A Facile Magnetic Extrusion Method for Preparing Endosome‐Derived Vesicles for Cancer Drug Delivery
Source abstract
Abstract
Abstract To date, the scaled‐up manufacturing and efficient drug loading of exosomes are two existing challenges limiting the clinical translation of exosome‐based drug delivery. Herein, a facile magnetic extrusion method is developed for preparing endosome‐derived vesicles, also known as exosome mimetics (EMs), which share the same biological origin and similar morphology, composition, and biofunctions with native exosomes. The high yield and consistency of this magnetic extrusion method help to overcome the manufacturing bottleneck in exosome research. Moreover, the proposed standardized multi‐step method readily facilitates the ammonium sulfate gradient approach to actively load chemodrugs such as doxorubicin into EMs. The engineered EMs developed and tested here exhibit comparable drug delivery properties as do native exosomes, and potently inhibit tumor growth by delivering doxorubicin in an orthotopic breast tumor model. These findings demonstrate that EMs can be prepared in a facile and scaled‐up manner as a promising biological nanomedicine for cancer drug delivery.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Extracellular vesicles in disease · Nanoparticle-Based Drug Delivery · RNA Interference and Gene Delivery
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Vascular Biology Program Boston Children's Hospital 300 Longwood Avenue Boston MA 02115 USA
Department of Surgery Boston Children's Hospital Harvard Medical School 300 Longwood Avenue Boston MA 02115 USA
Graduate School of Arts and Sciences Harvard University 1350 Massachusetts Avenue Cambridge MA 02138 USA
Funding
Breast Cancer Research Foundation · National Cancer Institute
References (41)
Show source-provided references
1. 10.1007/s10571-016-0366-z10.1007/s10571-016-0366-z ↗
2. 10.1038/s41571-018-0036-910.1038/s41571-018-0036-9 ↗
3. 10.1126/scitranslmed.aav852110.1126/scitranslmed.aav8521 ↗
4. 10.1080/20013078.2019.162716410.1080/20013078.2019.1627164 ↗
5. 10.1007/s10544-019-0396-710.1007/s10544-019-0396-7 ↗
6. 10.1080/20013078.2018.156080910.1080/20013078.2018.1560809 ↗
7. 10.1016/j.ymthe.2018.09.01510.1016/j.ymthe.2018.09.015 ↗
8. 10.3390/cells712027310.3390/cells7120273 ↗
9. 10.1016/j.molmed.2018.01.00610.1016/j.molmed.2018.01.006 ↗
10. 10.1016/j.tips.2020.08.00110.1016/j.tips.2020.08.001 ↗
11. 10.1016/j.jconrel.2013.08.01410.1016/j.jconrel.2013.08.014 ↗
12. 10.1021/acs.molpharmaceut.5b0036410.1021/acs.molpharmaceut.5b00364 ↗
13. 10.7150/thno.3709710.7150/thno.37097 ↗
14. 10.1038/s41551-019-0485-110.1038/s41551-019-0485-1 ↗
15. 10.1016/j.biomaterials.2016.06.02410.1016/j.biomaterials.2016.06.024 ↗
16. 10.1021/nn402232g10.1021/nn402232g ↗
17. 10.3390/nano1009181610.3390/nano10091816 ↗
18. 10.1038/s41598-020-67207-y10.1038/s41598-020-67207-y ↗
19. 10.1038/s41598-018-19628-z10.1038/s41598-018-19628-z ↗
20. 10.1016/0076-6879(90)82018-W10.1016/0076-6879(90)82018-W ↗
21. Graham J. M. · 199710.1093/oso/9780199634958.001.0001 ↗
22. Pryor P. R. · 2015
23. Wagner A. · J. Drug Delivery · 2010 · 2011
24. 10.2217/nnm.16.510.2217/nnm.16.5 ↗
25. 10.1038/nbt.333010.1038/nbt.3330 ↗
26. 10.3390/pharmaceutics1002005710.3390/pharmaceutics10020057 ↗
27. 10.1039/C7CS00230K10.1039/C7CS00230K ↗
28. 10.1016/0005-2736(93)90105-910.1016/0005-2736(93)90105-9 ↗
29. Haghiralsadat F. · Cell J. · 2017 · 19 · 55
30. 10.1007/s12195-016-0457-410.1007/s12195-016-0457-4 ↗
31. 10.1016/j.ymthe.2019.12.00710.1016/j.ymthe.2019.12.007 ↗
32. 10.3390/pharmaceutics1004021810.3390/pharmaceutics10040218 ↗
33. 10.1039/C4TB00811A10.1039/C4TB00811A ↗
34. 10.1021/acsnano.9b0439710.1021/acsnano.9b04397 ↗
35. 10.3390/ijms2111385110.3390/ijms21113851 ↗
36. 10.1016/j.biomaterials.2012.07.04310.1016/j.biomaterials.2012.07.043 ↗
37. 10.1021/acs.nanolett.7b0480110.1021/acs.nanolett.7b04801 ↗
38. 10.1126/sciadv.aav501010.1126/sciadv.aav5010 ↗
39. 10.1038/s41598-019-42643-710.1038/s41598-019-42643-7 ↗
40. 10.1038/s41467-017-02588-910.1038/s41467-017-02588-9 ↗
41. 10.1073/pnas.190469711610.1073/pnas.1904697116 ↗