Evidence map›Paper›PMID 41340279›Full record

ArticleThoracic research and practice2025

Nanoparticle-Based Therapeutic Strategies in Respiratory Diseases: Current Approaches and Future Perspectives.

Ozge Cinar, Ilgin Kimiz-Gebologlu, Suphi S Oncel

Abstract read
In one paragraph

Article in Thoracic research and practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Molecular Mechanisms Underlying Antimicrobial Resistance in Mycobacteria.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Review
  4. 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

3 authors.

Ozge CinarDepartment of Bioengineering, Faculty of Engineering, Ege University, Izmir, Türkiye.
Ilgin Kimiz-GebologluDepartment of Bioengineering, Faculty of Engineering, Ege University, Izmir, Türkiye.
Suphi S OncelDepartment of Bioengineering, Faculty of Engineering, Ege University, Izmir, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRespiratory diseases such as asthma, chronic obstructive pulmonary disease (COPD), lung cancer, tuberculosis, and acute respiratory distress syndrome (ARDS) remain major global health challenges, causing significant morbidity and mortality worldwide.

conclusionNanoparticle-based drug delivery systems provide a significant advancement in the treatment of respiratory diseases by overcoming the fundamental limitations of conventional therapies. Through their small size, tunable physicochemical properties, and ability to target specific lung regions, nanoparticles ensure improved bioavailability, controlled release, and reduced systemic toxicity. Studies on various nanocarriers -such as ROS-responsive and GSH-triggered nanoparticles, nanoliposomal salbutamol sulfate, PLA nanoparticles, and mannose-conjugated chitosan nanoparticles- have demonstrated promising outcomes in enhancing drug retention, reducing inflammation, and improving therapeutic efficacy in respiratory disorders. Despite these achievements, challenges such as mucus barrier penetration, long-term pulmonary toxicity, and large-scale reproducibility still remain. However, ongoing interdisciplinary research combining materials science, pharmacology, and pulmonary biology continues to improve the design, safety, and performance of nanoparticle systems. Collectively, these advancements indicate that nanotechnology can transform the current therapeutic landscape of respiratory medicine, making treatments more effective, safer, and more patient-centered. Future Perspectives: The future of nanoparticle-based pulmonary therapies lies in the development of next-generation smart and personalized nanomedicines. Stimuli-responsive nanoparticles capable of detecting disease-specific microenvironments, such as pH shifts, oxidative stress, or enzymatic activity, will enable localized and on-demand drug release, minimizing off-target effects. Personalized nanomedicine approaches will allow the design of patient-specific formulations that combine multiple therapeutic agents, offering synergistic efficacy for complex respiratory disorders. Hybrid nanoplatforms that integrate metallic nanoparticles (e.g., silver, gold) with natural bioactive compounds such as phycocyanin are expected to exhibit both therapeutic and diagnostic potential, enhancing the scope of precision medicine. Furthermore, advancements in inhalation device technology, aerosol engineering, and biocompatible excipient development will further support the translation of nanoparticle-based formulations from laboratory research to clinical application. As large-scale production, regulatory harmonization, and long-term safety validation advance, nanoparticle-based systems are expected to become a cornerstone of future respiratory therapies, offering precision, safety, and efficacy beyond the limitations of current treatments.

Indexed as

Nano-delivery systemsnanoparticlesrespiratory diseases

Identifiers

PMID41340279
PMCPMC12673190

What OpenQuestion holds

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LicenceCC BY-NC
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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.