Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/63613
Title: Cavity closure of 2-hydroxypropyl-β-cyclodextrin: Replica exchange molecular dynamics simulations
Authors: Khanittha Kerdpol
Jintawee Kicuntod
Peter Wolschann
Seiji Mori
Chompoonut Rungnim
Manaschai Kunaseth
Hisashi Okumura
Nawee Kungwan
Thanyada Rungrotmongkol
Keywords: Chemistry
Materials Science
Issue Date: 16-Jan-2019
Abstract: © 2019 by the authors. 2-Hydroxypropyl-β-cyclodextrin (HPβCD) has unique properties to enhance the stability and the solubility of low water-soluble compounds by inclusion complexation. An understanding of the structural properties of HPβCD and its derivatives, based on the number of 2-hydroxypropyl (HP) substituents at the α-D-glucopyranose subunits is rather important. In this work, replica exchange molecular dynamics simulations were performed to investigate the conformational changes of singleand double-sided HP-substitution, called 6-HPβCDs and 2,6-HPβCDs, respectively. The results show that the glucose subunits in both 6-HPβCDs and 2,6-HPβCDs have a lower chance of flipping than in βCD. Also, HP groups occasionally block the hydrophobic cavity of HPβCDs, thus hindering drug inclusion. We found that HPβCDs with a high number of HP-substitutions are more likely to be blocked, while HPβCDs with double-sided HP-substitutions have an even higher probability of being blocked. Overall, 6-HPβCDs with three and four HP-substitutions are highlighted as the most suitable structures for guest encapsulation, based on our conformational analyses, such as structural distortion, the radius of gyration, circularity, and cavity self-closure of the HPβCDs.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060147843&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/63613
ISSN: 20734360
Appears in Collections:CMUL: Journal Articles

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