Literature DB >> 20093181

Lyophilization of water-in-oil emulsions to prepare phospholipid-based anhydrous reverse micelles for oral peptide delivery.

Ting Wang1, Ning Wang, Aijun Hao, Xia He, Tiefu Li, Yingjie Deng.   

Abstract

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 nanoparticles, 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 24h. 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. Copyright 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20093181     DOI: 10.1016/j.ejps.2010.01.006

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  2 in total

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Authors:  Chih-Chien Lin; Chao-Hsun Yang; Nai-Fang Chang; Pey-Shiuan Wu; Yi-Shyan Chen; Shu-Mei Lee; Chiu-Wen Chen
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Review 2.  Recent Advancements in Non-Invasive Formulations for Protein Drug Delivery.

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Journal:  Comput Struct Biotechnol J       Date:  2019-09-11       Impact factor: 7.271

  2 in total

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