Evidence map›Paper›PMID 31823096›Full record

ArticlePharmaceutical research2019

Aerosol Pirfenidone Pharmacokinetics after Inhaled Delivery in Sheep: a Viable Approach to Treating Idiopathic Pulmonary Fibrosis.

Lisa M Kaminskas, Cornelia B Landersdorfer, Robert J Bischof, Nathania Leong, Jibriil Ibrahim, Andrew N Davies, Stephen Pham, Steven Beck, A Bruce Montgomery, Mark W Surber

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Pharmaceutical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Interstitial Lung Disease: Not So Fast.American journal of respiratory and critical care medicine · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Aerosol pulmonary immune engineering.Advanced drug delivery reviews · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Liposomes are Poorly AbsorbedFrontiers in pharmacology · 2022
    Article
  13. Article
  14. Antifibrotic drugs in lung transplantation and chronic lung allograft dysfunction: a review.European respiratory review : an official journal of the European Respiratory Society · 2021
    Review
  15. Review
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Lisa M KaminskasSchool of Biomedical Sciences, University of Queensland, QLD, St Lucia, 4072, Australia. L.kaminskas@uq.edu.au.ORCID http://orcid.org/0000-0003-4821-4262
Cornelia B LandersdorferCentre for Medicine Use and Safety, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC, 3052, Australia.
Robert J BischofAllergenix Pty Ltd, Melbourne, VIC, 3051, Australia.
Nathania LeongAllergenix Pty Ltd, Melbourne, VIC, 3051, Australia.
Jibriil IbrahimAllergenix Pty Ltd, Melbourne, VIC, 3051, Australia.
Andrew N DaviesAllergenix Pty Ltd, Melbourne, VIC, 3051, Australia.
Stephen PhamAvalyn Pharma Inc., 701 Pike Street, Suite 1500, Seattle, WA, 98101, USA.
Steven BeckAvalyn Pharma Inc., 701 Pike Street, Suite 1500, Seattle, WA, 98101, USA.
A Bruce MontgomeryAvalyn Pharma Inc., 701 Pike Street, Suite 1500, Seattle, WA, 98101, USA.
Mark W SurberAvalyn Pharma Inc., 701 Pike Street, Suite 1500, Seattle, WA, 98101, USA. msurber@avalynpharma.com.
Athira Pharma (United States) · USDiscovery Institute · USMonash University · AUThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeInhaled delivery of pirfenidone to the lungs of patients with idiopathic pulmonary fibrosis holds promise to eliminate oral-observed side effects while enhancing efficacy. This study aimed to comprehensively describe the pulmonary pharmacokinetics of inhaled aerosol pirfenidone in healthy adult sheep.

methodsPirfenidone concentrations were evaluated in plasma, lung-derived lymph and epithelial lining fluid (ELF) with data subjected to non-compartmental pharmacokinetic analysis.

resultsCompartmental pharmacokinetic evaluation indicated that a 49 mg lung-deposited dose delivered an ELF Cmax of 62 ± 23 mg/L, and plasma Cmax of 3.1 ± 1.7 mg/L. Further analysis revealed that plasma pirfenidone reached Tmax faster and at higher concentrations than in lymph. These results suggested inhaled pirfenidone was cleared from the alveolar interstitium via blood faster than the drug could equilibrate between the lung interstitial fluid and lung lymphatics. However, the data also suggested that a 'reservoir' of pirfenidone feeds into lung lymph at later time points (after it has largely been cleared from plasma), prolonging lung lymphatic exposure.

conclusionsThis study indicates inhaled pirfenidone efficiently deposits in ELF and is cleared from the lungs by initial absorption into plasma, followed by later equilibrium with lung interstitial and lymph fluid.

Indexed as

Administration, InhalationAnimalsAnti-Inflammatory Agents, Non-SteroidalFemaleIdiopathic Pulmonary FibrosisLungLymphPyridonesSheepAnti-Inflammatory Agents, Non-SteroidalpirfenidonePyridonesaerosolcompartmental modellingidiopathic pulmonary fibrosisinhalationlung lymphpharmacokineticspirfenidonesheep

Identifiers

PMID31823096
OpenAlexW2995296204

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.