Literature DB >> 11424894

Treating systemic diseases via the lung.

S Sanjar1, J Matthews.   

Abstract

Inhalation of pharmacologically active substances for medicinal, social, or recreational purposes has been prevalent for centuries but experience of exploiting the lung as a route of delivery for treatment of nonrespiratory diseases is limited. Despite the success of current applications such as anesthetics, the utility of the lung for drug delivery is not well appreciated, despite advantages such as rapid onset of action. Two drawbacks are the relatively poor efficiency of current inhalation devices, especially for large molecules, and the poor patient acceptability of inhalers. Advances now being made in pulmonary delivery technology may provide the impetus needed for the development of new inhaled presentations of drugs such as peptide hormones and other biologically derived molecules. Molecules of various sizes can be delivered in clinically relevant quantities via the lung. In vitro methods show that lipophilic drugs are absorbed through the alveolar membrane more quickly. Early work in animal models has already shown that absorption of analgesic and antiinflammatory drugs that are not well absorbed orally can be improved by delivering them by inhalation. This work may soon give rise to new formulations for therapeutic use.

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Mesh:

Year:  2001        PMID: 11424894     DOI: 10.1089/08942680150506349

Source DB:  PubMed          Journal:  J Aerosol Med        ISSN: 0894-2684


  7 in total

1.  Large porous particle impingement on lung epithelial cell monolayers--toward improved particle characterization in the lung.

Authors:  Jennifer Fiegel; Carsten Ehrhardt; Ulrich Friedrich Schaefer; Claus-Michael Lehr; Justin Hanes
Journal:  Pharm Res       Date:  2003-05       Impact factor: 4.200

Review 2.  Aerosol deposition in health and disease.

Authors:  Chantal Darquenne
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2012-06       Impact factor: 2.849

3.  Drug Permeation Characterization of Inhaled Dry Powder Formulations in Air-Liquid Interfaced Cell Layer Using an Improved, Simple Apparatus for Dispersion.

Authors:  Ayumu Asai; Tomoyuki Okuda; Erina Sonoda; Tomoyo Yamauchi; Saki Kato; Hirokazu Okamoto
Journal:  Pharm Res       Date:  2015-10-21       Impact factor: 4.200

4.  Administration of antibody to the lung protects mice against pneumonic plague.

Authors:  Jim Hill; Jim E Eyles; Stephen J Elvin; Gareth D Healey; Roman A Lukaszewski; Richard W Titball
Journal:  Infect Immun       Date:  2006-05       Impact factor: 3.441

5.  Regional distribution of aerosol deposition in rat lungs using magnetic resonance imaging.

Authors:  Jessica M Oakes; Miriam Scadeng; Ellen C Breen; G Kim Prisk; Chantal Darquenne
Journal:  Ann Biomed Eng       Date:  2013-01-25       Impact factor: 3.934

6.  Pulmonary delivery of deslorelin: large-porous PLGA particles and HPbetaCD complexes.

Authors:  Kavitha Koushik; Devender S Dhanda; Narayan P S Cheruvu; Uday B Kompella
Journal:  Pharm Res       Date:  2004-07       Impact factor: 4.200

7.  A dose-controlled system for air-liquid interface cell exposure and application to zinc oxide nanoparticles.

Authors:  Anke Gabriele Lenz; Erwin Karg; Bernd Lentner; Vlad Dittrich; Christina Brandenberger; Barbara Rothen-Rutishauser; Holger Schulz; George A Ferron; Otmar Schmid
Journal:  Part Fibre Toxicol       Date:  2009-12-16       Impact factor: 9.400

  7 in total

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