Record number :
1623716
Title of article :
Solubilization of haloperidol by acyclic succinoglycan oligosaccharides
Author/Authors :
Choi، نويسنده , , Jae-Min and Kim، نويسنده , , Hwanhee and Cho، نويسنده , , Eunae and Choi، نويسنده , , Youngjin and Lee، نويسنده , , Im Soon and Jung، نويسنده , , Seunho، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2012
Pages :
7
From page :
564
To page :
570
Abstract :
The isolated succinoglycan octasaccharide dimers isolated from Sinorhizobium meliloti 1021 have unique acyclic structures, displaying amphipathic properties against water. Thus, their potential usage as solubilizers of various water-insoluble drugs through non-covalent complexation are possible. In this study, we examined the solubility of a poorly water-soluble drug, haloperidol, in the presence of the acyclic form of succinoglycan dimers, and demonstrated that its solubility was increased up to 87 fold, Interestingly, the level of its solubility was even 7–10 fold higher than that achieved with β cyclodextrin or its derivatives that are cyclic forms, which is possibly due to the molecular flexibility of the acyclic structure of the dimers as well as the hydrophobic nature. Analyses of the stoichiometry and the stability constants for each complex were performed using phase solubility method, respectively. Additional analyses were also performed to confirm the formation of succinoglycan–drug complexes. Furthermore hypothetical 3-dimesional conformation of the complex was estimated through molecular docking simulations. Upon cytotoxicity test with a human cell line, the succinoglycan dimers displayed little effect up to 1000 μM, suggesting their potential usage to improve solubility and bioavailability of poorly soluble therapeutic agents.
Keywords :
Sinorhizobium meliloti , Haloperidol , Phase solubility , complexation , Succinoglycan , Solubilization
Journal title :
CARBOHYDRATE POLYMERS
Journal title :
CARBOHYDRATE POLYMERS
Serial Year :
2012
Link To Document :
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