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Introduction
  Description
  Executive Summary
Clinical Trial
Patents and Trademarks

PERFORMANCE

The emission performance of a dry-powder inhaler is measured by the amount of powder or drug delivered, under given conditions.

FlowCaps® operates at the nominal airflow rate of 35 litres per minute, which is half the flow rate used in most powder inhalers. It achieves this because of its design efficiency. FlowCaps® is able to disperse and entrain powder at much lower airflow rates than competing passive devices.

This allows FlowCaps® to be used by patients where the flow rate is lower, such as children and elderly patients affected by chronic obstructive pulmonary disease.

In terms of in-vitro performance, FlowCaps® delivers emitted doses typically in excess of 85%, and with very high reproducibility.

DOSE CONTENT UNIFORMITY
Salbutamol Sulphate - 200µg / cap

 
Emitted dose performance complies with FDA requirements.
 

ANDERSEN IMPACTOR PARTICLE SIZE DISTRIBUTION
Salbutamol Sulphate - Blend - 200µg / cap

 
The fine particle fraction (fraction of the emitted dose with particles < 5 µm) was 45.4%.
 

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