A convenient, bio-inspired approach to the synthesis of multi-functional, stable fluorescent silica nanoparticles using poly(ethylene-imine)
Source abstract
Abstract
Branched poly(ethylene-imine) can be tagged with luminescent dyes (e.g., fluorescein isothiocyanate and tetramethylrhodamine isothiocyanate) and used to precipitate spherical silica particles from 10s-to-100s of nm diameter size under mild conditions. These dye–PEI/SiO2 nanoparticles are highly compatible with polar solvents to give bright fluorescent suspensions, and detailed photophysical characterization reveals well-separated dye moieties with an approximately homogeneous dispersion of dye–PEI conjugate throughout the SiO2 matrix. Reaction of PEI amine groups incorporated at the particle surface affords a simple method for post-synthesis functionalization of these materials, and the formation of FITC/Eosin-Y fluorescence resonance energy transfer pair-tagged particles and SiO2@Au core–shell nanocomposites using this strategy is demonstrated. This bio-inspired approach to multi-functional SiO2 nanoparticles provides a range of potential advantages over traditional “inorganic” syntheses of similar materials, as it proceeds through a scalable, single-step reaction using inexpensive reagents, enables efficient incorporation of luminescent species into the resulting particles with very limited dye aggregation, and provides nanoparticles that do not require post-synthesis modification for further conjugation with species of interest. The method offers a simple means to generate complex nanocomposites, whereby a host of desired species can be incorporated both inside and on the surface of biocompatible SiO2 nanoparticles.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Diatoms and Algae Research · Advanced biosensing and bioanalysis techniques · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (55)
Show source-provided references
1. B. R. Masters , The Development of Fluorescence Microscopy, in Encyclopedia of Life Sciences (ELS), John Wiley & Sons, Chichester, 2010
2. J. R. Lackowicz , Principles of Fluorescence Spectroscopy, Springer, New York, 3rd edn, 200610.1007/978-0-387-46312-4 ↗
3. B. A. Kairdolf , A. M.Smith, T. H.Stokes, M. D.Wang, A. N.Young and S. M.Nie, in Annual Review of Analytical Chemistry, ed. R. G. Cooks and J. E. Pemberton, Annual Reviews, Palo Alto, 2013, vol. 6, pp. 143–162
4. Wegner · Chem. Soc. Rev. · 2015 · 44 · 479210.1039/C4CS00532E ↗
5. S. M. Borisov , T.Mayr, G.Mistlberger and I.Klimant, Dye-Doped Polymeric Particles for Sensing and Imaging, in Advanced Fluorescence Reporters in Chemistry and Biology II: Molecular Constructions, Polymers and Nanoparticles, Springer-Verlag, Berlin-Heidelberg, 2010, pp. 194–228
6. Tan · Med. Res. Rev. · 2004 · 24 · 62110.1002/med.20003 ↗
7. Tang · Adv. Mater. · 2012 · 24 · 150410.1002/adma.201104763 ↗
8. Montalti · Chem. Soc. Rev. · 2014 · 43 · 424310.1039/C3CS60433K ↗
9. Zhao · Adv. Mater. · 2004 · 16 · 17310.1002/adma.200305622 ↗
10. Wang · Nano Res. · 2008 · 1 · 9910.1007/s12274-008-8018-3 ↗
11. van Blaaderen · Langmuir · 1992 · 8 · 292110.1021/la00048a013 ↗
12. van Blaaderen · J. Colloid Interface Sci. · 1992 · 154 · 48110.1016/0021-9797(92)90163-G ↗
13. Imhof · J. Phys. Chem. B · 1999 · 103 · 140810.1021/jp983241q ↗
14. Nyffenegger · J. Colloid Interface Sci. · 1993 · 159 · 15010.1006/jcis.1993.1306 ↗
15. Ow · Nano Lett. · 2005 · 5 · 11310.1021/nl0482478 ↗
16. E. Herz , A.Burns, S.Lee, P.Sengupta, D.Bonner, H.Ow, C.Liddell, B.Baird and U.Wiesner, in Colloidal Quantum Dots for Biomedical Applications, ed. M. Osinski, K. Yamamoto and T. M. Jovin, Spie-Int Soc Optical Engineering, Bellingham, 2006, vol. 609610.1117/12.661782 ↗
17. Burns · Chem. Soc. Rev. · 2006 · 35 · 102810.1039/B600562B ↗
18. Phillips · Sci. Transl. Med. · 2014 · 6 · 110.1126/scitranslmed.3009524 ↗
19. Stöber · J. Colloid Interface Sci. · 1968 · 26 · 6210.1016/0021-9797(68)90272-5 ↗
20. Sumper · Science · 2002 · 295 · 243010.1126/science.1070026 ↗
21. Davis · Curr. Opin. Solid State Mater. Sci. · 2003 · 7 · 27310.1016/j.cossms.2003.09.013 ↗
22. Dickerson · Chem. Rev. · 2008 · 108 · 493510.1021/cr8002328 ↗
23. N. Kröger and N.Poulsen, in Annual Review of Genetics, Annual Reviews, Palo Alto, 2008, vol. 42, pp. 83–107
24. Belton · FEBS J. · 2012 · 279 · 171010.1111/j.1742-4658.2012.08531.x ↗
25. Kröger · Wiley Interdiscip. Rev.: Nanomed. Nanobiotechnol. · 2014 · 6 · 615
26. Bauer · Small · 2007 · 3 · 5810.1002/smll.200600352 ↗
27. Neville · Langmuir · 2011 · 27 · 27910.1021/la1033492 ↗
28. Neville · J. Chem. Educ. · 2012 · 89 · 94010.1021/ed200684s ↗
29. Kröger · Science · 2002 · 298 · 58410.1126/science.1076221 ↗
30. Duff · Langmuir · 1993 · 9 · 230110.1021/la00033a010 ↗
31. Nune · Expert Opin. Drug Delivery · 2009 · 6 · 117510.1517/17425240903229031 ↗
32. Salvati · Nanomedicine · 2015 · 10 · 349510.2217/nnm.15.180 ↗
33. He · Nanotechnology · 2008 · 19 · 7
34. Choosakoonkriang · J. Pharm. Sci. · 2003 · 92 · 171010.1002/jps.10437 ↗
35. Bagwe · Langmuir · 2004 · 20 · 833610.1021/la049137j ↗
36. Kim · Chem. Mater. · 2007 · 19 · 565010.1021/cm071273x ↗
37. Sumper · Angew. Chem., Int. Ed. · 2003 · 42 · 519210.1002/anie.200352212 ↗
38. Brunner · Phys. Chem. Chem. Phys. · 2004 · 6 · 85410.1039/b313261g ↗
39. Rodriguez · Biomacromolecules · 2004 · 5 · 26110.1021/bm034232c ↗
40. Bernecker · J. Am. Chem. Soc. · 2010 · 132 · 102310.1021/ja9061163 ↗
41. Neville · Langmuir · 2013 · 29 · 1468110.1021/la403040u ↗
42. Han · Nanoscale · 2015 · 7 · 1203810.1039/C5NR01407G ↗
43. Jakhmola · Adv. Healthcare Mater. · 2015 · 4 · 268810.1002/adhm.201500588 ↗
44. Pinheiro · Materials · 2013 · 6 · 321310.3390/ma6083213 ↗
45. Klonis · Photochem. Photobiol. · 2003 · 77 · 50210.1562/0031-8655(2003)077<0502:TTGMTF>2.0.CO;2 ↗
46. Martin · J. Lumin.. · 1975 · 10 · 38110.1016/0022-2313(75)90003-4 ↗
47. B. Valeur , Molecular Fluorescence: Principles and Applications, Wiley-VCH Verlag GmbH, Weinheim, 200110.1002/3527600248 ↗
48. Alvarez-Pez · J. Phys. Chem. A · 2001 · 105 · 632010.1021/jp010372+ ↗
49. Swindlehurst · Biophys. J. · 1991 · 59 · 61910.1016/S0006-3495(91)82277-9 ↗
50. Rodrigues · J. Phys. Chem. B · 2013 · 117 · 1410810.1021/jp408616r ↗
51. Arbeloa · J. Chem. Soc., Faraday Trans. 2 · 1981 · 77 · 173510.1039/F29817701735 ↗
52. Burns · Small · 2006 · 2 · 72310.1002/smll.200600017 ↗
53. Neville · Collids Surf. A · 2013 · 431 · 4210.1016/j.colsurfa.2013.04.022 ↗
54. Bohlen · Arch. Biochem. Biophys. · 1973 · 155 · 21310.1016/S0003-9861(73)80023-2 ↗
55. Alvarez · J. Phys. Chem. B · 1997 · 101 · 370610.1021/jp962922n ↗