302
Mizobuchi Y, Tanaka M, Shono T (1980) Preparation and sorption behaviour of cyclodextrin polyurethane resins. J Chromatogr A 194:153–161. https://doi.org/10.1016/S0021-9673(00)87291-X
Mocanu G, Vizitiu D, Carpov A (2001) Cyclodextrin polymers. J Bioact Compat Polym
16:315–342. https://doi.org/10.1106/JJUV-8F2K-JGYF-HNGF
Moya-Ortega MD, Alvarez-Lorenzo C, Concheiro A, Loftsson T (2012) Cyclodextrin-based nanogels for pharmaceutical and biomedical applications. Int J Pharm 428:152–163. https://doi.
org/10.1016/j.ijpharm.2012.02.038
Nozaki T, Maeda Y, Ito K, Kitano H (1995) Cyclodextrins modified with polymer chains which
are responsive to external stimuli. Macromolecules 28:522–524. https://doi.org/10.1021/
ma00106a016
Oliveira MF, Suarez D, Rocha JCB, De Carvalho Teixeira AVN, Cortés ME, De Sousa FB,
Sinisterra RD (2015) Electrospun nanofibers of polycyclodextrin/PMAA polymers and their
potential application as drug delivery system. Mater Sci Eng C 54:252–261. https://doi.
org/10.1016/j.msec.2015.04.042
Osmani RAM, Bhosale RR, Hani U, Vaghela R, Kulkarni PK (2015) Cyclodextrin based nanosponges: impending carters in drug delivery and nanotherapeutics. Curr Drug Ther 10:3–19.
https://doi.org/10.2174/157488551001150825095513
Palomino-Durand C, Lopez M, Cazaux F, Martel B, Blanchemain N, Chai F (2019) Influence of the
soluble-insoluble ratios of cyclodextrins polymers on the viscoelastic properties of injectable
chitosan-based hydrogels for biomedical application. Polymers:11. https://doi.org/10.3390/
polym11020214
Peng L, Liu S, Feng A, Yuan J (2017) Polymeric nanocarriers based on cyclodextrins for drug
delivery: host-guest interaction as stimuli responsive linker. Mol Pharm 14:2475–2486. https://
doi.org/10.1021/acs.molpharmaceut.7b00160
Piletsky SA, Andersson HS, Nicholls IA (1998) The rational use of hydrophobic effect-based recognition in molecularly imprinted polymers. J Mol Recognit 11:94–97. https://doi.org/10.1002/
(SICI)1099-1352(199812)11:1/6<94::AID-JMR398>3.0.CO;2-C
Pitha J, Harman SM, Michel ME (1986) Hydrophilic cyclodextrin derivatives enable effective
oral administration of steroidal hormones. J Pharm Sci 75:165–167. https://doi.org/10.1002/
jps.2600750213
Plackett DV, Holm VK, Johansen P, Ndoni S, Nielsen PV, Sipilainen-Malm T, Södergård A,
Verstichel S (2006) Characterization of L-polylactide and L-polylactide-polycaprolactone
co- polymer films for use in cheese-packaging applications. Packag Technol Sci 19:1–24.
https://doi.org/10.1002/pts.704
Pöpping B, Deratani A (1992) Synthesis of cyclodextrins with pendant chlorinated groups.
Reaction of β-cyclodextrin with epichlorohydrin in acidic medium. Die Makromol Chemie
Rapid Commun 13:237–241. https://doi.org/10.1002/marc.1992.030130409
Prabaharan M, Mano JF (2005) Hydroxypropyl chitosan bearing β-cyclodextrin cavities: synthesis
and slow release of its inclusion complex with a model hydrophobic drug. Macromol Biosci
5:965–973. https://doi.org/10.1002/mabi.200500087
Renard E, Deratani A, Volet G, Sebille B (1997) Preparation and characterization of water soluble high molecular weight β-cyclodextrin-epichlorohydrin polymers. Eur Polym J 33:49–57.
https://doi.org/10.1016/S0014-3057(96)00123-1
Reuscher H, Hirsenkorn R, Haas W (1998) Cyclodextrin derivatives having at least one nitrogencontaining heterocycle, their preparation and use. US Patent 5728823
Romo A, Peñas FJ, Sevillano X, Isasi JR (2006) Application of factorial experimental design to the
study of the suspension polymerisation of β-cyclodextrin and epichlorohydrin. J Appl Polym
Sci 100:3393–3402. https://doi.org/10.1002/app.23778
Shaw PE, Buslig BS (1986) Selective removal of bitter compounds from grapefruit juice and from
aqueous solution with cyclodextrin polymers and with Amberlite XAD-4. J Agric Food Chem
34:837–840. https://doi.org/10.1021/jf00071a018
M. Petitjean et al.
Mizobuchi Y, Tanaka M, Shono T (1980) Preparation and sorption behaviour of cyclodextrin polyurethane resins. J Chromatogr A 194:153–161. https://doi.org/10.1016/S0021-9673(00)87291-X
Mocanu G, Vizitiu D, Carpov A (2001) Cyclodextrin polymers. J Bioact Compat Polym
16:315–342. https://doi.org/10.1106/JJUV-8F2K-JGYF-HNGF
Moya-Ortega MD, Alvarez-Lorenzo C, Concheiro A, Loftsson T (2012) Cyclodextrin-based nanogels for pharmaceutical and biomedical applications. Int J Pharm 428:152–163. https://doi.
org/10.1016/j.ijpharm.2012.02.038
Nozaki T, Maeda Y, Ito K, Kitano H (1995) Cyclodextrins modified with polymer chains which
are responsive to external stimuli. Macromolecules 28:522–524. https://doi.org/10.1021/
ma00106a016
Oliveira MF, Suarez D, Rocha JCB, De Carvalho Teixeira AVN, Cortés ME, De Sousa FB,
Sinisterra RD (2015) Electrospun nanofibers of polycyclodextrin/PMAA polymers and their
potential application as drug delivery system. Mater Sci Eng C 54:252–261. https://doi.
org/10.1016/j.msec.2015.04.042
Osmani RAM, Bhosale RR, Hani U, Vaghela R, Kulkarni PK (2015) Cyclodextrin based nanosponges: impending carters in drug delivery and nanotherapeutics. Curr Drug Ther 10:3–19.
https://doi.org/10.2174/157488551001150825095513
Palomino-Durand C, Lopez M, Cazaux F, Martel B, Blanchemain N, Chai F (2019) Influence of the
soluble-insoluble ratios of cyclodextrins polymers on the viscoelastic properties of injectable
chitosan-based hydrogels for biomedical application. Polymers:11. https://doi.org/10.3390/
polym11020214
Peng L, Liu S, Feng A, Yuan J (2017) Polymeric nanocarriers based on cyclodextrins for drug
delivery: host-guest interaction as stimuli responsive linker. Mol Pharm 14:2475–2486. https://
doi.org/10.1021/acs.molpharmaceut.7b00160
Piletsky SA, Andersson HS, Nicholls IA (1998) The rational use of hydrophobic effect-based recognition in molecularly imprinted polymers. J Mol Recognit 11:94–97. https://doi.org/10.1002/
(SICI)1099-1352(199812)11:1/6<94::AID-JMR398>3.0.CO;2-C
Pitha J, Harman SM, Michel ME (1986) Hydrophilic cyclodextrin derivatives enable effective
oral administration of steroidal hormones. J Pharm Sci 75:165–167. https://doi.org/10.1002/
jps.2600750213
Plackett DV, Holm VK, Johansen P, Ndoni S, Nielsen PV, Sipilainen-Malm T, Södergård A,
Verstichel S (2006) Characterization of L-polylactide and L-polylactide-polycaprolactone
co- polymer films for use in cheese-packaging applications. Packag Technol Sci 19:1–24.
https://doi.org/10.1002/pts.704
Pöpping B, Deratani A (1992) Synthesis of cyclodextrins with pendant chlorinated groups.
Reaction of β-cyclodextrin with epichlorohydrin in acidic medium. Die Makromol Chemie
Rapid Commun 13:237–241. https://doi.org/10.1002/marc.1992.030130409
Prabaharan M, Mano JF (2005) Hydroxypropyl chitosan bearing β-cyclodextrin cavities: synthesis
and slow release of its inclusion complex with a model hydrophobic drug. Macromol Biosci
5:965–973. https://doi.org/10.1002/mabi.200500087
Renard E, Deratani A, Volet G, Sebille B (1997) Preparation and characterization of water soluble high molecular weight β-cyclodextrin-epichlorohydrin polymers. Eur Polym J 33:49–57.
https://doi.org/10.1016/S0014-3057(96)00123-1
Reuscher H, Hirsenkorn R, Haas W (1998) Cyclodextrin derivatives having at least one nitrogencontaining heterocycle, their preparation and use. US Patent 5728823
Romo A, Peñas FJ, Sevillano X, Isasi JR (2006) Application of factorial experimental design to the
study of the suspension polymerisation of β-cyclodextrin and epichlorohydrin. J Appl Polym
Sci 100:3393–3402. https://doi.org/10.1002/app.23778
Shaw PE, Buslig BS (1986) Selective removal of bitter compounds from grapefruit juice and from
aqueous solution with cyclodextrin polymers and with Amberlite XAD-4. J Agric Food Chem
34:837–840. https://doi.org/10.1021/jf00071a018
M. Petitjean et al.