In Vitro Tests for Aerosol Deposition. V: Using Realistic Testing to Estimate Variations in Aerosol Properties at the Trachea
Journal of aerosol medicine and pulmonary drug delivery, 2017•liebertpub.com
Background: The dose and aerodynamic particle size distribution (APSD) of drug aerosols'
exiting models of the mouth and throat (MT) during a realistic inhalation profile (IP) may be
estimated in vitro and designated Total Lung Dose, TLD in vitro, and APSDTLD in vitro,
respectively. These aerosol characteristics likely define the drug's regional distribution in the
lung. Methods: A general method was evaluated to enable the simultaneous determination
of TLD in vitro and APSDTLD in vitro for budesonide aerosols' exiting small, medium and …
exiting models of the mouth and throat (MT) during a realistic inhalation profile (IP) may be
estimated in vitro and designated Total Lung Dose, TLD in vitro, and APSDTLD in vitro,
respectively. These aerosol characteristics likely define the drug's regional distribution in the
lung. Methods: A general method was evaluated to enable the simultaneous determination
of TLD in vitro and APSDTLD in vitro for budesonide aerosols' exiting small, medium and …
Abstract
Background: The dose and aerodynamic particle size distribution (APSD) of drug aerosols' exiting models of the mouth and throat (MT) during a realistic inhalation profile (IP) may be estimated in vitro and designated Total Lung Dose, TLDin vitro, and APSDTLDin vitro, respectively. These aerosol characteristics likely define the drug's regional distribution in the lung.
Methods: A general method was evaluated to enable the simultaneous determination of TLDin vitro and APSDTLDin vitro for budesonide aerosols' exiting small, medium and large VCU-MT models. Following calibration of the modified next generation pharmaceutical impactor (NGI) at 140 L/min, variations in aerosol dose and size exiting MT were determined from Budelin® Novolizer® across the IPs reported by Newman et al., who assessed drug deposition from this inhaler by scintigraphy.
Results: Values for TLDin vitro from the test inhaler determined by the general method were found to be statistically comparable to those using a filter capture method. Using new stage cutoffs determined by calibration of the modified NGI at 140 L/min, APSDTLDin vitro profiles and mass median aerodynamic diameters at the MT exit (MMADTLDin vitro) were determined as functions of MT geometric size across Newman's IPs. The range of mean values (n ≥ 5) for TLDin vitro and MMADTLDin vitro for this inhaler extended from 6.2 to 103.0 μg (3.1%–51.5% of label claim) and from 1.7 to 3.6 μm, respectively.
Conclusions: The method enables reliable determination of TLDin vitro and APSDTLDin vitro for aerosols likely to enter the trachea of test subjects in the clinic. By simulating realistic IPs and testing in different MT models, the effects of major variables on TLDin vitro and APSDTLDin vitro may be studied using the general method described in this study.
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