298
Binello A, Cravotto G, Nano GM, Spagliardi P (2004) Synthesis of chitosan-cyclodextrin adducts
and evaluation of their bitter-masking properties. Flavour Fragr J 19:394–400. https://doi.
org/10.1002/ffj.1434
Blanchemain N, Haulon S, Martel B, Traisnel M, Morcellet M, Hildebrand HF (2005) Vascular PET
prostheses surface modification with cyclodextrin coating: development of a new drug delivery
system. Eur J Vasc Endovasc Surg 29:628–632. https://doi.org/10.1016/j.ejvs.2005.02.020
Buckler SA, Martel RF, Moshy RJ (1969) Schardinger dextrins. US Patent Office 3472835
Caldera F, Tannous M, Cavalli R, Zanetti M, Trotta F (2017) Evolution of Cyclodextrin
Nanosponges. Int J Pharm 531:470–479. https://doi.org/10.1016/j.ijpharm.2017.06.072
Cammas S, Béar M-M, Moine L, Escalup R, Ponchel G, Kataoka K, Guérin P (1999) Polymers of
malic acid and 3-alkylmalic acid as synthetic PHAs in the design of biocompatible hydrolyzable
devices. Int J Biol Macromol 25:273–282. https://doi.org/10.1016/S0141-8130(99)00042-2
Celebioglu A, Yildiz ZI, Uyar T (2018) Fabrication of electrospun eugenol/cyclodextrin inclusion
complex nanofibrous webs for enhanced antioxidant property, water solubility, and high temperature stability. J Agric Food Chem 66:457–466. https://doi.org/10.1021/acs.jafc.7b04312
Cheng J, Davis ME, Khin KT (2013) Cyclodextrin-based polymers for therapeutic delivery US
Patent Office 8389499
Choi HS, Yamashita A, Ooya T, Yui N, Akita H, Kogure K, Ito R, Harashima H (2005) Sunflowershaped cyclodextrin-conjugated poly(ε-lysine) polyplex as a controlled intracellular trafficking
device. Chembiochem 6:1986–1990. https://doi.org/10.1002/cbic.200500242
Ciobanu A, Mallard I, Landy D, Brabie G, Nistor D, Fourmentin S (2012) Inclusion interactions of
cyclodextrins and crosslinked cyclodextrin polymers with linalool and camphor in Lavandula
angustifolia essential oil. Carbohydr Polym 87:1963–1970. https://doi.org/10.1016/j.
carbpol.2011.10.005
Conte C, Caldera F, Catanzano O, D’Angelo I, Ungaro F, Miro A, Pellosi DS, Trotta F, Quaglia F
(2014) β-cyclodextrin nanosponges as multifunctional ingredient in water-containing semisolid
formulations for skin delivery. J Pharm Sci 103:3941–3949. https://doi.org/10.1002/jps.24203
Costoya A, Concheiro A, Alvarez-Lorenzo C (2017) Electrospun fibers of cyclodextrins and
poly(cyclodextrins). Molecules 22. https://doi.org/10.3390/molecules22020230
Crini
G,
Morcellet
M
(2002)
Synthesis
and
applications
of
adsorbents
containing
cyclodextrins.
J
Sep
Sci
25:789–813.
https://doi.
org/10.1002/1615-9314(20020901)25:13<789::AID-JSSC789>3.0.CO;2-J
Crini G, Lekchiri Y, Morcellet M (1995) Separation of structural isomers using cyclodextrinpolymers coated on silica beads. Chromatographia 40:296–302. https://doi.org/10.1007/
BF02290360
Crini C, Janus L, Morcellet M, Torri G, Naggi A, Bertini S, Vecchi C (1998a) Macroporous polyamines containing cyclodextrin: synthesis, characterization, and sorption properties. J Appl
Polym Sci 69:1419–1427. https://doi.org/10.1002/(SICI)1097-4628(19980815)69:7<1419::
AID-APP17>3.0.CO;2-O
Crini G, Cosentino C, Bertini S, Naggi A, Torri G, Vecchi C, Janus L, Morcellet M (1998b) Solid
state NMR spectroscopy study of molecular motion in cyclomaltoheptaose (β-cyclodextrin)
crosslinked with epichlorohydrin. Carbohydr Res 308:37–45. https://doi.org/10.1016/
S0008-6215(98)00077-9
Crini G, Bourdonneau M, Martel B, Piotto M, Morcellet M, Richert T, Vebrel J, Torri G, Morin
N (2000) Solid-state NMR characterization of cyclomaltoheptaose (β-cyclodextrin) polymers
using high-resolution magic angle spinning with gradients. J Appl Polym Sci 75:1288–1295.
https://doi.org/10.1002/(SICI)1097-4628(20000307)75:10<1288::AID-APP10>3.0.CO;2-J
Cusola O, Tabary N, Belgacem MN, Bras J (2013) Cyclodextrin functionalization of several cellulosic substrates for prolonged release of antibacterial agents. J Appl Polym Sci 129:604–613.
https://doi.org/10.1002/app.38748
Das S, Subuddhi U (2015) pH-responsive guar gum hydrogels for controlled delivery of dexamethasone to the intestine. Int J Biol Macromol 79:856–863. https://doi.org/10.1016/j.
ijbiomac.2015.06.008
M. Petitjean et al.
Binello A, Cravotto G, Nano GM, Spagliardi P (2004) Synthesis of chitosan-cyclodextrin adducts
and evaluation of their bitter-masking properties. Flavour Fragr J 19:394–400. https://doi.
org/10.1002/ffj.1434
Blanchemain N, Haulon S, Martel B, Traisnel M, Morcellet M, Hildebrand HF (2005) Vascular PET
prostheses surface modification with cyclodextrin coating: development of a new drug delivery
system. Eur J Vasc Endovasc Surg 29:628–632. https://doi.org/10.1016/j.ejvs.2005.02.020
Buckler SA, Martel RF, Moshy RJ (1969) Schardinger dextrins. US Patent Office 3472835
Caldera F, Tannous M, Cavalli R, Zanetti M, Trotta F (2017) Evolution of Cyclodextrin
Nanosponges. Int J Pharm 531:470–479. https://doi.org/10.1016/j.ijpharm.2017.06.072
Cammas S, Béar M-M, Moine L, Escalup R, Ponchel G, Kataoka K, Guérin P (1999) Polymers of
malic acid and 3-alkylmalic acid as synthetic PHAs in the design of biocompatible hydrolyzable
devices. Int J Biol Macromol 25:273–282. https://doi.org/10.1016/S0141-8130(99)00042-2
Celebioglu A, Yildiz ZI, Uyar T (2018) Fabrication of electrospun eugenol/cyclodextrin inclusion
complex nanofibrous webs for enhanced antioxidant property, water solubility, and high temperature stability. J Agric Food Chem 66:457–466. https://doi.org/10.1021/acs.jafc.7b04312
Cheng J, Davis ME, Khin KT (2013) Cyclodextrin-based polymers for therapeutic delivery US
Patent Office 8389499
Choi HS, Yamashita A, Ooya T, Yui N, Akita H, Kogure K, Ito R, Harashima H (2005) Sunflowershaped cyclodextrin-conjugated poly(ε-lysine) polyplex as a controlled intracellular trafficking
device. Chembiochem 6:1986–1990. https://doi.org/10.1002/cbic.200500242
Ciobanu A, Mallard I, Landy D, Brabie G, Nistor D, Fourmentin S (2012) Inclusion interactions of
cyclodextrins and crosslinked cyclodextrin polymers with linalool and camphor in Lavandula
angustifolia essential oil. Carbohydr Polym 87:1963–1970. https://doi.org/10.1016/j.
carbpol.2011.10.005
Conte C, Caldera F, Catanzano O, D’Angelo I, Ungaro F, Miro A, Pellosi DS, Trotta F, Quaglia F
(2014) β-cyclodextrin nanosponges as multifunctional ingredient in water-containing semisolid
formulations for skin delivery. J Pharm Sci 103:3941–3949. https://doi.org/10.1002/jps.24203
Costoya A, Concheiro A, Alvarez-Lorenzo C (2017) Electrospun fibers of cyclodextrins and
poly(cyclodextrins). Molecules 22. https://doi.org/10.3390/molecules22020230
Crini
G,
Morcellet
M
(2002)
Synthesis
and
applications
of
adsorbents
containing
cyclodextrins.
J
Sep
Sci
25:789–813.
https://doi.
org/10.1002/1615-9314(20020901)25:13<789::AID-JSSC789>3.0.CO;2-J
Crini G, Lekchiri Y, Morcellet M (1995) Separation of structural isomers using cyclodextrinpolymers coated on silica beads. Chromatographia 40:296–302. https://doi.org/10.1007/
BF02290360
Crini C, Janus L, Morcellet M, Torri G, Naggi A, Bertini S, Vecchi C (1998a) Macroporous polyamines containing cyclodextrin: synthesis, characterization, and sorption properties. J Appl
Polym Sci 69:1419–1427. https://doi.org/10.1002/(SICI)1097-4628(19980815)69:7<1419::
AID-APP17>3.0.CO;2-O
Crini G, Cosentino C, Bertini S, Naggi A, Torri G, Vecchi C, Janus L, Morcellet M (1998b) Solid
state NMR spectroscopy study of molecular motion in cyclomaltoheptaose (β-cyclodextrin)
crosslinked with epichlorohydrin. Carbohydr Res 308:37–45. https://doi.org/10.1016/
S0008-6215(98)00077-9
Crini G, Bourdonneau M, Martel B, Piotto M, Morcellet M, Richert T, Vebrel J, Torri G, Morin
N (2000) Solid-state NMR characterization of cyclomaltoheptaose (β-cyclodextrin) polymers
using high-resolution magic angle spinning with gradients. J Appl Polym Sci 75:1288–1295.
https://doi.org/10.1002/(SICI)1097-4628(20000307)75:10<1288::AID-APP10>3.0.CO;2-J
Cusola O, Tabary N, Belgacem MN, Bras J (2013) Cyclodextrin functionalization of several cellulosic substrates for prolonged release of antibacterial agents. J Appl Polym Sci 129:604–613.
https://doi.org/10.1002/app.38748
Das S, Subuddhi U (2015) pH-responsive guar gum hydrogels for controlled delivery of dexamethasone to the intestine. Int J Biol Macromol 79:856–863. https://doi.org/10.1016/j.
ijbiomac.2015.06.008
M. Petitjean et al.