Evidence map›Paper›PMID 41004077›Full record

ArticleDrug delivery and translational research2026

Clinically translatable anti-fibrotic nanosuspension for inhaled treatment of idiopathic pulmonary fibrosis.

Daiheon Lee, Byoungjae Kong, Gijung Kwak, Bokyung Kang, Carter Swaby, Rachel Fanaroff, Venkataramana Sidhaye, Jung Soo Suk

Abstract read
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In one paragraph

Article in Drug delivery and translational research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

8 authors.

Daiheon LeeDepartment of Neurosurgery, School of Medicine, University of Maryland, 21201, Baltimore, MD, USA.
Byoungjae KongDepartment of Neurosurgery, School of Medicine, University of Maryland, 21201, Baltimore, MD, USA.
Gijung KwakDepartment of Neurosurgery, School of Medicine, University of Maryland, 21201, Baltimore, MD, USA.
Bokyung KangDepartment of Neurosurgery, School of Medicine, University of Maryland, 21201, Baltimore, MD, USA.
Carter SwabyDivision of Pulmonary and Critical Care, Department of Medicine, School of Medicine, Johns Hopkins University, 21205, Baltimore, MD, USA.
Rachel FanaroffDepartment of Pathology, School of Medicine, University of Maryland, 21201, Baltimore, MD, USA.
Venkataramana SidhayeDivision of Pulmonary and Critical Care, Department of Medicine, School of Medicine, Johns Hopkins University, 21205, Baltimore, MD, USA.
Jung Soo SukDepartment of Neurosurgery, School of Medicine, University of Maryland, 21201, Baltimore, MD, USA.

Funding

Maryland Technology Development Corporation Maryland Technology Development Corporation
6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease characterized by chronic pulmonary fibrosis, irreversible lung function decline, and high mortality rate. Oral nintedanib (NTB) is one of the rare anti-fibrotic drugs clinically available for managing the condition but suffers from poor bioavailability and lung delivery efficiency as well as numerous off-target adverse effects. To address these critical limitations, we developed a nanosuspension (NS) formulation of NTB (NTB-NS) for inhaled treatment of IPF. The formulation is composed entirely of FDA-approved materials, including NTB and polysorbate 80, a surfactant approved for respiratory use in a clinic, and can be freeze-dried to a powder form for long-term storage and remote shipping without perturbing the physicochemical properties and drug activity. NTB-NS locally administered via oropharyngeal administration exhibited favorable pharmacokinetics over the standard oral administration of nintedanib esylate (NTB-esy), resulting in comprehensive anti-inflammatory and anti-fibrotic effects in a mouse model of bleomycin-induced pulmonary fibrosis. Notably, locally administered NTB-NS, but not oral NTB-esy, normalized several key lung function parameters in the model despite the use of 60-fold and 3-fold lower dose and dosing frequency, respectively. The findings here may open a new avenue for the treatment of IPF and potentially other fibrotic lung diseases in the clinic.

Indexed as

Antifibrotic AgentsIdiopathic Pulmonary FibrosisIndolesNanoparticlesAdministration, InhalationAnimalsBleomycinDisease Models, AnimalHumansLungMaleMiceMice, Inbred C57BLPolysorbatesSuspensionsAntifibrotic AgentsBleomycinIndolesnintedanibPolysorbatesSuspensionsAnti-fibrotic drugInhaled therapyNanoformulationPharmacokineticsPulmonary fibrosis

Identifiers

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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.