79
Hedges AR, Shieh WJ, Sikorski CT (1995) Use of cyclodextrins for encapsulation in the use
and treatment of food products. In: Risch SJ, Reineccius GA (eds) Encapsulation and controlled release of food ingredients, ACS symposium series 590. American Chemical Society,
Washington, DC, pp 60–71
Hess K, Trogus M, Ulmann M (1933) Information on the modifications of alpha-dextrin by F
Schardinger. Z Phys Chem Abt B 21:1–6
Higashi T (2019) Cyclodextrin-based molecular accessories for drug discovery and drug delivery.
Chem Pharm Bull 67:289–298. https://doi.org/10.1248/cpb.c18-00735
Higashi T, Iohara D, Motoyama K, Arima H (2018) Supramolecular pharmaceutical sciences: a
novel concept combining pharmaceutical sciences and supramolecular chemistry with a focus
on cyclodextrin-based supermolecules. Chem Pharm Bull 66:207–216
Higuchi T, Connors KA (1965) Phase solubility techniques. Adv Anal Chem Instrum 4:117–212
Higuchi S, Tanaka K, Tanaka S (1982) Raman circular intensity differential spectra of methyl
orange induced by inclusion in cyclodextrin. Chem Lett 11:635–638. https://doi.org/10.1246/
cl.1982.635
Hinze WL (1981) Applications of cyclodextrins in chromatographic separations and purification
methods. Sep Purif Methods 10:159–237
Hirakawa H, Tomita H (2013) Interference of bacterial cell-to-cell communication: a new concept
of antimicrobial chemotherapy breaks antibiotic resistance. Front Microbiol 4:114. https://doi.
org/10.3389/fmicb.2013.00114
Hirayama F, Uekama K, Koinuma H (1980) Molecular dynamics of prostaglandin F 2α -cyclodextrin
complexes in aqueous solution. Chem Pharm Bull 28:1975–1980
Hiroshi K (1981) Edible film. Japan Patent JPS 5618555
Hoesslin H, Pringsheim H (1923) Physiology of the polyamyloses. II. Glycogen formation and
animal combustion. Hoppe-Seiler’s Z Physiol Chem 131:168–176
Horikoshi K (1979) Production and industrial applications of beta-cyclodextrin. Process Biochem
14:26–30
Hou XS, Ke CF, Stoddart JF (2016) Cooperative capture synthesis: yet another playground for
copper-free click chemistry. Chem Soc Rev 45:3766–3780. https://doi.org/10.1039/c6cs00055j
Hybl A, Rundle RE, Williams DE (1965) The crystal and molecular structure of the
cyclohexaamylose- potassium acetate complex. J Am Chem Soc 87:2779–2788. https://doi.
org/10.1021/ja01091a001
Irvine JC, Pringsheim H, MacDonald J (1924) CXIV.– The constitution of polysaccharides. Part
VIII. The molecular structure of β-hexa-amylose. J Chem Soc Trans 125:942–947
Irvine JC, Pringsheim H, Skinner AF (1929) Die methylierung der α-tetra-amylose. Ber Dtsch
Chem Ges 62:2372–2378. https://doi.org/10.1002/cber.19290620873
Ito K (2017) Slide-ring materials using cyclodextrin. Chem Pharm Bull 65:326–329. https://doi.
org/10.1248/cpb.c16-00874
James WJ, French D, Rundle RE (1959) Studies on the Schardinger dextrins. 9. Structure of the
cyclohexaamylose-iodine complex. Acta Crystallogr 12:385–389. https://doi.org/10.1107/
S0365110X59001141
Jansook P, Ogawa N, Loftsson T (2018) Cyclodextrins: structure, physicochemical properties and pharmaceutical applications. Int J Pharm 535:272–284. https://doi.org/10.1016/j.
ijpharm.2017.11.018
Jiang L, Liu C, Mayumi K, Kato K, Yokoyama H, Ito K (2018) Highly stretchable and instantly
recoverable slide-ring gels consisting of enzymatically synthesized polyrotaxane with low host
coverage. Chem Mater 30:5013–5019. https://doi.org/0.1021/acs.chemmater.8b01208
Jicsinszky L, Fenyvesi É, Hashimoto H, Ueno A (1996) Chapter 4: Cyclodextrin derivatives. In:
Atwood JL, Davies JE, DD MN, Vögtle F, Szejtli J, Osa T (eds) Comprehensive supramolecular chemistry, vol 3. Elsevier Science Ltd, London, pp 57–188. ISBN: 978-008-0912-844
Junthip J, Tabary N, Chai F, Leclercq L, Maton M, Cazaux F, Neut C, Paccou L, Guinet Y, Staelens
JN, Bria M, Landy D, Hedoux A, Blanchemain N, Martel B (2016) Layer-by-layer coating of
1 History of Cyclodextrins
Hedges AR, Shieh WJ, Sikorski CT (1995) Use of cyclodextrins for encapsulation in the use
and treatment of food products. In: Risch SJ, Reineccius GA (eds) Encapsulation and controlled release of food ingredients, ACS symposium series 590. American Chemical Society,
Washington, DC, pp 60–71
Hess K, Trogus M, Ulmann M (1933) Information on the modifications of alpha-dextrin by F
Schardinger. Z Phys Chem Abt B 21:1–6
Higashi T (2019) Cyclodextrin-based molecular accessories for drug discovery and drug delivery.
Chem Pharm Bull 67:289–298. https://doi.org/10.1248/cpb.c18-00735
Higashi T, Iohara D, Motoyama K, Arima H (2018) Supramolecular pharmaceutical sciences: a
novel concept combining pharmaceutical sciences and supramolecular chemistry with a focus
on cyclodextrin-based supermolecules. Chem Pharm Bull 66:207–216
Higuchi T, Connors KA (1965) Phase solubility techniques. Adv Anal Chem Instrum 4:117–212
Higuchi S, Tanaka K, Tanaka S (1982) Raman circular intensity differential spectra of methyl
orange induced by inclusion in cyclodextrin. Chem Lett 11:635–638. https://doi.org/10.1246/
cl.1982.635
Hinze WL (1981) Applications of cyclodextrins in chromatographic separations and purification
methods. Sep Purif Methods 10:159–237
Hirakawa H, Tomita H (2013) Interference of bacterial cell-to-cell communication: a new concept
of antimicrobial chemotherapy breaks antibiotic resistance. Front Microbiol 4:114. https://doi.
org/10.3389/fmicb.2013.00114
Hirayama F, Uekama K, Koinuma H (1980) Molecular dynamics of prostaglandin F 2α -cyclodextrin
complexes in aqueous solution. Chem Pharm Bull 28:1975–1980
Hiroshi K (1981) Edible film. Japan Patent JPS 5618555
Hoesslin H, Pringsheim H (1923) Physiology of the polyamyloses. II. Glycogen formation and
animal combustion. Hoppe-Seiler’s Z Physiol Chem 131:168–176
Horikoshi K (1979) Production and industrial applications of beta-cyclodextrin. Process Biochem
14:26–30
Hou XS, Ke CF, Stoddart JF (2016) Cooperative capture synthesis: yet another playground for
copper-free click chemistry. Chem Soc Rev 45:3766–3780. https://doi.org/10.1039/c6cs00055j
Hybl A, Rundle RE, Williams DE (1965) The crystal and molecular structure of the
cyclohexaamylose- potassium acetate complex. J Am Chem Soc 87:2779–2788. https://doi.
org/10.1021/ja01091a001
Irvine JC, Pringsheim H, MacDonald J (1924) CXIV.– The constitution of polysaccharides. Part
VIII. The molecular structure of β-hexa-amylose. J Chem Soc Trans 125:942–947
Irvine JC, Pringsheim H, Skinner AF (1929) Die methylierung der α-tetra-amylose. Ber Dtsch
Chem Ges 62:2372–2378. https://doi.org/10.1002/cber.19290620873
Ito K (2017) Slide-ring materials using cyclodextrin. Chem Pharm Bull 65:326–329. https://doi.
org/10.1248/cpb.c16-00874
James WJ, French D, Rundle RE (1959) Studies on the Schardinger dextrins. 9. Structure of the
cyclohexaamylose-iodine complex. Acta Crystallogr 12:385–389. https://doi.org/10.1107/
S0365110X59001141
Jansook P, Ogawa N, Loftsson T (2018) Cyclodextrins: structure, physicochemical properties and pharmaceutical applications. Int J Pharm 535:272–284. https://doi.org/10.1016/j.
ijpharm.2017.11.018
Jiang L, Liu C, Mayumi K, Kato K, Yokoyama H, Ito K (2018) Highly stretchable and instantly
recoverable slide-ring gels consisting of enzymatically synthesized polyrotaxane with low host
coverage. Chem Mater 30:5013–5019. https://doi.org/0.1021/acs.chemmater.8b01208
Jicsinszky L, Fenyvesi É, Hashimoto H, Ueno A (1996) Chapter 4: Cyclodextrin derivatives. In:
Atwood JL, Davies JE, DD MN, Vögtle F, Szejtli J, Osa T (eds) Comprehensive supramolecular chemistry, vol 3. Elsevier Science Ltd, London, pp 57–188. ISBN: 978-008-0912-844
Junthip J, Tabary N, Chai F, Leclercq L, Maton M, Cazaux F, Neut C, Paccou L, Guinet Y, Staelens
JN, Bria M, Landy D, Hedoux A, Blanchemain N, Martel B (2016) Layer-by-layer coating of
1 History of Cyclodextrins