基于粉的化纳米颗粒的开发,用于安福特里辛B的输送
Yonas Brhane1, Anteneh Belete1, Stefaan C De Smedt2
1Department of Pharmaceutics and Industrial Pharmacy, School of Pharmacy, College of Health Sciences, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia; Center for Innovative Drug Development and Therapeutic Trials for Africa (CDT-AFRICA), College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
International journal of pharmaceutics
|November 17, 2025
概括
研究人员开发了低成本,生物相容的粉纳米颗粒来输送安福特里辛B,为昂贵的脂质体配方提供了潜在的替代品. 这些新型纳米粒子显示了可比的药物释放和稳定性.
科学领域:
- 制药纳米技术 制药纳米技术
- 药物输送系统 药物输送系统
- 材料科学 材料科学 材料科学
背景情况:
- 氨酸B是一种重要的抗真菌药物,但其毒性和脂质体配方 (AmBisome®) 的高成本限制了其可获得性.
- 开发成本效益高,更安全的安二乙药物输送系统至关重要,特别是对于低收入和中等收入国家.
研究的目的:
- 开发一种新的,低成本的,生物相容的,稳定的基于粉的纳米载体,用于安福特里辛B的输送.
- 通过响应表面方法 (RSM) 和中央复合材料设计 (CCD) 来优化这些粉纳米颗粒的配方.
主要方法:
- 使用溶剂乳化扩散技术制备了化 Dioscorea abyssinica 粉纳米颗粒 (PDASNPs).
- 使用响应表面方法 (RSM) 和中央复合材料设计 (CCD) 来优化表面活性剂度,均质化速度和时间.
- 评估了粒子大小,多分散性指数 (PDI),泽塔潜力 (ζ),形态,体外释放和稳定性.
主要成果:
- 优化的PDASNP可以达到149nm的粒子大小,PDI为0.22,而zeta电位为-20mV.
- 在体外释放药物的AMPHOTERICIN B装载PDASNP的概况与AMBISOME®相似.
- 开发的纳米载体在4°C下至少3个月表现出稳定性.
结论:
- 化迪奥斯科雷亚亚亚比西尼卡粉纳米颗粒 (PDASNPs) 代表了一种有希望的,具有成本效益的纳米载体,用于安福特里辛B的输送.
- 这种配方提供了一个潜在的替代现有的脂肪体安二B,解决成本和可访问性障碍.
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