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在有既定和新型推进剂的加压计量吸入器中使用粗糙脂质微粒的可行性。

On the Feasibility of Rugose Lipid Microparticles in Pressurized Metered Dose Inhalers with Established and New Propellants.

机构信息

Donadeo Innovation Centre for Engineering (DICE), 9211 116 Street NW, Edmonton, Alberta, T6G1H9, Canada.

Department of Mechanical Engineering, University of Alberta, Edmonton, Alberta, T6G1H9, Canada.

出版信息

AAPS PharmSciTech. 2024 Apr 10;25(4):82. doi: 10.1208/s12249-024-02776-z.

DOI:10.1208/s12249-024-02776-z
PMID:38600288
Abstract

Pressurized metered dose inhalers (pMDIs) require optimized formulations to provide stable, consistent lung delivery. This study investigates the feasibility of novel rugose lipid particles (RLPs) as potential drug carriers in pMDI formulations. The physical stability of RLPs was assessed in three different propellants: the established HFA-134a and HFA-227ea and the new low global-warming-potential (GWP) propellant HFO-1234ze. A feedstock containing DSPC and calcium chloride was prepared without pore forming agent to spray dry two RLP batches at inlet temperatures of 55 °C (RLP55) and 75 °C (RLP75). RLPs performance in pMDI formulations was compared to two reference samples that exhibit significantly different performance when suspended in propellants: well-established engineered porous particles and particles containing 80% trehalose and 20% leucine (80T20L). An accelerated stability study at 40 °C and relative humidity of 7% ± 5% was conducted over 3 months. At different time points, a shadowgraphic imaging technique was used to evaluate the colloidal stability of particles in pMDIs. Field emission electron microscopy with energy dispersive X-ray spectroscopy was used to evaluate the morphology and elemental composition of particles extracted from the pMDIs. After 2 weeks, all 80T20L formulations rapidly aggregated upon agitation and exhibited significantly inferior colloidal stability compared to the other samples. In comparison, both the RLP55 and RLP75 formulations, regardless of the propellant used, retained their rugose structure and demonstrated excellent suspension stability comparable with the engineered porous particles. The studied RLPs demonstrate great potential for use in pMDI formulations with HFA propellants and the next-generation low-GWP propellant HFO-1234ze.

摘要

加压定量吸入器 (pMDI) 需要优化的配方,以提供稳定、一致的肺部输送。本研究探讨了新型粗糙脂质颗粒 (RLP) 作为 pMDI 配方中潜在药物载体的可行性。在三种不同推进剂中评估了 RLP 的物理稳定性:已建立的 HFA-134a 和 HFA-227ea 以及新型低全球变暖潜能值 (GWP) 推进剂 HFO-1234ze。含有 DSPC 和氯化钙的原料在没有成孔剂的情况下制备,以在 55°C (RLP55) 和 75°C (RLP75) 的入口温度下喷雾干燥两个 RLP 批次。RLP 在 pMDI 配方中的性能与两个参考样品进行了比较,这两个参考样品在悬浮在推进剂中时表现出明显不同的性能:成熟的工程多孔颗粒和含有 80%海藻糖和 20%亮氨酸的颗粒 (80T20L)。在 40°C 和相对湿度为 7%±5%的条件下进行了为期 3 个月的加速稳定性研究。在不同的时间点,使用阴影成像技术评估 pMDI 中颗粒的胶体稳定性。用场发射电子显微镜和能量色散 X 射线光谱法评估从 pMDI 中提取的颗粒的形态和元素组成。在 2 周后,所有 80T20L 配方在搅拌时迅速聚集,与其他样品相比,胶体稳定性明显较差。相比之下,无论使用哪种推进剂,RLP55 和 RLP75 配方都保留了其粗糙结构,并表现出与工程多孔颗粒相当的优异悬浮稳定性。研究中的 RLP 具有在 HFA 推进剂和下一代低 GWP 推进剂 HFO-1234ze 中用于 pMDI 配方的巨大潜力。

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本文引用的文献

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On the Physical Stability of Leucine-Containing Spray-Dried Powders for Respiratory Drug Delivery.用于呼吸道药物递送的含亮氨酸喷雾干燥粉末的物理稳定性
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Spray Dried Rugose Lipid Particle Platform for Respiratory Drug Delivery.
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The Climate is Changing for Metered-Dose Inhalers and Action is Needed.定量吸入器的气候正在改变,需要采取行动。
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