journal article·2018-06-27

pH-Induced Charge-Reversal Amphiphile with Cancer Cell-Selective Membrane-Disrupting Activity

Yincheng Chang, Zehuan Huang, Yang Jiao, Jiang-Fei Xu, Xi Zhang

ACS Applied Materials & Interfaces· Volume 10· Issue 25
Publisher page

Abstract

A charge-reversal amphiphile exhibiting charge conversion from negative to positive induced by pH is reported. It selectively kills cancer cells through cell membrane disruption. This amphiphile comprising an alkyl chain and anionic headgroup of acid-labile β-carboxylic amide (C16N-DCA) was prepared. In the microenvironment of normal cells with pH 7.4, the negatively charged C16N-DCA exhibited considerably reduced cytotoxicity. However, in the acidic microenvironment of cancer cells with pH 6.5-6.8, the headgroup charge of C16N-DCA changed from negative to positive under hydrolysis of the acid-labile amide group. As a result, the generated cationic amphiphile displayed significant killing of cancer cells by disrupting their cell membranes. Such pH-selective cell killing bioactivity represents a new route of chemotherapy for anticancer strategies.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: RNA Interference and Gene Delivery · Supramolecular Self-Assembly in Materials · Metal-Organic Frameworks: Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Key Lab of Organic Optoelectronics & Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084, China

Funding

Ministry of Science and Technology of the People's Republic of China · China Postdoctoral Science Foundation

References (37)

Show source-provided references
1. 10.1002/anie.19880113110.1002/anie.198801131 ↗
2. 10.1021/acsami.8b0087510.1021/acsami.8b00875 ↗
3. 10.1021/acsami.7b1928110.1021/acsami.7b19281 ↗
4. 10.1021/cr400431410.1021/cr4004314 ↗
5. 10.1002/anie.20170329810.1002/anie.201703298 ↗
6. 10.1002/anie.20140644210.1002/anie.201406442 ↗
7. 10.1021/acsami.5b1184610.1021/acsami.5b11846 ↗
8. 10.1021/acsnano.7b0237610.1021/acsnano.7b02376 ↗
9. 10.1002/adfm.20170308310.1002/adfm.201703083 ↗
10. 10.1021/jacs.5b0997410.1021/jacs.5b09974 ↗
11. 10.1021/jacs.7b0280110.1021/jacs.7b02801 ↗
12. 10.1039/c6cc03637f10.1039/c6cc03637f ↗
13. 10.1021/acsami.6b0829510.1021/acsami.6b08295 ↗
14. 10.1021/acsami.7b0115710.1021/acsami.7b01157 ↗
15. 10.1021/acsami.7b1978410.1021/acsami.7b19784 ↗
16. 10.1016/j.addr.2009.03.00510.1016/j.addr.2009.03.005 ↗
17. 10.1002/adma.20080327610.1002/adma.200803276 ↗
18. 10.1002/anie.20170114610.1002/anie.201701146 ↗
19. 10.1021/jacs.6b0421810.1021/jacs.6b04218 ↗
20. 10.1021/acs.jmedchem.5b0137510.1021/acs.jmedchem.5b01375 ↗
21. 10.1002/anie.20150456610.1002/anie.201504566 ↗
22. 10.1021/acs.langmuir.5b0143010.1021/acs.langmuir.5b01430 ↗
23. 10.1038/pj.2017.7210.1038/pj.2017.72 ↗
24. 10.1021/jacs.7b1146810.1021/jacs.7b11468 ↗
25. 10.1021/ja500367u10.1021/ja500367u ↗
26. 10.1021/la203974f10.1021/la203974f ↗
27. 10.1002/anie.20080096310.1002/anie.200800963 ↗
28. 10.1002/adfm.20090082510.1002/adfm.200900825 ↗
29. 10.1021/acs.nanolett.6b0539610.1021/acs.nanolett.6b05396 ↗
30. 10.1021/bm400358z10.1021/bm400358z ↗
31. Tannock I. F. · Cancer Res. · 1989 · 49 · 4373
32. 10.1021/jacs.5b0689210.1021/jacs.5b06892 ↗
33. 10.1021/ja210569f10.1021/ja210569f ↗
34. 10.1002/anie.20170759810.1002/anie.201707598 ↗
35. 10.1021/jacs.7b1113310.1021/jacs.7b11133 ↗
36. 10.1002/anie.20131124510.1002/anie.201311245 ↗
37. 10.1021/bi300836r10.1021/bi300836r ↗