journal article·2015-06-03

Graphene Oxide Based Nanocarrier Combined with a pH-Sensitive Tracer: A Vehicle for Concurrent pH Sensing and pH-Responsive Oligonucleotide Delivery

Chia-Jung Hsieh, Yu-Cheng Chen, Pei-Ying Hsieh, Shi-Rong Liu, Shu-Pao Wu, You-Zung Hsieh, Hsin-Yun Hsu

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Abstract

We chemically tuned the oxidation status of graphene oxide (GO) and constructed a GO-based nanoplatform combined with a pH-sensitive fluorescence tracer that is designed for both pH sensing and pH-responsive drug delivery. A series of GOs oxidized to distinct degrees were examined to optimize the adsorption of the model drug, poly dT30. We determined that highly oxidized GO was a superior drug-carrier candidate in vitro when compared to GOs oxidized to lesser degrees. In the cell experiment, the synthesized pH-sensitive rhodamine dye was first applied to monitor cellular pH; under acidic conditions, protonated rhodamine fluoresces at 588 nm (λex=561 nm). When the dT30-GO nanocarrier was introduced into cells, a rhodamine-triggered competition reaction occurred, and this led to the release of the oligonucleotides and the quenching of rhodamine fluorescence by GO. Our results indicate high drug loading (FAM-dT30/GO=25/50 μg/mL) and rapid cellular uptake (<0.5 h) of the nanocarrier which can potentially be used for targeted RNAi delivery to the acidic milieu of tumors.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Graphene and Nanomaterials Applications · Advanced biosensing and bioanalysis techniques · Carbon and Quantum Dots Applications

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

Affiliations

Department of Applied Chemistry, ‡Center for Interdisciplinary Science (CIS), and §Institute of Molecular Science, National Chiao-Tung University, No. 1001 Ta-Hsueh Road, Hsinchu 30010, Taiwan

Funding

Ministry of Science and Technology, Taiwan · Ministry of Education, Taiwan

References (39)

Show source-provided references
1. Yang Z. · Cancer Gene Ther. · 2007 · 14 · 59910.1038/sj.cgt.7701054 ↗
2. Naldini L. · Science · 1996 · 272 · 26310.1126/science.272.5259.263 ↗
3. Zhang L. · Small · 2010 · 6 · 53710.1002/smll.200901680 ↗
4. Choi D. · Analyst · 2014 · 139 · 133110.1039/c3an02197a ↗
5. Sun X. · Nano Res. · 2008 · 1 · 20310.1007/s12274-008-8021-8 ↗
6. Lin D. · Anal. Chem. · 2012 · 84 · 366210.1021/ac3001435 ↗
7. Lu C.-H. · Chem. Commun. (Cambridge, U. K.) · 2010 · 46 · 311610.1039/b926893f ↗
8. Tang Z. · Small · 2010 · 6 · 120510.1002/smll.201000024 ↗
9. Feng L. · Nanoscale · 2011 · 3 · 125210.1039/c0nr00680g ↗
10. Chen B. · J. Mater. Chem. · 2011 · 21 · 773610.1039/c1jm10341e ↗
11. Kim H. · Small · 2014 · 10 · 11710.1002/smll.201202636 ↗
12. Stubbs M. · Mol. Med. Today · 2000 · 6 · 1510.1016/S1357-4310(99)01615-9 ↗
13. Yu J. · Chem. Commun. (Cambridge, U. K.) · 2014 · 50 · 1161410.1039/C4CC03984J ↗
14. Goenka S. · J. Controlled Release · 2014 · 173 · 7510.1016/j.jconrel.2013.10.017 ↗
15. He X. · Ther. Delivery · 2013 · 4 · 149910.4155/tde.13.120 ↗
16. Yang X. · J. Mater. Chem. · 2011 · 21 · 344810.1039/C0JM02494E ↗
17. Kavitha T. · Phys. Chem. Chem. Phys. · 2013 · 15 · 517610.1039/c3cp00008g ↗
18. Fan X. · J. Mater. Chem. B · 2013 · 1 · 265810.1039/c3tb00493g ↗
19. Rana V. K. · Macromol. Mater. Eng. · 2011 · 296 · 13110.1002/mame.201000307 ↗
20. Tao C.-a. · J. Mater. Chem. · 2012 · 22 · 2485610.1039/c2jm34461k ↗
21. Zhu L. · Biosens. Bioelectron. · 2012 · 35 · 50710.1016/j.bios.2012.03.026 ↗
22. Wang X.-Y. · Biosens. Bioelectron. · 2013 · 48 · 12010.1016/j.bios.2013.04.003 ↗
23. Song Y. · Adv. Mater. · 2010 · 22 · 220610.1002/adma.200903783 ↗
24. Chang H. · Anal. Chem. · 2010 · 82 · 234110.1021/ac9025384 ↗
25. Song J. · ACS Appl. Mater. Interfaces · 2014 · 6 · 2180610.1021/am502138n ↗
26. Viraka Nellore B. P. · Bioconjugate Chem. · 2015 · 26 · 23510.1021/bc500503e ↗
27. Chen R. J. · J. Phys. Chem. B · 2006 · 110 · 5410.1021/jp055044e ↗
28. Liu S.-R. · Sens. Actuators, B · 2012 · 171 · 111010.1016/j.snb.2012.06.041 ↗
29. Hummers W. S. · J. Am. Chem. Soc. · 1958 · 80 · 133910.1021/ja01539a017 ↗
30. Premkumar T. · Prog. Polym. Sci. · 2012 · 37 · 51510.1016/j.progpolymsci.2011.08.003 ↗
31. Park J. S. · Analyst · 2013 · 138 · 174510.1039/c3an36493c ↗
32. Wu M. · Langmuir · 2011 · 27 · 273110.1021/la1037926 ↗
33. Chen X. · Chem. Rev. · 2011 · 112 · 191010.1021/cr200201z ↗
34. Li S. · ACS Appl. Mater. Interfaces · 2012 · 4 · 706910.1021/am302704a ↗
35. Wang Y. · J. Am. Chem. Soc. · 2010 · 132 · 927410.1021/ja103169v ↗
36. Hong B. J. · Small · 2012 · 8 · 246910.1002/smll.201200264 ↗
37. Tan X. · Anal. Chem. · 2012 · 84 · 862210.1021/ac301657f ↗
38. Liu Z. · J. Am. Chem. Soc. · 2008 · 130 · 1087610.1021/ja803688x ↗
39. Chen T.-T. · J. Am. Chem. Soc. · 2015 · 137 · 98210.1021/ja511988w ↗