83
Malanga M, Seggio M, Kirejev V, Fraix A, Di Bari I, Fenyvesi É, Ericson MB, Sortino S (2019)
A phototherapeutic fluorescent β-cyclodextrin branched polymer delivering nitric oxide.
Biomater Sci 7:2272–2276. https://doi.org/10.1039/C9BM00395A
Matzuzawa M, Kawano M, Nakamura N, Horikoshi K (1975) An improved method for the
preparation of Schardinger β-dextrin on an industrial scale by cyclodextrin glycosyl transferase of an alkalophilic Bacillus sp. Starch/Die Stärke 27:410–413. https://doi.org/10.1002/
star.19750271204
Mavridis IM, Yannakopoulou K (2015) Anionic cyclodextrins as versatile hosts for pharmaceutical nanotechnology: synthesis, drug delivery, enantioselectivity, contrast agents for MRI. Int J
Pharm 492:275–290. https://doi.org/10.1016/j.ijpharm.2015.06.004
McClenahan WS, Tilden EB, Hudson CS (1942) A study of the products obtained from starch by
the action of the amylase of Bacillus macerans. J Am Chem Soc 64:2139–2144
McMullan RK, Saenger W, Fayos J, Mootz D (1973a) Topography of cyclodextrin inclusion complexes. 1. Classification of crystallographic data of alpha-cyclodextrin inclusion complexes.
Carbohydr Res 31:37–46
McMullan RK, Saenger W, Fayos J, Mootz D (1973b) Topography of cyclodextrin inclusion complexes. 2. Iodine-cyclohexaamylose tetrahydrate complex. Its molecular geometry and cagetype crystal-structure. Carbohydr Res 31:211–227
Melotti A, Mas C, Kuciak M, Lorente-Trigos A, Borges I, Ruiz i Altaba A (2014) The river blindness drug ivermectin and related macrocyclic lactones inhibit WNT-TCF pathway responses
in human cancer. EMBO Mol Med 6:1263–1278. https://doi.org/10.15252/emmm.201404084
Menezes PD, Andrade TD, Frank LA, de Souza EPBSS, Trindade GDG, Trindade IAS, Serafini
MR, Guterres SS, Araujo AAD (2019) Advances of nanosystems containing cyclodextrins
and their applications in pharmaceuticals. Int J Pharm 559:312–328. https://doi.org/10.1016/j.
ijpharm.2019.01.041
Menges RA, Armstrong DW (1991) Chiral separations using native and functionalized cyclodextrinbonded stationary phases in high-pressure liquid-chromatography. ACS Symp Ser 471:67–100
Miekeley A (1930) Über die fragliche existenz der sog. α-diamylose. Ber Dtsch Chem Ges
63:1957–1961
Miekeley A (1932) Bemerkung zür existenz des α-diamylose. Ber Dtsch Chem Ges 65:69–69
Miller KP, Wang L, Chen YP, Pellechia PJ, Benicewicz BC, Decho AW (2015) Engineering
nanoparticles to silence bacterial communication. Front Microbiol 6:189. https://doi.
org/10.3389/fmicb.2015.00189
Mitchell CR, Armstrong DW (2004) Cyclodextrin-based chiral stationary phases for liquid chromatography: a twenty-year overview. In: Gübitz G, Schmid MG (eds) Chiral separations –
methods and protocols, Methods in molecular biology, vol 243. Humana Press Inc, Totowa,
pp 61–112. ISBN: 1-58829-150-2
Miyazawa I, Ueda H, Nagase H, Endo T, Kobayashi S, Nagai T (1995) Physicochemical properties
and inclusion complex formation of δ-cyclodextrin. Eur J Pharm Sci 3:153–162
Mocanu G, Vizitiu D, Carpov A (2001) Cyclodextrin polymers. J Bioact Compat Polym 16:315–342
Morillo E (2006) Chapter 16: Application of cyclodextrins in agrochemistry. In: Dodziuk H (ed)
Cyclodextrins and their complexes. Chemistry, analytical methods, applications. Wiley-VCH,
Verlag GmbH & Co. KGaA, Weinheim, pp 459–467
Morin-Crini N, Fourmentin S, Crini G (eds) (2015) Cyclodextrines. PUFC, Besançon, 370 p.
ISBN: 978-2-84867-520-6
Morin-Crini N, Fourmentin M, Fourmentin S, Torri G, Crini G (2018) Synthesis of silica materials containing cyclodextrin and their applications in wastewater treatment. Environ Chem Lett
16:1361–1375. https://doi.org/10.1007/s10311-018-00818-0
Morohoshi T, Tokita K, Ito S, Saito Y, Maeda S, Kato K, Ikeda T (2013) Inhibition of quorum
sensing in gram-negative bacteria by alkylamine-modified cyclodextrins. J Biosci Bioeng
116:175–179. https://doi.org/10.1016/j.jbiosc.2013.01.022
1 History of Cyclodextrins
Malanga M, Seggio M, Kirejev V, Fraix A, Di Bari I, Fenyvesi É, Ericson MB, Sortino S (2019)
A phototherapeutic fluorescent β-cyclodextrin branched polymer delivering nitric oxide.
Biomater Sci 7:2272–2276. https://doi.org/10.1039/C9BM00395A
Matzuzawa M, Kawano M, Nakamura N, Horikoshi K (1975) An improved method for the
preparation of Schardinger β-dextrin on an industrial scale by cyclodextrin glycosyl transferase of an alkalophilic Bacillus sp. Starch/Die Stärke 27:410–413. https://doi.org/10.1002/
star.19750271204
Mavridis IM, Yannakopoulou K (2015) Anionic cyclodextrins as versatile hosts for pharmaceutical nanotechnology: synthesis, drug delivery, enantioselectivity, contrast agents for MRI. Int J
Pharm 492:275–290. https://doi.org/10.1016/j.ijpharm.2015.06.004
McClenahan WS, Tilden EB, Hudson CS (1942) A study of the products obtained from starch by
the action of the amylase of Bacillus macerans. J Am Chem Soc 64:2139–2144
McMullan RK, Saenger W, Fayos J, Mootz D (1973a) Topography of cyclodextrin inclusion complexes. 1. Classification of crystallographic data of alpha-cyclodextrin inclusion complexes.
Carbohydr Res 31:37–46
McMullan RK, Saenger W, Fayos J, Mootz D (1973b) Topography of cyclodextrin inclusion complexes. 2. Iodine-cyclohexaamylose tetrahydrate complex. Its molecular geometry and cagetype crystal-structure. Carbohydr Res 31:211–227
Melotti A, Mas C, Kuciak M, Lorente-Trigos A, Borges I, Ruiz i Altaba A (2014) The river blindness drug ivermectin and related macrocyclic lactones inhibit WNT-TCF pathway responses
in human cancer. EMBO Mol Med 6:1263–1278. https://doi.org/10.15252/emmm.201404084
Menezes PD, Andrade TD, Frank LA, de Souza EPBSS, Trindade GDG, Trindade IAS, Serafini
MR, Guterres SS, Araujo AAD (2019) Advances of nanosystems containing cyclodextrins
and their applications in pharmaceuticals. Int J Pharm 559:312–328. https://doi.org/10.1016/j.
ijpharm.2019.01.041
Menges RA, Armstrong DW (1991) Chiral separations using native and functionalized cyclodextrinbonded stationary phases in high-pressure liquid-chromatography. ACS Symp Ser 471:67–100
Miekeley A (1930) Über die fragliche existenz der sog. α-diamylose. Ber Dtsch Chem Ges
63:1957–1961
Miekeley A (1932) Bemerkung zür existenz des α-diamylose. Ber Dtsch Chem Ges 65:69–69
Miller KP, Wang L, Chen YP, Pellechia PJ, Benicewicz BC, Decho AW (2015) Engineering
nanoparticles to silence bacterial communication. Front Microbiol 6:189. https://doi.
org/10.3389/fmicb.2015.00189
Mitchell CR, Armstrong DW (2004) Cyclodextrin-based chiral stationary phases for liquid chromatography: a twenty-year overview. In: Gübitz G, Schmid MG (eds) Chiral separations –
methods and protocols, Methods in molecular biology, vol 243. Humana Press Inc, Totowa,
pp 61–112. ISBN: 1-58829-150-2
Miyazawa I, Ueda H, Nagase H, Endo T, Kobayashi S, Nagai T (1995) Physicochemical properties
and inclusion complex formation of δ-cyclodextrin. Eur J Pharm Sci 3:153–162
Mocanu G, Vizitiu D, Carpov A (2001) Cyclodextrin polymers. J Bioact Compat Polym 16:315–342
Morillo E (2006) Chapter 16: Application of cyclodextrins in agrochemistry. In: Dodziuk H (ed)
Cyclodextrins and their complexes. Chemistry, analytical methods, applications. Wiley-VCH,
Verlag GmbH & Co. KGaA, Weinheim, pp 459–467
Morin-Crini N, Fourmentin S, Crini G (eds) (2015) Cyclodextrines. PUFC, Besançon, 370 p.
ISBN: 978-2-84867-520-6
Morin-Crini N, Fourmentin M, Fourmentin S, Torri G, Crini G (2018) Synthesis of silica materials containing cyclodextrin and their applications in wastewater treatment. Environ Chem Lett
16:1361–1375. https://doi.org/10.1007/s10311-018-00818-0
Morohoshi T, Tokita K, Ito S, Saito Y, Maeda S, Kato K, Ikeda T (2013) Inhibition of quorum
sensing in gram-negative bacteria by alkylamine-modified cyclodextrins. J Biosci Bioeng
116:175–179. https://doi.org/10.1016/j.jbiosc.2013.01.022
1 History of Cyclodextrins