Inclusion complex of water-soluble arbutin with n-cyclodextrin: Computer modeling and experimental studies

被引:0
作者
Paiboon, Narin [1 ]
Rujipairoj, Supawan [2 ]
Surassmo, Suvimol [3 ]
Ruktanonchai, Uracha Rungsardthong [3 ]
Phunpee, Sarunya [3 ]
Ali, Saba [4 ]
Darai, Nitchakan [5 ]
Rungrotmongkol, Thanyada [4 ,6 ]
Soottitantawat, Apinan [2 ]
机构
[1] King Mongkuts Inst Technol Ladkrabang, Sch Food Ind, Program Food Proc Engn, Bangkok 10520, Thailand
[2] Chulalongkorn Univ, Fac Engn, Ctr Excellence Particle & Mat Proc Technol, Dept Chem Engn, Bangkok 10330, Thailand
[3] Natl Sci & Technol Dev Agcy NSTDA, Natl Nanotechnol Ctr NANOTEC, Pathum Thani 12120, Thailand
[4] Chulalongkorn Univ, Fac Sci, Ctr Excellence Struct & Computat Biol, Dept Biochem, Bangkok 10330, Thailand
[5] Walailak Univ, Futurist Sci Res Ctr, Sch Sci, Nakhon Si Thammarat 80160, Thailand
[6] Chulalongkorn Univ, Grad Sch, Program Bioinformat & Computat Biol, Bangkok 10330, Thailand
来源
CARBOHYDRATE POLYMER TECHNOLOGIES AND APPLICATIONS | 2025年 / 9卷
关键词
Arbutin; n-cyclodextrin; Inclusion complex; Water-soluble guest molecules; Molecular dynamics simulation; PERACETYLATED-BETA-CYCLODEXTRIN; ENHANCING SOLUBILITY; MOLECULAR-DYNAMICS; DRUG; STABILITY; BINDING; ENCAPSULATION; DERIVATIVES; ACID;
D O I
10.1016/j.carpta.2025.100662
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A water-soluble arbutin was investigated for its potential to form an inclusion complex with n-cyclodextrin (n-CD). Molecular modeling tests confirmed that arbutin can be accommodated within the cavity of n-CD primarily through Van der Waals forces rather than electrostatic interactions. The structure of the arbutin-n-CD inclusion complex was characterized using Differential Scanning Calorimetry (DSC), and Proton Nuclear Magnetic Resonance Spectroscopy (1H NMR). The inclusion complex prepared at a mole ratio of 1:1 (arbutin: n-CD) exhibited the highest encapsulation efficiency at 43.72 %. The study findings affirm that encapsulation of arbutin within n-CD does not reduce its inherent antioxidant activity and its inhibitory effects against tyrosinase enzyme activity. Moreover, the complexation of arbutin with n-CD resulted in a notably slower release rate, indicating the role of n-CD in modulating substance release kinetics. Furthermore, encapsulation of arbutin within n-CD demonstrated a reduction in hydrolysis from arbutin to hydroquinone by Staphylococcus epidermidis, highlighting the potential of the inclusion complex to mitigate enzymatic conversion processes.
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页数:12
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