共 7 条
Lyophilization of water-in-oil emulsions to prepare phospholipid-based anhydrous reverse micelles for oral peptide delivery
被引:30
|作者:
Wang, Ting
[1
]
Wang, Ning
[1
]
Hao, Aijun
[2
]
He, Xia
[1
]
Li, Tiefu
[3
]
Deng, Yingjie
[3
]
机构:
[1] Jining Med Coll, Dept Pharm, Sunshine City 276826, Shandong, Peoples R China
[2] Liaoning Univ, Sch Pharm, Shenyang 110036, Liaoning, Peoples R China
[3] Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Liaoning, Peoples R China
关键词:
Solubilization;
Insulin;
Oily formulation;
Nanoparticle;
Drug release;
Blood glucose reduction;
X-RAY-SCATTERING;
DRUG-DELIVERY;
PHARMACEUTICAL APPLICATIONS;
DICLOFENAC SODIUM;
INSULIN DELIVERY;
LIPOSOMES;
SYSTEM;
NANOPARTICLES;
SOLUBILITY;
PHOSPHATIDYLCHOLINE;
D O I:
10.1016/j.ejps.2010.01.006
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
A novel procedure for the preparation of hydrophilic peptide-containing oily formulations involving the freeze-drying of water-in-oil emulsions (FWE) is described. A mixture of an aqueous phase containing insulin and oil phase containing phosphatidylcholine was emulsified to prepare water-in-oil emulsions, which were subsequently lyophilized. Upon addition of oil, the lyophilates formed a clear oily solution which was considered as an anhydrous reverse micelle (ARM) system since it contained no water but 20-nm insulin nanoparticles, as revealed by dynamic light scattering. The 20-nm insulin nanopartides, existing in a crystal form, were also contained in the lyophilates, as proved by scanning electron microscopy, small angle X-ray scattering and differential scanning calorimetry analysis. The drug release from the oily formulation of SPC/insulin (10:1) was slow and less than 12% of the total insulin was released after 24 h. A significant reduction in the plasma glucose level of fasting diabetic rats after oral administration of insulin-containing ARMs confirmed the bioactivity of the drug and the potential usefulness of phospholipid-based oily formulations. Both the ARMs and lyophilates were stable and could be stored at 4 degrees C for at least 6 months. Thus, this simple FWE procedure is suitable for the solubilization of hydrophilic peptides in oil to produce stable products for therapeutic applications. (C) 2010 Elsevier BM. All rights reserved.
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页码:373 / 379
页数:7
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