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Characterization, stability and solubility of co-amorphous systems of glibenclamide and L-arginine at different pH
被引:0
|作者:
Aragon-Aburto, Salma O.
[1
,2
]
Mondragon-Vasquez, Karina
[1
]
Valerio-Alfaro, Gerardo
[2
]
Dominguez-Chavez, Jorge G.
[1
]
机构:
[1] Univ Veracruzana, Fac Bioanal Reg Veracruz, Agustin De Iturbide 91700, Mexico
[2] Tecnol Nacl Mexico IT Veracruz, UNIDA, Miguel A de Quevedo 2779, Veracruz 91860, Mexico
关键词:
Co-amorphous;
Glibenclamide;
L-Arginine;
Solubility;
Stability;
AMINO-ACIDS;
DISSOLUTION;
BIOAVAILABILITY;
STABILIZATION;
PROTEIN;
DRUGS;
D O I:
10.4314/tjpr.v21i7.1
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Purpose: To investigate the stability and solubility of co-amorphous systems of glibenclamide (GBC) with L-arginine (L-Arg) at different pH values. Methods: Three co-amorphous solids of GBC and L-Arg were obtained by fast solvent evaporation using 2:1, 1:1 and 1:2 stoichiometries. All co-amorphous systems were characterized by XRPD, FTIR, RAMAN and NMR-solid state as well as thermal techniques such as DSC and TGA. The stability of co-amorphous systems was evaluated by indicative stability and stability in relevant physiological media was measured at different pH values. Results: The chemical characterization suggest that there was no proton transference between L-Arg and GBC indicative of co-amorphous solids. Stability studies showed that all the co-amorphous solids are unstable under humid conditions and only the co-amorphous system of GBC: L-Arg 1:2 was stable in all the pH values tested. Solubility studies at different pH values showed that the co-amorphous GBC: L-Arg 1:1 and 1:2, showed increasing solubility values even at pH < 7 (0.6468 mg/mL at pH 1.2 for co-amorphous GBC: L-Arg 1:2 at the first hour) where free GBC was not soluble. Conclusion: Co-amorphous systems of GBC and L-Arg, is an interesting strategy to increase the solubility of poorly-soluble drugs at acidic pH values
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页码:1355 / 1364
页数:10
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