72
Benkovics G, Afonso D, Darcsi A, Béni S, Conoci S, Fenyvesi É, Szente L, Malanga M, Sortino S
(2017) Novel β-cyclodextrin-eosin conjugates. Beilstein J Org Chem 13:543–551. https://doi.
org/10.3762/bjoc.13.52
Bergeron RJ (1984) Chapter 12: Cycloamylose-substrate binding. In: Atwood JL, JED D, DD MN
(eds) Inclusion compounds, vol 3. Academic, London, pp 391–443
Bergeron RJ, McPhie P (1979) Circular dichroism studies on the structure of p-nitro-phenolatecycloamylose complexes. Bioorg Chem 6:465–436
Bilensoy E (ed) (2011) Cyclodextrins in pharmaceutics, cosmetics and biomedicine. Current
and future industrial applications. John Wiley & Sons, Inc., Hoboken, 395 p. https://doi.
org/10.1002/9780470926819
Biltz W (1913) Über den osmotischen druck der kolloide. Fünfte mitteilung: zur kolloidchemie der
dextrine (On the osmotic pressure of colloids. Fitfh announcement: on the colloid chemistry of
dextrins). Z Phys Chem 83:683–707. https://doi.org/10.1515/zpch-1913-8348
Biltz W, Truthe W (1913) Über die molekulargrösse von dextrin β (The molecular size of β-dextrin).
Ber Dtsch Chem Ges 46:1377–1380. https://doi.org/10.1002/cber.19130460217
Blinc M (1941) Gewinnung des enzyms von Bacillus macerans und seine wirkungsweise. Arch
Mikrobiol 12:183–191
Blinc M (1942) Experiments to concentrate the macerans enzyme. Kolloid Z 101:126–128
Borchert W (1948) Röntgenographische untersuchungen an Shardinger-dextrinen. Z Naturforsch
B 3:464–465
Brackman G, Garcia-Fernandez MJ, Lenoir J, De Meyer L, Remon JP, De Beer T, Concheiro
A, Alvarez-Lorenzo C, Coenye T (2016) Dressings loaded with cyclodextrin-hamamelitannin
complexes increase Staphylococcus aureus susceptibility toward antibiotics both in single as
well as in mixed biofilm communities. Macromol Biosci 16:859–869. https://doi.org/10.1002/
mabi.201500437
Brauns U, Müller BW (1983) Pharmaceutical compositions drugs which are unstable or sparingly
soluble in water, and methods for their preparation. European Patent No. 149197, 21 March
1990, with priority from German Patent DE No. 3346123, 21 December 1983
Breslow R (1979) Biomimetic chemistry in oriented systems. Isr J Chem 18:187–191
Breslow R, Dong SD (1998) Biomimetic reactions catalyzed by cyclodextrins and their derivatives. Chem Rev 98:1997–2012. https://doi.org/10.1021/cr970011j
Breslow R, Czarniecki MF, Emert J, Hamaguchi H (1980) Improved acylation rates within cyclodextrin complexes from flexible capping of the cyclodextrin and from adjustment of the substrate geometry. J Am Chem Soc 102:762–770
Brewster ME, Loftsson T (2002) The use of chemically modified cyclodextrins in the development
of formulations for chemical delivery systems. Pharmazie 57:94–101
Brewster ME, Loftsson T (2007) Cyclodextrins as pharmaceutical solubilizers. Adv Drug Deliv
Rev 59:645–666. https://doi.org/10.1016/j.addr.2007.05.012
Brewster ME, Loftsson T, Bodor N (2004) Applications of chemically-modified cyclodextrins: use
of hydroxypropyl-beta-cyclodextrin as an enabling excipient for brain targeting, redox-based
derivatives of estradiol a review of preclinical and clinical findings. J Drug Del Sci Technol
14:32–34
Buschmann HJ, Schollmeyer EJ (2002) Applications of cyclodextrins in cosmetic products: a
review. J Cosmet Sci 53:185–191
Buschmann HJ, Schollmeyer E (2004) Cosmetic textiles: a new functionality of clothes. Cosmet
Toiletries 11:105–112
Buschmann HJ, Denter U, Knittel D, Schollmeyer E (1998) The use of cyclodextrins in textile
processes – an overview. J Text Inst 89:554–561. https://doi.org/10.1080/00405009808658641
Cael JJ, Koenig JL, Blackwell J (1973) Infrared and Raman spectroscopy of carbohydrates.
III. Raman spectra of the polymorphic forms of amylose. Carbohydr Res 29:123–134
Caesar GV (1968) Chapter 5: The Schardinger dextrins. In: Radley JA (ed) Starch and its derivatives, 4th edn. Chapman and Hall Ltd., EC4, London, pp 290–305
N. Morin-Crini et al.
Benkovics G, Afonso D, Darcsi A, Béni S, Conoci S, Fenyvesi É, Szente L, Malanga M, Sortino S
(2017) Novel β-cyclodextrin-eosin conjugates. Beilstein J Org Chem 13:543–551. https://doi.
org/10.3762/bjoc.13.52
Bergeron RJ (1984) Chapter 12: Cycloamylose-substrate binding. In: Atwood JL, JED D, DD MN
(eds) Inclusion compounds, vol 3. Academic, London, pp 391–443
Bergeron RJ, McPhie P (1979) Circular dichroism studies on the structure of p-nitro-phenolatecycloamylose complexes. Bioorg Chem 6:465–436
Bilensoy E (ed) (2011) Cyclodextrins in pharmaceutics, cosmetics and biomedicine. Current
and future industrial applications. John Wiley & Sons, Inc., Hoboken, 395 p. https://doi.
org/10.1002/9780470926819
Biltz W (1913) Über den osmotischen druck der kolloide. Fünfte mitteilung: zur kolloidchemie der
dextrine (On the osmotic pressure of colloids. Fitfh announcement: on the colloid chemistry of
dextrins). Z Phys Chem 83:683–707. https://doi.org/10.1515/zpch-1913-8348
Biltz W, Truthe W (1913) Über die molekulargrösse von dextrin β (The molecular size of β-dextrin).
Ber Dtsch Chem Ges 46:1377–1380. https://doi.org/10.1002/cber.19130460217
Blinc M (1941) Gewinnung des enzyms von Bacillus macerans und seine wirkungsweise. Arch
Mikrobiol 12:183–191
Blinc M (1942) Experiments to concentrate the macerans enzyme. Kolloid Z 101:126–128
Borchert W (1948) Röntgenographische untersuchungen an Shardinger-dextrinen. Z Naturforsch
B 3:464–465
Brackman G, Garcia-Fernandez MJ, Lenoir J, De Meyer L, Remon JP, De Beer T, Concheiro
A, Alvarez-Lorenzo C, Coenye T (2016) Dressings loaded with cyclodextrin-hamamelitannin
complexes increase Staphylococcus aureus susceptibility toward antibiotics both in single as
well as in mixed biofilm communities. Macromol Biosci 16:859–869. https://doi.org/10.1002/
mabi.201500437
Brauns U, Müller BW (1983) Pharmaceutical compositions drugs which are unstable or sparingly
soluble in water, and methods for their preparation. European Patent No. 149197, 21 March
1990, with priority from German Patent DE No. 3346123, 21 December 1983
Breslow R (1979) Biomimetic chemistry in oriented systems. Isr J Chem 18:187–191
Breslow R, Dong SD (1998) Biomimetic reactions catalyzed by cyclodextrins and their derivatives. Chem Rev 98:1997–2012. https://doi.org/10.1021/cr970011j
Breslow R, Czarniecki MF, Emert J, Hamaguchi H (1980) Improved acylation rates within cyclodextrin complexes from flexible capping of the cyclodextrin and from adjustment of the substrate geometry. J Am Chem Soc 102:762–770
Brewster ME, Loftsson T (2002) The use of chemically modified cyclodextrins in the development
of formulations for chemical delivery systems. Pharmazie 57:94–101
Brewster ME, Loftsson T (2007) Cyclodextrins as pharmaceutical solubilizers. Adv Drug Deliv
Rev 59:645–666. https://doi.org/10.1016/j.addr.2007.05.012
Brewster ME, Loftsson T, Bodor N (2004) Applications of chemically-modified cyclodextrins: use
of hydroxypropyl-beta-cyclodextrin as an enabling excipient for brain targeting, redox-based
derivatives of estradiol a review of preclinical and clinical findings. J Drug Del Sci Technol
14:32–34
Buschmann HJ, Schollmeyer EJ (2002) Applications of cyclodextrins in cosmetic products: a
review. J Cosmet Sci 53:185–191
Buschmann HJ, Schollmeyer E (2004) Cosmetic textiles: a new functionality of clothes. Cosmet
Toiletries 11:105–112
Buschmann HJ, Denter U, Knittel D, Schollmeyer E (1998) The use of cyclodextrins in textile
processes – an overview. J Text Inst 89:554–561. https://doi.org/10.1080/00405009808658641
Cael JJ, Koenig JL, Blackwell J (1973) Infrared and Raman spectroscopy of carbohydrates.
III. Raman spectra of the polymorphic forms of amylose. Carbohydr Res 29:123–134
Caesar GV (1968) Chapter 5: The Schardinger dextrins. In: Radley JA (ed) Starch and its derivatives, 4th edn. Chapman and Hall Ltd., EC4, London, pp 290–305
N. Morin-Crini et al.