84
Motoyama K, Onodera R, Tanaka N, Kameyama K, Higashi T, Kariya R, Okada S, Arima H (2015)
Evaluation of antitumor effects of folate-conjugated methyl-β-cyclodextrin in melanoma. Biol
Pharm Bull 38:374–379. https://doi.org/10.1248/bpb.b14-00531
Muankaew C, Loftsson T (2018) Cyclodextrin-based formulations: a non-invasive platform for
targeted drug delivery. Basic Clin Pharmacol Toxicol 122:46–55. https://doi.org/10.1111/
bcpt.12917
Müller S, Estour F, Kalakuntla RK, Le P, Romain LO, Worek F, Thiermann H, Reiter G (2013)
New modified beta-cyclodextrin derivatives as detoxifying agents of chemicalwarfare agents
(II). In vitro detoxification of cyclosarin (GF): general screening and toxicokineticaspects of
OP scavengers. Toxicol Lett 216:206–212
Myrbäck K (1938) Beta-dextrin and starch. I. Announcement. Biochem Z 297:160–171
Myrbäck K (1942) Article on border dextrin and starch. XVI. On the nature of alpha-dextrin.
Biochem Z 311:242–246
Myrbäck K (1949a) On the action of Bacillus macerans amylase. Acta Chem Scand 3:91–93
Myrbäck K (1949b) Nonoxidative, nonproteolytic enzymes. Annu Rev Biochem 18:59–86
Myrbäck K, Ahlborg K (1940) About limit dextrin and starch. VIII. Announcement: constitution of
starch limit dextrin. Evidence of alpha-glycoside 1,6-bindings in dextrin and starch. Biochem
Z 307:69–78
Myrbäck K, Gjörling LG (1945) Über die starkespaltung durch Bacillus macerans. Ark Kemi Min
Och Geol 20:1–13
Nepogodiev S, Stoddart FJ (1998) Cyclodextrin-based catenanes and rotaxanes. Chem Rev
98:1959–1576. https://doi.org/10.1021/cr970049w
Neva T, Mellet CO, Fernandez JMG, Benito JM (2019) Multiply-linked cyclodextrin- aromatic
hybrids: caps, hinges and clips. J Carbohydr Chem. https://doi.org/10.1080/0732830
3.2019.1609020
Nociari MM, Lehmann GL, Perez Bay AE, Radu RA, Jiang Z, Goicochea S, Schreiner R, Warren
JD, Shan J, de Beaumais SA, Ménand M, Sollogoub M, Maxfield FR, Rodriguez-Boulan E
(2014) Beta cyclodextrins bind, stabilize, and remove lipofuscin bisretinoids from retinal
pigment epithelium. Proc Natl Acad Sci U S A 111:E1402–E1408. https://doi.org/10.1073/
pnas.1400530111
Norberg E, French D (1950) Studies on the Schardinger dextrins. III. Redistribution reactions of
Macerans amylase. J Am Chem Soc 72:1202–1205. https://doi.org/10.1021/ja01159a036
Okada S (1979) Application of cyclodextrin glycosyltransferase – review. Hakkokogaku Kaishi J
Soc Ferment Technol 57:396–406
Okano C, Nasuno E, Iimura K, Kato N (2016) Cyclodextrin-immobilized microspheres for uptake
of the quorum-sensing signaling molecule N-acylhomoserine lactone. J Appl Polym Sci
133:43198. https://doi.org/10.1002/app.43198
Oliveri V, Vecchio G (2016) Cyclodextrins as protective agents of protein aggregation: an overview. Chem Asian J 11:1648–1657. https://doi.org/10.1002/asia.201600259
Osa T, Matsue T, Fujihira M (1977) Cyclodextrin-nitrophenol systems studied by polarography.
Heterocycles 6:1833–1839
Osaki M (2019) Functionalization of cyclodextrin derivatives to create supramolecular pharmaceutical materials. J Pharm Soc Japan 139:165–173
Pawar S, Shende P (2019) A comprehensive patent review on beta-cyclodextrin cross-linked nanosponges for multiple applications. Recent Pat Nanotechnol 14(1):75–89. https://doi.org/10.217
4/1872210513666190603083930
Perez-Anes A, Gargouri M, Laure W, Van Den Berghe H, Courcot E, Sobocinski J, Tabary N,
Chai F, Blach JF, Addad A, Woisel P, Douroumis D, Martel B, Blanchemain N, Lyskawa J
(2015) Bioinspired titanium drug eluting platforms based on a poly-beta-cyclodextrin-chitosan
layer-by-layer self-assembly targeting infections. ACS Appl Mater Interfaces 7:12882–12893.
https://doi.org/10.1021/acsami.5b02402
Pictet A, Jahn R (1922) Sur un nouveau produit de dépolymérisation de l’amidon. Helv Chim Acta
5:640–644. https://doi.org/10.1002/hlca.19220050503
N. Morin-Crini et al.
Motoyama K, Onodera R, Tanaka N, Kameyama K, Higashi T, Kariya R, Okada S, Arima H (2015)
Evaluation of antitumor effects of folate-conjugated methyl-β-cyclodextrin in melanoma. Biol
Pharm Bull 38:374–379. https://doi.org/10.1248/bpb.b14-00531
Muankaew C, Loftsson T (2018) Cyclodextrin-based formulations: a non-invasive platform for
targeted drug delivery. Basic Clin Pharmacol Toxicol 122:46–55. https://doi.org/10.1111/
bcpt.12917
Müller S, Estour F, Kalakuntla RK, Le P, Romain LO, Worek F, Thiermann H, Reiter G (2013)
New modified beta-cyclodextrin derivatives as detoxifying agents of chemicalwarfare agents
(II). In vitro detoxification of cyclosarin (GF): general screening and toxicokineticaspects of
OP scavengers. Toxicol Lett 216:206–212
Myrbäck K (1938) Beta-dextrin and starch. I. Announcement. Biochem Z 297:160–171
Myrbäck K (1942) Article on border dextrin and starch. XVI. On the nature of alpha-dextrin.
Biochem Z 311:242–246
Myrbäck K (1949a) On the action of Bacillus macerans amylase. Acta Chem Scand 3:91–93
Myrbäck K (1949b) Nonoxidative, nonproteolytic enzymes. Annu Rev Biochem 18:59–86
Myrbäck K, Ahlborg K (1940) About limit dextrin and starch. VIII. Announcement: constitution of
starch limit dextrin. Evidence of alpha-glycoside 1,6-bindings in dextrin and starch. Biochem
Z 307:69–78
Myrbäck K, Gjörling LG (1945) Über die starkespaltung durch Bacillus macerans. Ark Kemi Min
Och Geol 20:1–13
Nepogodiev S, Stoddart FJ (1998) Cyclodextrin-based catenanes and rotaxanes. Chem Rev
98:1959–1576. https://doi.org/10.1021/cr970049w
Neva T, Mellet CO, Fernandez JMG, Benito JM (2019) Multiply-linked cyclodextrin- aromatic
hybrids: caps, hinges and clips. J Carbohydr Chem. https://doi.org/10.1080/0732830
3.2019.1609020
Nociari MM, Lehmann GL, Perez Bay AE, Radu RA, Jiang Z, Goicochea S, Schreiner R, Warren
JD, Shan J, de Beaumais SA, Ménand M, Sollogoub M, Maxfield FR, Rodriguez-Boulan E
(2014) Beta cyclodextrins bind, stabilize, and remove lipofuscin bisretinoids from retinal
pigment epithelium. Proc Natl Acad Sci U S A 111:E1402–E1408. https://doi.org/10.1073/
pnas.1400530111
Norberg E, French D (1950) Studies on the Schardinger dextrins. III. Redistribution reactions of
Macerans amylase. J Am Chem Soc 72:1202–1205. https://doi.org/10.1021/ja01159a036
Okada S (1979) Application of cyclodextrin glycosyltransferase – review. Hakkokogaku Kaishi J
Soc Ferment Technol 57:396–406
Okano C, Nasuno E, Iimura K, Kato N (2016) Cyclodextrin-immobilized microspheres for uptake
of the quorum-sensing signaling molecule N-acylhomoserine lactone. J Appl Polym Sci
133:43198. https://doi.org/10.1002/app.43198
Oliveri V, Vecchio G (2016) Cyclodextrins as protective agents of protein aggregation: an overview. Chem Asian J 11:1648–1657. https://doi.org/10.1002/asia.201600259
Osa T, Matsue T, Fujihira M (1977) Cyclodextrin-nitrophenol systems studied by polarography.
Heterocycles 6:1833–1839
Osaki M (2019) Functionalization of cyclodextrin derivatives to create supramolecular pharmaceutical materials. J Pharm Soc Japan 139:165–173
Pawar S, Shende P (2019) A comprehensive patent review on beta-cyclodextrin cross-linked nanosponges for multiple applications. Recent Pat Nanotechnol 14(1):75–89. https://doi.org/10.217
4/1872210513666190603083930
Perez-Anes A, Gargouri M, Laure W, Van Den Berghe H, Courcot E, Sobocinski J, Tabary N,
Chai F, Blach JF, Addad A, Woisel P, Douroumis D, Martel B, Blanchemain N, Lyskawa J
(2015) Bioinspired titanium drug eluting platforms based on a poly-beta-cyclodextrin-chitosan
layer-by-layer self-assembly targeting infections. ACS Appl Mater Interfaces 7:12882–12893.
https://doi.org/10.1021/acsami.5b02402
Pictet A, Jahn R (1922) Sur un nouveau produit de dépolymérisation de l’amidon. Helv Chim Acta
5:640–644. https://doi.org/10.1002/hlca.19220050503
N. Morin-Crini et al.