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首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Design and evaluation of novel inhalable sildenafil citrate spray-dried microparticles for pulmonary arterial hypertension
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Design and evaluation of novel inhalable sildenafil citrate spray-dried microparticles for pulmonary arterial hypertension

机译:新型吸入西地那非柠檬酸盐喷雾干燥微粒的设计与评价,用于肺动脉高压

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摘要

Pulmonary delivery of vasodilators is a promising alternative for the intravenous and oral treatment of pulmonary arterial hypertension (PAH). The aim of this study was to design and evaluate hydrogel microparticles as a carrier for sustained pulmonary delivery of sildenafil citrate. Spray dried hydrogel microparticles containing biodegradable sodium carboxymethyl cellulose, sodium alginate, and sodium hyaluronate polymers at variable concentrations were prepared. A design of experiment using the "Extreme Vertices Mixture" design was executed. The design was used to study the influence of polymer concentration and their interactions on the physicochemical properties of the formulations in terms of particle size, particle size distribution, product yield, entrapment efficiency, and in-vitro drug release. Selected formulations were also evaluated for swelling, biodegradation, moisture content, in-vitro aerodynamic performance, and cytotoxicity. In addition, a lung deposition and pharmacokinetic study was conducted in rats to study drug accumulation in lungs and blood after intratracheal administration of the spray dried inhalable hydrogel microparticles in comparison to orally administered Viagra (R). The results demonstrated that formulated microparticles had a mean geometric particle size between 2 and 5 mu m entrapment efficiency of > 80%, and yield ranging between 47 and 66% w/w. The in-vitro drug release profiles showed a sustained drug release of sildenafil citrate for over 24 h. The statistical design showed a significant influence of the microparticulate composition on the physicochemical properties. Furthermore, selected formulations were evaluated for their aerodynamic properties. The aerodynamic properties included fine particle fraction ranging between 24 and 30%, dose recovery percent of 68-8 5%, and average mass median aerodynamic diameter of 4.6-4.8 mu m. The in-vivo pharmacokinetic study showed that inhaled spray dried hydrogel microparticles (M6) form
机译:血管扩张器的肺部递送是肺动脉高血压(PAH)的静脉内和口服治疗的有希望的替代方案。本研究的目的是设计和评估水凝胶微粒作为载体持续肺递送柠檬酸盐。制备含有可生物降解的羧甲基纤维素,藻酸钠和透明质酸钠聚合物的喷雾干燥的水凝胶微粒在可变浓度下进行。执行使用“极端顶点混合物”设计的实验设计。该设计用于研究聚合物浓度及其相互作用对粒径,粒度分布,产物产率,熵效率和体外药物释放方面的制剂的物理化学性质的影响。还评估所选制剂用于溶胀,生物降解,水分含量,体外空气动力学性能和细胞毒性。此外,在大鼠中进行肺沉积和药代动力学研究,以研究喷雾干燥的可吸入水凝胶微粒的肺部和血液中的肺部和血液中的血液中的血液相比,与口服给予的viaga(r)相比。结果表明,配制的微粒的平均几何粒度为2至5μm捕获效率> 80%,并在47和66%w / w之间的产率范围。体外药物释放型材显示出Sildenafil柠檬酸盐的持续释放含量超过24小时。统计设计表明微粒组合物对物理化学性质的显着影响。此外,评估所选制剂的空气动力学性质。空气动力学特性包括24至30%的细颗粒分数,剂量回收率为68-8 5%,平均质量中值的气体动力直径为4.6-4.8μm。体内药代动力学研究显示吸入喷雾干燥水凝胶微粒(M6)形式

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