262
D. Makieła and Z. Gburski
7. Li Z, Wang L, Li Y, Feng Y, Feng W (2019) Carbon-based functional nanomaterials: preparation, properties and applications, Compos Sci Technol 179:10–40. https://doi.org/10.1016/j.
compscitech.2019.04.028
8. Gburski Z, Górny K, Raczy´ nski P (2010) The impact of a carbon nanotube on the cholesterol
domain localized on a protein surface. Solid State Commun 150:415–418. https://doi.org/10.
1016/j.ssc.2009.12.005
9. Li G, Xiao P, Hou S, Huang Y (2019) Graphene based self-healing materials. Carbon 146:371–
387. https://doi.org/10.1016/j.carbon.2019.02.011
10. Fernandez MA, Silva F, Vico RV, de Rossi RH (2019) Complex systems that incorporate
cyclodextrins to get materials for some specific applications. Carbohydr Res 480:12–34. https://
doi.org/10.1016/j.carres.2019.05.006
11. Dawid A, Górny K, Gburski Z (2015) The influence of distribution of hydroxyl groups on
vibrational spectra of fullerenol C-60(OH)(24) isomers: DFT study. Spectrochim Acta Part A
Mol Biomol Spectrosc 136:1993–1997. https://doi.org/10.1016/j.saa.2014.08.023
12. Szente L, Fenyvesi E (2017) Cyclodextrin-lipid complexes: cavity size matters. Struct Chem
28:479–492. https://doi.org/10.1007/s11224-016-0884-9
13. Roux M, Auzely-Velty R, Djedaini-Pilard F, Perly B (2002) Cyclodextrin-induced lipid lateral
separation in DMPC membranes: 2 H nuclear magnetic resonance study. Biophys J 82:813–822.
https://doi.org/10.1016/s0006-3495(02)75443-x
14. Grachev MK, Malenkovskaya MA, Vasyanina LK (2015) NMR study of inclusion complexes
formation between amphiphilic dimeric β-cyclodextrin derivative and some pharmacologically
important compounds. J Incl Phenom Macrocycl Chem 83:209–214. https://doi.org/10.1007/
s10847-015-0548-1
15. Dawid A, Gburski Z (2003) Rayleigh light scattering in fullerene covered by a spherical argon
film—a molecular dynamics study. J Phys Condens Matter 15:2399–2405. https://doi.org/10.
1088/0953-8984/15/14/315
16. Litz JP, Thakkar N, Portet T, Keller SL (2016) Depletion with cyclodextrin reveals two populations of cholesterol in model lipid membranes. Biophys J 110:635–645. https://doi.org/10.
1016/j.bpj.2015.11.021
17. Joset A, Grammenos A, Hoebeke M, Leyh B (2015) Investigation of the interaction between
a β-cyclodextrin and DMPC liposomes: a small angle neutron scattering study. J Incl Phenom
Macrocycl Chem 83:227–238. https://doi.org/10.1007/s10847-015-0558-z
18. Gburski Z, Gray CG, Sullivan DE (1983) Information theory of line shape in collision-induced
absorption. Chem Phys Lett 100:383–386. https://doi.org/10.1016/0009-2614(83)80292-9
19. Mascetti J, Castano S, Cavagnat D, Desbat B (2008) Organization of β-cyclodextrin under
pure cholesterol, DMPC, or DMPG and mixed cholesterol/phospholipid monolayers. Langmuir
24:9616–9622. https://doi.org/10.1021/la8004294
20. Tsamaloukas A, Szadkowska H, Slotte PJ, Heerklotz H (2005) Interactions of cholesterol with
lipid membranes and cyclodextrin characterized by calorimetry. Biophys J 89:1109–1119.
https://doi.org/10.1529/biophysj.105.061846
21. Gwizdała W, Górny K, Gburski Z (2008) Molecular dynamics and dielectric loss in 4-cyano-4n-pentylbiphenyl (5CB) mesogene film surrounding carbon nanotube—computer simulation.
J Mol Struct 887:148–151. https://doi.org/10.1016/j.molstruc.2007.12.045
22. Loftsson T, Vogensen SB, Brewster ME, Konráðsdóttir F (2007) Effects of cyclodextrins on
drug delivery through biological membranes. J Pharm Sci 96:2532–2546. https://doi.org/10.
1002/jps.20992
23. Puglisi G, Fresta M, Ventura CA (1996) Interaction of natural and modified β-cyclodextrins
with a biological membrane model of dipalmitoylphosphatidylcholine. J Colloid Interface Sci
180:542–547. https://doi.org/10.1006/jcis.1996.0335
24. Piatek A, Dawid A, Gburski Z (2011) The properties of small fullerenol cluster (C60(OH)(24))(7): computer simulation. Spectrochim Acta Part A Mol Biomol Spectrosc
79:819–823. https://doi.org/10.1016/j.saa.2010.08.059
25. Menezes P, Andrade T, Frank LA, Souza EPBS, Trindade GG, Trindade IAS, Serafinni MS,
Guterres SS, Araujo AA (2019) Advances of nanosystems containing cyclodextrins and their
D. Makieła and Z. Gburski
7. Li Z, Wang L, Li Y, Feng Y, Feng W (2019) Carbon-based functional nanomaterials: preparation, properties and applications, Compos Sci Technol 179:10–40. https://doi.org/10.1016/j.
compscitech.2019.04.028
8. Gburski Z, Górny K, Raczy´ nski P (2010) The impact of a carbon nanotube on the cholesterol
domain localized on a protein surface. Solid State Commun 150:415–418. https://doi.org/10.
1016/j.ssc.2009.12.005
9. Li G, Xiao P, Hou S, Huang Y (2019) Graphene based self-healing materials. Carbon 146:371–
387. https://doi.org/10.1016/j.carbon.2019.02.011
10. Fernandez MA, Silva F, Vico RV, de Rossi RH (2019) Complex systems that incorporate
cyclodextrins to get materials for some specific applications. Carbohydr Res 480:12–34. https://
doi.org/10.1016/j.carres.2019.05.006
11. Dawid A, Górny K, Gburski Z (2015) The influence of distribution of hydroxyl groups on
vibrational spectra of fullerenol C-60(OH)(24) isomers: DFT study. Spectrochim Acta Part A
Mol Biomol Spectrosc 136:1993–1997. https://doi.org/10.1016/j.saa.2014.08.023
12. Szente L, Fenyvesi E (2017) Cyclodextrin-lipid complexes: cavity size matters. Struct Chem
28:479–492. https://doi.org/10.1007/s11224-016-0884-9
13. Roux M, Auzely-Velty R, Djedaini-Pilard F, Perly B (2002) Cyclodextrin-induced lipid lateral
separation in DMPC membranes: 2 H nuclear magnetic resonance study. Biophys J 82:813–822.
https://doi.org/10.1016/s0006-3495(02)75443-x
14. Grachev MK, Malenkovskaya MA, Vasyanina LK (2015) NMR study of inclusion complexes
formation between amphiphilic dimeric β-cyclodextrin derivative and some pharmacologically
important compounds. J Incl Phenom Macrocycl Chem 83:209–214. https://doi.org/10.1007/
s10847-015-0548-1
15. Dawid A, Gburski Z (2003) Rayleigh light scattering in fullerene covered by a spherical argon
film—a molecular dynamics study. J Phys Condens Matter 15:2399–2405. https://doi.org/10.
1088/0953-8984/15/14/315
16. Litz JP, Thakkar N, Portet T, Keller SL (2016) Depletion with cyclodextrin reveals two populations of cholesterol in model lipid membranes. Biophys J 110:635–645. https://doi.org/10.
1016/j.bpj.2015.11.021
17. Joset A, Grammenos A, Hoebeke M, Leyh B (2015) Investigation of the interaction between
a β-cyclodextrin and DMPC liposomes: a small angle neutron scattering study. J Incl Phenom
Macrocycl Chem 83:227–238. https://doi.org/10.1007/s10847-015-0558-z
18. Gburski Z, Gray CG, Sullivan DE (1983) Information theory of line shape in collision-induced
absorption. Chem Phys Lett 100:383–386. https://doi.org/10.1016/0009-2614(83)80292-9
19. Mascetti J, Castano S, Cavagnat D, Desbat B (2008) Organization of β-cyclodextrin under
pure cholesterol, DMPC, or DMPG and mixed cholesterol/phospholipid monolayers. Langmuir
24:9616–9622. https://doi.org/10.1021/la8004294
20. Tsamaloukas A, Szadkowska H, Slotte PJ, Heerklotz H (2005) Interactions of cholesterol with
lipid membranes and cyclodextrin characterized by calorimetry. Biophys J 89:1109–1119.
https://doi.org/10.1529/biophysj.105.061846
21. Gwizdała W, Górny K, Gburski Z (2008) Molecular dynamics and dielectric loss in 4-cyano-4n-pentylbiphenyl (5CB) mesogene film surrounding carbon nanotube—computer simulation.
J Mol Struct 887:148–151. https://doi.org/10.1016/j.molstruc.2007.12.045
22. Loftsson T, Vogensen SB, Brewster ME, Konráðsdóttir F (2007) Effects of cyclodextrins on
drug delivery through biological membranes. J Pharm Sci 96:2532–2546. https://doi.org/10.
1002/jps.20992
23. Puglisi G, Fresta M, Ventura CA (1996) Interaction of natural and modified β-cyclodextrins
with a biological membrane model of dipalmitoylphosphatidylcholine. J Colloid Interface Sci
180:542–547. https://doi.org/10.1006/jcis.1996.0335
24. Piatek A, Dawid A, Gburski Z (2011) The properties of small fullerenol cluster (C60(OH)(24))(7): computer simulation. Spectrochim Acta Part A Mol Biomol Spectrosc
79:819–823. https://doi.org/10.1016/j.saa.2010.08.059
25. Menezes P, Andrade T, Frank LA, Souza EPBS, Trindade GG, Trindade IAS, Serafinni MS,
Guterres SS, Araujo AA (2019) Advances of nanosystems containing cyclodextrins and their