1995
DOI: 10.1080/02786829408959756
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Characterization of Medical Aerosols: Physical and Clinical Requirements for New Inhalers

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Cited by 16 publications
(11 citation statements)
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“…An assortment of different spacer tubes, valved holding chambers and mouthpiece extensions have been developed to eliminate co‐ordination requirements, reduce the ‘cold Freon ® ’ effect (when the below‐freezing spray temperature causes some patients to stop inhaling) and reduce the amount of drug deposited in the oropharynx by decreasing the particle size distribution and slowing the aerosol's velocity. The aerosol from a MDI and holding chamber is finer than that with the MDI alone, with an approximate 25% decrease in the MMAD compared with the original aerosol [19, 20]. This finer aerosol is more uniformly distributed in the normal lung, with increased delivery to the peripheral airway.…”
Section: Pulmonary Delivery Devicesmentioning
confidence: 99%
See 1 more Smart Citation
“…An assortment of different spacer tubes, valved holding chambers and mouthpiece extensions have been developed to eliminate co‐ordination requirements, reduce the ‘cold Freon ® ’ effect (when the below‐freezing spray temperature causes some patients to stop inhaling) and reduce the amount of drug deposited in the oropharynx by decreasing the particle size distribution and slowing the aerosol's velocity. The aerosol from a MDI and holding chamber is finer than that with the MDI alone, with an approximate 25% decrease in the MMAD compared with the original aerosol [19, 20]. This finer aerosol is more uniformly distributed in the normal lung, with increased delivery to the peripheral airway.…”
Section: Pulmonary Delivery Devicesmentioning
confidence: 99%
“…By adding either a battery‐driven propeller that aids in the dispersion of the powder (Spiros; Dura Pharmaceuticals, San Diego, CA, USA) or using compressed air to aerosolize the powder and converting it into a standing cloud in a holding chamber, the generation of a respirable aerosol becomes independent of a patient's inspiratory effort (Inhance Pulmonary Delivery System, Inhale Therapeutic Systems, San Carlos, CA, USA). However, DPIs in use today are breath actuated and are dependent on a patient's IFR of 30–130 l min −1 to achieve an aerosol within the respirable range [19].…”
Section: Pulmonary Delivery Devicesmentioning
confidence: 99%
“…The majority of currently marketed dry powder inhalers (DPIs) utilise the energy of the patient_s inspiration to generate an effective dry powder aerosol for delivery to the lungs (1). For many of these inhalers the aerosol particle size distribution is influenced by the inhaled flow rate, inspiration time and inhaled volume (2,3), and initial rate of inspiration (4Y7).…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3] The MDI device, comprised of the formulation, a metering valve, container (can), and actuator, is delivered to the patient as an aerosol of fine droplets by the atomization of the liquid phase of the formulation. The driving force for atomization is provided by the evaporation of the propellant within the actuator nozzle.…”
Section: Introductionmentioning
confidence: 99%