78
Grachev MK, Kurochkina GI, Popkov AV (2019) The features of synthesis and chemical behavior
of some silicon-containing cyclodextrin derivatives. Russ Chem Bull 68:708–716. https://doi.
org/10.1007/s11172-019-2477-4
Gramera R (1969) Cyclodextrin polyethers and their production. US Patent No. 3459731,
October 1969
Griffiths DW, Bender ML (1973) Cycloamyloses as catalysts. Adv Catal 23:209–261. https://doi.
org/10.1016/S0360-0564(08)60302-8
Gruenhut NS, Cushing ML, Caesar GV (1948) Alpha and beta-Schardinger dextrin nitrates. J Am
Chem Soc 70:424–425
Gruiz K, Molnar M, Fenyvesi É, Cs H, Atkari A, Barkacs K (2011) Cyclodextrins in innovative
engineering tools for risk-based environmental management. J Incl Phenom Macrocycl Chem
70:299–306. https://doi.org/10.1007/s10847-010-9909-y
Gruiz K, Meggyes T, Fenyvesi É (eds) (2019) Engineering tools for environmental risk management. Volume 4. Risk reduction technologies and case studies. CRC Press, Boca Raton. https://
doi.org/10.1201/b20405
Guo J, Russell EG, Darcy R, Cotter TG, McKenna SL, Cahill MR, O’Driscoll CM (2017)
Antibody-targeted cyclodextrin-based nanoparticles for siRNA Delivery in the treatment of
acute myeloid leukemia: physicochemical characteristics, in vitro mechanistic studies, and
ex vivo patient derived therapeutic efficacy. Mol Pharm 14:940–952. https://doi.org/10.1021/
acs.molpharmaceut.6b01150
Hale WS, Rawlins LC (1951) Amylase of Bacillus macerans. Cereal Chem 28:49–58
Hamada Y, Nambu N, Nagai T (1975) Pharmaceutical interactions in dosage forms and processing.
III. Interactions of α- and β-cyclodextrin with several nonsteroidal antiinflammatory drugs in
aqueous solution. Chem Pharm Bull 23:1205–1211
Hammoud Z, Khreich N, Auezova L, Fourmentin S, Elaissari A, Greige-Gerges H (2019)
Cyclodextrin-membrane interaction in drug delivery and membrane structure maintenance. Int
J Pharm 564:59–76. https://doi.org/10.1016/j.ijpharm.2019.03.063
Han JH (2005) Innovations in food packaging. Food science and technology, international series.
Academic, Amsterdam, 503 p. ISBN: 0-12-311632-5
Han SM, Armstrong DW (1989) Chapter 10: HPLC separation of enantiomers and other isomers
with cyclodextrin-bonded phases: rules for chiral recognition. In: Krstulovic AM (ed) Chiral
separations by HPLC. Ellis Horwood Limited/Wiley, New York, pp 208–284
Han YY, Liu WCJ, Huang JW, Qiu SR, Zhong H, Liu D, Liu JQ (2018) Cyclodextrin-based metalorganic frameworks (CD-MOFs) in pharmaceutics and biomedicine. Pharmaceutics 10:271.
https://doi.org/10.3390/pharmaceutics10040271
Hanes CS (1937) The action of amylases in relation to the structure of starch and its metabolism in
the plant. Parts IV-VII. New Phytol 36:189–239
Hapiot F, Bricout H, Menuel S, Tilloy S, Monflier E (2014) Recent breakthroughs in aqueous
cyclodextrin-assisted supramolecular catalysis. Cat Sci Technol 4:1899–1908. https://doi.
org/10.1039/C4CY00005F
Harata K, Uedaira H (1975) Structure of α-cyclodextrin-p-iodoaniline complex. Nature
253:190–191
Harvey AE, Manning DL (1950) Spectrophotometric methods of establishing empirical formulas
of colored complexes in solution. J Am Chem Soc 72:4488–4493
Hashimoto HJ (1996) Cyclodextrins in foods, cosmetics, and toiletries. In: Szejtli J, Osa T (eds)
Comprehensive supramolecular chemistry, vol 3. Pergamon, London/Oxford, pp 483–502
Hashimoto HJ (2002) Present status of industrial applications of cyclodextrins in Japan. J Incl
Phenom Macrocycl Chem 44:57–62
Hashimoto H (2006) Chapter 16: Cyclodextrin applications in food, cosmetic, toiletry, textile and
wrapping materiel fields. In: Dodziuk H (ed) Cyclodextrins and their complexes. Chemistry,
analytical methods, applications. Wiley-VCH/Verlag GmbH & Co. KGaA, Weinheim,
pp 452–459. https://doi.org/10.1002/3527608982.ch16
Hedges AR (1998) Industrial applications of cyclodextrins. Chem Rev 98:2035–2044
N. Morin-Crini et al.
Grachev MK, Kurochkina GI, Popkov AV (2019) The features of synthesis and chemical behavior
of some silicon-containing cyclodextrin derivatives. Russ Chem Bull 68:708–716. https://doi.
org/10.1007/s11172-019-2477-4
Gramera R (1969) Cyclodextrin polyethers and their production. US Patent No. 3459731,
October 1969
Griffiths DW, Bender ML (1973) Cycloamyloses as catalysts. Adv Catal 23:209–261. https://doi.
org/10.1016/S0360-0564(08)60302-8
Gruenhut NS, Cushing ML, Caesar GV (1948) Alpha and beta-Schardinger dextrin nitrates. J Am
Chem Soc 70:424–425
Gruiz K, Molnar M, Fenyvesi É, Cs H, Atkari A, Barkacs K (2011) Cyclodextrins in innovative
engineering tools for risk-based environmental management. J Incl Phenom Macrocycl Chem
70:299–306. https://doi.org/10.1007/s10847-010-9909-y
Gruiz K, Meggyes T, Fenyvesi É (eds) (2019) Engineering tools for environmental risk management. Volume 4. Risk reduction technologies and case studies. CRC Press, Boca Raton. https://
doi.org/10.1201/b20405
Guo J, Russell EG, Darcy R, Cotter TG, McKenna SL, Cahill MR, O’Driscoll CM (2017)
Antibody-targeted cyclodextrin-based nanoparticles for siRNA Delivery in the treatment of
acute myeloid leukemia: physicochemical characteristics, in vitro mechanistic studies, and
ex vivo patient derived therapeutic efficacy. Mol Pharm 14:940–952. https://doi.org/10.1021/
acs.molpharmaceut.6b01150
Hale WS, Rawlins LC (1951) Amylase of Bacillus macerans. Cereal Chem 28:49–58
Hamada Y, Nambu N, Nagai T (1975) Pharmaceutical interactions in dosage forms and processing.
III. Interactions of α- and β-cyclodextrin with several nonsteroidal antiinflammatory drugs in
aqueous solution. Chem Pharm Bull 23:1205–1211
Hammoud Z, Khreich N, Auezova L, Fourmentin S, Elaissari A, Greige-Gerges H (2019)
Cyclodextrin-membrane interaction in drug delivery and membrane structure maintenance. Int
J Pharm 564:59–76. https://doi.org/10.1016/j.ijpharm.2019.03.063
Han JH (2005) Innovations in food packaging. Food science and technology, international series.
Academic, Amsterdam, 503 p. ISBN: 0-12-311632-5
Han SM, Armstrong DW (1989) Chapter 10: HPLC separation of enantiomers and other isomers
with cyclodextrin-bonded phases: rules for chiral recognition. In: Krstulovic AM (ed) Chiral
separations by HPLC. Ellis Horwood Limited/Wiley, New York, pp 208–284
Han YY, Liu WCJ, Huang JW, Qiu SR, Zhong H, Liu D, Liu JQ (2018) Cyclodextrin-based metalorganic frameworks (CD-MOFs) in pharmaceutics and biomedicine. Pharmaceutics 10:271.
https://doi.org/10.3390/pharmaceutics10040271
Hanes CS (1937) The action of amylases in relation to the structure of starch and its metabolism in
the plant. Parts IV-VII. New Phytol 36:189–239
Hapiot F, Bricout H, Menuel S, Tilloy S, Monflier E (2014) Recent breakthroughs in aqueous
cyclodextrin-assisted supramolecular catalysis. Cat Sci Technol 4:1899–1908. https://doi.
org/10.1039/C4CY00005F
Harata K, Uedaira H (1975) Structure of α-cyclodextrin-p-iodoaniline complex. Nature
253:190–191
Harvey AE, Manning DL (1950) Spectrophotometric methods of establishing empirical formulas
of colored complexes in solution. J Am Chem Soc 72:4488–4493
Hashimoto HJ (1996) Cyclodextrins in foods, cosmetics, and toiletries. In: Szejtli J, Osa T (eds)
Comprehensive supramolecular chemistry, vol 3. Pergamon, London/Oxford, pp 483–502
Hashimoto HJ (2002) Present status of industrial applications of cyclodextrins in Japan. J Incl
Phenom Macrocycl Chem 44:57–62
Hashimoto H (2006) Chapter 16: Cyclodextrin applications in food, cosmetic, toiletry, textile and
wrapping materiel fields. In: Dodziuk H (ed) Cyclodextrins and their complexes. Chemistry,
analytical methods, applications. Wiley-VCH/Verlag GmbH & Co. KGaA, Weinheim,
pp 452–459. https://doi.org/10.1002/3527608982.ch16
Hedges AR (1998) Industrial applications of cyclodextrins. Chem Rev 98:2035–2044
N. Morin-Crini et al.