journal article·2014-05-28

Vitamin B1 Derived Blue and Green Fluorescent Carbon Nanoparticles for Cell-Imaging Application

Susanta Kumar Bhunia, Nibedita Pradhan, Nikhil R. Jana

Publisher page

Abstract

A carbon-based fluorescent nanoparticle is considered to be a new generation nontoxic nanoprobe suitable for various bioimaging and sensing applications. However, the synthesis of such a high-quality nanoparticle is challenging, and its application potential is mostly unexplored. Here we report a vitamin B1 carbonization-based approach for blue and green fluorescent carbon nanoparticles of <10 nm size with a fluorescence quantum of up to 76%. We found that carbonization of vitamin B1 in the presence of phosphate salt at ∼90-130 °C for about 2 h produces highly fluorescent carbon nanoparticles of 1-6 nm size. The particle size and fluorescence property can be controlled by varying the reaction temperature and nature of phosphate salt. Elemental analysis shows the incorporation of a large percentage (up to 48 wt %) of other elements (such as nitrogen, oxygen, phophorus, and sulfur) in the carbon matrix. The chemical structure of vitamin B1 (thiamine) is unique in a sense that it consists of a large number of heteroatoms along with unsaturated bonds and offers low-temperature carbonization with the formation of a nanoparticle having an optimum ratio of sp(2) and sp(3) carbon atoms. These carbon nanoparticles have high colloidal stability and stable fluorescence and have been used as fluorescent imaging probes.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Carbon and Quantum Dots Applications · Electrochemical sensors and biosensors · Luminescence and Fluorescent Materials

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

Affiliations

Centre for Advanced Materials, Indian Association for the Cultivation of Science, Kolkata 700032, India

References (53)

Show source-provided references
1. Baker S. N. · Angew. Chem., Int. Ed. · 2010 · 49 · 672610.1002/anie.200906623 ↗
2. Cao L. · J. Am. Chem. Soc. · 2007 · 129 · 1131810.1021/ja073527l ↗
3. Yang S. T. · J. Am. Chem. Soc. · 2009 · 131 · 1130810.1021/ja904843x ↗
4. Michalet X. · Science · 2005 · 307 · 53810.1126/science.1104274 ↗
5. Peng Z. A. · J. Am. Chem. Soc. · 2001 · 123 · 18310.1021/ja003633m ↗
6. Medintz I. L. · Nat. Mater. · 2005 · 4 · 43510.1038/nmat1390 ↗
7. Pelley J. L. · Toxicol. Sci. · 2009 · 112 · 27610.1093/toxsci/kfp188 ↗
8. Tasis D. · Chem. Rev. · 2006 · 106 · 110510.1021/cr050569o ↗
9. Diederich F. · Science · 1996 · 271 · 31710.1126/science.271.5247.317 ↗
10. Dreyer D. R. · Chem. Soc. Rev. · 2010 · 39 · 22810.1039/B917103G ↗
11. Zhang X. Q. · Nanoscale · 2013 · 5 · 14710.1039/C2NR32698A ↗
12. Zhang X. Q. · Polym. Chem. · 2013 · 4 · 506010.1039/c3py00860f ↗
13. Zhang X. Q. · Colloid Surf. B · 2013 · 112 · 8110.1016/j.colsurfb.2013.07.052 ↗
14. Zhang X. Q. · Polym. Chem. · 2014 · 5 · 31810.1039/C3PY01143G ↗
15. Zhang X. Q. · Polym. Chem. · 2014 · 5 · 68310.1039/C3PY01348K ↗
16. Zhang X. Q. · J. Mater. Chem. C · 2014 · 2 · 81610.1039/C3TC31852D ↗
17. Zhang X. Y. · ACS Appl. Mater. Interfaces · 2013 · 5 · 194310.1021/am302512u ↗
18. Zhang X. Y. · Polym. Chem. · 2013 · 4 · 431710.1039/c3py00712j ↗
19. Zhang X. Y. · RSC Adv. · 2013 · 3 · 963310.1039/c3ra41578c ↗
20. Das P. · Nanoscale · 2013 · 5 · 573210.1039/c3nr00932g ↗
21. Palmal S. · Chem.—Eur. J. · 2013 · 19 · 94310.1002/chem.201203083 ↗
22. Maity A. R. · Nanoscale · 2013 · 5 · 550610.1039/c3nr00549f ↗
23. Li H. T. · Angew. Chem., Int. Ed. · 2010 · 49 · 443010.1002/anie.200906154 ↗
24. Suda Y. · Thin Solid Films · 2002 · 415 · 1510.1016/S0040-6090(02)00532-1 ↗
25. Liu H. P. · Angew. Chem., Int. Ed. · 2007 · 46 · 647310.1002/anie.200701271 ↗
26. Fortunato M. E. · Chem. Mater. · 2010 · 22 · 161010.1021/cm100075j ↗
27. Yang Z. C. · Chem. Commun. · 2011 · 47 · 1161510.1039/c1cc14860e ↗
28. Zhu H. · Chem. Commun. · 2009 · 511810.1039/b907612c ↗
29. Bhunia S. K. · Sci. Rep. · 2013 · 3 · 147310.1038/srep01473 ↗
30. Pan D. Y. · Chem. Commun. · 2010 · 46 · 368110.1039/c000114g ↗
31. Liu R. L. · Angew. Chem., Int. Ed. · 2009 · 48 · 459810.1002/anie.200900652 ↗
32. Wang X. H. · J. Mater. Chem. · 2011 · 21 · 244510.1039/c0jm02963g ↗
33. Jiang J. · Chem. Commun. · 2012 · 48 · 963410.1039/c2cc34612e ↗
34. Wei W. · Sci. Rep. · 2014 · 4 · 356410.1038/srep03564 ↗
35. Yang Z. C. · Carbon · 2011 · 49 · 520710.1016/j.carbon.2011.07.038 ↗
36. Sun Y. P. · J. Am. Chem. Soc. · 2006 · 128 · 775610.1021/ja062677d ↗
37. Ray S. C. · J. Phys. Chem. C · 2009 · 113 · 1854610.1021/jp905912n ↗
38. Felten A. · J. Nanotechnol. · 2006 · 17 · 195410.1088/0957-4484/17/8/026 ↗
39. Choi H. C. · J. Phys. Chem. B · 2005 · 109 · 168310.1021/jp046098b ↗
40. Kapteijn F. · Carbon · 1999 · 37 · 114310.1016/S0008-6223(98)00312-1 ↗
41. Baltrusaitis J. · Phys. Chem. Chem. Phys. · 2009 · 11 · 829510.1039/b907584d ↗
42. Yue Z. R. · Carbon · 1999 · 37 · 178510.1016/S0008-6223(99)00047-0 ↗
43. Laszlo K. · Carbon · 2001 · 39 · 121710.1016/S0008-6223(00)00245-1 ↗
44. Thomas L. C. · Spectrochim. Acta · 1964 · 20 · 46710.1016/0371-1951(64)80043-6 ↗
45. Zhou J. · RSC Adv. · 2014 · 4 · 546510.1039/c3ra45294h ↗
46. Maity A. R. · J. Phys. Chem. C · 2011 · 115 · 13710.1021/jp108828c ↗
47. Oyewumi M. O. · Bioconjugate Chem. · 2003 · 14 · 40410.1021/bc0340013 ↗
48. Derfus A. M. · Nano Lett. · 2004 · 4 · 1110.1021/nl0347334 ↗
49. Thornalley P. J. · Curr. Diabetes Rev. · 2005 · 1 · 28710.2174/157339905774574383 ↗
50. Meador K. · J. Geriatr. Psych. Neurol. · 1993 · 6 · 22210.1177/089198879300600408 ↗
51. Mimori Y. · Metab. Brain Dis. · 1996 · 11 · 8910.1007/BF02080934 ↗
52. Shils M. E. · 2006
53. Stanbury J. B. · 1983