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赤藓糖醇与乳糖一水合物作为吸入载体的比较研究:原子力显微镜及体外相关性

Comparative study of erythritol and lactose monohydrate as carriers for inhalation: atomic force microscopy and in vitro correlation.

作者信息

Traini Daniela, Young Paul M, Jones Matthew, Edge Stephen, Price Robert

机构信息

Advanced Drug Delivery Group, Faculty of Pharmacy (A15), University of Sydney, NSW 2006, Australia.

出版信息

Eur J Pharm Sci. 2006 Feb;27(2-3):243-51. doi: 10.1016/j.ejps.2005.10.005. Epub 2005 Dec 5.

DOI:10.1016/j.ejps.2005.10.005
PMID:16330191
Abstract

The adhesion of micronised salbutamol sulphate to two carrier excipients, lactose monohydrate and erythritol, was investigated using the atomic force microscope (AFM) colloid probe technique and correlated with their respective physico-mechanical properties and aerosolisation performance. The particle size, morphology and moisture sorption properties of the carriers were similar thereby allowing direct comparison of functionality. AFM force measurements (n = 1024 force curves) were obtained between salbutamol sulphate drug probes (n = 4) and the excipients, as 63-90 microm sieve fractions and atomically smooth crystals. In general, significant differences in drug adhesion to lactose monohydrate and erythritol were observed (ANOVA, p<0.05), with erythritol exhibiting relatively greater adhesiveness. A linear relationship between drug probe adhesion to lactose monohydrate and drug probe adhesion to erythritol was established with salbutamol sulphate-lactose monohydrate adhesion being 60-70% of that of the erythritol system. In vitro analysis suggested good correlation with the adhesion measurements. The aerosolisation of salbutamol sulphate from erythritol carrier particles was significantly less (ANOVA, p<0.05) than from lactose monohydrate, with a fine particle dose (<6.4 microm) of 41.9 +/- 7.4 microg and 24.9 +/- 3.1 microg for the lactose monohydrate and erythritol carriers, respectively (n = 3).

摘要

使用原子力显微镜(AFM)胶体探针技术研究了微粉化硫酸沙丁胺醇与两种载体辅料一水乳糖和赤藓糖醇的粘附情况,并将其与各自的物理机械性能和气雾化性能相关联。载体的粒径、形态和吸湿性能相似,从而可以直接比较其功能。在硫酸沙丁胺醇药物探针(n = 4)与辅料之间进行了AFM力测量(n = 1024条力曲线),辅料为63 - 90微米筛分级分和原子级光滑晶体。总体而言,观察到硫酸沙丁胺醇与一水乳糖和赤藓糖醇的药物粘附存在显著差异(方差分析,p<0.05),赤藓糖醇表现出相对更强的粘附性。建立了药物探针与一水乳糖的粘附和药物探针与赤藓糖醇的粘附之间的线性关系,硫酸沙丁胺醇 - 一水乳糖的粘附力为赤藓糖醇体系的60 - 70%。体外分析表明与粘附测量结果具有良好的相关性。硫酸沙丁胺醇从赤藓糖醇载体颗粒中的气雾化明显少于从一水乳糖中的气雾化(方差分析,p<0.05),一水乳糖和赤藓糖醇载体的细颗粒剂量(<6.4微米)分别为41.9 +/- 7.4微克和24.9 +/- 3.1微克(n = 3)。

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