91
Topuz F, Uyar T (2019) Electrospinning of cyclodextrin functional nanofibers for drug delivery
applications. Pharmaceutics 11:1–35. https://doi.org/10.3390/pharmaceutics11010006
Uekama K, Hirayama F (1978) Inclusion complexation of prostaglandin F 2α with α- and
β-cyclodextrins in aqueous solution. Chem Pharm Bull 26:1195–1200
Uekama K, Otagiri M (1987) Cyclodextrins in drug carrier systems. Crit Rev Ther Drug Carrier
Syst 3:1–40
Uekama K, Fujise A, Hirayama F, Otagiri M, Inaba K (1984) Improvement of dissolution characteristics and chemical stability of prostaglandins E 1 by γ-cyclodextrin complexation. Chem
Pharm Bull 32:275–279
Uekama K, Hirayama F, Irie T (1998) Cyclodextrin drug carrier systems. Chem Rev 98:2045–2076
Ueno A, Takahashi K, Osa T (1980) One host/two guest complexation between γ-cyclodextrin
and sodium α-naphthylacetate as shown by excimer fluorescence. J Chem Soc Chem Commun
19:921–922. https://doi.org/10.1039/C39800000921
Ulmann M (1932) The molecular size of the alpha-dextrin of F Schardinger. Biochem Z
251:458–477
Ulmann M, Trogus M, Hess K (1932) Zur kenntnis des α-dextrins von F. Schardinger (information
on the α-dextrins by F. Schardinger). Ber Dtsch Chem Ges 65:682–686
Valente AJM, Söderman O (2014) The formation of host-guest complexes between surfactants and
cyclodextrins. Adv Colloid Interface 205:156–176. https://doi.org/10.1016/j.cis.2013.08.001
Van de Manakker F, Vermonden T, Van Nostrum CF, Hennink WE (2009) Cyclodextrin-based
polymeric materials: synthesis, properties, and pharmaceutical/biomedical applications.
Biomacromolecules 10:3157–3175. https://doi.org/10.1021/bm901065f
van Etten RL, Sebastian JF, Clowes GA, Bender ML (1967a) Acceleration of phenyl ester cleavage
by cycloamyloses: a model for enzymatic specificity. J Am Chem Soc 89:3242–3253
van Etten RL, Clowes GA, Sebastian JF, Bender ML (1967b) The mechanism of the cycloamyloseaccelerated cleavage of phenyl esters. J Am Chem Soc 89:3253–3262
van Hooidonk C, Breebaart-Hansen CAE (1970) Stereospecific reaction of isopropyl methylphosphonofluoridated (sarin) with α-cyclodextrin: a model for enzyme inhibition. Rec Trav Chim
89:289–299. https://doi.org/10.1002/recl.19700890309
van Hooidonk C, Breebaart-Hansen CAE (1972) Model studies for enzyme inhibition. Part IV: the
association of some alkyl methylphosphonates with α-cyclodextrin in an aqueous medium. Rec
Trav Chim 91:958–964. https://doi.org/10.1002/recl.19720910811
Vaution C, Hutin M, Glomot F, Duchêne D (1987) Chapter 8: The use of cyclodextrins in various
industries. In: Duchêne D (ed) Cyclodextrins and their industrial uses. Éditions de Santé, Paris,
pp 299–350
Vermet G, Degoutin S, Chai F, Maton M, Danjou PE, Martel B, Blanchemain N (2017) Cyclodextrin
modified PLLA parietal reinforcement implant with prolonged antibacterial activity. Acta
Biomater 53:222–232. https://doi.org/10.1016/j.actbio.2017.02.017
Vetter W, Bester K (2006) Chapter 6: Gas chromatographic enantioseparation of chiral pollutants – techniques and results. In: Busch KW, Busch MA (eds) Chiral separation. Elsevier,
Amsterdam, pp 131–228
Villalonga R, Cao R, Fragoso A (2007) Supramolecular chemistry of cyclodextrin in enzyme technology. Chem Rev 107:3088–3116. https://doi.org/10.1021/cr050253g
Villiers A (1891a) Sur la transformation de la fécule en dextrine par le ferment butyrique. Chimie
Organique – Compte Rendus des Séances de l’Académie des Sciences (France) Février, CXII,
pp 435–437
Villiers A (1891b) Sur la transformation de la fécule en dextrine par le ferment butyrique. Bulletin
de la Société Chimique de Paris. 1
er semestre, 3
ème série, tome V, vol 45, pp 468–470
Villiers A (1891c) Sur la fermentation de la fécule par l’action du ferment butyrique. Chimie
Organique – Compte Rendus des Séances de l’Académie des Sciences (France) Juin, CXII,
pp 536–538
Villiers A (1891d) Sur la fermentation de la fécule par l’action du ferment butyrique. Bulletin de la
Société Chimique de Paris. 1
er semestre, 3
ème série, tome V, vol 46, pp 470–472
1 History of Cyclodextrins
Topuz F, Uyar T (2019) Electrospinning of cyclodextrin functional nanofibers for drug delivery
applications. Pharmaceutics 11:1–35. https://doi.org/10.3390/pharmaceutics11010006
Uekama K, Hirayama F (1978) Inclusion complexation of prostaglandin F 2α with α- and
β-cyclodextrins in aqueous solution. Chem Pharm Bull 26:1195–1200
Uekama K, Otagiri M (1987) Cyclodextrins in drug carrier systems. Crit Rev Ther Drug Carrier
Syst 3:1–40
Uekama K, Fujise A, Hirayama F, Otagiri M, Inaba K (1984) Improvement of dissolution characteristics and chemical stability of prostaglandins E 1 by γ-cyclodextrin complexation. Chem
Pharm Bull 32:275–279
Uekama K, Hirayama F, Irie T (1998) Cyclodextrin drug carrier systems. Chem Rev 98:2045–2076
Ueno A, Takahashi K, Osa T (1980) One host/two guest complexation between γ-cyclodextrin
and sodium α-naphthylacetate as shown by excimer fluorescence. J Chem Soc Chem Commun
19:921–922. https://doi.org/10.1039/C39800000921
Ulmann M (1932) The molecular size of the alpha-dextrin of F Schardinger. Biochem Z
251:458–477
Ulmann M, Trogus M, Hess K (1932) Zur kenntnis des α-dextrins von F. Schardinger (information
on the α-dextrins by F. Schardinger). Ber Dtsch Chem Ges 65:682–686
Valente AJM, Söderman O (2014) The formation of host-guest complexes between surfactants and
cyclodextrins. Adv Colloid Interface 205:156–176. https://doi.org/10.1016/j.cis.2013.08.001
Van de Manakker F, Vermonden T, Van Nostrum CF, Hennink WE (2009) Cyclodextrin-based
polymeric materials: synthesis, properties, and pharmaceutical/biomedical applications.
Biomacromolecules 10:3157–3175. https://doi.org/10.1021/bm901065f
van Etten RL, Sebastian JF, Clowes GA, Bender ML (1967a) Acceleration of phenyl ester cleavage
by cycloamyloses: a model for enzymatic specificity. J Am Chem Soc 89:3242–3253
van Etten RL, Clowes GA, Sebastian JF, Bender ML (1967b) The mechanism of the cycloamyloseaccelerated cleavage of phenyl esters. J Am Chem Soc 89:3253–3262
van Hooidonk C, Breebaart-Hansen CAE (1970) Stereospecific reaction of isopropyl methylphosphonofluoridated (sarin) with α-cyclodextrin: a model for enzyme inhibition. Rec Trav Chim
89:289–299. https://doi.org/10.1002/recl.19700890309
van Hooidonk C, Breebaart-Hansen CAE (1972) Model studies for enzyme inhibition. Part IV: the
association of some alkyl methylphosphonates with α-cyclodextrin in an aqueous medium. Rec
Trav Chim 91:958–964. https://doi.org/10.1002/recl.19720910811
Vaution C, Hutin M, Glomot F, Duchêne D (1987) Chapter 8: The use of cyclodextrins in various
industries. In: Duchêne D (ed) Cyclodextrins and their industrial uses. Éditions de Santé, Paris,
pp 299–350
Vermet G, Degoutin S, Chai F, Maton M, Danjou PE, Martel B, Blanchemain N (2017) Cyclodextrin
modified PLLA parietal reinforcement implant with prolonged antibacterial activity. Acta
Biomater 53:222–232. https://doi.org/10.1016/j.actbio.2017.02.017
Vetter W, Bester K (2006) Chapter 6: Gas chromatographic enantioseparation of chiral pollutants – techniques and results. In: Busch KW, Busch MA (eds) Chiral separation. Elsevier,
Amsterdam, pp 131–228
Villalonga R, Cao R, Fragoso A (2007) Supramolecular chemistry of cyclodextrin in enzyme technology. Chem Rev 107:3088–3116. https://doi.org/10.1021/cr050253g
Villiers A (1891a) Sur la transformation de la fécule en dextrine par le ferment butyrique. Chimie
Organique – Compte Rendus des Séances de l’Académie des Sciences (France) Février, CXII,
pp 435–437
Villiers A (1891b) Sur la transformation de la fécule en dextrine par le ferment butyrique. Bulletin
de la Société Chimique de Paris. 1
er semestre, 3
ème série, tome V, vol 45, pp 468–470
Villiers A (1891c) Sur la fermentation de la fécule par l’action du ferment butyrique. Chimie
Organique – Compte Rendus des Séances de l’Académie des Sciences (France) Juin, CXII,
pp 536–538
Villiers A (1891d) Sur la fermentation de la fécule par l’action du ferment butyrique. Bulletin de la
Société Chimique de Paris. 1
er semestre, 3
ème série, tome V, vol 46, pp 470–472
1 History of Cyclodextrins