Evidence mapPaperPMID 40488002Full record

ArticleACS omega2025

Codelivery of Paclitaxel and Cannabidiol in Lipid Nanoparticles Enhances Cytotoxicity against Melanoma Cells.

Fabíola V de Carvalho, Gabriela Geronimo, Ludmilla D de Moura, Talita C Mendonça, Márcia Cristina Breitkreitz, Eneida de Paula, Gustavo H Rodrigues da Silva

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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

7 authors.

Fabíola V de CarvalhoDepartment of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas (UNICAMP), 13083-862 Campinas, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-4450-0563
Gabriela GeronimoDepartment of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas (UNICAMP), 13083-862 Campinas, São Paulo, Brazil.
Ludmilla D de MouraDepartment of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas (UNICAMP), 13083-862 Campinas, São Paulo, Brazil.
Talita C MendonçaDepartment of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas (UNICAMP), 13083-862 Campinas, São Paulo, Brazil.
Márcia Cristina BreitkreitzDepartment of Analytical Chemistry, Institute of Chemistry, University of Campinas (UNICAMP), 13083-970 Campinas, São Paulo, Brazil.
Eneida de PaulaDepartment of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas (UNICAMP), 13083-862 Campinas, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-4504-5723
Gustavo H Rodrigues da SilvaDepartment of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas (UNICAMP), 13083-862 Campinas, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-7377-8532

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although chemotherapy regimens are well-established in clinical practice, chemoresistance and adverse side effects pose significant obstacles in cancer treatment. Paclitaxel (PTX), a widely used chemotherapeutic agent, faces formulation challenges due to its poor solubility and permeability. Research suggests that the phytochemical Cannabidiol (CBD) holds potential not only in targeting cancer cells but also in alleviating pain and nausea, thereby improving the quality of life for cancer patients. However, CBD's clinical application is also limited by its poor solubility, low bioavailability, and susceptibility to oxidation. Nanostructured lipid carriers (NLCs) represent a promising drug delivery system for hydrophobic compounds like PTX and CBD and allow their coencapsulation. Nonetheless, achieving a stable formulation requires the identification of suitable preparation methods and excipients. The aim of this study was to develop and optimize an NLC formulation for the coencapsulation of PTX and CBD. Using factorial design, an optimized formulation was obtained with homogeneous particle sizes (200 nm), negative ZPs (-16.1 mV), a particle concentration of 10

Identifiers

PMID40488002
PMCPMC12138705

What Socratic holds

Textmetadata
LicenceCC BY
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.