Evidence map›Paper›PMID 40842623›Full record

ArticleAdvances in pharmacological and pharmaceutical sciences2025

Encapsulation of Curcumin and Gemcitabine: Cytotoxic Effect and Mechanisms of Death in Lung Cancer.

Oscar Alberto Alvarez-Quezada, Norma Cesilia Arellano-Rodríguez, Mara Valeria Rodríguez-Rodríguez, Moisés Armides Franco-Molina, Diana Ginette Zarate-Triviño, Diana Elisa Zamora-Ávila, Claudia Lucía Vargas-Requena, Pablo Zapata-Benavides, María Cristina Rodríguez-Padilla

Abstract read
In one paragraph

Article in Advances in pharmacological and pharmaceutical sciences, 2025. 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

9 authors.

Oscar Alberto Alvarez-QuezadaDepartamento de Microbiología e Inmunología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León (UANL), San Nicolás de los Garza 66450, Nuevo León, Mexico.ORCID https://orcid.org/0000-0003-0753-3099
Norma Cesilia Arellano-RodríguezDepartamento de Microbiología e Inmunología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León (UANL), San Nicolás de los Garza 66450, Nuevo León, Mexico.ORCID https://orcid.org/0000-0002-9691-2412
Mara Valeria Rodríguez-RodríguezDepartamento de Microbiología e Inmunología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León (UANL), San Nicolás de los Garza 66450, Nuevo León, Mexico.ORCID https://orcid.org/0009-0006-1172-7936
Moisés Armides Franco-MolinaDepartamento de Microbiología e Inmunología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León (UANL), San Nicolás de los Garza 66450, Nuevo León, Mexico.ORCID https://orcid.org/0000-0002-0522-6637
Diana Ginette Zarate-TriviñoDepartamento de Microbiología e Inmunología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León (UANL), San Nicolás de los Garza 66450, Nuevo León, Mexico.ORCID https://orcid.org/0000-0003-0177-6022
Diana Elisa Zamora-ÁvilaDepartamento de Genética, Facultad de Medicina Veterinaria, Universidad Autónoma de Nuevo León (UANL), General Escobedo 66050, Nuevo León, Mexico.ORCID https://orcid.org/0000-0002-2225-0495
Claudia Lucía Vargas-RequenaDepartamento de Ciencias Químico-Biológicas, Instituto de Ciencias Biomédicas, Universidad Autónoma de Ciudad Juárez (UACJ), Ciudad Juárez 32310, Chihuahua, Mexico.ORCID https://orcid.org/0000-0001-7612-1616
Pablo Zapata-BenavidesDepartamento de Microbiología e Inmunología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León (UANL), San Nicolás de los Garza 66450, Nuevo León, Mexico.ORCID https://orcid.org/0000-0002-2986-0755
María Cristina Rodríguez-PadillaDepartamento de Microbiología e Inmunología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León (UANL), San Nicolás de los Garza 66450, Nuevo León, Mexico.ORCID https://orcid.org/0000-0001-5469-8449

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the second most common type of cancer and the leading cause of cancer-related deaths worldwide. Some chemotherapeutic agents, such as curcumin and gemcitabine, have low bioavailability due to their hydrophobicity or the need for specialized transporters. This limits their cytotoxic potential against tumor cells but can be addressed through nanoencapsulation. This study evaluated the effects of nanometric encapsulation of curcumin and gemcitabine in chitosan, a biocompatible polymer, on the A549 lung cancer cell line and B16F10 murine melanoma cells. The chemical properties of the synthesized nanoparticles were characterized using UV-vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, and scanning electron microscopy (SEM). The nanoparticles ranged in size from 180 to 197 nm, with a positive surface charge between 11.8 and 16.3 mV. Cytotoxicity assays were conducted on the A549 and B16F10 cell lines, along with morphological analyses of apoptosis and flow cytometry to assess cell death mechanisms. Compared to the free drugs, the nanometric encapsulation of curcumin and gemcitabine did not always enhance the cytotoxic effects, but it did induce pronounced apoptosis in the lung cancer cells. These findings suggest that this approach could optimize drug delivery, reduce the required doses, and minimize side effects, thereby improving the overall efficacy of lung cancer treatment.

Indexed as

curcumincytotoxic effectgemcitabinelung cancernanoparticles

Identifiers

PMID40842623
PMCPMC12367379

What OpenQuestion holds

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Registered trials

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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.