Stabilization of Neutral Polyfluorene in Aqueous Solution through Their Interaction with Phospholipids and Sol–Gel Encapsulation
Source abstract
Abstract
Interaction between poly[9,9-bis(6'-bromohexyl)-2,7-fluorene-co-alt-1,4-phenylene] (PFPBr2), a neutral conjugated polyfluorene which is completely insoluble in water, and zwitterionic phospholipids has been investigated in order to generate new fluorescent structures which are stable in aqueous media as a means of extending the biological applications of these kinds of polymers. Two types of differently shaped and composed fluorescent structures were identified and then isolated and characterized separately using different biophysical techniques. The first structure type, corresponding to liposomal complexes, showed a fluorescence band centered around 405 nm and maximum absorption at 345 nm, while the second, corresponding to polymer-phospholipid aggregates of variable sizes with lower lipid content, absorbed at longer wavelengths and displayed a well resolved fluorescence spectrum with a maximum centered at 424 nm. Both structures were stable in a large range of pH, and their fluorescence intensity remained practically unaltered for 10 days; it then began to decrease, which was probably because of aggregation. Encapsulation of these structures within the pores of a sol-gel matrix did not affect their fluorescent properties but increased their stability, avoiding further aggregation and subsequent precipitation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Conducting polymers and applications · Polydiacetylene-based materials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Instituto de Biología Molecular y Celular, Universidad Miguel Hernández de Elche, Edificio Torregaitán. Avda. de la Universidad s/n, Alicante 03202, Elche, Spain
References (39)
Show source-provided references
1. Gunes S. · Chem. Rev. · 2007 · 107 · 132410.1021/cr050149z ↗
2. Thomas S. W. · Chem. Rev. · 2007 · 107 · 133910.1021/cr0501339 ↗
3. Hoven C. · Adv. Mater. · 2008 · 20 · 379310.1002/adma.200800533 ↗
4. Scherf U. · Adv. Mater. · 2002 · 14 · 47710.1002/1521-4095(20020404)14:7<477::AID-ADMA477>3.0.CO;2-9 ↗
5. Grimsdale A. C. · Chem. Rev. · 2009 · 109 · 89710.1021/cr000013v ↗
6. Chochos C. L. · Prog. Polym. Sci. · 2011 · 36 · 132610.1016/j.progpolymsci.2011.04.003 ↗
7. An L. · Asian J. Chem. · 2009 · 4 · 119610.1002/asia.200900148 ↗
8. Tapia M. J. · Adv. Colloid Interface Sci. · 2010 · 158 · 9410.1016/j.cis.2009.09.001 ↗
9. Zhu C. · Chem. Rev. · 2012 · 112 · 468710.1021/cr200263w ↗
10. Jiang H. · Angew. Chem., Int. Ed. · 2009 · 48 · 430010.1002/anie.200805456 ↗
11. Scherf, U.; Neher, D.Polyfluorenes;Springer-Verlag:Heidelberg, Germany, 2008; p274.10.1007/978-3-540-68734-4 ↗
12. Liu B. · J. Am. Chem. Soc. · 2006 · 128 · 118810.1021/ja055382t ↗
13. Huang F. · Polymer · 2005 · 46 · 1201010.1016/j.polymer.2005.10.034 ↗
14. Mallavia R. · Bol. Soc. Esp. Ceram. Vidrio · 2004 · 43 · 32710.3989/cyv.2004.v43.i2.532 ↗
15. Liu B. · J. Am. Chem. Soc. · 2003 · 125 · 670510.1021/ja028961w ↗
16. Chen Q. · Biomacromolecules · 2010 · 11 · 1310.1021/bm901165n ↗
17. Burrows H. D. · Macromolecules · 2004 · 37 · 742510.1021/ma048780+ ↗
18. Farcas A. · Eur. Polym. J. · 2009 · 45 · 79510.1016/j.eurpolymj.2008.11.047 ↗
19. Tapia M. J. · Langmuir · 2006 · 22 · 1017010.1021/la0612217 ↗
20. Infante M. R. · Colloids Surf., A · 1997 · 123 · 4910.1016/S0927-7757(96)03793-4 ↗
21. Pérez L. · Prog. Colloid Polym. Sci. · 2004 · 123 · 210
22. Immordino M. L. · Int. J. Nanomed. · 2006 · 1 · 29710.2217/17435889.1.3.297 ↗
23. Mallavia R. · Proc. SPIE-Int. Soc. Opt. Eng. · 2007 · 6592 · 659213
24. Tapia M. J. · J. Phys. Chem. B · 2011 · 115 · 579410.1021/jp2010666 ↗
25. Mallavia R. · Macromolecules · 2005 · 38 · 318510.1021/ma0477955 ↗
26. Molina R. · Macromolecules · 2009 · 42 · 547110.1021/ma900850w ↗
27. Driessen A. J. · Proc. Natl. Acad. Sci. U.S.A. · 1985 · 82 · 755510.1073/pnas.82.22.7555 ↗
28. Yamamura H. · J. Appl. Microbiol. · 2003 · 95 · 67710.1046/j.1365-2672.2003.02025.x ↗
29. Martínez-Tomé M. J. · J. Fluoresc. · 2013 · 23 · 17110.1007/s10895-012-1130-5 ↗
30. Martínez-Tomé M. J. · Biomacromolecules · 2011 · 11 · 149410.1021/bm100123t ↗
31. Attar H. A. · J. Phys. Chem. B · 2007 · 111 · 1241810.1021/jp070827g ↗
32. Montilla F. · J. Phys. Chem. C · 2007 · 11 · 18045
33. Molina R. · Macromolecules · 2007 · 40 · 304210.1021/ma062013o ↗
34. Livage J. · J. Phys.: Condens. Matter · 2001 · 13 · R673
35. Pastor I. · J. Phys. Chem. B · 2007 · 111 · 1160310.1021/jp074790b ↗
36. Menaa B. · Int. J. Nanotechnol. · 2010 · 7 · 110.1504/IJNT.2010.029546 ↗
37. Salinas-Castillo A. · Biosens. Bioelectron. · 2008 · 24 · 105310.1016/j.bios.2008.07.052 ↗
38. R. Esquembre R. · Soft Matter · 2012 · 8 · 40810.1039/C1SM06264F ↗
39. Evans R. C. · Adv. Mater. · 2010 · 22 · 303210.1002/adma.200904377 ↗