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.
引用
收藏
页码:373 / 379
页数:7
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