73
Campos EVR, de Oliveira JL, Fraceto LF, Singh B (2015) Polysaccharides as safer release systems
for agrochemicals. Agron Sustain Dev 35:47–66. https://doi.org/10.1007/s13593-014-0263-0
Carneiro SB, Duarte FIC, Heimfarth L, Quintans JDS, Quintans LJ, da Veiga VF, de Lima AAN
(2019) Cyclodextrin-drug inclusion complexes: in vivo and in vitro approaches. Int J Mol Sci
20:642. https://doi.org/10.3390/ijms20030642
Casu B (1964) Spectrometric identification of organic compounds. Chim Ind 46:1425–1429
Casu B (1966) Recent contributions to knowledge of amylose and cyclodextrins structure. Chim
Ind 48:921–923
Casu B, Reggiani M (1964) Infrared spectra of amylose and its oligomers. J Polym Sci Part C
7:171–185
Casu B, Reggiani M (1966) Conformation of amylose and its derived products. I. Infrared spectra of amylose and its oligomers in the amorphous solid phase and in solution. Starch/Stärke
18:218–229. https://doi.org/10.1002/star.19660180704
Casu B, Reggiani M, Gallo GG, Vigevani A (1964) Hydroxyl proton resonances of sugars in
dimethylsulphoxide solution. Tetrahedron Lett 39-4:2839–2284
Casu B, Reggiani M, Gallo GG, Vigevani A (1965) NMR spectra and conformation of glucose and
some related carbohydrates in dimethylsulphoxide solution. Tetrahedron Lett 27:2253–2259
Casu B, Gallo GG, Reggiani M, Vigevani A (1968a) Applications of magnetic resonance spectroscopy of hydroxyl protons to analysis of starch-derived products. Starch/Stärke 20:387–391.
https://doi.org/10.1002/star.19680201202
Casu B, Reggiani M, Gallo GG, Vigevani A (1968b) Applications of magnetic resonance spectroscopy of the hydroxyl protons to the analysis of starch-derived products. X Congress of the
Italian Chemical Society, Padova, Italy, June 1968
Casu B, Reggiani M, Gallo GG, Vigevani A (1968c) Conformation of O-methylated amylose and
cyclodextrins. Tetrahedron 24:803–821. https://doi.org/10.1016/0040-4020(68)88030-5
Casu B, Reggiani M, Gallo GG, Vigevani A (1970) Conformation of acetylated cyclodextrins and
Amylose. Carbohydr Res 12(2):157–170
Celebioglu A, Uyar T (2012) Electrospinning of nanofibers from non-polymeric systems: polymerfree nanofibers from cyclodextrin derivatives. Nanoscale 4:621–631. https://doi.org/10.1039/
c1nr11364j
Celebioglu A, Uyar T (2013) Electrospinning of nanofibers from non-polymeric systems: electrospun nanofibers from native cyclodextrins. J Colloid Interface Sci 404:1–7. https://doi.
org/10.1016/j.jcis.2013.04.034
Celebioglu A, Sen HS, Durgun E, Uyar T (2016) Molecular entrapment of volatile organic compounds (VOCs) by electrospun cyclodextrin nanofibers. Chemosphere 144:736–744. https://
doi.org/10.1016/j.chemosphere.2015.09.029
Chacko KK, Saenger W (1981) Topography of cyclodextrin inclusion complexes. Crystal
and molecular structure of the cyclohexaamylose 7.57 water complex. J Am Chem Soc
103:1708–1715
Chai F, Maton M, Degoutin S, Vermet G, Simon N, Rousseaux C, Martel B, Blanchemain N
(2019) In vivo evaluation of post-operative pain reduction on rat model after implantation of
intraperitoneal PET meshes functionalized with cyclodextrins and loaded with ropivacaine.
Biomaterials 192:260–270. https://doi.org/10.1016/j.biomaterials.2018.07.032
Chankvetadze B (2004) Combined approach using capillary electrophoresis and NMR spectroscopy for an understanding of enantioselective recognition mechanisms by cyclodextrins. Chem
Soc Rev 33(6):337–347. https://doi.org/10.1039/b111412n
Chen YQ, Gui X, Duan ZB, Zhu LJ, Xiang YZ, Xia DH (2019) Transition metal catalyzed organic
reaction involving cyclodextrin. Chin J Org Chem 39:1284–1292. https://doi.org/10.6023/
cjoc201809012
Chilajwar SV, Pednekar PP, Jadhav KR, Gupta GJC, Kadam VJ (2014) Cyclodextrin-based
nanosponges: a propitious platform for enhancing drug delivery. Expert Opin Drug Deliv
11:111–120. https://doi.org/10.1517/17425247.2014.865013
1 History of Cyclodextrins
Campos EVR, de Oliveira JL, Fraceto LF, Singh B (2015) Polysaccharides as safer release systems
for agrochemicals. Agron Sustain Dev 35:47–66. https://doi.org/10.1007/s13593-014-0263-0
Carneiro SB, Duarte FIC, Heimfarth L, Quintans JDS, Quintans LJ, da Veiga VF, de Lima AAN
(2019) Cyclodextrin-drug inclusion complexes: in vivo and in vitro approaches. Int J Mol Sci
20:642. https://doi.org/10.3390/ijms20030642
Casu B (1964) Spectrometric identification of organic compounds. Chim Ind 46:1425–1429
Casu B (1966) Recent contributions to knowledge of amylose and cyclodextrins structure. Chim
Ind 48:921–923
Casu B, Reggiani M (1964) Infrared spectra of amylose and its oligomers. J Polym Sci Part C
7:171–185
Casu B, Reggiani M (1966) Conformation of amylose and its derived products. I. Infrared spectra of amylose and its oligomers in the amorphous solid phase and in solution. Starch/Stärke
18:218–229. https://doi.org/10.1002/star.19660180704
Casu B, Reggiani M, Gallo GG, Vigevani A (1964) Hydroxyl proton resonances of sugars in
dimethylsulphoxide solution. Tetrahedron Lett 39-4:2839–2284
Casu B, Reggiani M, Gallo GG, Vigevani A (1965) NMR spectra and conformation of glucose and
some related carbohydrates in dimethylsulphoxide solution. Tetrahedron Lett 27:2253–2259
Casu B, Gallo GG, Reggiani M, Vigevani A (1968a) Applications of magnetic resonance spectroscopy of hydroxyl protons to analysis of starch-derived products. Starch/Stärke 20:387–391.
https://doi.org/10.1002/star.19680201202
Casu B, Reggiani M, Gallo GG, Vigevani A (1968b) Applications of magnetic resonance spectroscopy of the hydroxyl protons to the analysis of starch-derived products. X Congress of the
Italian Chemical Society, Padova, Italy, June 1968
Casu B, Reggiani M, Gallo GG, Vigevani A (1968c) Conformation of O-methylated amylose and
cyclodextrins. Tetrahedron 24:803–821. https://doi.org/10.1016/0040-4020(68)88030-5
Casu B, Reggiani M, Gallo GG, Vigevani A (1970) Conformation of acetylated cyclodextrins and
Amylose. Carbohydr Res 12(2):157–170
Celebioglu A, Uyar T (2012) Electrospinning of nanofibers from non-polymeric systems: polymerfree nanofibers from cyclodextrin derivatives. Nanoscale 4:621–631. https://doi.org/10.1039/
c1nr11364j
Celebioglu A, Uyar T (2013) Electrospinning of nanofibers from non-polymeric systems: electrospun nanofibers from native cyclodextrins. J Colloid Interface Sci 404:1–7. https://doi.
org/10.1016/j.jcis.2013.04.034
Celebioglu A, Sen HS, Durgun E, Uyar T (2016) Molecular entrapment of volatile organic compounds (VOCs) by electrospun cyclodextrin nanofibers. Chemosphere 144:736–744. https://
doi.org/10.1016/j.chemosphere.2015.09.029
Chacko KK, Saenger W (1981) Topography of cyclodextrin inclusion complexes. Crystal
and molecular structure of the cyclohexaamylose 7.57 water complex. J Am Chem Soc
103:1708–1715
Chai F, Maton M, Degoutin S, Vermet G, Simon N, Rousseaux C, Martel B, Blanchemain N
(2019) In vivo evaluation of post-operative pain reduction on rat model after implantation of
intraperitoneal PET meshes functionalized with cyclodextrins and loaded with ropivacaine.
Biomaterials 192:260–270. https://doi.org/10.1016/j.biomaterials.2018.07.032
Chankvetadze B (2004) Combined approach using capillary electrophoresis and NMR spectroscopy for an understanding of enantioselective recognition mechanisms by cyclodextrins. Chem
Soc Rev 33(6):337–347. https://doi.org/10.1039/b111412n
Chen YQ, Gui X, Duan ZB, Zhu LJ, Xiang YZ, Xia DH (2019) Transition metal catalyzed organic
reaction involving cyclodextrin. Chin J Org Chem 39:1284–1292. https://doi.org/10.6023/
cjoc201809012
Chilajwar SV, Pednekar PP, Jadhav KR, Gupta GJC, Kadam VJ (2014) Cyclodextrin-based
nanosponges: a propitious platform for enhancing drug delivery. Expert Opin Drug Deliv
11:111–120. https://doi.org/10.1517/17425247.2014.865013
1 History of Cyclodextrins