Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/29189
Title: Dry amorphisation of mangiferin, a poorly water-soluble compound, using mesoporous silica
Authors: Baan, Adrienn
ADRIAENSENS, Peter 
Lammens, Joris
Delgado Hernandez, Rene
Vanden Berghe, Wim
Pieters, Luc
Vervaet, Chris
Kiekens, Filip
Issue Date: 2019
Publisher: ELSEVIER
Source: EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 141, p. 172-179
Abstract: Mangiferin, a poorly water soluble compound, was processed via a dry amorphisation technique (ball milling) in combination with mesoporous silica to enhance the solubility of mangiferin. The amorphous samples were prepared by mixing 1:1 (w/w) Syloid (R) XDP 3050 silica-mangiferin mixtures using a planetary mono mill at different milling speeds and milling times according to a 32 full factorial experimental design. The prepared samples were characterized for dissolution profile, particle size distribution using laser diffraction particle size analyzer, thermal characteristics using DSC, crystalline characteristics using XRD and molecular interactions using FTIR and ss-NMR. The samples were tested for stability at stress conditions (40 degrees C/75%RH) for up to 6 months in open and closed containers. To improve stability of the samples, mixtures of 1:1:2 mangiferin-polymer (Soluplus or HPMC)-silica samples were also prepared and analyzed. Amorphisation of mangiferin is possible using dry amorphisation by ball milling with mesoporous silica in a short amount of time. The amorphisation rate of the samples improved with the energy input of the milling process. The samples prepared with high energy input resulted in amorphous samples and showed a better stability at the stress conditions for up to 3 months. Solubility of these samples increased from 0.32 to 0.50 mg/ml and the particle size decreased from 35.5 mu m to around 7 mu m. The spectral analysis suggest presence of interactions between the silica material and the compound. The amorphous stability was improved with addition of polymer, even though the solubility of the samples was lower.
Notes: [Baan, Adrienn; Kiekens, Filip] Univ Antwerp, Dept Pharmaceut Technol & Biopharm, Univ Pl 1, B-2610 Antwerp, Belgium. [Adriaensens, Peter] Univ Hasselt, Inst Mat Res, Agoralaan Bldg D, B-3590 Diepenbeek, Belgium. [Lammens, Joris; Vervaet, Chris] Univ Ghent, Lab Pharmaceut Technol, Ottergemsesteenweg 460, B-9000 Ghent, Belgium. [Delgado Hernandez, Rene] Univ La Habana, Inst Farm & Alimentos, Havana 222, Cuba. [Vanden Berghe, Wim] Univ Antwerp, Dept Biomed Sci, Univ Pl 1, B-2610 Antwerp, Belgium. [Pieters, Luc] Univ Antwerp, Dept Pharmaceut Sci, Univ Pl 1, B-2610 Antwerp, Belgium.
Keywords: Mesoporous silica; Solid dispersions; Dry amorphisation; Co-milling; Drug formulation; Solubility improvement;Mesoporous silica; Solid dispersions; Dry amorphisation; Co-milling; Drug formulation; Solubility improvement
Document URI: http://hdl.handle.net/1942/29189
ISSN: 0939-6411
e-ISSN: 1873-3441
DOI: 10.1016/j.ejpb.2019.05.026
ISI #: 000476961600017
Rights: 2019 Elsevier B.V. All rights reserved.
Category: A1
Type: Journal Contribution
Validations: ecoom 2020
Appears in Collections:Research publications

Files in This Item:
File Description SizeFormat 
baan 1.pdf
  Restricted Access
Published version1.9 MBAdobe PDFView/Open    Request a copy
Show full item record

SCOPUSTM   
Citations

1
checked on Sep 3, 2020

WEB OF SCIENCETM
Citations

15
checked on Apr 24, 2024

Page view(s)

24
checked on Sep 7, 2022

Download(s)

4
checked on Sep 7, 2022

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.