Literature DB >> 25725254

Efficient mechanochemical complexation of various steroid compounds with α-, β- and γ-cyclodextrin.

Laura Rinaldi1, Arianna Binello2, Achim Stolle3, Massimo Curini4, Giancarlo Cravotto2.   

Abstract

Mechanochemical technology enables solvent-free micronized solid dispersions and efficient molecular host-guest inclusion complexes to be formed in matrices which contain cyclodextrins (CDs). This type of complexation has been studied using α-, β- and γ-cyclodextrin with the dual aims of improving overall solubility and enhancing the bioavailability of common steroid compounds, such as cholic acids and β-sitosterols or lowering cholesterol content in products of animal origin. Several parameters have been studied and optimized: CD/compound molar ratio (1:1, 1:2, 2:1 and 3:1) in function of the cavity sizes of the three different CDs, milling time (from 5 to 40 min) and rotation speed (from 100 to 300 rpm). DSC (differential scanning calorimetry) analyses have revealed that inclusion complexes were efficiently formed after 40 min milling (200 rpm) for β-CD/cholesterol and β-CD/ugrsodeoxycholic acid (encapsulation efficiency 96% and 77% respectively). Besides steroid encapsulation/vehiculation, the mechanochemical technique may pave the way for new ideas in solventless steroid extraction from vegetal matrices with CDs.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Bile acids; Cholesterol; Cyclodextrins; Inclusion complexes; Planetary ball mill; β-Sitosterol

Mesh:

Substances:

Year:  2015        PMID: 25725254     DOI: 10.1016/j.steroids.2015.02.016

Source DB:  PubMed          Journal:  Steroids        ISSN: 0039-128X            Impact factor:   2.668


  4 in total

1.  Efficient mechanochemical synthesis of regioselective persubstituted cyclodextrins.

Authors:  Laszlo Jicsinszky; Marina Caporaso; Katia Martina; Emanuela Calcio Gaudino; Giancarlo Cravotto
Journal:  Beilstein J Org Chem       Date:  2016-11-10       Impact factor: 2.883

2.  Synthesis of Randomly Substituted Anionic Cyclodextrins in Ball Milling.

Authors:  László Jicsinszky; Marina Caporaso; Emanuela Calcio Gaudino; Cristina Giovannoli; Giancarlo Cravotto
Journal:  Molecules       Date:  2017-03-19       Impact factor: 4.411

Review 3.  Enabling technologies and green processes in cyclodextrin chemistry.

Authors:  Giancarlo Cravotto; Marina Caporaso; Laszlo Jicsinszky; Katia Martina
Journal:  Beilstein J Org Chem       Date:  2016-02-15       Impact factor: 2.883

4.  Influence of the milling parameters on the nucleophilic substitution reaction of activated β-cyclodextrins.

Authors:  László Jicsinszky; Kata Tuza; Giancarlo Cravotto; Andrea Porcheddu; Francesco Delogu; Evelina Colacino
Journal:  Beilstein J Org Chem       Date:  2017-09-07       Impact factor: 2.883

  4 in total

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