Abstract

A method of radiolabelling micronised salbutamol with 99mTc and blending it with lactose, for use in a multidose dry powder inhaler (Pulvinal, Chiesi) was developed. In vitro experiments with a multistage liquid impinger demonstrated that the labelling process did not affect the particle size distribution of the drug, and that the radiolabel was a marker for the drug substance across a range of particle sizes. Gamma scintigraphy was used to measure the in vivo deposition of salbutamol in 10 healthy volunteers, at a fast peak inhaled flow rate (mean 46.0 l/min) and at a slow peak inhaled flow rate (27.8 l/min). A significantly higher percentage of the dose ( p=0.05) was deposited in the lungs at the fast flow rate (14.1 ± 3.2%) compared to the slow flow rate (11.7 ± 2.3%). Deposition patterns within the lung regions were similar at the two flow rates. The major site of deposition was the oropharynx, and approx. 1% of the dose was exhaled. The deposition patterns from the Pulvinal inhaler were similar to those observed previously both for other powder inhalers and for pressurised metered dose inhalers.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.