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首页> 外文期刊>Journal of Aerosol Medicine and Pulmonary Drug Delivery >Changes in Performance of the Pari eFlow® Rapid and Pari LC Plus™ during 6 Months Use by CF Patients
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Changes in Performance of the Pari eFlow® Rapid and Pari LC Plus™ during 6 Months Use by CF Patients

机译:CF患者使用6个月内ParieFlow®Rapid和Pari LC Plus™的性能变化

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Conclusions: New eFlows produce larger droplets and in a narrower size range compared to new LC Plus nebulizers for TOBI, and therefore both devices are not equivalent. Theoretically a larger portion of the aerosol from eFlow is likely to be deposited in the upper airways. The performance of both tested nebulizers decreases after 6 months of use. For the eFlow, timely replacement of the mesh is necessary. These in vitro results underscore the importance of registration studies of new drug–device combinations.
机译:结论:与用于TOBI的新型LC Plus雾化器相比,新型eFlow产生的液滴更大,粒径范围更窄,因此这两种设备并不等效。从理论上讲,来自eFlow的大部分气溶胶可能会沉积在上呼吸道中。在使用6个月后,两种经过测试的雾化器的性能都会下降。对于eFlow,必须及时更换网格。这些体外结果强调了对新药设备组合进行注册研究的重要性。

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    Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, The Netherlands.;

    Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, The Netherlands.;

    Novartis Pharma, Arnhem, The Netherlands.;

    Department of Pulmonology, Haga Teaching Hospital, The Hague, The Netherlands.;

    Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, The Netherlands.;

    Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, The Netherlands.;

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