Literature DB >> 9516895

Effects of airway calibre on lung delivery of nebulised salbutamol.

B J Lipworth1, D J Clark.   

Abstract

BACKGROUND: A study was undertaken to test the hypothesis that airway calibre may alter lung deposition and therefore lung bioavailability of inhaled drugs as a result of narrowed airways reducing peripheral drug delivery. This was evaluated using the early lung absorption profile of salbutamol over the first 30 minutes after inhalation.
METHODS: Three groups were compared: (1) 10 normal subjects with mean forced expiratory volume in one second (FEV1) 109.5% predicted and mid forced expiratory flow (FEF25-75) 103.0%, (2) 10 mild asthmatic patients with FEV1 102.0% and FEF25-75 82.6%, and (3) 10 severe asthmatic patients with FEV1 49.2% and FEF25-75 27.5% predicted. Each subject had one study visit where a single dose of nebulised salbutamol was given (40 micrograms/kg) via a Ventstream nebuliser with mouthpiece followed by mouth rinsing. Plasma salbutamol levels were measured at five, 10, 20, and 30 minutes after the end of nebulisation with calculation of maximal (Cmax) and average (Cav) concentration over 0-30 minutes. Systemic beta 2 responses (plasma potassium, tremor and heart rate) and airway responses (FEV1, FEF25-75) were measured before and 30 minutes after nebulisation.
RESULTS: For Cav over 0-30 minutes the severe asthmatic patients had a lower plasma salbutamol concentration (1.31 ng/ml) than either the normal subjects (2.40 ng/ml) or those with mild asthma (2.45 ng/ml): normal subjects versus severe asthmatics 95% CI 0.30 to 1.88, mild versus severe asthmatics 95% CI 0.07 to 2.21. Airway responses as delta FEF25-75 were lower in the severe asthmatic subjects (0.30 l/s) than in either the normal subjects (0.69 l/s) or those with mild asthma (0.74 l/s): normal subjects versus severe asthmatic subjects 95% CI 0.09 to 0.88, mild versus severe asthmatics 95% CI 0.04 to 0.93. Values for delta log tremor also showed attenuated responses in those with severe asthma (1.22 mg2/s) compared with normal subjects (2.00 mg2/s) or those with mild asthma (2.02 mg2/s): normal subjects versus those with severe asthma 95% CI -0.02 to 3.30, mild versus severe asthmatics 95% CI 0.02 to 3.30.
CONCLUSIONS: These results show that baseline airway calibre significantly alters the early lung absorption profile of salbutamol in patients with severe asthma. This may have implications in terms of optimising dose and delivery of inhaled beta 2 agonists in these patients.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9516895      PMCID: PMC1758465          DOI: 10.1136/thx.52.12.1036

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  12 in total

1.  Lung bioavailability of generic and innovator salbutamol MDIs.

Authors:  H Chrystyn; S A Corlett; V Silkstone
Journal:  Thorax       Date:  1996-06       Impact factor: 9.139

2.  Lung bioavailability of chlorofluorocarbon free, dry powder and chlorofluorocarbon containing formulations of salbutamol.

Authors:  D J Clark; B J Lipworth
Journal:  Br J Clin Pharmacol       Date:  1996-03       Impact factor: 4.335

3.  Effect of multiple actuations, delayed inhalation and antistatic treatment on the lung bioavailability of salbutamol via a spacer device.

Authors:  D J Clark; B J Lipworth
Journal:  Thorax       Date:  1996-10       Impact factor: 9.139

4.  Beta-adrenoceptor responses to inhaled salbutamol in normal subjects.

Authors:  B J Lipworth; D G McDevitt
Journal:  Eur J Clin Pharmacol       Date:  1989       Impact factor: 2.953

5.  Lung bioavailability of generic and innovator salbutamol metered dose inhalers.

Authors:  D J Clark; J Gordon-Smith; G McPhate; G Clark; B J Lipworth
Journal:  Thorax       Date:  1996-03       Impact factor: 9.139

6.  Comparison of the relative airways and systemic potencies of inhaled fenoterol and salbutamol in asthmatic patients.

Authors:  B J Lipworth; D M Newnham; R A Clark; D P Dhillon; J H Winter; D G McDevitt
Journal:  Thorax       Date:  1995-01       Impact factor: 9.139

7.  Uptake of disodium cromoglycate in obstructive airways disease.

Authors:  M K Benson; S H Curry; G G Mills; D T Hughes
Journal:  Clin Allergy       Date:  1973-12

8.  Effect of lung function and mode of inhalation on penetration of aerosol into the human lung.

Authors:  D Pavia; M L Thomson; S W Clarke; H S Shannon
Journal:  Thorax       Date:  1977-04       Impact factor: 9.139

9.  Single dosing comparison of the relative cardiac beta 1/beta 2 activity of inhaled fenoterol and salbutamol in normal subjects.

Authors:  D M Newnham; N M Wheeldon; B J Lipworth; D G McDevitt
Journal:  Thorax       Date:  1993-06       Impact factor: 9.139

10.  Lung deposition patterns of directly labelled salbutamol in normal subjects and in patients with reversible airflow obstruction.

Authors:  R Melchor; M F Biddiscombe; V H Mak; M D Short; S G Spiro
Journal:  Thorax       Date:  1993-05       Impact factor: 9.139

View more
  23 in total

1.  Comparison of the systemic availability of fluticasone propionate in healthy volunteers and patients with asthma.

Authors:  P T Daley-Yates; J Tournant; R L Kunka
Journal:  Clin Pharmacokinet       Date:  2000       Impact factor: 6.447

2.  Relative bioavailability of salbutamol to the lung following inhalation when administration is prolonged.

Authors:  V L Silkstone; H S Tomlinson; S A Corlett; H Chrystyn
Journal:  Br J Clin Pharmacol       Date:  2000-09       Impact factor: 4.335

Review 3.  Methods to identify drug deposition in the lungs following inhalation.

Authors:  H Chrystyn
Journal:  Br J Clin Pharmacol       Date:  2001-04       Impact factor: 4.335

4.  Dose-response relationship and reproducibility of urinary salbutamol excretion during the first 30 min after an inhalation.

Authors:  H S Tomlinson; S A Corlett; H Chrystyn
Journal:  Br J Clin Pharmacol       Date:  2003-08       Impact factor: 4.335

5.  Determination of the relative bioavailability of salbutamol to the lungs and systemic circulation following nebulization.

Authors:  V L Silkstone; S A Corlett; H Chrystyn
Journal:  Br J Clin Pharmacol       Date:  2002-08       Impact factor: 4.335

6.  Age dependent systemic exposure to inhaled salbutamol.

Authors:  Klaus Bønnelykke; Jakob Jessing Jespersen; Hans Bisgaard
Journal:  Br J Clin Pharmacol       Date:  2007-03-01       Impact factor: 4.335

Review 7.  Deposition and effects of inhaled corticosteroids.

Authors:  Stephen P Newman
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

8.  Bisphenol A exposure is associated with decreased lung function.

Authors:  Adam J Spanier; Elizabeth K Fiorino; Leonardo Trasande
Journal:  J Pediatr       Date:  2014-03-20       Impact factor: 4.406

Review 9.  The pharmacokinetics of levosalbutamol: what are the clinical implications?

Authors:  D W Boulton; J P Fawcett
Journal:  Clin Pharmacokinet       Date:  2001-01       Impact factor: 6.447

10.  Desensitisation of mast cell beta2-adrenoceptor-mediated responses by salmeterol and formoterol.

Authors:  Anne-Marie Scola; Lee K Chong; S Kim Suvarna; Russell Chess-Williams; Peter T Peachell
Journal:  Br J Pharmacol       Date:  2003-12-08       Impact factor: 8.739

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.