Functional Modification of Bacteria during Plasmolysis and Deplasmolysis for Tumor Diagnosis and Treatment
Source abstract
Abstract
Bacteria have been widely used as biotherapeutics or drug delivery carriers, due to their unique biological functions. However, the clinical translation of living bacteria for biomedical applications is largely limited by their inevitable side effects and poor therapeutic efficacy. Here, we report a simple, but effective method for the functional enhancement of bacteria based on plasmolysis and deplasmolysis (P/deP) to entangle functional polymer chains with the bacterial walls. It was found that the modified efficiency by this method was 2–3-fold higher than traditional methods, such as the Huisgen cycloaddition reaction and carbodiimide reaction. Moreover, this method did not require expensive or toxic reagents and could modify a variety of functional polymers on the bacterial surface in one step. Importantly, modified bacteria achieved effective tumor imaging and 95% tumor growth inhibition. This simple and universal method might open a new window for the construction of modified bacteria for disease diagnosis and treatment.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Cancer Research and Treatments · Nanoplatforms for cancer theranostics · Bacteriophages and microbial interactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Biomedical Polymers of Ministry of Education & Department of Chemistry, Wuhan University, Wuhan 430072, People’s Republic of China
Wuhan Research Centre for Infectious Diseases and Cancer, Chinese Academy of Medical Sciences, Wuhan 430071, People’s Republic of China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (45)
Show source-provided references
1. 10.1038/nrc.2017.1310.1038/nrc.2017.13 ↗
2. 10.1021/acsnano.8b0223510.1021/acsnano.8b02235 ↗
3. 10.1038/s41467-019-11390-810.1038/s41467-019-11390-8 ↗
4. 10.1038/s41551-019-0423-210.1038/s41551-019-0423-2 ↗
5. 10.1038/d41586-020-00199-x10.1038/d41586-020-00199-x ↗
6. 10.1155/2022/999992510.1155/2022/9999925 ↗
7. 10.3390/antibiotics1104048010.3390/antibiotics11040480 ↗
8. 10.1038/nrurol.2014.1510.1038/nrurol.2014.15 ↗
9. 10.1126/scitranslmed.aak953710.1126/scitranslmed.aak9537 ↗
10. 10.1038/nnano.2007.14910.1038/nnano.2007.149 ↗
11. 10.1038/nprot.2008.3210.1038/nprot.2008.32 ↗
12. 10.1002/anie.20200264910.1002/anie.202002649 ↗
13. 10.1126/scitranslmed.300898210.1126/scitranslmed.3008982 ↗
14. 10.1038/cgt.2011.5710.1038/cgt.2011.57 ↗
15. 10.1002/ijc.2304710.1002/ijc.23047 ↗
16. 10.1007/s40820-020-00560-910.1007/s40820-020-00560-9 ↗
17. 10.1021/acsnano.0c1014410.1021/acsnano.0c10144 ↗
18. 10.1016/j.addr.2016.09.00710.1016/j.addr.2016.09.007 ↗
19. 10.31635/ccschem.021.20210095710.31635/ccschem.021.202100957 ↗
20. 10.1039/D0CS01571G10.1039/D0CS01571G ↗
21. 10.1016/j.addr.2022.11429610.1016/j.addr.2022.114296 ↗
22. 10.1007/s11426-022-1243-510.1007/s11426-022-1243-5 ↗
23. 10.1002/adma.20180827810.1002/adma.201808278 ↗
24. 10.1002/adma.20210258010.1002/adma.202102580 ↗
25. 10.1021/cb600322810.1021/cb6003228 ↗
26. 10.1038/nchembio0605-1310.1038/nchembio0605-13 ↗
27. 10.1073/pnas.80.18.548010.1073/pnas.80.18.5480 ↗
28. 10.1038/s41467-021-26956-810.1038/s41467-021-26956-8 ↗
29. 10.1002/adma.20160327010.1002/adma.201603270 ↗
30. 10.1021/la903738n10.1021/la903738n ↗
31. 10.1111/j.1469-8137.1994.tb02952.x10.1111/j.1469-8137.1994.tb02952.x ↗
32. 10.1099/13500872-141-12-316110.1099/13500872-141-12-3161 ↗
33. 10.1073/pnas.051018210310.1073/pnas.0510182103 ↗
34. 10.1007/s00253-010-2606-310.1007/s00253-010-2606-3 ↗
35. 10.1038/s41563-020-00857-510.1038/s41563-020-00857-5 ↗
36. 10.1093/nsr/nwaa16010.1093/nsr/nwaa160 ↗
37. 10.1002/adma.20200452910.1002/adma.202004529 ↗
38. 10.1021/acsmaterialslett.0c0025910.1021/acsmaterialslett.0c00259 ↗
39. 10.1038/nrc107110.1038/nrc1071 ↗
40. 10.1002/anie.20191438410.1002/anie.201914384 ↗
41. 10.1021/acsnano.9b0030010.1021/acsnano.9b00300 ↗
42. 10.1016/0003-2697(83)90270-110.1016/0003-2697(83)90270-1 ↗
43. 10.1021/acs.nanolett.9b0521010.1021/acs.nanolett.9b05210 ↗
44. 10.1016/j.freeradbiomed.2009.06.01310.1016/j.freeradbiomed.2009.06.013 ↗
45. 10.1002/adfm.20190980610.1002/adfm.201909806 ↗