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.

译文

描述了一种制备含亲水性肽的油性制剂的新方法,该方法涉及油包水乳液 (FWE) 的冷冻干燥。将含有胰岛素的水相和含有磷脂酰胆碱的油相的混合物乳化以制备油包水乳液,随后将其冻干。加入油后,冻干物形成透明的油状溶液,该溶液被认为是无水反胶束 (ARM) 系统,因为它不含水,但含有20 nm的胰岛素纳米颗粒,如动态光散射所示。通过扫描电子显微镜,小角度x射线散射和差示扫描量热法分析证明,以晶体形式存在的20nm胰岛素纳米颗粒也包含在冻干物中。从SPC/胰岛素 (10:1) 的油性制剂中释放药物缓慢,并且在24小时后释放少于总胰岛素的12%。口服含胰岛素的手臂后,空腹糖尿病大鼠的血浆葡萄糖水平显着降低,证实了该药物的生物活性以及基于磷脂的油性制剂的潜在用途。臂和冻干物都是稳定的,可以在4 ℃ 下储存至少6个月。因此,这种简单的FWE程序适用于油中的亲水性肽的溶解,以生产用于治疗应用的稳定产品。

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