journal article·2020-10-27

Precisely Regulated Luminescent Gold Nanoparticles for Identification of Cancer Metastases

Yue Tan, Kui He, Bing Tang, Huarui Chen, Zhipeng Zhao, Chengqian Zhang, Li Lin, Jinbin Liu

ACS Nano· Volume 14· Issue 10
Publisher page

Abstract

The nanoprobes for identification of cancer metastases in the mononuclear phagocyte system (MPS) organs are of significant importance but are limited due to the long-standing challenge of low tumor-targeting specificity with inadequate targeting efficiency and high nonspecific accumulation. Here, we report a surface regulation strategy that integrates the tumor-acidity-activated charge-reversal behavior and precise control in both hydrodynamic diameter (HD) and surface charge on ultrasmall luminescent gold nanoparticles (AuNPs) to achieve significantly high tumor-targeting specificity. The precise regulation of AuNPs to a rational HD and surface charge could rapidly and selectively recognize small metastatic tumors (∼1 mm) in liver and lung with high signal-to-noise ratios of 4.6 and 4.5, respectively. These results help further understand the in vivo transport of nanoprobes and provide guidance for design of translatable nanosized nanomedicines in cancer metastasis theranostics.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Nanoparticle-Based Drug Delivery · Advanced biosensing and bioanalysis techniques

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

Affiliations

Key Laboratory of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640, China

Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China

Funding

National Natural Science Foundation of China · Guangzhou Science and Technology Project · Guangdong Natural Science Funds for Distinguished Young Scholars

References (36)

Show source-provided references
1. 10.1038/nrc.2016.2510.1038/nrc.2016.25 ↗
2. 10.1038/nature2079110.1038/nature20791 ↗
3. 10.1021/acs.chemrev.5b0010010.1021/acs.chemrev.5b00100 ↗
4. 10.1002/anie.20180784710.1002/anie.201807847 ↗
5. 10.1021/acsnano.9b0999110.1021/acsnano.9b09991 ↗
6. 10.1021/jacs.9b1101310.1021/jacs.9b11013 ↗
7. 10.1038/s41467-017-00153-y10.1038/s41467-017-00153-y ↗
8. 10.1002/anie.20190564310.1002/anie.201905643 ↗
9. 10.1002/anie.20200094710.1002/anie.202000947 ↗
10. 10.1002/anie.20130446510.1002/anie.201304465 ↗
11. 10.1002/adma.20190260410.1002/adma.201902604 ↗
12. 10.1002/adma.20200005510.1002/adma.202000055 ↗
13. 10.1038/s41467-020-14972-z10.1038/s41467-020-14972-z ↗
14. 10.1002/adma.20200117210.1002/adma.202001172 ↗
15. 10.1002/adma.20120229610.1002/adma.201202296 ↗
16. 10.1021/acsnano.0c0026910.1021/acsnano.0c00269 ↗
17. 10.1021/ja401612x10.1021/ja401612x ↗
18. 10.1016/j.mattod.2013.11.00310.1016/j.mattod.2013.11.003 ↗
19. 10.1002/anie.20141029510.1002/anie.201410295 ↗
20. 10.1038/nbt134010.1038/nbt1340 ↗
21. 10.1038/s41578-018-0038-310.1038/s41578-018-0038-3 ↗
22. 10.1002/adma.20140086610.1002/adma.201400866 ↗
23. 10.1016/j.nucmedbio.2008.12.01110.1016/j.nucmedbio.2008.12.011 ↗
24. 10.1126/scitranslmed.300952410.1126/scitranslmed.3009524 ↗
25. 10.1021/acsnano.8b0810310.1021/acsnano.8b08103 ↗
26. 10.1002/adom.20170132410.1002/adom.201701324 ↗
27. 10.1002/anie.20161264710.1002/anie.201612647 ↗
28. 10.1021/acsami.6b0505710.1021/acsami.6b05057 ↗
29. 10.1021/acsnano.5b0720010.1021/acsnano.5b07200 ↗
30. 10.1038/natrevmats.2016.1410.1038/natrevmats.2016.14 ↗
31. 10.1038/nnano.2016.7210.1038/nnano.2016.72 ↗
32. 10.1007/s11095-013-1142-010.1007/s11095-013-1142-0 ↗
33. 10.1021/acsnano.9b0143610.1021/acsnano.9b01436 ↗
34. 10.1021/jacs.8b1202610.1021/jacs.8b12026 ↗
35. 10.1111/j.1751-1097.1999.tb08277.x10.1111/j.1751-1097.1999.tb08277.x ↗
36. 10.1186/1471-2407-8-22810.1186/1471-2407-8-228 ↗