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乳糖的球形团聚体作为吸入用潜在载体。

Spherical agglomerates of lactose as potential carriers for inhalation.

机构信息

Research Center Pharmaceutical Engineering (RCPE) GmbH, Inffeldgasse 13, 8010 Graz, Austria.

Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Ljubljana, Aškerčeva cesta 7, 1000 Ljubljana, Slovenia.

出版信息

Eur J Pharm Biopharm. 2021 Feb;159:11-20. doi: 10.1016/j.ejpb.2020.12.015. Epub 2020 Dec 27.

DOI:10.1016/j.ejpb.2020.12.015
PMID:33358941
Abstract

We report here on spherical lactose agglomerates as potential carriers for inhalation applications. Micromeritic properties of three spherical lactose agglomerates (SA-A, SA-B, SA-C) and a standard lactose inhalation grade carrier (Lactohale 100; LH100) were evaluated and compared. Ordered mixtures with micronized salbutamol sulfate as the model active pharmaceutical ingredient (API) and lactose carriers at two drug loadings (2 wt%, 5 wt%) were prepared, and in-vitro aerosolization performance was assessed. The spherical crystallization process led to particles with tailored micromeritic properties. These had larger specific surface area and greater fine fraction < 10 µm, compared to LH100, due to their coarse morphology. Their properties were reflected in the flowability parameters, where two types of spherical agglomerates of lactose showed more cohesive behavior compared to the other lactose grades. Blend uniformity showed improved homogeneous distribution of the API at higher drug load. In-vitro aerosolization tests showed that the spherical agglomerates of lactose enhanced the dose of API, compared to LH100. SA-B and SA-C showed significantly higher fine particle fractions at low drug load compared to the others, whereas overall, the largest fine particle fraction was for SA-B at high drug load. The carrier material attributes related to particle size, specific surface area, compressibility, flowability (cohesion, flow function), and air permeability were critical for aerosolization performance.

摘要

我们在此报告了球形乳糖团聚体作为吸入应用潜在载体的研究。评估并比较了三种球形乳糖团聚体(SA-A、SA-B、SA-C)和一种标准乳糖吸入级载体(Lactohale 100;LH100)的微粉学特性。制备了载有微米化硫酸沙丁胺醇作为模型药物活性成分(API)和乳糖载体的有序混合物,并在两种药物载药量(2wt%,5wt%)下评估了其体外雾化性能。球形结晶过程导致颗粒具有定制的微粉学特性。与 LH100 相比,由于其粗糙的形态,这些颗粒具有更大的比表面积和更大的<10μm细颗粒分数。它们的性质反映在流动性参数中,其中两种类型的乳糖球形团聚体表现出比其他乳糖级更具粘性的行为。混合均匀度显示,在较高药物载药量下,API 的均匀分布得到了改善。体外雾化测试表明,与 LH100 相比,乳糖球形团聚体增强了 API 的剂量。与其他乳糖相比,SA-B 和 SA-C 在低药物载药量下表现出明显更高的细颗粒分数,而在高药物载药量下,SA-B 的总细颗粒分数最大。与粒径、比表面积、可压缩性、流动性(粘性、流动函数)和透气性相关的载体材料特性对于雾化性能至关重要。

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