Multivariable Response of Semiconductor Nanocrystal-Dye Sensors: The Case of pH
Source abstract
Abstract
Emissive semiconductor nanocrystals can be efficient FRET donors to chemically responsive organic fluorophores; conjugating the two creates a ratiometric (or self-calibrating) sensor. Given that the organic component engenders chemical and/or biological sensitivity, it is natural to assume that the NC−dye response is reflective of the photochemical properties of the neat dye. In the case of a pH sensor like fluorescein, the dye emission can be analytically described by the Henderson−Hasselbalch equation. Our research demonstrates that the ratiometric sensing response of CdS/ZnS−fluorescein pH sensors, however, does not directly reflect the Henderson−Hasselbalch relationship and is difficult to predict. The reasons for this complexity are the alternations of the dye microenvironment within the nanoscale architecture and the nature of energy transfer from the NC donor to the acceptor dye.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Advanced biosensing and bioanalysis techniques · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061, United States
References (48)
Show source-provided references
1. Zhang F. · Anal. Bioanal. Chem · 2010 · 397 · 93510.1007/s00216-010-3609-8 ↗
2. Somers R. C. · Chem. Soc. Rev. · 2007 · 36 · 57910.1039/b517613c ↗
3. Willard D. M. · Anal. Bioanal. Chem · 2006 · 384 · 56410.1007/s00216-005-0250-z ↗
4. Medintz I. L. · Nat. Mater. · 2005 · 4 · 43510.1038/nmat1390 ↗
5. Bruchez M. · Science · 1998 · 281 · 201310.1126/science.281.5385.2013 ↗
6. Chan W. C. W. · Science · 1998 · 281 · 201610.1126/science.281.5385.2016 ↗
7. Bharali D. J. · J. Am. Chem. Soc. · 2005 · 127 · 1136410.1021/ja051455x ↗
8. Kim S. W. · J. Am. Chem. Soc. · 2005 · 127 · 1052610.1021/ja0434331 ↗
9. Pradhan N. · Nano Lett. · 2007 · 7 · 31210.1021/nl062336y ↗
10. Michalet X. · Science · 2005 · 307 · 53810.1126/science.1104274 ↗
11. Delehanty J. B. · Anal. Bioanal. Chem. · 2009 · 393 · 109110.1007/s00216-008-2410-4 ↗
12. Derfus A. M. · Adv. Mater. · 2004 · 16 · 96110.1002/adma.200306111 ↗
13. Medintz I. L. · Bioconjugate Chem. · 2008 · 19 · 178510.1021/bc800089r ↗
14. Rozenzhak S. M. · Chem. Commun. · 2005 · 221710.1039/b418454h ↗
15. Yezhelyev M. V. · J. Am. Chem. Soc. · 2008 · 130 · 900610.1021/ja800086u ↗
16. Delehanty J. B. · Integr. Biol. · 2010 · 2 · 26510.1039/c0ib00002g ↗
17. Hines M. A. · J. Phys. Chem. · 1996 · 100 · 46810.1021/jp9530562 ↗
18. Dabbousi B. O. · J. Phys. Chem. B · 1997 · 101 · 946310.1021/jp971091y ↗
19. Grynkiewicz G. · J. Biol. Chem. · 1985 · 260 · 344010.1016/S0021-9258(19)83641-4 ↗
20. Rink T. J. · FEBS Lett. · 1982 · 148 · 2110.1016/0014-5793(82)81234-9 ↗
21. Rink T. J. · J. Cell Biol. · 1982 · 95 · 18910.1083/jcb.95.1.189 ↗
22. Burdette S. C. · Proc. Natl. Acad. Sci., U. S. A. · 2003 · 100 · 360510.1073/pnas.0637711100 ↗
23. Domaille D. W. · J. Am. Chem. Soc. · 2010 · 132 · 119410.1021/ja907778b ↗
24. Willard D. M. · Nano Lett. · 2001 · 1 · 46910.1021/nl015565n ↗
25. Snee P. T. · J. Am. Chem. Soc. · 2006 · 128 · 1332010.1021/ja0618999 ↗
26. Goldman E. R. · J. Am. Chem. Soc. · 2005 · 127 · 674410.1021/ja043677l ↗
27. Medintz I. L. · Nat. Mater. · 2003 · 2 · 63010.1038/nmat961 ↗
28. Förster T. · Ann. Phys. · 1948 · 437 · 5510.1002/andp.19484370105 ↗
29. Zhong X. H. · J. Am. Chem. Soc. · 2003 · 125 · 1355910.1021/ja036683a ↗
30. Steckel J. S. · Angew. Chem., Int. Ed. · 2004 · 43 · 215410.1002/anie.200453728 ↗
31. Chen Y. · J. Am. Chem. Soc. · 2008 · 130 · 374410.1021/ja711252n ↗
32. Shen H. Y. · ACS Nano · 2009 · 3 · 91510.1021/nn800870r ↗
33. Medintz I. L. · Nano Lett. · 2007 · 7 · 174110.1021/nl070782v ↗
34. Haughland R. P. · 2005
35. Chiefari J. · Macromolecules · 1998 · 31 · 555910.1021/ma9804951 ↗
36. Bogert M. T. · J. Am. Chem. Soc. · 1905 · 27 · 131010.1021/ja01988a015 ↗
37. McKinney R. M. · J. Org. Chem. · 1962 · 27 · 398610.1021/jo01058a055 ↗
38. Haugland, R. P.Fluorescent labeling reagents containing the fluorescein and eosin chromophores. U.S. Patent 4,213,904, July 22, 1980.
39. Lavis L. D. · Anal. Chem. · 2007 · 79 · 677510.1021/ac070907g ↗
40. Henderson L. J. · Am. J. Physiol. · 1905 · 21 · 17310.1152/ajplegacy.1908.21.2.173 ↗
41. Hasselbalch K. A. · Biochemische Zeitschrift · 1917 · 78 · 112
42. Pellegrino T. · Nano Lett. · 2004 · 4 · 70310.1021/nl035172j ↗
43. Wu X. Y. · Nat. Biotechnol. · 2003 · 21 · 4110.1038/nbt764 ↗
44. Elliott J. E. · Polymer · 2004 · 45 · 150310.1016/j.polymer.2003.12.040 ↗
45. Pons T. · Nano Lett. · 2007 · 7 · 315710.1021/nl071729+ ↗
46. Sjoback R. · Spectrochim. Acta, Part A · 1995 · 51 · L710.1016/0584-8539(95)01421-P ↗
47. Smith A. M. · J. Am. Chem. Soc. · 2008 · 130 · 1127810.1021/ja804306c ↗
48. Liu W. H. · J. Am. Chem. Soc. · 2010 · 132 · 47210.1021/ja908137d ↗