92
Voncina B (2011) Chapter 17: application of cyclodextrins in textile dyeing. In: Hauser P (ed)
Textile dyeing. InTech, Tijeka, pp 373–392. ISBN: 978-953-307-565-5
Ward TJ, Armstrong DW (1986) Improved cyclodextrin chiral phases – a comparison and review.
J Liq Chromatogr 9:407–423. https://doi.org/10.1080/01483918608076644
Ward TJ, Armstrong DW (1988) Chapter 5: Cyclodextrin-stationary phases. In: Zief M, Crane LJ
(eds) Chromatographic chiral separations. Marcel Dekker Inc, New York, pp 131–163
Wenz G (1994) Cyclodextrins as building blocks for supramolecular structures and functional
units. Angew Chem Int Ed 33:803–822
Wenz G, Han BH, Müller A (2006) Cyclodextrin rotaxanes and polyrotaxanes. Chem Rev
106:782–817. https://doi.org/10.1021/cr970027+
West C (2014) Enantioselective separations with supercritical fluids – review. Curr Anal Chem
10:99–120. https://doi.org/10.2174/1573411011410010009
Whelan WJ, Manners DJ, Rosenfeld E, Gottschalk A, French D, Bell DJ, Courtois JE, Hasside
WZ (1960) Determination of starch structure by enzymes – discussion. Bull Soc Chim Biol
42:1690–1700
Wiedenhoff N, Lammers JNJJ (1968) Properties of cyclodextrins: part II. Preparation of a stable
β-cyclodextrin hydrate and determination of its water content and enthalpy of solution in water
from 15-30°. Carbohydr Res 7:1–6. https://doi.org/10.1016/S0008-6215(00)81426-3
Wilson EJ, Schoch TJ, Hudson CS (1943) The action of macerans amylase on the fractions from
starch. J Am Chem Soc 65:1380–1383
Wood DJ, Hrsuka FE, Saenger W (1977) 1H NMR study of the inclusion of aromatic molecules in
α-cyclodextrin. J Am Chem Soc 99:1735–1740
Wu ZL, Song N, Menz R, Pingali B, Yang YW, Zheng YB (2015) Nanoparticles functionalized
with supramolecular host-guest systems for nanomedicine and healthcare. Nanomedicine
10:1493–1514. https://doi.org/10.2217/NNM.15.1
Xiao Y, Ng SC, Tan TTY, Wang Y (2012) Recent development of cyclodextrin chiral stationary
phases and their applications in chromatography. J Chromatogr A 1269:52–68. https://doi.
org/10.1016/j.chroma.2012.08.049
Xu J, Wu L, Guo T, Zhang G, Wang C, Li H, Li X, Singh V, Chen W, Gref R, Zhang J (2019)
A “ship-in-a-bottle” strategy to create folic acid nanoclusters inside the nanocages of
γ-cyclodextrin metal-organic frameworks. Int J Pharm 556:89–96. https://doi.org/10.1016/j.
ijpharm.2018.11.074
Yamagiwa T, Kawaguchi AT, Saito T, Inoue S, Morita S, Watanabe K, Kitagishi H, Koji K,
Inokuchi S (2014) Supramolecular ferric porphyrins and a cyclodextrin dimer as antidotes for
cyanide poisoning. Hum Exp Toxicol 33:360–368. https://doi.org/10.1177/0960327113499041
Yamamoto Y, Inoue Y (1989) NMR-studies of cyclodextrin inclusion complex. J Carbohydr Chem
8:29–46. https://doi.org/10.1080/07328308908047990
Yang JS, Yang L (2013) Preparation and application of cyclodextrin immobilized polysaccharides.
J Mater Chem B 1:909–918. https://doi.org/10.1039/c2tb00107a
Yao XK, Huang P, Nie ZH (2019) Cyclodextrin-based polymer materials: from controlled synthesis
to applications. Prog Polym Sci 93:1–35. https://doi.org/10.1016/j.progpolymsci.2019.03.004
Yokoo M, Kubota Y, Motoyama K, Higashi T, Taniyoshi M, Tokommaru H, Nishiyama R, Tabe
Y, Mochinaga S, Sato A, Sueoka-Aragane N, Sueoka E, Arima H, Irie T, Kimura S (2015)
2-Hydroxypropyl-β-cyclodextrin acts as a novel anticancer agent. PlosOne 10:e0141946.
https://doi.org/10.1371/journal.pone.0141946
Yuan Z, Zhang L (2016) Photoinduced controlled-release drug delivery systems for applications in nanomedicine. Curr Org Chem 20:1768–1785. https://doi.org/10.217
4/1385272820666160112001944
Yusoff SNM, Kamari A, Aljafree NFA (2016) A review of materials used as carrier agents in
pesticide formulations. Int J Environ Sci Technol 13:2977–2994. https://doi.org/10.1007/
s13762-016-1096-y
Zacherov JP (1930) Some morphological and physiological characteristics of Bacillus macerans.
Zentrabl Bakteriol Parasitenkd Infektionskrankh Hyg Abt 80:205–218
N. Morin-Crini et al.
Voncina B (2011) Chapter 17: application of cyclodextrins in textile dyeing. In: Hauser P (ed)
Textile dyeing. InTech, Tijeka, pp 373–392. ISBN: 978-953-307-565-5
Ward TJ, Armstrong DW (1986) Improved cyclodextrin chiral phases – a comparison and review.
J Liq Chromatogr 9:407–423. https://doi.org/10.1080/01483918608076644
Ward TJ, Armstrong DW (1988) Chapter 5: Cyclodextrin-stationary phases. In: Zief M, Crane LJ
(eds) Chromatographic chiral separations. Marcel Dekker Inc, New York, pp 131–163
Wenz G (1994) Cyclodextrins as building blocks for supramolecular structures and functional
units. Angew Chem Int Ed 33:803–822
Wenz G, Han BH, Müller A (2006) Cyclodextrin rotaxanes and polyrotaxanes. Chem Rev
106:782–817. https://doi.org/10.1021/cr970027+
West C (2014) Enantioselective separations with supercritical fluids – review. Curr Anal Chem
10:99–120. https://doi.org/10.2174/1573411011410010009
Whelan WJ, Manners DJ, Rosenfeld E, Gottschalk A, French D, Bell DJ, Courtois JE, Hasside
WZ (1960) Determination of starch structure by enzymes – discussion. Bull Soc Chim Biol
42:1690–1700
Wiedenhoff N, Lammers JNJJ (1968) Properties of cyclodextrins: part II. Preparation of a stable
β-cyclodextrin hydrate and determination of its water content and enthalpy of solution in water
from 15-30°. Carbohydr Res 7:1–6. https://doi.org/10.1016/S0008-6215(00)81426-3
Wilson EJ, Schoch TJ, Hudson CS (1943) The action of macerans amylase on the fractions from
starch. J Am Chem Soc 65:1380–1383
Wood DJ, Hrsuka FE, Saenger W (1977) 1H NMR study of the inclusion of aromatic molecules in
α-cyclodextrin. J Am Chem Soc 99:1735–1740
Wu ZL, Song N, Menz R, Pingali B, Yang YW, Zheng YB (2015) Nanoparticles functionalized
with supramolecular host-guest systems for nanomedicine and healthcare. Nanomedicine
10:1493–1514. https://doi.org/10.2217/NNM.15.1
Xiao Y, Ng SC, Tan TTY, Wang Y (2012) Recent development of cyclodextrin chiral stationary
phases and their applications in chromatography. J Chromatogr A 1269:52–68. https://doi.
org/10.1016/j.chroma.2012.08.049
Xu J, Wu L, Guo T, Zhang G, Wang C, Li H, Li X, Singh V, Chen W, Gref R, Zhang J (2019)
A “ship-in-a-bottle” strategy to create folic acid nanoclusters inside the nanocages of
γ-cyclodextrin metal-organic frameworks. Int J Pharm 556:89–96. https://doi.org/10.1016/j.
ijpharm.2018.11.074
Yamagiwa T, Kawaguchi AT, Saito T, Inoue S, Morita S, Watanabe K, Kitagishi H, Koji K,
Inokuchi S (2014) Supramolecular ferric porphyrins and a cyclodextrin dimer as antidotes for
cyanide poisoning. Hum Exp Toxicol 33:360–368. https://doi.org/10.1177/0960327113499041
Yamamoto Y, Inoue Y (1989) NMR-studies of cyclodextrin inclusion complex. J Carbohydr Chem
8:29–46. https://doi.org/10.1080/07328308908047990
Yang JS, Yang L (2013) Preparation and application of cyclodextrin immobilized polysaccharides.
J Mater Chem B 1:909–918. https://doi.org/10.1039/c2tb00107a
Yao XK, Huang P, Nie ZH (2019) Cyclodextrin-based polymer materials: from controlled synthesis
to applications. Prog Polym Sci 93:1–35. https://doi.org/10.1016/j.progpolymsci.2019.03.004
Yokoo M, Kubota Y, Motoyama K, Higashi T, Taniyoshi M, Tokommaru H, Nishiyama R, Tabe
Y, Mochinaga S, Sato A, Sueoka-Aragane N, Sueoka E, Arima H, Irie T, Kimura S (2015)
2-Hydroxypropyl-β-cyclodextrin acts as a novel anticancer agent. PlosOne 10:e0141946.
https://doi.org/10.1371/journal.pone.0141946
Yuan Z, Zhang L (2016) Photoinduced controlled-release drug delivery systems for applications in nanomedicine. Curr Org Chem 20:1768–1785. https://doi.org/10.217
4/1385272820666160112001944
Yusoff SNM, Kamari A, Aljafree NFA (2016) A review of materials used as carrier agents in
pesticide formulations. Int J Environ Sci Technol 13:2977–2994. https://doi.org/10.1007/
s13762-016-1096-y
Zacherov JP (1930) Some morphological and physiological characteristics of Bacillus macerans.
Zentrabl Bakteriol Parasitenkd Infektionskrankh Hyg Abt 80:205–218
N. Morin-Crini et al.