Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2006 Aug;23(8):1665-74.
doi: 10.1007/s11095-006-9012-7.

The influence of fine excipient particles on the performance of carrier-based dry powder inhalation formulations

Affiliations
Review

The influence of fine excipient particles on the performance of carrier-based dry powder inhalation formulations

Matthew D Jones et al. Pharm Res. 2006 Aug.

Abstract

The inclusion of a small amount of fine particle excipient in a carrier-based dry powder inhalation system is a well researched technique to improve formulation performance and is employed in the pharmaceutical industry. The removal of intrinsic fines from a lactose carrier has been found to decrease formulation performance, whereas adding fines of many different materials into formulations increased performance. Changing the particle size of these fines, the amount added and the technique by which they were prepared also affected formulation behaviour. Despite this body of research, there is disagreement as to the mechanism by which fines improved formulation performance, with two main hypotheses presented in the literature. The first hypothesis suggested that fines prevent the drug from adhering to the strongest binding sites on the carrier, whilst the second proposed that fine particles of drug and excipient form mixed agglomerates that are more easily dispersed and deaggregated during aerosolisation. The evidence in support of each hypothesis is limited and it is clear that future research should aim to produce stronger mechanistic evidence. The investigation of interparticulate interactions using techniques such as atomic force microscopy and inverse gas chromatography may prove useful in achieving this aim.

PubMed Disclaimer

References

    1. Eur J Pharm Biopharm. 2004 Nov;58(3):595-606 - PubMed
    1. AAPS PharmSciTech. 2004 Aug 09;5(4):e65 - PubMed
    1. Int J Pharm. 1999 May 25;182(2):133-44 - PubMed
    1. Int J Pharm. 2006 Feb 17;309(1-2):51-9 - PubMed
    1. Int J Pharm. 1999 Nov 25;191(1):1-14 - PubMed

LinkOut - more resources