Dipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF), Università degli Studi di Palermo, Via Archirafi 32, 90123 Palermo, Italy.
Istituto di Biomedicina e Immunologia Molecolare (IBIM), CNR, Via Ugo La Malfa 153, 90146 Palermo, Italy.
Nanomedicine (Lond). 2017 Oct;12(19):2287-2302. doi: 10.2217/nnm-2017-0072. Epub 2017 Sep 4.
Therapeutic efficacy of pulmonary diseases is often limited and drug delivery systems offer new solutions to clinical problems. Solid lipid microparticles (SLMs) are suggested as systems for the delivery of therapeutics to the lung as, because of their size, they are able to deposit into secondary bronchi.
MATERIALS & METHODS: Here, we describe two novel different SLMs using chitosan and alginate such as mucoadhesive polymers and we also studied their biocompatibility and their effectiveness compared with the free drug in controlling senescence and inflammatory processes in cigarette smoke extracts.
Data reported show that fluticasone propionate (FP)-loaded SLMs are more effective than FP alone in controlling oxidative stress.
The therapeutic approach using FP-loaded microparticles could be a promising strategy for the treatment of the chronic inflammatory pulmonary diseases.
肺部疾病的治疗效果往往有限,而药物输送系统为临床问题提供了新的解决方案。固体脂质微粒(SLM)被认为是一种向肺部输送治疗药物的系统,因为其粒径较小,能够沉积到次级支气管中。
在这里,我们描述了两种新型的 SLM,分别使用壳聚糖和海藻酸盐作为黏附聚合物,并研究了它们与游离药物相比在控制香烟烟雾提取物中衰老和炎症过程方面的生物相容性和效果。
报告的数据显示,负载氟替卡松丙酸酯(FP)的 SLM 在控制氧化应激方面比单独使用 FP 更有效。
使用负载 FP 的微粒的治疗方法可能是治疗慢性炎症性肺部疾病的一种有前途的策略。