Monitoring mesoglobules formation in PNIPAm solutions using Nile Red solvatochromism

Colloid and Polymer Science

Volumn 291, Issue 12, 2013, Pages 2911-2916

  Locatelli Champagne, Clémentine ^a,b   Cloitre, Michel ^a  

^a PSL RESEARCH UNIVERSITY   (France)

^b ARKEMA   (France)

Author keywords

Lower critical solubility temperature; Mesoglobule; Nile Red; PNIPAm; Solvatochromism; Thermosensitive polymer

Indexed keywords

AMIDES; MOLECULES; PHASE SEPARATION;

LOWER CRITICAL SOLUBILITY TEMPERATURES; MESOGLOBULE; NILE RED; PNIPAM; SOLVATOCHROMISMS; THERMO-SENSITIVE POLYMER;

FLUORESCENCE;

ACRYLAMIDE DERIVATIVE;

ARTICLE; FLUORESCENCE; MEASUREMENT; MOLECULE; MONITORING; PRIORITY JOURNAL; SOLUTION AND SOLUBILITY; TEMPERATURE;

EID: 84892370218     PISSN: 0303402X     EISSN: 14351536     Source Type: Journal    
DOI: 10.1007/s00396-013-3035-5     Document Type: Article

References (29)

1. Schild HG (1992) Poly(N-isopropylacrylamide): experiment, theory and application. Prog Polym Sci 17:163-249. doi:10.1016/0079-6700(92)90023-R
2. Zhang G, Wu C (2006) Folding and formation of mesoglobules in dilute copolymer solutions. Adv Polym Sci 195:101-176. doi:10. 1007/12-050
3. Aseyev V, Hietala S, Laukkanen A, NuopponenM, Confortini O, Du Prez FE, Tenhu H (2005) Mesoglobules of thermoresponsive polymers in dilute aqueous solutions above the LCST. Polymer 46:7118-7131. doi:10.1016/j.polymer.2005.05. 097
4. Chan K, Pelton R, Zhang J (1999) On the formation of colloidally dispersed phase separated poly(N-isopropylacrylamide). Langmuir 15:4018-4020. doi:10.1021/la9812673
5. Kujawa P, Aseyev V, Tenhu H, Winnik FM (2006) Temperaturesensitive properties of poly(N-isopropylacrylamide) mesoglobules formed in dilute aqueous solutions heated above their demixing point. Macromolecules 39:7686-7693. doi:10.1021/ma061604b
6. Balu C, Delsanti M, Guenoun P,Monti F, CloitreM(2007) Colloidal phase separation of concentrated PNIPAm solutions. Langmuir 23:2404-2407. doi:10.1021/la0627821
7. Monti F, Fu S-Y, Iliopoulos I, Cloitre M (2008) Doubly responsive polymer-microgel composites: rheology and structure. Langmuir 24:11474-11482. doi:10.1021/la8018056
8. Yushmanov PV, Furó I, Iliopoulos I (2006) Kinetics of demixing and remixing transitions in aqueous solutions of poly(N-isopropylacrylamide): a temperature-jump 1H NMR study. Macromol Chem Phys 207:1972-1979. doi:10.1002/macp.200600394
9. Greenspan P, Mayer EP, Fowler SD (1985) Nile Red: a selective fluorescent stain for intracellular lipid droplets. J Cell Biol 100:965-973. doi:10.1083/jcb.100.3.965
10. Sarkar N, Das K, Nath DN, Bhattacharyya K (1994) Twisted charge transfer processes of Nile Red in homogeneous solutions and in Faujasite zeolite. Langmuir 10:326-329. doi:10.1021/la00013a048
11. Dutta AK, Kamada K, Ohta KJ (1996) Spectroscopic studies of Nile Red in organic solvents and polymers. Photochem Photobiol A: Chem 93:57-64. doi:10.1016/1010-6030(95) 04140-0
12. Polverini E, Cugini G, Annoni F, Abbruzzetti S, Viappiani C, Gensch T (2006) Molten globule formation in apomyoglobin monitored by the fluorescent probe Nile Red. Biochemistry 45:5111-5121. doi:10. 1021/bi051905y
13. Hawe A, Sutter M, Jiskott W (2008) Extrinsic fluorescent dyes as tools for protein characterization. Pharm Res 25:1487-1499. doi:10. 1007/s11095-007-9516-9
14. Haidekker MA, Theodorakis EA (2010) Environment-sensitive behavior of fluorescent molecular rotors. J Biol Eng 4:1-14. doi:10. 1186/1754-1611-4-11
15. Neves Silva JP, Real Oliveira MECD, Coutinho PJG (2009) Characterization of mixed DODAB/monoolein aggregates using Nile Red as a solvatochromic and anisotropy fluorescent probe. J Photochem PhotobiolA: Chem 203:32-39. doi:10.1016/j. jphotochem.2008.12.016
16. Krishan MMG (1999) Excited-state kinetics of the hydrophobic probe nile red in membranes and micelles. J Phys Chem A 103:3589-3595. doi:10.1021/ jp984620m
17. Hazra P, Chakrabarty D, Chakraborty A, Sarkar N (2004) Intramolecular charge transfer and solvation dynamics of Nile Red in the nanocavity of cyclodextrins. Chem Phys Lett 388:150-157. doi:10. 1016/j.cplett.2004.02.078
18. Lin C, Zhao J, Jiang R (2008) Nile red probing for the micelle-tovesicle transition of AOT in aqueous solution. Chem Phys Lett 464:77-81. doi:10.1016/j.cplett.2008.09.001
19. Hungerford G, Castanheira EMS, Real Oliveira MECD, da Graca MM, Burrows HD (2002) Monitoring ternary systems of C12E5/ water/tetradecane via the fluorescence of solvatochromic probes. J Phys Chem B 106:4061-4069. doi:10.1021/jp013047v
20. Stuart MCA, van de Pas JC, Engberts JBFN (2005) The use of Nile Red to monitor the aggregation behaviour in ternary surfactant-water-organic solvent systems. J Phys Org Chem 18:929-934. doi:10.1002/poc.919
21. Mueller W, Koynov K, Fischer K, Hartmann S, Pierrat S, Basche T, Maskos M (2009) Hydrophobic shell loading of PB-b-PEO vesicles. Macromolecules 42:357-361. doi:10.1021/ma801954y
22. Lin C, Zhao J (2010) Nile red probing for sphere-to-rod-to-wormlike micelle transition in aqueous surfactant solution. Dye Pigment 84:223-228. doi:10.1016/ j.dyepig.2009.09.006
23. Dutta AK, Kamada K, Ohta K (1996) Langmuir-Blodgett films of Nile Red: a steady-state and time-resolved fluorescence study. Chem Phys Lett 258:369-375. doi:10.1016/0009-2614(96)00628-8
24. Levitsky I, Krivoshlykov SG (2001) Rational design of a Nile Red/ polymer composite film for fluorescence sensing of organophosphonate vapors using hydrogen bond acidic polymers. Anal Chem 73:3441-3448. doi:10.1021/ac0014966
25. Cser A, NagyK, Biczk L (2002) Fluorescence lifetime of Nile Red as a probe for the hydrogen bonding strength with its microenvironment. Chem Phys Lett 360:473-478. doi:10.1016/S0009-2614(02)00784-4
26. Jee A-Y, Park S, Kwon H, Lee M (2009) Excited state dynamics of Nile Red in polymers. Chem Phys Lett 477:112-115. doi:10.1016/j. cplett.2009.06.088
27. Bokias G, Durand A, Hourdet D (1998) Molar mass control of poly(N-isopropylacrylamide) and poly(acrylic acid) in aqueous polymerizations initiated by redox initiators based on persulfates. Macromol Chem Phys 199:1387-1392. doi:10.1002/(SICI)1521-3935(19980701)199:7<1387::AID- MACP1387>3.0.CO;2-K
28. Locatelli C, PhD thesis (Université Pierre et Marie Curie, 2011
29. Patrenostre M, Meyer O, Grabielle-Madelmont C, Lesieur S, Ghanam M, Ollivon M (1995) Partition coefficient of a surfactant between aggregates and solution: application to the micelle-vesicle transition of egg phosphatidylcholine and octyl beta-Dglucopyranoside. Biophys J 69:2476-2488. doi:10.1016/S0006-3495(95)80118-9