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RESEARCH PRODUCT

Lung Deposition Using the Respimat® Soft Mist™ Inhaler Mono and Fixed-Dose Combination Therapies: An In Vitro/In Silico Analysis

Mark DennyHerbert WachtelAm CicilianiPeter LangguthThomas Voshaar

subject

Pulmonary and Respiratory MedicineCOPDRespimatLungbusiness.industryInhalerFixed-dose combinationOlodaterolrespiratory systemPharmacologymedicine.diseaseIn vitrorespiratory tract diseases03 medical and health scienceschemistry.chemical_compound0302 clinical medicinemedicine.anatomical_structure030228 respiratory systemchemistryDrug deliveryMedicine030212 general & internal medicinebusiness

description

Tiotropium and olodaterol are mainstay treatments for chronic obstructive pulmonary disease (COPD) and yield important clinical improvements, especially when used in fixed-dose combination. Whilst previous studies have shown consistent delivery of tiotropium to the lungs with the Respimat® inhaler, no such study has been carried out for olodaterol or the components of their fixed-dose combination (TIO/OLO). Combining in vitro and in silico models, we measured the amount of drug retained in the mouth–throat area, entering the trachea and reaching the lung periphery. We applied a hybrid deposition model that considered the experimentally determined output of an Alberta throat model (in vitro – dose to lung) combined with a computational fluid dynamic model of the lungs (in silico). Regardless of the COPD breathing pattern, ≥50% of the nominal dose of either tiotropium, olodaterol, or TIO and OLO in the fixed-dose combination reached the lung. Of the dose reaching the lungs, greater than 50% is deposited in the lung periphery (from generation 8 onwards). Our study demonstrated that aerosol delivery via the Respimat inhaler achieved high deposition deep into the lung periphery with all formulations evaluated.

https://doi.org/10.1080/15412555.2020.1853091