Evidence map›Paper›PMID 38078921›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2024

Advances in nano-based drug delivery systems for the management of cytokine influx-mediated inflammation in lung diseases.

Nisha Gulati, Dinesh Kumar Chellappan, Ronan MacLoughlin, Gaurav Gupta, Sachin Kumar Singh, Brian G Oliver, Kamal Dua, Harish Dureja

Abstract readReview
PubMed Publisher
In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. A Combined Extract fromAntioxidants (Basel, Switzerland) · 2024
    Article
  5. Review
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 at 6 institutions in 4 countries.

Nisha GulatiDepartment of Pharmaceutical Sciences, Maharshi Dayanand University, Rohtak, 124001, India.
Dinesh Kumar ChellappanDepartment of Life Sciences, School of Pharmacy, International Medical University, 57000, Bukit Jalil, Kuala Lumpur, Malaysia.
Ronan MacLoughlinResearch and Development, Science and Emerging Technologies, Aerogen Limited, Galway Business Park, Galway, H91 HE94, Ireland.
Gaurav GuptaSchool of Pharmacy, Suresh Gyan Vihar University, Mahal Road, Jagatpura, Jaipur, India.
Sachin Kumar SinghSchool of Pharmaceutical Sciences, Lovely Professional University, Phagwara, 144411, Punjab, India.
Brian G OliverFaculty of Science, School of Life Sciences, University of Technology Sydney, Sydney, NSW, 2007, Australia.
Kamal DuaDepartment of Pharmaceutical Sciences, Maharshi Dayanand University, Rohtak, 124001, India. kamal.dua@uts.edu.au.
Harish DurejaDepartment of Pharmaceutical Sciences, Maharshi Dayanand University, Rohtak, 124001, India. harishdureja@mdurohtak.ac.in.
Maharshi Dayanand University · INUniversity of Technology Sydney · AUAerogen (Ireland) · IEInternational Medical University · MYThe University of Sydney · AUUttaranchal University · IN

Funding

Maharshi Dayanand University Rohtak FO/UGC/22/1200 dated 27-5-22
6 · The paper itself

Abstract

Asthma, lung cancer, cystic fibrosis, tuberculosis, acute respiratory distress syndrome, chronic obstructive pulmonary disease, and COVID-19 are few examples of inflammatory lung conditions that cause cytokine release syndrome. It can initiate a widespread inflammatory response and may activate several inflammatory pathways that cause multiple organ failures leading to increased number of deaths and increased prevalence rates around the world. Nanotechnology-based therapeutic modalities such as nanoparticles, liposomes, nanosuspension, monoclonal antibodies, and vaccines can be used in the effective treatment of inflammatory lung diseases at both cellular and molecular levels. This would also help significantly in the reduction of patient mortality. Therefore, nanotechnology could be a potent platform for repurposing current medications in the treatment of inflammatory lung diseases. The aim and approach of this article are to highlight the clinical manifestations of cytokine storm in inflammatory lung diseases along with the advances and potential applications of nanotechnology-based therapeutics in the management of cytokine storm. Further in-depth studies are required to understand the molecular pathophysiology, and how nanotechnology-based therapeutics can help to effectively combat this problem.

Indexed as

CytokinesLung DiseasesAnimalsCOVID-19Cytokine Release SyndromeDrug Delivery SystemsHumansInflammationNanoparticle Drug Delivery SystemNanoparticlesCytokinesNanoparticle Drug Delivery SystemCytokine stormInflammatory lung diseaseNanomedicines

Identifiers

PMID38078921
OpenAlexW4389570914

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.