81
Komiyama M (1996) Cyclodextrins as enzyme models. In: Szejtli J, Osa T (eds) Comprehensive
supramolecular chemistry, vol 3. Pergamon Oxford, London, pp 401–422
Komiyama M, Hirai H (1981) Carbon 13 NMR study on the cyclodextrin inclusion complexes in
solution. Bull Chem Soc Jpn 54:828–831
Kozlowski CA, Sliwa W (2010) Use of cyclodextrin polymers in separation of organic species,
Polymer science and technology series. Nova Science Publishers, Inc, New York
Krysl S, Smolková-Keulemansová E (1985) Cyclodextrins and their utilization in chromatographic
methods. Chem List 79:919–942
Kumar S, Rao R (2019) Analytical tools for cyclodextrin nanosponges in pharmaceutical field: a
review. J Incl Phenom Macrocycl Chem 94:11–30. https://doi.org/10.1007/s10847-019-00903-z
Kurkov SV, Loftsson T (2013) Cyclodextrins. Int J Pharm 453:167–180. https://doi.org/10.1016/j.
ijpharm.2012.06.055
Kurozumi M, Nambu N, Nagai T (1975) Inclusion compounds of non-steroidal anti-inflammatory
and other slightly water soluble drugs with α- and β-cyclodextrins in powdered form. Chem
Pharm Bull 23:3062–3068
Lach JL, Chin TF (1964) Interaction of pharmaceuticals with Schardinger dextrins. III. J Pharm
Sci 53:69–73
Lach JL, Cohen J (1963) Interaction of pharmaceuticals with Schardinger dextrins. II. J Pharm
Sci 52:137–142
Lammers JNJJ (1967) A new purity criterion for α- and β-cyclodextrin using partition chromatography on cellulose columns. Die Stärke 19:70–73. https://doi.org/10.1002/star.19670190304
Landy D, Mallard I, Ponchel A, Monflier E, Fourmentin S (2012) Remediation technologies
using cyclodextrins: an overview. Environ Chem Lett 10:225–237. https://doi.org/10.1007/
s10311-011-0351-1
Lange F (1925) Verfahren zur gewinnung von polyamylosen. German Patent, Patentschrift n°
442963, I.G. Farbenindustrie Akt.-Ges. In Frankfurt
Larsen KL (2002) Large cyclodextrins. J Incl Phenom 43:1–13. https://doi.org/10.102
3/A:1020494503684
Lau EV, Gan SY, Ng HK, Poh PE (2014) Extraction agents for the removal of polycyclic aromatic
hydrocarbons (PAHs) from soil in soil washing technologies. Environ Pollut 184:640–649.
https://doi.org/10.1016/j.envpol.2013.09.010
Lau MT, Manion J, Littleboy JB, Oyston L, Khuong TM, Wang QP, Nguyen DT, Hesselson
D, Seymour J, Neely GG (2019) Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote. Nat Commun 10:1655. https://doi.org/10.1038/
s41467-019-09681-1
Lautsch W, von Wiechert R, Lehman H (1954) Tosyl- and mesyl derivative der cyclodextrine.
Kollloid Z 135:134–136
Lay S, Ni XF, Yu HN, Shen SR (2016) State-of-the-art applications of cyclodextrins as functional
monomers in molecular imprinting techniques: a review. J Sep Sci 39:2321–2331. https://doi.
org/10.1002/jssc.201600003
Lee SB, Robyt JF (2001) Trapping of a covalent enzyme intermediate in the reaction of Bacillus
macerans cyclomaltodextrin glucanyltransferase with cyclomaltohexaose. Carbohydr Res
336:47–53. https://doi.org/10.1016/S0008-6215(01)00247-6
Lepage ML, Schneider JP, Bodlenner A, Compain P (2015) Toward a molecular Lego approach for
the diversity-oriented synthesis of cyclodextrin analogues designed as scaffolds for multivalent
systems. J Organomet Chem 80:10719–10733. https://doi.org/10.1021/acs.joc.5b01938
Lewis EA, Hansen LD (1973) Thermodynamics of binding of guest molecules to α- and
β-cyclodextrins. J Chem Soc Perkin Trans II:2081–2085
Li J (2009) Cyclodextrin inclusion polymers forming hydrogels. In: Wenz G (ed) Inclusion polymers, Advances in polymer science, vol 222, pp 79–112. https://doi.org/10.1007/12_2008_9
Li S, Purdy WC (1992) Cyclodextrins and their applications in analytical chemistry. Chem Rev
92:1457–1470
1 History of Cyclodextrins
Komiyama M (1996) Cyclodextrins as enzyme models. In: Szejtli J, Osa T (eds) Comprehensive
supramolecular chemistry, vol 3. Pergamon Oxford, London, pp 401–422
Komiyama M, Hirai H (1981) Carbon 13 NMR study on the cyclodextrin inclusion complexes in
solution. Bull Chem Soc Jpn 54:828–831
Kozlowski CA, Sliwa W (2010) Use of cyclodextrin polymers in separation of organic species,
Polymer science and technology series. Nova Science Publishers, Inc, New York
Krysl S, Smolková-Keulemansová E (1985) Cyclodextrins and their utilization in chromatographic
methods. Chem List 79:919–942
Kumar S, Rao R (2019) Analytical tools for cyclodextrin nanosponges in pharmaceutical field: a
review. J Incl Phenom Macrocycl Chem 94:11–30. https://doi.org/10.1007/s10847-019-00903-z
Kurkov SV, Loftsson T (2013) Cyclodextrins. Int J Pharm 453:167–180. https://doi.org/10.1016/j.
ijpharm.2012.06.055
Kurozumi M, Nambu N, Nagai T (1975) Inclusion compounds of non-steroidal anti-inflammatory
and other slightly water soluble drugs with α- and β-cyclodextrins in powdered form. Chem
Pharm Bull 23:3062–3068
Lach JL, Chin TF (1964) Interaction of pharmaceuticals with Schardinger dextrins. III. J Pharm
Sci 53:69–73
Lach JL, Cohen J (1963) Interaction of pharmaceuticals with Schardinger dextrins. II. J Pharm
Sci 52:137–142
Lammers JNJJ (1967) A new purity criterion for α- and β-cyclodextrin using partition chromatography on cellulose columns. Die Stärke 19:70–73. https://doi.org/10.1002/star.19670190304
Landy D, Mallard I, Ponchel A, Monflier E, Fourmentin S (2012) Remediation technologies
using cyclodextrins: an overview. Environ Chem Lett 10:225–237. https://doi.org/10.1007/
s10311-011-0351-1
Lange F (1925) Verfahren zur gewinnung von polyamylosen. German Patent, Patentschrift n°
442963, I.G. Farbenindustrie Akt.-Ges. In Frankfurt
Larsen KL (2002) Large cyclodextrins. J Incl Phenom 43:1–13. https://doi.org/10.102
3/A:1020494503684
Lau EV, Gan SY, Ng HK, Poh PE (2014) Extraction agents for the removal of polycyclic aromatic
hydrocarbons (PAHs) from soil in soil washing technologies. Environ Pollut 184:640–649.
https://doi.org/10.1016/j.envpol.2013.09.010
Lau MT, Manion J, Littleboy JB, Oyston L, Khuong TM, Wang QP, Nguyen DT, Hesselson
D, Seymour J, Neely GG (2019) Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote. Nat Commun 10:1655. https://doi.org/10.1038/
s41467-019-09681-1
Lautsch W, von Wiechert R, Lehman H (1954) Tosyl- and mesyl derivative der cyclodextrine.
Kollloid Z 135:134–136
Lay S, Ni XF, Yu HN, Shen SR (2016) State-of-the-art applications of cyclodextrins as functional
monomers in molecular imprinting techniques: a review. J Sep Sci 39:2321–2331. https://doi.
org/10.1002/jssc.201600003
Lee SB, Robyt JF (2001) Trapping of a covalent enzyme intermediate in the reaction of Bacillus
macerans cyclomaltodextrin glucanyltransferase with cyclomaltohexaose. Carbohydr Res
336:47–53. https://doi.org/10.1016/S0008-6215(01)00247-6
Lepage ML, Schneider JP, Bodlenner A, Compain P (2015) Toward a molecular Lego approach for
the diversity-oriented synthesis of cyclodextrin analogues designed as scaffolds for multivalent
systems. J Organomet Chem 80:10719–10733. https://doi.org/10.1021/acs.joc.5b01938
Lewis EA, Hansen LD (1973) Thermodynamics of binding of guest molecules to α- and
β-cyclodextrins. J Chem Soc Perkin Trans II:2081–2085
Li J (2009) Cyclodextrin inclusion polymers forming hydrogels. In: Wenz G (ed) Inclusion polymers, Advances in polymer science, vol 222, pp 79–112. https://doi.org/10.1007/12_2008_9
Li S, Purdy WC (1992) Cyclodextrins and their applications in analytical chemistry. Chem Rev
92:1457–1470
1 History of Cyclodextrins