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他达拉非纳米复合材料作为干粉吸入制剂,用于肺动脉高压治疗的新策略。

Tadalafil nanocomposites as a dry powder formulation for inhalation, a new strategy for pulmonary arterial hypertension treatment.

机构信息

Department of Pharmaceutics, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Students' Research Committee, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Department of Pharmaceutics, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Eur J Pharm Sci. 2019 May 15;133:275-286. doi: 10.1016/j.ejps.2019.04.001. Epub 2019 Apr 3.

Abstract

Tadalafil (a phosphodiesterase-5 inhibitor) is a choice for treatment of pulmonary arterial hypertension (PAH) that is known as an increase in mean pulmonary arterial pressure ≥25 mmHg at rest and ≥30 mmHg during exercise with reduced cardiac output. The aim of this study was to prepare inhalable tadalafil nanocomposites as a dry powder formulation by spray drying technique for increasing bioavailability and treatment efficacy, as well as decreasing systemic side effects. The D-optimal design was used for optimization of formulation parameters. Microparticle size, morphology, crystallinity, density, solubility, redispersion (%), and in-vitro inhalation performance of tadalafil nanocomposites were investigated as physicochemical characteristics. Pharmacokinetic parameters were also evaluated in plasma and lung tissue of Wistar rats after intratracheal insufflation and compared with a control group receiving an oral tadalafil marketed product (dose = 10 mg/kg). The suggested optimum formulation contained stable amorphous particles with almost rounded shape and corrugated surface that were completely redispersed in the lung simulated medium with the mass median geometric diameter of 3.2 μm, density of 1.4 g/cm, fine particle fraction based on emitted dose (%) of 57.2 ± 6.5%, and 13.7-fold enhancement in dissolution rate. In-vivo studies showed that the ratio of AUC/AUC, achieved in the treated group after intratracheal insufflation, was significantly higher than the control group that means high local drug concentration and more efficacy. Besides, plasma data analysis indicated high value of MRT (2.3-fold) and t (3.7-fold) after intratracheal insufflation of tadalafil nanocomposites in comparison with the conventional oral route, indicating longer retention of tadalafil molecules in the lungs and their slower entry to the systemic blood circulation. In conclusion, it seems that inhalable tadalafil nanocomposites can be introduced as an alternative to oral tadalafil in the treatment of PAH.

摘要

他达拉非(一种磷酸二酯酶-5 抑制剂)是治疗肺动脉高压(PAH)的选择,其定义为静息时平均肺动脉压升高≥25mmHg,运动时降低心输出量时升高≥30mmHg。本研究的目的是通过喷雾干燥技术制备可吸入他达拉非纳米复合材料作为干粉制剂,以提高生物利用度和治疗效果,并减少全身副作用。采用 D-最优设计优化制剂参数。研究了他达拉非纳米复合材料的微粒子大小、形态、结晶度、密度、溶解度、再分散(%)和体外吸入性能等理化特性。还通过气管内滴注给药,在 Wistar 大鼠的血浆和肺组织中评价了药代动力学参数,并与口服市售他达拉非产品(剂量=10mg/kg)的对照组进行了比较。建议的最佳制剂含有稳定的无定形颗粒,几乎为圆形,表面有波纹,在模拟肺部的介质中完全再分散,质量中值几何直径为 3.2μm,密度为 1.4g/cm,基于发射剂量的细颗粒分数为 57.2%±6.5%,溶解速率提高了 13.7 倍。体内研究表明,气管内滴注后治疗组的 AUC/AUC 比值明显高于对照组,这意味着局部药物浓度高,疗效好。此外,与口服常规途径相比,气管内滴注他达拉非纳米复合材料后血浆数据分析表明,MRT(2.3 倍)和 t(3.7 倍)值较高,表明他达拉非分子在肺部的滞留时间较长,进入全身血液循环的速度较慢。总之,可吸入他达拉非纳米复合材料可作为口服他达拉非治疗 PAH 的替代药物。

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