Evidence map›Paper›PMID 41057843›Full record

ArticleBMC cancer2025

Innovative inhalable dry powder: nanoparticles loaded with Crizotinib for targeted lung cancer therapy.

Faiza Naureen, Yasar Shah, Maqsood Ur Rehman, Fazli Nasir Fazli Nasir, Abdul Saboor Pirzada, Jamelah Saleh Al-Otaibi, Maria Daglia, Haroon Khan

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Vismodegib-loaded ufasomes inhaler for treatment of non-small cell lung cancer.Naunyn-Schmiedeberg's archives of pharmacology · 2026
    Article
  2. 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.

Faiza NaureenDepartment of Pharmacy, Abdul Wali Khan University Mardan, 23200, Mardan, Pakistan.
Yasar ShahDepartment of Pharmacy, Abdul Wali Khan University Mardan, 23200, Mardan, Pakistan. shah.yasar@awkum.edu.pk.
Maqsood Ur RehmanDepartment of Pharmacy, University of Malakand, Lower Dir, Chakdara, Pakistan.
Fazli Nasir Fazli NasirDepartment of Pharmacy,, University of Peshawar, Peshawar, Pakistan.
Abdul Saboor PirzadaDepartment of Pharmacy, Abdul Wali Khan University Mardan, 23200, Mardan, Pakistan.
Jamelah Saleh Al-OtaibiDepartment of Chemistry, College of Science, Princess Nourah Bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Kingdom of Saudi Arabia.
Maria DagliaDepartment of Pharmacy, University of Napoli Federico II, Via D. Montesano 49, NA, 80131 Naples, Italy.
Haroon KhanDepartment of Pharmacy, Abdul Wali Khan University Mardan, 23200, Mardan, Pakistan. haroonkhan@awkum.edu.pk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Crizotinib is a targeted therapy for metastatic non-small cell lung cancer (NSCLC) that is ALK- or ROS1-positive, as well as for conditions such as ALK-positive anaplastic large cell lymphoma and inflammatory myofibroblastic tumor. However, the associated toxicity poses a significant challenge to its use. To mitigate this issue, a novel dry powder inhalation formulation was developed using Crizotinib-loaded polyethylene glycol-based polymeric nanoparticles (NPs). These nanoparticles were created through a nanoprecipitation approach and improved employing central composite design. The capabilities of the formulation were assessed with Anderson Cascade Impactor, revealing a fine particle fraction of 56.2% and a mass median aerodynamic diameter of around 1.5 μm, indicating appropriate aerodynamic characteristics for inhalation. Key properties of the optimized nanoparticles included Encapsulation efficiency (82.3%, Zeta potential (-31.9 mV), Particle size (167 nm), Polydispersity index (0.462) and Release efficiency (60.6%) In vitro studies indicated that the polymeric nanoparticles exhibited greater anticancer activity compared to free Crizotinib. Additional characterization using techniques like XRD, DSC, FTIR, and SEM confirmed that the polymeric nanoparticle formulation has promising physicochemical properties, suggesting it could enhance local drug delivery and efficacy in lung cancer treatment while potentially reducing systemic toxicity.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsNanoparticlesProtein Kinase InhibitorsPyrazolesPyridinesAdministration, InhalationCell Line, TumorCrizotinibDry Powder InhalersHumansParticle SizePolyethylene GlycolsPowdersAntineoplastic AgentsCrizotinibPolyethylene GlycolsPowdersProtein Kinase InhibitorsPyrazolesPyridinesCrizotinibInhalable dry powderLung cancerOptimizationPolymeric nanoparticlesPulmonary delivery

Identifiers

PMID41057843
PMCPMC12506271

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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.