共 60 条
Comparison of fenofibrate-mesoporous silica drug-loading processes for enhanced drug delivery
被引:98
作者:
Ahern, Robert J.
[1
]
Hanrahan, John P.
[2
]
Tobin, Joseph M.
[2
]
Ryan, Katie B.
[1
]
Crean, Abina M.
[1
]
机构:
[1] Natl Univ Ireland Univ Coll Cork, Sch Pharm, Cork, Ireland
[2] Natl Univ Ireland Univ Coll Cork, Environm Res Inst, Glantreo Ltd, Cork, Ireland
基金:
爱尔兰科学基金会;
关键词:
SBA-15;
Fenofibrate;
Supercritical CO2;
Poorly water-soluble;
Amorphous;
Drug-loading;
SUPERCRITICAL CARBON-DIOXIDE;
AMORPHOUS STATE;
PHYSICAL STATE;
PORE-SIZE;
SBA-15;
MCM-41;
IBUPROFEN;
RELEASE;
DISSOLUTION;
FORMULATION;
D O I:
10.1016/j.ejps.2013.08.026
中图分类号:
R9 [药学];
学科分类号:
100702 [药剂学];
摘要:
Loading a poorly water-soluble drug onto a high surface area carrier such as mesoporous silica (SBA-15) can increase the drug's dissolution rate and oral bioavailability. The loading method can influence subsequent drug properties including solid state structure and release rate. The objective of this research was to compare several loading processes in terms of drug distribution throughout the mesoporous silica matrix, drug solid state form and drug release properties. A model poorly water-soluble drug fenabrate was loaded onto SBA-15 using; (i) physical mixing, (ii) melt, (iii) solvent impregnation, (iv) liquid CO2 and (v) supercritical CO2 methods. Physical mixing resulted in heterogeneous drug-loading, with no evidence of drug in the mesopores and the retention of the drug in its crystalline state. The other loading processes yielded more homogeneous drug-loading; the drug was deposited into the mesopores of the SBA-15 and was non-crystalline. All the processing methods resulted in enhanced drug release compared to the unprocessed drug with the impregnation, liquid and SC-CO2 producing the greatest increase at t=30 min. (C) 2013 Elsevier B.V. All rights reserved.
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页码:400 / 409
页数:10
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