Flexible Modulation of Cellular Activities with Cationic Photosensitizers: Insights of Alkyl Chain Length on Reactive Oxygen Species Antimicrobial Mechanisms
Source abstract
Abstract
Abstract Cationic photosensitizers have good binding ability with negatively charged bacteria and fungi, exhibiting broad applications potential in antimicrobial photodynamic therapy (aPDT). However, cationic photosensitizers often display unsatisfactory transkingdom selectivity between mammalian cells and pathogens, especially for eukaryotic fungi. It is unclear which biomolecular sites are more efficient for photodynamic damage, owing to the lack of systematic research with the same photosensitizer system. Herein, a series of cationic aggregation‐induced emission (AIE) derivatives (CABs) (using berberine (BBR) as the photosensitizers core) with different length alkyl chains are successfully designed and synthesized for flexible modulation of cellular activities. The BBR core can efficiently produce reactive oxygen species (ROS) and achieve high‐performance aPDT . Through the precise regulation of alkyl chain length, different bindings, localizations, and photodynamic killing effects of CABs are achieved and investigated systematically among bacteria, fungi, and mammalian cells. It is found that intracellular active substances, not membranes, are more efficient damage sites of aPDT. Moderate length alkyl chains enable CABs to effectively kill Gram‐negative bacteria and fungi with light, while still maintaining excellent mammalian cell and blood compatibility. This study is expected to provide systematic theoretical and strategic research guidance for the construction of high‐performance cationic photosensitizers with good transkingdom selectivity.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Antimicrobial Peptides and Activities · Photodynamic Therapy Research Studies · Nanoplatforms for cancer theranostics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Chemical Resource Engineering Key Lab of Biomedical Materials of Natural Macromolecules (Beijing University of Chemical Technology Ministry of Education) and Laboratory of Biomedical Materials College of Materials Science and Engineering Beijing University of Chemical Technology Beijing 100029 China
College of Medical Engineering & the Key Laboratory for Medical Functional Nanomaterials Jining Medical University Jining 272067 China
Funding
National Natural Science Foundation of China
References (46)
Show source-provided references
1. 10.1021/acsnano.1c0350810.1021/acsnano.1c03508 ↗
2. 10.1002/smtd.20200004610.1002/smtd.202000046 ↗
3. 10.1038/s41551-016-000810.1038/s41551-016-0008 ↗
4. 10.1073/pnas.161119311310.1073/pnas.1611193113 ↗
5. 10.1002/adfm.20210359110.1002/adfm.202103591 ↗
6. 10.1039/D0CS00729C10.1039/D0CS00729C ↗
7. 10.1002/anie.20220077810.1002/anie.202200778 ↗
8. 10.1021/jp045553110.1021/jp0455531 ↗
9. 10.1073/pnas.061132810410.1073/pnas.0611328104 ↗
10. 10.1021/acs.chemrev.8b0055410.1021/acs.chemrev.8b00554 ↗
11. 10.1021/acsnano.2c0582110.1021/acsnano.2c05821 ↗
12. 10.1021/jacs.0c1077110.1021/jacs.0c10771 ↗
13. 10.1016/j.chempr.2020.05.01810.1016/j.chempr.2020.05.018 ↗
14. 10.1021/acsnano.2c0172110.1021/acsnano.2c01721 ↗
15. 10.1039/D1CS00647A10.1039/D1CS00647A ↗
16. 10.3892/ol.2021.1262010.3892/ol.2021.12620 ↗
17. 10.1039/C8SC01635F10.1039/C8SC01635F ↗
18. 10.1039/C9QM00242A10.1039/C9QM00242A ↗
19. 10.1002/smll.20190235210.1002/smll.201902352 ↗
20. 10.1021/jacs.9b0716210.1021/jacs.9b07162 ↗
21. 10.1080/1040841X.2018.146787610.1080/1040841X.2018.1467876 ↗
22. 10.1016/j.biomaterials.2020.12059810.1016/j.biomaterials.2020.120598 ↗
23. 10.1021/acs.langmuir.9b0212810.1021/acs.langmuir.9b02128 ↗
24. 10.1021/jacs.1c1065910.1021/jacs.1c10659 ↗
25. 10.1038/s41579-021-00638-010.1038/s41579-021-00638-0 ↗
26. 10.1021/acschembio.5b0054710.1021/acschembio.5b00547 ↗
27. 10.1002/anie.20190734310.1002/anie.201907343 ↗
28. 10.1021/jacs.9b1293610.1021/jacs.9b12936 ↗
29. 10.1021/jacs.8b0501410.1021/jacs.8b05014 ↗
30. 10.1039/C8BM01483C10.1039/C8BM01483C ↗
31. 10.1002/smll.20180229010.1002/smll.201802290 ↗
32. 10.1039/D1NR04512A10.1039/D1NR04512A ↗
33. 10.1021/acs.chemrev.0c0019910.1021/acs.chemrev.0c00199 ↗
34. 10.1016/S0196-9781(01)00502-210.1016/S0196-9781(01)00502-2 ↗
35. 10.1021/acsinfecdis.0c0072110.1021/acsinfecdis.0c00721 ↗
36. 10.1002/anie.20201495910.1002/anie.202014959 ↗
37. 10.1124/pr.55.1.210.1124/pr.55.1.2 ↗
38. 10.1038/252047a010.1038/252047a0 ↗
39. 10.1016/j.bpj.2016.05.03910.1016/j.bpj.2016.05.039 ↗
40. 10.1021/acs.chemrev.8b0060810.1021/acs.chemrev.8b00608 ↗
41. 10.1063/1.502403610.1063/1.5024036 ↗
42. 10.1021/ja211929h10.1021/ja211929h ↗
43. 10.1002/anie.20171303610.1002/anie.201713036 ↗
44. 10.1002/adfm.20200925810.1002/adfm.202009258 ↗
45. 10.1016/j.jconrel.2020.04.01410.1016/j.jconrel.2020.04.014 ↗
46. 10.1016/j.jconrel.2020.06.01310.1016/j.jconrel.2020.06.013 ↗