Evidence map›Paper›PMID 37774084›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2023

Characteristics and Cytotoxic Effects of Nano-Liposomal Paclitaxel on Gastric Cancer Cells.

Zahra Abedi Cham Heidari, Parizad Ghanbarikondori, Elham Mortazavi Mamaghani, Ali Hheidari, Elham Saberian, Elaheh Mozaffari, Mohsen Alizadeh, Mohammadreza Allahyartorkaman

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Advances in nanomedicine and delivery systems for gastric cancer research.Frontiers in bioengineering and biotechnology · 2025
    Review
  5. Review
  6. Review
  7. Review
  8. Metal-based nanoparticle in cancer treatment: lessons learned and challenges.Frontiers in bioengineering and biotechnology · 2024
    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 4 institutions in 1 country.

Zahra Abedi Cham HeidariDepartment of Nursing, Karaj Branch, Islamic Azad University, Karaj, Iran.
Parizad GhanbarikondoriDepartment of Pharmaceutics, Pharmaceutical Sciences Branch, Islamic Azad University (IAU), Tehran, Iran.
Elham Mortazavi MamaghaniDepartment of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID 0009-0004-6913-4629
Ali HheidariDepartment of Mechanical Engineering, Islamic Azad University, Science and Research Branch, Tehran, Iran.
Elham SaberianMDDr., PhD and Specialty Student, Pavol Jozef Safarik University, Klinika Bacikova, Kosice, Slovakia.
Elaheh MozaffariDepartment of Neurology, School of Medicine, Boushehr University of Medical Sciences, Boushehr, Iran.
Mohsen AlizadehDepartment of Chemistry Engineering, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Mohammadreza AllahyartorkamanDepartment of life Science, College of Life Science, National Taiwan University, Taipei, Taiwan.
Iran University of Medical Sciences · IRIslamic Azad University, Karaj · IRIslamic Azad University Pharmaceutical Sciences Branch · IRIslamic Azad University, Science and Research Branch · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAddressing both the initial treatment response and subsequent paclitaxel resistance is a pivotal concern. Nano drug delivery, an emerging approach, presents a cutting-edge alternative to conventional chemotherapy.

methodsThis investigation synthesized PEGylated nanoparticles (NPs) via the Reverse Phase Evaporation technique for liposomal NPs. Characteristics such as zeta potential, size, drug release and polydispersity index (PDI) were subjected to evaluation. Subsequently, cytotoxicity assays were conducted on gastric cancer cells (AGS) following 24 and 48-hour incubation periods.

resultsIn this study, the liposomal NPs had a zeta potential of -22 mV and a particle size of 285 nm. The Entrapment efficiency was determined as 41% that occurred physically. Additionally, the liposomal NPs demonstrated a high drug retention rate (39% remained after 72 hours), and they exhibited significantly increased cytotoxicity compared to the free drug, confirming their effectiveness as a suitable carrier for paclitaxel during both incubation periods (P<0.05).

conclusionThese findings collectively advocate the potential of liposomal NPs as promising contenders for effective nano-drug application in propelling chemotherapy forward.

Indexed as

Antineoplastic AgentsNanoparticlesStomach NeoplasmsDrug CarriersHumansLiposomesPaclitaxelParticle SizeAntineoplastic AgentsDrug CarriersLiposomesPaclitaxelGastric cancerLiposomal nanoparticleNano drug deliveryPaclitaxel

Identifiers

PMID37774084
PMCPMC10762764
OpenAlexW4387164471

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.