A nanoscale study of particle friction in a pharmaceutical system

被引:9
作者
Bunker, Matthew J.
Roberts, Clive J. [1 ]
Davies, Martyn C.
James, Michael B.
机构
[1] Univ Nottingham, Sch Pharm, Lab Biophys & Surface Anal, Nottingham NG7 2RD, England
[2] GlaxoSmithKline, Inhaled Prod Dev, Ware SG12 0DP, Herts, England
基金
英国工程与自然科学研究理事会;
关键词
atomic force microscopy; dry powder inhaler; particle interactions; friction; lactose;
D O I
10.1016/j.ijpharm.2006.06.024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Studies of single particle interactions in dry powder inhaler (DPI) formulations using atomic force microscopy (AFM) have recently grown in popularity. Currently, these experiments are all based on measuring particle adhesion forces. We broaden this approach by presenting a novel AFM friction study of single particles in a pharmaceutical system, to examine forces acting parallel to a surface. The sliding friction signal of lactose particles attached to AFM cantilevers was recorded in lateral force (LF) mode over 5 mu m x 5 mu m areas on five different surfaces chosen to represent both relevant inter-particle and particle-surface interactions. A ranking of friction forces was obtained as follows: glass approximate to zanamivir > zanamivir-magnesium stearate (99.5%/0.5%, w/w) blend approximate to magnesium stearate approximate to PTFE. The addition of magnesium stearate to the zanamivir surface dominated and significantly reduced the friction (Kruskal-Wallis test, P < 0.001). AFM images of the contacting asperities of the lactose particles show changes in contact morphology due to two processes. Firstly the asperity wears flat due to abrasion and secondly small magnesium stearate particles transfer onto the asperity. It is proposed that in combination with AFM particle adhesion measurements, this method could be used to screen new formulations and the effectiveness of tertiary components in modifying carrier-drug interactions. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:163 / 171
页数:9
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