299
Delval F, Crini G, Bertini S, Morin-Crini N, Badot PM, Vebrel J, Torri G (2004) Characterization
of crosslinked starch materials with spectroscopic techniques. J Appl Polym Sci 93:2650–2663.
https://doi.org/10.1002/app.20851
Ding Y, Shen SZ, Sun H, Sun K, Liu F, Qi Y, Yan J (2015) Design and construction of polymerisedchitosan coated Fe 3 O 4 magnetic nanoparticles and its application for hydrophobic drug delivery. Mater Sci Eng C Mater Biol Appl 48:487–498. https://doi.org/10.1016/j.msec.2014.12.036
dos Santos J-FR, Alvarez-Lorenzo C, Silva M, Balsa L, Couceiro J, Torres-Labandeira
J-J, Concheiro A (2009) Soft contact lenses functionalized with pendant cyclodextrins for controlled drug delivery. Biomaterials 30:1348–1355. https://doi.org/10.1016/j.
biomaterials.2008.11.016
Dumitriu S (1996) Polysaccharides in medicinal applications, 1st edn. Routledge, CRC Press,
New York, 816p. ISBN 9780824795405
Dumoulin Y, Alex S, Szabo P, Cartilier L, Mateescu MA (1998) Cross-linked amylose as
matrix for drug controlled release. X-ray and FT-IR structural analysis. Carbohydr Polym
37:361–370. https://doi.org/10.1016/S0144-8617(98)00058-7
El Ghoul Y, Blanchemain N, Laurent T, Campagne C, El Achari A, Roudesli S, Morcellet M,
Martel B, Hildebrand HF (2008) Chemical, biological and microbiological evaluation of
cyclodextrin finished polyamide inguinal meshes. Acta Biomater 4:1392–1400. https://doi.
org/10.1016/j.actbio.2008.02.019
Felméray I, Fenyvesi É, Neumark T, Takács J, Gerlóczy A, Szejtli J (1996) Effect of Cyclodextrin
bead polymer on wound healing. Proc Eighth Int Symp Cyclodextrins:491–494. https://doi.
org/10.1007/978-94-011-5448-2_108
Feng G, Ping W, Qin XX, Liu J, Zhu X (2015) Ionic-liquid-loaded β-cyclodextrin-cross-linked
polymer solid-phase extraction for the separation/analysis of linuron in fruit and vegetable
samples. Food Anal Methods 8:2315–2320. https://doi.org/10.1007/s12161-015-0118-6
Fenyvesi E (1988) Cyclodextrin polymers in the pharmaceutical industry. J Incl Phenom
6:537–545. https://doi.org/10.1007/BF00660751
Fenyvesi E, Shirakura O, Szejtli J, Nagai T (1984) Properties of cyclodextrin polymer as a tableting aid. Chem Pharm Bull 32:665–669
Fenyvesi É, Ujházy A, Szejtli J, Pütter S, Gan TG (1996) Controlled release of drugs from cyclodextrin polymers substituted with ionic groups. J Incl Phenom Mol Recognit Chem 25:185–189.
https://doi.org/10.1007/BF01041566
Friedman RB (1988) Controlled release agent for cetylpyridinium chloride US Patent
Office 4774329
Friedman RB, Hedges AR, Black FL, Gottneid DJ (1989) Complexation of aromatic compounds
with, and their release from, cyclomaltoheptaose-containing polymers, hydroxyethylcyclomaltoheptaose, and cyclomaltoheptaose. Carbohydr Res 192:283–289
Fujiyoshi T, Carrez O, Imizcoz M, Zornoza A, Isasi JR (2019) Interpenetrated polymer networks
of poly(β-cyclodextrin)and polyvinylpyrrolidone with synergistic and selective sorption capacities. Carbohydr Polym 219:105–112. https://doi.org/10.1016/j.carbpol.2019.05.027
Furue M, Harada A, Nozakura S (1975) Preparation of cyclodextrin-containing polymers and their
catalysis in ester-hydrolysis. J Polym Sci Polym Lett Ed 13:357–360. https://doi.org/10.1002/
pol.1975.130130608
García-Zubiri ÍX (2005) Sorption of naphthalenes in beta-cyclodextrin polymers. PhD thesis.
University of Navarra
Gidwani B, Vyas A (2015) A comprehensive review on cyclodextrin based carriers for delivery
of chemotherapeutic cytotoxic anticancer drugs. Biomed Res Int 2015:198268. https://doi.
org/10.1155/2015/198268
Gil ES, Li J, Xiao H, Lowe TL (2009) Quaternary ammonium β-cyclodextrin nanoparticles for
enhancing doxorubicin permeability across the in vitro blood-brain barrier. Biomacromolecules
10:505–516. https://doi.org/10.1021/bm801026k
6 Cyclodextrin-Based Polymers for Food and Pharmaceutical Applications…
Delval F, Crini G, Bertini S, Morin-Crini N, Badot PM, Vebrel J, Torri G (2004) Characterization
of crosslinked starch materials with spectroscopic techniques. J Appl Polym Sci 93:2650–2663.
https://doi.org/10.1002/app.20851
Ding Y, Shen SZ, Sun H, Sun K, Liu F, Qi Y, Yan J (2015) Design and construction of polymerisedchitosan coated Fe 3 O 4 magnetic nanoparticles and its application for hydrophobic drug delivery. Mater Sci Eng C Mater Biol Appl 48:487–498. https://doi.org/10.1016/j.msec.2014.12.036
dos Santos J-FR, Alvarez-Lorenzo C, Silva M, Balsa L, Couceiro J, Torres-Labandeira
J-J, Concheiro A (2009) Soft contact lenses functionalized with pendant cyclodextrins for controlled drug delivery. Biomaterials 30:1348–1355. https://doi.org/10.1016/j.
biomaterials.2008.11.016
Dumitriu S (1996) Polysaccharides in medicinal applications, 1st edn. Routledge, CRC Press,
New York, 816p. ISBN 9780824795405
Dumoulin Y, Alex S, Szabo P, Cartilier L, Mateescu MA (1998) Cross-linked amylose as
matrix for drug controlled release. X-ray and FT-IR structural analysis. Carbohydr Polym
37:361–370. https://doi.org/10.1016/S0144-8617(98)00058-7
El Ghoul Y, Blanchemain N, Laurent T, Campagne C, El Achari A, Roudesli S, Morcellet M,
Martel B, Hildebrand HF (2008) Chemical, biological and microbiological evaluation of
cyclodextrin finished polyamide inguinal meshes. Acta Biomater 4:1392–1400. https://doi.
org/10.1016/j.actbio.2008.02.019
Felméray I, Fenyvesi É, Neumark T, Takács J, Gerlóczy A, Szejtli J (1996) Effect of Cyclodextrin
bead polymer on wound healing. Proc Eighth Int Symp Cyclodextrins:491–494. https://doi.
org/10.1007/978-94-011-5448-2_108
Feng G, Ping W, Qin XX, Liu J, Zhu X (2015) Ionic-liquid-loaded β-cyclodextrin-cross-linked
polymer solid-phase extraction for the separation/analysis of linuron in fruit and vegetable
samples. Food Anal Methods 8:2315–2320. https://doi.org/10.1007/s12161-015-0118-6
Fenyvesi E (1988) Cyclodextrin polymers in the pharmaceutical industry. J Incl Phenom
6:537–545. https://doi.org/10.1007/BF00660751
Fenyvesi E, Shirakura O, Szejtli J, Nagai T (1984) Properties of cyclodextrin polymer as a tableting aid. Chem Pharm Bull 32:665–669
Fenyvesi É, Ujházy A, Szejtli J, Pütter S, Gan TG (1996) Controlled release of drugs from cyclodextrin polymers substituted with ionic groups. J Incl Phenom Mol Recognit Chem 25:185–189.
https://doi.org/10.1007/BF01041566
Friedman RB (1988) Controlled release agent for cetylpyridinium chloride US Patent
Office 4774329
Friedman RB, Hedges AR, Black FL, Gottneid DJ (1989) Complexation of aromatic compounds
with, and their release from, cyclomaltoheptaose-containing polymers, hydroxyethylcyclomaltoheptaose, and cyclomaltoheptaose. Carbohydr Res 192:283–289
Fujiyoshi T, Carrez O, Imizcoz M, Zornoza A, Isasi JR (2019) Interpenetrated polymer networks
of poly(β-cyclodextrin)and polyvinylpyrrolidone with synergistic and selective sorption capacities. Carbohydr Polym 219:105–112. https://doi.org/10.1016/j.carbpol.2019.05.027
Furue M, Harada A, Nozakura S (1975) Preparation of cyclodextrin-containing polymers and their
catalysis in ester-hydrolysis. J Polym Sci Polym Lett Ed 13:357–360. https://doi.org/10.1002/
pol.1975.130130608
García-Zubiri ÍX (2005) Sorption of naphthalenes in beta-cyclodextrin polymers. PhD thesis.
University of Navarra
Gidwani B, Vyas A (2015) A comprehensive review on cyclodextrin based carriers for delivery
of chemotherapeutic cytotoxic anticancer drugs. Biomed Res Int 2015:198268. https://doi.
org/10.1155/2015/198268
Gil ES, Li J, Xiao H, Lowe TL (2009) Quaternary ammonium β-cyclodextrin nanoparticles for
enhancing doxorubicin permeability across the in vitro blood-brain barrier. Biomacromolecules
10:505–516. https://doi.org/10.1021/bm801026k
6 Cyclodextrin-Based Polymers for Food and Pharmaceutical Applications…