Trends Cancer 6, 745–756 (2020).10.1016/j.trecan.2020.06.002 ↗
14. Han, S. et al. Isolation and analysis of extracellular vesicles in a Morpho butterfly wing-integrated microvortex biochip. Biosens. Bioelectron. 154, 112073 (2020).10.1016/j.bios.2020.112073 ↗
15. Song, Y., Fan, J. B., Li, X., Liang, X. & Wang, S. pH-regulated heterostructure porous particles enable similarly sized protein separation. Adv. Mater. 31, 1900391 (2019).10.1002/adma.201900391 ↗
16. Tian, Y. et al. Quality and efficiency assessment of six extracellular vesicle isolation methods by nano-flow cytometry. J. Extracell. Vesicles 9, 1697028 (2020).10.1080/20013078.2019.1697028 ↗
17. Qi, H. et al. Blood exosomes endowed with magnetic and targeting properties for cancer therapy. ACS Nano 10, 3323–3333 (2016).10.1021/acsnano.5b06939 ↗
18. Xu, H., Liao, C., Zuo, P., Liu, Z. & Ye, B. C. E. Magnetic-based microfluidic device for on-chip isolation and detection of tumor-derived exosomes. Anal. Chem. 90, 13451–13458 (2018).10.1021/acs.analchem.8b03272 ↗
19. Ma, X. et al. P-glycoprotein antibody decorated porous hydrogel particles for capture and release of drug-resistant tumor cells. Adv. Health Mater. 8, 1900136 (2019).10.1002/adhm.201900136 ↗
20. Ma, Q. et al. Cell-inspired all-aqueous microfluidics: from intracellular liquid-liquid phase separation toward advanced biomaterials. Adv. Sci. 7, 1903359 (2020).10.1002/advs.201903359 ↗
21. Wan, Y. et al. Rapid magnetic isolation of extracellular vesicles via lipid-based nanoprobes. Nat. Biomed. Eng. 1, 1–11 (2017).10.1038/s41551-017-0058 ↗
22. Liao, Z., Lei, Dong & Wang, C. Modulating, instead of suppressing, foreign body responses for biomaterials design. Eng. Regen. 2, 91–95 (2021).
23. Zhu, S. et al. Rapid multilevel compartmentalization of stable all-aqueous blastosomes by interfacial aqueous-phase separation. ACS nano 14, 11215–11224 (2020).10.1021/acsnano.0c02923 ↗
24. Liu, L. et al. A versatile dynamic mussel-inspired biointerface: from specific cell behavior modulation to selective cell isolation. Angew. Chem. 130, 8004–8008 (2018).10.1002/ange.201804802 ↗
25. Wang, L., Liu, H., Zhang, F., Li, G. & Wang, S. Smart thin hydrogel coatings harnessing hydrophobicity and topography to capture and release cancer cells. Small 12, 4697–4701 (2016).10.1002/smll.201601275 ↗
26. Zhang, X., Wang, Y., Chi, J. & Zhao, Y. Smart microneedles for therapy and diagnosis. Research 2020, 7462915 (2020).10.34133/2020/7462915 ↗
27. Yan, Y. et al. Euryale ferox seed-inspired superlubricated nanoparticles for treatment of osteoarthritis. Adv. Funct. Mater. 29, 1807559 (2019).10.1002/adfm.201807559 ↗
28. Li, H. et al. Bioinspired micropatterned superhydrophilic Au-areoles for surface-enhanced Raman scattering (SERS) trace detection. Adv. Funct. Mater. 28, 1800448 (2018).10.1002/adfm.201800448 ↗
29. Liu, Z. et al. Multifunctional nanohybrid based on porous silicon nanoparticles, gold nanoparticles, and acetalated dextran for liver regeneration and acute liver failure theranostics. Adv. Mater. 30, 1703393 (2018).10.1002/adma.201703393 ↗
30. Tang, H., Zhao, X. & Jiang, X. Synthetic multi-layer nanoparticles for CRISPR-Cas9 genome editing. Adv. Drug Deliv. Rev. 168, 55–78 (2020).10.1016/j.addr.2020.03.001 ↗
31. Liu, Y. et al. Bioinspired structural color particles with multi-layer graphene oxide encapsulated nanoparticle components. Bioact. Mater. 5, 917–923 (2020).10.1016/j.bioactmat.2020.06.013 ↗
32. Hou, Jue, Li, M. & Song, Y. Recent advances in colloidal photonic crystal sensors: Materials, structures and analysis methods. Nano Today 22, 132–144 (2018).10.1016/j.nantod.2018.08.008 ↗
33. Maus, A., Strait, L. & Zhu, D. Nanoparticles as delivery vehicles for antiviral therapeutic drugs. Eng. Regen. 2, 31–46 (2021).
34. Nie, M. et al. Bio-inspired adhesive porous particles with human MSCs encapsulation for systemic lupus erythematosus treatment. Bioact. Mater. 6, 84–90 (2020).10.1016/j.bioactmat.2020.07.018 ↗
35. Zhang, H. et al. Fabrication of a multifunctional Nano-in-micro drug delivery platform by microfluidic templated encapsulation of porous silicon in polymer matrix. Adv. Mater. 26, 4497–4503 (2014).10.1002/adma.201400953 ↗
36. Shin, M. K. et al. Synthesis of Fe3O4@ nickel-silicate core-shell nanoparticles for His-tagged enzyme immobilizing agents. Nanotechnology 27, 495705 (2016).10.1088/0957-4484/27/49/495705 ↗
37. Fang, Q., Xuan, S., Jiang, W. & Gong, X. Yolk-like micro/nanoparticles with superparamagnetic iron oxide cores and hierarchical nickel silicate shells. Adv. Funct. Mater. 21, 1902–1909 (2011).10.1002/adfm.201002191 ↗
38. Yang, J. et al. Biologically modified nanoparticles as theranostic bionanomaterials. Prog. Mater. Sci. 118, 100768 (2020).10.1016/j.pmatsci.2020.100768 ↗
39. Yu, Q. et al. Copper silicate hollow microspheres-incorporated scaffolds for chemo-photothermal therapy of melanoma and tissue healing. ACS Nano 12, 2695–2707 (2018).10.1021/acsnano.7b08928 ↗
40. Zhang, P. et al. Ultrasensit.ive detection of circulating exosomes with a 3D-nanopatterned microfluidic chip. Nat. Biomed. Eng. 3, 438–451 (2019).10.1038/s41551-019-0356-9 ↗
41. Wang, Y. & Gu, H. Core-shell-type magnetic mesoporous silica nanocomposites for bioimaging and therapeutic agent delivery. Adv. Mater. 27, 576–585 (2015).10.1002/adma.201401124 ↗