Solubility and release modulation effect of sulfamerazine ternary complexes with cyclodextrins and meglumine


Autoria(s): Aloisio, Carolina; Oliveira, Anselmo Gomes de; Longhi, Marcela
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

18/03/2015

18/03/2015

01/11/2014

Resumo

This study investigated the effect on solubility and release of ternary complexes of sulfamerazine (SMR) with beta-(beta CD), methyl-(M beta CD) and hydroxypropyl-P-cyclodextrin (HP beta CD) using meglumine (MEG) as the ternary component. The combination of MEG with M beta CD resulted the best approach, with an increased effect (29-fold) of the aqueous solubility of SMR. The mode of inclusion was supported by 2D NMR, which indicated that real ternary complexes were formed between SMR, MEG and M beta CD or HP beta CD. Solid state analysis was performed using Fourier-transform infrared spectroscopy (FT IR), differential scanning calorimetry (DSC) and powder X-ray diffraction (XRD), which demonstrated that different interactions occurred among SMR, MEG and M beta CD or HP beta CD in the ternary lyophilized systems. The ternary complexes with beta CD and M beta CD produced an additional retention effect on the release of SMR compared to the corresponding binary complexes, implying that they were clearly superior in terms of solubility and release modulation. (C) 2014 Elsevier B.V. All rights reserved.

Formato

64-73

Identificador

http://dx.doi.org/10.1016/j.jpba.2014.07.008

Journal Of Pharmaceutical And Biomedical Analysis. Amsterdam: Elsevier Science Bv, v. 100, p. 64-73, 2014.

0731-7085

http://hdl.handle.net/11449/116632

10.1016/j.jpba.2014.07.008

WOS:000343021100009

Idioma(s)

eng

Publicador

Elsevier B.V.

Relação

Journal Of Pharmaceutical And Biomedical Analysis

Direitos

closedAccess

Palavras-Chave #Sulfamerazine #Cyclodextrin #Ternary complex #Solubility #In vitro-release
Tipo

info:eu-repo/semantics/article