Evidence map›Paper›PMID 27842973›Full record

ArticleJournal of pharmaceutical sciences2017

Pharmacokinetics of Ethionamide Delivered in Spray-Dried Microparticles to the Lungs of Guinea Pigs.

Lucila Garcia-Contreras, Danielle J Padilla-Carlin, Jean Sung, Jarod VerBerkmoes, Pavan Muttil, Katharina Elbert, Charles Peloquin, David Edwards, Anthony Hickey

Open access · bronzeAbstract read
In one paragraph

Article in Journal of pharmaceutical sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

6 citing papers in PubMed, 22 citations in OpenAlex.

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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

9 authors at 7 institutions in 1 country.

Lucila Garcia-ContrerasDepartment of Pharmaceutical Sciences, College of Pharmacy, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104. Electronic address: lucila-garcia-contreras@ouhsc.edu.
Danielle J Padilla-CarlinCenter of Risk and Integrated Sciences, Division of Extramural Research and Training, National Institute of Environmental Health Sciences, RTP, Durham, North Carolina 27709.
Jean SungBiomedical Engineering, John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138; Department of Pharmaceutical Development, Pulmatrix, Lexington, Massachusetts 02421.
Jarod VerBerkmoesBiomedical Engineering, John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138.
Pavan MuttilDepartment of Pharmaceutical Sciences, College of Pharmacy, University of New Mexico, Albuquerque, New Mexico 87131.
Katharina ElbertBiomedical Engineering, John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138.
Charles PeloquinDepartment of Pharmacotherapy and Translational Research, University of Florida, Gainesville, Florida 32611.
David EdwardsBiomedical Engineering, John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138.
Anthony HickeyDiscovery Science and Technology, RTI International, RTP, Durham, North Carolina 27709.
Harvard University · USNational Institute of Environmental Health Sciences · USPulmatrix (United States) · USRTI International · USUniversity of Florida · USUniversity of New Mexico · USUniversity of Oklahoma Health Sciences Center · US

Funding

Inhaled Large Porous Particles for Treatment of MDR-TBU01AI061336 · NIAID · HARVARD UNIVERSITY · PI EDWARDS, DAVID A · 2004 to 2006
$3.3M
NIAID NIH HHS U01 AI061336
6 · The paper itself

Abstract

The use of ethionamide (ETH) in treating multidrug-resistant tuberculosis is limited by severe side effects. ETH disposition after pulmonary administration in spray-dried particles might minimize systemic exposure and side effects. To explore this hypothesis, spray-dried ETH particles were optimized for performance in a dry powder aerosol generator and exposure chamber. ETH particles were administered by the intravenous (IV), oral, or pulmonary routes to guinea pigs. ETH appearance in plasma, bronchoalveolar lavage, and lung tissues was measured and subjected to noncompartmental pharmacokinetic analysis. Dry powder aerosol generator dispersion of 20% ETH particles gave the highest dose at the exposure chamber ports and fine particle fraction of 72.3%. Pulmonary ETH was absorbed more rapidly and to a greater extent than orally administered drug. At T

Indexed as

Administration, InhalationAdministration, IntravenousAdministration, OralAerosolsAnimalsAntitubercular AgentsDesiccationDry Powder InhalersEthionamideGuinea PigsLungMaleParticle SizePorosityPowdersAerosolsAntitubercular AgentsEthionamidePowdersbioavailabilityethionamidepharmacokinetics and pulmonary absorptionporous particlestuberculosis

Identifiers

PMID27842973
PMCPMC5637532
OpenAlexW2552896031

What OpenQuestion holds

Textmetadata
LicenceTDM
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.