Effect of mechanochemical inclusion of triamterene into sulfobutylether-β-cyclodextrin and its improved dissolution behavior

Maeda, Hideko; Shiobara, Ryoma; Tanaka, Masafumi; Kajinami, Akihiko

doi:10.1080/03639045.2020.1850759

Cited by 6 publications

(1 citation statement)

References 34 publications

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“…2,6-DMCD 2.0 molar substitution per glucose unit; product code, H0513-5G and randomly substituted dimethyl-β -CD RDMCD, 2.0 molar substitution per glucose unit; product code, 02157320-CF, lot no., SR01729 were obtained from Sigma-Aldrich Japan, Tokyo, Japan and MP Biomedicals, LLC, Illkirch, France, respectively. α -CD, β -CD, γ -CD, methyl-β -CD Mβ -CD, 2.2 molar substitution per glucose unit 21 , trimethyl-β -CD TMβ -CD, 3.0 molar substitution per glucose unit and hydroxypropyl-β -CD Hβ -CD, 6.7 molar substitution per CD unit 22 were purchased from TCI Co. Ltd. Tokyo, Japan .…”

Section: Experimental Procedures 21 Materialsmentioning

confidence: 99%

Clarification of the Complexation Behaviour of 2,6-di-O-Methylated β-Cyclodextrin and Vitamin E and Radical Scavenging Ability of the Complex in Aqueous Solution

et al. 2021

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IntroductionCyclodextrin CD is a cyclic oligosaccharide that typically consists of six, seven or eight glucose residues linked by an α-1,4 glycosidic bond 1 3 . Because of the presence of a hydrophobic internal cavity, CDs form inclusion complexes with vitamin E α -tocopherol; Toc , a representative lipophilic anti-oxidant in nature 4 7 . Toc, which comprises a chromanol head and a phytyl tail, is known to interfere with one or more propagation steps of the lipid peroxidation process 8 11 , and its complexation or encapsulation with CDs has been widely studied to expand its applicability in water-mixed systems 7, 12 20 .

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Section: Experimental Procedures 21 Materialsmentioning

confidence: 99%