Literature DB >> 8582466

Acute safety of the CFC-free propellant HFA-134a from a pressurized metered dose inhaler.

D Donnell1, L I Harrison, S Ward, N M Klinger, B P Ekholm, K M Cooper, I Porietis, J McEwen.   

Abstract

The acute safety of the alternative chlorofluorocarbon-free (CFC-free) propellant HFA-134a from a pressurized metered-dose inhaler (MDI) was assessed in 12 healthy male subjects according to a double-blind, randomized, crossover design. On each of three consecutive days, cumulative doses of 1,2,4,8 and 16 inhalations were administered 30 min apart from one of three MDIs. The three MDIs contained either the HFA-134a CFC-free system without drug (HFA-Placebo), the CFC-free system with salbutamol sulphate (HFA-Salbutamol), or a conventional CFC propellant mixture without drug (CFC-Placebo). Pulmonary function (FEV1, FEF25-75%), cardiovascular performance (heart rate and blood pressure), objective tremor measurements and serum potassium were measured after each incremental dose. Similar responses for pulmonary function, cardiovascular performance, tremor and serum potassium were observed between the HFA-Placebo and CFC-Placebo groups. No statistically significant difference was seen in change from baseline of any parameter between the two propellant systems. The administration of HFA-Salbutamol produced statistically significant dose-related increases in heart rate, systolic blood pressure and tremor and a significant dose-related decrease in serum potassium; these responses were expected based on cumulative doses of active drug. Blood samples for HFA-134a analysis were collected to measure systemic absorption of this propellant. Levels of HFA-134a between 200 and 700 ng.ml-1 were detected in all subjects given the CFC-free system. This study shows that acute inhalation of HFA-134a in a CFC-free system is as safe as a CFC propellant system. Salbutamol sulphate in the CFC-free system can be delivered in a dose-linear fashion, without any noticeable change in the safety profile of active drug.

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Year:  1995        PMID: 8582466     DOI: 10.1007/bf00194337

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  16 in total

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Journal:  Science       Date:  1990-07-06       Impact factor: 47.728

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Journal:  Am Rev Respir Dis       Date:  1987-11

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Authors:  T Foucard; G Lönnerholm
Journal:  Eur Respir J       Date:  1991-11       Impact factor: 16.671

5.  Determination of the chlorofluorocarbon substitute 1,1,1,2-tetrafluoroethane (HFA-134a) in human and animal blood using gas chromatography with headspace analysis.

Authors:  K M Cooper; S F Chang; L I Harrison
Journal:  J Chromatogr B Biomed Appl       Date:  1995-05-05

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Authors:  C Teale; J F Morrison; R L Page; S B Pearson
Journal:  Postgrad Med J       Date:  1991-08       Impact factor: 2.401

9.  Dynamic monitoring of total-body absorption by 19F NMR spectroscopy: one hour ventilation of HFA-134a in male and female rats.

Authors:  J R Finch; E J Dadey; S L Smith; L I Harrison; G A Digenis
Journal:  Magn Reson Med       Date:  1995-03       Impact factor: 4.668

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Authors:  L B Sheiner; S L Beal; N C Sambol
Journal:  Clin Pharmacol Ther       Date:  1989-07       Impact factor: 6.875

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  4 in total

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2.  One-Year Evaluation of the Safety and Efficacy of Ipratropium Bromide HFA and CFC Inhalation Aerosols in Patients with Chronic Obstructive Pulmonary Disease.

Authors:  Shari A Brazinsky; Robert J Lapidus; Laurence A Weiss; Mo Ghafouri; Nora M Fagan; Theodore J Witek
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4.  Asthma pressurised metered dose inhaler performance: propellant effect studies in delivery systems.

Authors:  William F S Sellers
Journal:  Allergy Asthma Clin Immunol       Date:  2017-06-29       Impact factor: 3.406

  4 in total

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