用伊特拉科纳装载的聚烯酸纳米粒子凝用于增强通过皮肤传递:开发,表征和体外评估
Sajjad Hussain1,2, Nadia Shamshad Malik1, Ume Ruqia Tulain3
1Faculty of Pharmacy, Capital University of Science and Technology, Islamabad, Pakistan.
International journal of nanomedicine
|December 30, 2025
概括
碳聚凝中的聚烯酸 (PCL) 纳米颗粒增强了通过皮肤输送伊特拉可纳 (ITZ). 这种配方改善了药物释放和皮肤透,为抗真菌治疗提供了有前途的方法.
科学领域:
- 制药科学 制药科学
- 材料科学 材料科学 材料科学
- 生物医学工程 生物医学工程
背景情况:
- 伊特拉科纳 (ITZ) 是一种BCSII类的抗真菌药物,具有较差的水溶性和可变的口服生物可用性,这给配方带来了挑战.
- 通过皮肤递送药物提供了一种替代途径,以克服口服生物可用性问题并提高治疗疗效.
研究的目的:
- 开发和表征聚烯 (PCL) 纳米颗粒,以增强通过皮肤输送伊特拉可纳 (ITZ).
- 为提升皮肤透度和持续释放药物的ITZ装载PCL纳米粒子凝配制.
主要方法:
- 纳米颗粒使用修改的纳米沉方法制备,优化的配方被纳入碳烯凝中.
- 特性包括颗粒大小,PDI,泽塔潜力,封装效率 (EE),体外释放,体外透,皮肤刺激和稳定性研究.
主要成果:
- 优化的PCL纳米粒子 (F2) 呈现出有利的特征:154.6nm大小,0.378PDI,-10.7mV泽塔电位,和88.4%的EE.
- 凝配方在pH值为5.5和7.4时显著增强透皮透 (增加了2.32倍) 和持续的药物释放 (24小时内80.41-94.34%).
- 该配方在三个月内是不刺激和稳定的,ITZ在无形状态下证实没有相互作用.
结论:
- 一种生物相容的PCL基凝已成功开发,用于增强伊特拉科纳的通过皮肤输送.
- 该配方提供持续的药物释放和改善的皮肤透性,代表ITZ透皮治疗的有效策略.
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