British Journal of Clinical Pharmacology · 2005 · 14 citations · 6 references
PharmacyPharmacokineticsPharmacologyBioavailabilityDrug DeliveryPulmonary Drug DeliveryBioavailability AnalysisInhalation Dosage FormsInhalation Drug DeliveryLung DepositionOral BioavailabilityPulmonary PharmacokineticsFine Particle DoseIn-vitro CharacterizationInhalation BioavailabilityJet NebulizersLung Deposition MeasurementNebulized Drug Deposition
AIMS: To determine the bioavailability of gentamicin to the lung following inhalation from two jet nebulizers. METHODS: Serial urine samples were obtained from 10 volunteers after a 80 mg dose given orally, nebulized from a Pari LC + (PARI) and MicroNeb III (MN) devices, or after a 40 mg intravenous dose. In vitro aerodynamic characteristics of the nebulized doses were also determined. RESULTS: The mean (SD) absolute gentamicin lung bioavailalibility following delivery by PARI and MN devices was 1.4 (0.4) and 1.7 (0.5) %. The mass median aerodynamic diameter (MMAD) of the drug particles from the PARI and MN systems was 8.6 (0.6) and 6.7 (0.5) microm and the corresponding fine particle doses (FPD) were 10.2 (2.8) and 11.7 (1.5) mg. CONCLUSIONS: The MMAD and FPD data reflect the poor lung deposition of gentamicin identified by urinary excretion.
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European Respiratory Society Guidelines on the use of nebulizers
John Dennis, B. Ronan O’Driscoll, Torsten Bauer et al. · European Respiratory Journal · 2001 · 277 citations · Full text
Inhalation of a Dry Powder Tobramycin PulmoSphere Formulation in Healthy Volunteers
Michael T. Newhouse, Peter H. Hirst, Sarma P. Duddu et al. · CHEST Journal · 2003 · 191 citations
Pharmacy, Pharmacology, Toxicology +13
Abdulsalam I Al-Amoud, Brian J. Clark, Henry Chrystyn · Journal of Chromatography B · 2002 · 60 citations