Evidence map›Paper›PMID 39470612›Full record

ReviewAmerican journal of physiology. Lung cellular and molecular physiology2024

Nanoparticles to target asthma.

Samantha K Hamrick, Michael A Thompson, Vincent M Rotello, Y S Prakash, Christina M Pabelick

Abstract readReview
In one paragraph

Review in American journal of physiology. Lung cellular and molecular physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Samantha K HamrickDepartment of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0002-8680-2906
Michael A ThompsonDepartment of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, United States.
Vincent M RotelloDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts, United States.
Y S PrakashDepartment of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0002-2968-224X
Christina M PabelickDepartment of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0002-4632-2174

Funding

NEURAL REGULATION OF AIRWAYS DURING POSTNATAL MATURATIONR01HL056470 · NHLBI · MAYO CLINIC ROCHESTER · PI PRAKASH, Y. S. · 1996 to 2025
$10.5M
Targeting of Bio-orthogonal Chemotherapeutic Nanozymes to Tumor-Associated MacrophagesR01EB022641 · NIBIB · UNIVERSITY OF MASSACHUSETTS AMHERST · PI ROTELLO, VINCENT M. · 2017 to 2024
$3.0M
Hydrogen Sulfide in Neonatal Airway DiseaseR01HL160570 · NHLBI · MAYO CLINIC ROCHESTER · PI Christina Maria Pabelick, Y. S. Prakash · 2023 to 2026
$2.4M
Aryl hydrocarbon receptor signaling in Airway InflammationR01HL171245 · NHLBI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Rodney Britt, Sathish Venkatachalem · 2024 to 2026
$1.8M
Identification of Biomarkers in Zebrafish AgingR03AG022641 · NIA · DANA-FARBER CANCER INSTITUTE · PI KISHI, SHUJI · 2004 to 2005
$171k
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL056470HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL160570HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL171245HHS | NIH | National Institute of Biomedical Imaging and Bioengineering (NIBIB) EB022641NHLBI NIH HHS R01 HL056470NHLBI NIH HHS R01 HL160570NHLBI NIH HHS R01 HL171245NIBIB NIH HHS R01 EB022641
6 · The paper itself

Abstract

Asthma is a heterogeneous chronic lung disease that affects nearly 340 million people globally. Airway hyperresponsiveness, remodeling (thickening and fibrosis), and mucus hypersecretion are some hallmarks of asthma. With several current treatments having serious side effects from long-term use and a proportion of patients with uncontrolled asthma, there is an urgent need for new therapies. With an increasing understanding of asthma pathophysiology, there is a recognized need to target therapies to specific cell types of the airway, which necessitates the identification of delivery systems that can overcome increased mucus and thickened airways. Nanoparticles (NPs) that are highly customizable (material, size, charge, and surface modification) are a potential solution for delivery systems of a wide variety of cargoes (nucleic acids, proteins, and/or small molecules), as well as sole therapeutics for asthma. However, there is a need to consider the safety of the NPs in terms of potential for inflammation, toxicity, nonspecific targets, and accumulation in organs. Ongoing clinical trials using NPs, some FDA-approved for therapeutics in other diseases, provide confidence regarding the potential safety and efficacy of NPs in asthma treatment. This review highlights the current state of the use of NPs in asthma, identifying opportunities for further improvements in NP design and utilization for targeting this chronic lung disease.

Indexed as

AsthmaNanoparticlesAnimalsAnti-Asthmatic AgentsDrug Delivery SystemsHumansAnti-Asthmatic Agentsasthmalung diseasenanoparticlestherapeutic target

Identifiers

PMID39470612
PMCPMC11684954

What Socratic 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 Socratic graph.