局部和持续的巴里西提尼布通过含有可逆硫胺酸的可注射水凝向皮肤输送
Leo L Wang1, Spencer Tuohy1,2, Karen L Xu2,3
1Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, 1053 Biomedical Research Building, 421 Curie Blvd, Philadelphia, PA, 19104, USA.
Advanced healthcare materials
|January 11, 2024
概括
可注射的水凝将巴里丁尼布 (一种Janus激酶抑制剂) 直接输送到皮肤上,降低了全身毒性. 这种局部药物输送有效地治疗小鼠的牛皮状皮肤炎症.
科学领域:
- 生物材料科学 生物材料科学
- 皮肤病学 皮肤病学
- 药理学 药理学是指药理学的学科.
背景情况:
- 简氏激酶 (JAK) 抑制剂治疗皮肤疾病,但导致全身毒性.
- 当地药物输送系统可以克服这些局限性.
研究的目的:
- 设计可注射的水凝,以持续,局部输送巴里西提尼布.
- 在前临床牛皮病模型中评估含巴里西提尼布的水凝的疗效.
主要方法:
- 水凝是使用硫化物交叉连接硫酸化氨酸而形成的.
- 巴里西提尼布通过动态胺酸键与水凝结合.
- 评估了体外药物释放和JAK信号抑制.
- 在体内有效性被测试在一只因伊米奎莫德诱导的牛皮的小鼠模型中.
主要成果:
- 在体外,巴里西提尼布的释放可以在六周内调整.
- 水凝配方在基于细胞的测定中抑制了JAK信号传递.
- 在小鼠体内注射巴里西提尼布水凝抑制了因伊米奎莫德诱导的表皮加厚.
结论:
- 可注射的胺酸结合凝可提供巴里西提尼布的持续局部输送.
- 这种方法显示了治疗炎症性皮肤疾病的翻译潜力,并降低了全身毒性.
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