针对性肺纤维化治疗的新兴交付方法
Rimpy Diwan1, Himanshu N Bhatt1, Elfa Beaven1
1Department of Pharmaceutical Sciences, School of Pharmacy, The University of Texas El Paso, El Paso, TX 79902, United States; Department of Biomedical Engineering, College of Engineering, The University of Texas El Paso, El Paso, TX 79968, United States.
肺纤维化 (PF) 导致不可逆转的肺痕. 目前的治疗方法在临床前研究中显示出前景,但有副作用;新型药物输送系统和临床试验为有效的PF疗法提供了新的希望.
科学领域:
- 肺部病理学 肺部病理学
- 病理学 病理学 病理学
- 药理学 药理学是指药理学的学科.
背景情况:
- 肺纤维化 (PF) 是一种渐进的,不可逆转的间歇性肺病,其特征是肺部痕.
- 病理特征包括上皮细胞损伤,免疫细胞透和异常的细胞外基质沉积.
- 目前对PF的治疗选择有限,在逆转潜在疾病病理方面缺乏有效性.
研究的目的:
- 审查了解PF病理学,机制和治疗目标方面的最新进展.
- 探索开发用于PF治疗的多种药物输送系统.
- 总结新型PF疗法临床试验的进展情况.
主要方法:
- 对肺纤维化前临床和临床研究的文献综述.
- 分析新兴的治疗策略和药物输送系统.
- 对PF治疗的当前临床试验数据的评估.
主要成果:
- 临床前研究表明,在治疗PF时,各种抑制剂 (例如,罗激酶,Smad信号) 有潜力.
- 使用小分子,RNA,,抗体,外体和干细胞的药物递送系统正在开发中.
- 尽管临床前的承诺,治疗分子往往表现出毒性由于非选择性.
结论:
- 在了解PF机制和确定治疗点方面取得了重大进展.
- 新型药物输送系统和正在进行的临床试验代表了推进PF治疗的有希望的途径.
- 解决毒性和提高特异性对于开发有效的PF疗法至关重要.
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