journal article·2019-03-13

Polyelectrolyte-Mediated Nontoxic AgGaxIn1–xS2 QDs/Low-Density Lipoprotein Nanoprobe for Selective 3D Fluorescence Imaging of Cancer Stem Cells

Jiangluqi Song, Yan Zhang, Yiwen Dai, Jinhang Hu, Lixin Zhu, Xiaoliang Xu, Yue Yu, Huan Li, Bo Yao, Huixin Zhou

ACS Applied Materials & Interfaces· Volume 11· Issue 10
Publisher page

Abstract

Cancer stem cells, which are a population of cancer cells sharing common properties with normal stem cells, have strong self-renewal ability and multi-lineage differentiation potential to trigger tumor proliferation, metastases, and recurrence. From this, targeted therapy for cancer stem cells may be one of the most promising strategies for comprehensive treatment of tumors in the future. We design a facile approach to establish the colon cancer stem cells-selective fluorescent probe based on the low-density lipoprotein (LDL) and the novel AgGaxIn(1–x)S2 quantum dots (AGIS QDs). The AGIS QDs with a high crystallinity are obtained for the first time via cation-exchange protocol of Ga3+ to In3+ starting from parent AgInS2 QDs. Photoluminescence peak of AGIS QDs can be turned from 502 to 719 nm by regulating the reaction conditions, with the highest quantum yield up to 37%. Subsequently, AGIS QDs-conjugated LDL nanocomposites (NCs) are fabricated, in which a cationic polyelectrolyte was used as a coupling reagent to guarantee the electrostatic self-assembly. The structural integrity and physicochemical properties of the LDL–QDs NCs are found to be maintained in vitro, and the NCs exhibit remarkable biocompatibility. The LDL–QDs can be selectively delivered into cancer stem cells that overexpress LDL receptor, and three-dimensional imaging of cancer stem cells is realized. The results of this study not only demonstrate the versatility of nature-derived lipoprotein nanoparticles, but also confirm the feasibility of electrostatic conjugation using cationic polyelectrolyte, allowing reseachers to design nanoarchitectures for targeted diagnosis and treatment of cancer.
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Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Advanced biosensing and bioanalysis techniques · Nanocluster Synthesis and Applications

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

Affiliations

School of Physics and Optoelectronic Engineering, Xidian University, Xi’an 710071, China

Central Laboratory, First Affiliated Hospital of Anhui Medical University, Hefei 230022, China

Department of General Surgery, The Second Hospital of Anhui Medical University, Hefei 230601, China

Shaanxi Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Shaanxi University of Chinese Medicine, Xianyang 712046, China

Key Laboratory of Strongly-Coupled Quantum Matter Physics, Chinese Academy of Sciences, and Department of Physics, University of Science and Technology of China, Hefei, Anhui 230026, China

Funding

National Natural Science Foundation of China · State Administration of Foreign Experts Affairs · Natural Science Foundation of Shaanxi Province · Ministry of Education of the People's Republic of China

References (50)

Show source-provided references
1. 10.1038/nrc.2017.8810.1038/nrc.2017.88 ↗
2. 10.1038/nature2330210.1038/nature23302 ↗
3. 10.1038/ncb271710.1038/ncb2717 ↗
4. 10.1016/j.pharmthera.2013.01.01410.1016/j.pharmthera.2013.01.014 ↗
5. 10.1016/j.drudis.2016.03.00410.1016/j.drudis.2016.03.004 ↗
6. 10.1021/acs.chemrev.8b0034010.1021/acs.chemrev.8b00340 ↗
7. 10.1002/adfm.20177022010.1002/adfm.201770220 ↗
8. 10.1039/C7CS00219J10.1039/C7CS00219J ↗
9. 10.1021/acsami.6b1391110.1021/acsami.6b13911 ↗
10. 10.1002/adma.20180530810.1002/adma.201805308 ↗
11. 10.1016/j.biomaterials.2018.03.05410.1016/j.biomaterials.2018.03.054 ↗
12. 10.1039/C1CS15188F10.1039/C1CS15188F ↗
13. 10.1038/s41565-018-0147-610.1038/s41565-018-0147-6 ↗
14. 10.1016/j.addr.2016.04.02010.1016/j.addr.2016.04.020 ↗
15. 10.1038/s41598-017-00685-910.1038/s41598-017-00685-9 ↗
16. 10.1021/nn403258w10.1021/nn403258w ↗
17. 10.1039/C7CS00492C10.1039/C7CS00492C ↗
18. Krieger, M. In Methods Enzymology; Academic Press, 1986; Vol. 128, pp 608–613.10.1016/0076-6879(86)28094-5 ↗
19. 10.1021/acs.chemrev.6b0029010.1021/acs.chemrev.6b00290 ↗
20. 10.1002/anie.20180149510.1002/anie.201801495 ↗
21. 10.1021/acs.chemrev.6b0016910.1021/acs.chemrev.6b00169 ↗
22. 10.1002/adma.20160443610.1002/adma.201604436 ↗
23. 10.1016/j.aquatox.2007.11.01310.1016/j.aquatox.2007.11.013 ↗
24. 10.1021/cm903602310.1021/cm9036023 ↗
25. 10.1021/jp046481g10.1021/jp046481g ↗
26. 10.1021/acs.analchem.8b0000610.1021/acs.analchem.8b00006 ↗
27. 10.1063/1.310376810.1063/1.3103768 ↗
28. 10.1039/C4RA05677A10.1039/C4RA05677A ↗
29. 10.1021/jp207711p10.1021/jp207711p ↗
30. 10.1021/acsami.5b0066410.1021/acsami.5b00664 ↗
31. 10.1039/c4cc01778a10.1039/c4cc01778a ↗
32. 10.1039/c3nr04765b10.1039/c3nr04765b ↗
33. 10.1172/JCI10318210.1172/JCI103182 ↗
34. 10.1021/ja017002j10.1021/ja017002j ↗
35. 10.1021/jp405989z10.1021/jp405989z ↗
36. 10.1021/acsami.6b0776810.1021/acsami.6b07768 ↗
37. Haynes W. M. · 2012
38. 10.1021/nn505786d10.1021/nn505786d ↗
39. 10.1021/jp201118310.1021/jp2011183 ↗
40. 10.1021/ic502600u10.1021/ic502600u ↗
41. 10.1088/0957-4484/24/5/05570610.1088/0957-4484/24/5/055706 ↗
42. 10.1039/C6TB02297A10.1039/C6TB02297A ↗
43. 10.1126/science.110375510.1126/science.1103755 ↗
44. 10.1016/j.commatsci.2005.12.04310.1016/j.commatsci.2005.12.043 ↗
45. 10.1021/jp309202g10.1021/jp309202g ↗
46. 10.1021/nl404606910.1021/nl4046069 ↗
47. 10.1039/C2CS35241A10.1039/C2CS35241A ↗
48. 10.1016/j.memsci.2010.05.02110.1016/j.memsci.2010.05.021 ↗
49. 10.1002/anie.20170467410.1002/anie.201704674 ↗
50. 10.1042/bj256077510.1042/bj2560775 ↗