Literature DB >> 22691109

Dose emission characteristics of placebo PulmoSphere® particles are unaffected by a subject's inhalation maneuver.

Jeffry Weers1, Keith Ung, John Le, Nagaraja Rao, Brian Ament, George Axford, David Maltz, Leo Chan.   

Abstract

BACKGROUND: Good compliance to the prescribed dosing regimen and inhaler instructions for use are critical for asthma/chronic obstructive pulmonary disease (COPD) patients to achieve good control of their disease. We investigated the extent to which a system comprising porous particles delivered with a passive dry powder inhaler could be designed to achieve significant reductions in dose inhalation errors.
METHODS: Porous placebo particles were prepared by an emulsion-based spray-drying method (PulmoSphere® technology). The formulations were administered as dry powders with a portable, blister-based dry powder inhaler (Simoon Inhaler). The inhalation profiles of 69 asthma/COPD subjects were determined with an inhaler simulator with resistance comparable to that of the Simoon Inhaler. Powder emptying from the device was assessed by laser photometry. Aerosol performance was assessed on a Next Generation Impactor, and with the idealized Alberta mouth-throat model using both square-wave and subject-inhalation profiles generated in the breathing study.
RESULTS: Virtually all subjects could achieve a pressure drop of at least 1 kPa and an inhaled volume of at least 500 mL with the Simoon Inhaler. In vitro measures of particle deposition were found to be largely independent of the inhalation maneuver (flow rate, inhaled volume, ramp time) across the broad range of inhalation profiles observed in the breathing study. The rapid emptying of powder from the Simoon Inhaler minimizes the impact of dose-related errors, such as failure to exhale before inhalation and failure to breath-hold post inhalation.
CONCLUSIONS: Inertial impaction that is largely independent of a subject's inhalation maneuver can be achieved with a drug/device combination product comprising a porous particle formulation and blister-based inhaler.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22691109     DOI: 10.1089/jamp.2012.0973

Source DB:  PubMed          Journal:  J Aerosol Med Pulm Drug Deliv        ISSN: 1941-2711            Impact factor:   2.849


  6 in total

Review 1.  The Impact of Inspiratory Flow Rate on Drug Delivery to the Lungs with Dry Powder Inhalers.

Authors:  Jeffry Weers; Andy Clark
Journal:  Pharm Res       Date:  2016-10-13       Impact factor: 4.200

2.  Development of an Inline Dry Powder Inhaler for Oral or Trans-Nasal Aerosol Administration to Children.

Authors:  Dale Farkas; Michael Hindle; Serena Bonasera; Karl Bass; Worth Longest
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2019-08-29       Impact factor: 2.849

3.  Can Patients with Parkinson's Disease Use Dry Powder Inhalers during Off Periods?

Authors:  M Luinstra; A W F Rutgers; H Dijkstra; F Grasmeijer; P Hagedoorn; J M J Vogelzang; H W Frijlink; A H de Boer
Journal:  PLoS One       Date:  2015-07-14       Impact factor: 3.240

Review 4.  Inhaled Biologicals for the Treatment of Cystic Fibrosis.

Authors:  Valentina Sala; Alessandra Murabito; Alessandra Ghigo
Journal:  Recent Pat Inflamm Allergy Drug Discov       Date:  2019

Review 5.  The Confusing World of Dry Powder Inhalers: It Is All About Inspiratory Pressures, Not Inspiratory Flow Rates.

Authors:  Andrew R Clark; Jeffry G Weers; Rajiv Dhand
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2019-10-31       Impact factor: 2.849

Review 6.  Lung Deposition and Inspiratory Flow Rate in Patients with Chronic Obstructive Pulmonary Disease Using Different Inhalation Devices: A Systematic Literature Review and Expert Opinion.

Authors:  Adolfo Baloira; Araceli Abad; Antonia Fuster; Juan Luis García Rivero; Patricia García-Sidro; Eduardo Márquez-Martín; Marta Palop; Néstor Soler; J L Velasco; Fernando González-Torralba
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2021-04-19
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.