<i>In Vitro</i> Tests for Aerosol Deposition. VI: Realistic Testing with Different Mouth–Throat Models and <i>In Vitro—In Vivo</i> Correlations for a Dry Powder Inhaler, Metered Dose Inhaler, and Soft Mist Inhaler

Xiangyin Wei, Michael Hindle, Anubhav Kaviratna, Bao K. Huynh, Renishkumar Delvadia, Dennis Sandell, Peter R. Byron

Journal of Aerosol Medicine and Pulmonary Drug Delivery · 2018 · 71 citations · 29 references

Abstract

<b><i>Background:</i></b><i>In vitro-in vivo</i> correlations (IVIVC) for lung deposition may be established by testing inhalers <i>in vitro</i> with realistic mouth-throat (MT) models and inhalation profiles (IP). This study was designed to compare the currently available MT models and their ability to predict <i>in vivo</i> lung deposition. <b><i>Methods:</i></b> Budelin<sup>®</sup> Novolizer<sup>®</sup>, Ventolin<sup>®</sup> Evohaler<sup>®</sup>, and Respimat<sup>®</sup> fenoterol were chosen to represent a dry powder inhaler (DPI), metered dose inhaler (MDI), and soft mist inhaler (SMI) in tests using eight MT models: small, medium, and large Virginia Commonwealth University (VCU) models; small, medium, and large oropharyngeal consortium (OPC) models, the medium adult Alberta Idealized Throat (AIT), and the United States Pharmacopeia (USP) Induction Port, with IPs that simulated those used by volunteers in lung scintigraphy studies. Drug deposition in MT was compared across the models, and IVIVCs evaluated by comparing values for total lung dose <i>in vitro</i> (TLD<sub><i>in vitro</i></sub>) to those reported in the clinic. <b><i>Results:</i></b> MT deposition was dependent on both the flow condition and MT geometry for all the inhalers, while the deposition rank order was independent of both factors. The overall ranking was USP <OPC<sub>L</sub> <AIT <VCU<sub>L</sub> <VCU<sub>M</sub> <OPC<sub>M</sub> <VCU<sub>S</sub> <OPC<sub>S</sub>. All model groups (VCU, OPC, AIT, and USP) produced TLD<sub><i>in vitro</i></sub> comparable with TLD<sub><i>in vivo</i></sub> for the DPI, where flow conditions dominated aerosol deposition. Only the VCU and OPC models produced good IVIVCs for the MDI, where MT geometry dominated deposition. <i>In vitro</i> tests with the SMI at 15-45 L/min underestimated MT deposition and overestimated lung deposition with all MT models except OPCs, although testing at higher flow rates showed good agreement with <i>in vivo</i> results. <b><i>Conclusions:</i></b> While realistic <i>in vitro</i> tests may produce results that correspond to drug deposition <i>in vivo</i>, MT model selection was most important for the MDI and SMI, but much less important than inhalation strength for the DPI.

References

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