Evidence map›Paper›PMID 39240502›Full record

ReviewDiscover nano2024

Advances, limitations and perspectives in the use of celecoxib-loaded nanocarriers in therapeutics of cancer.

Miguel de Jesus Oliveira Santos, Jéssica Teles-Souza, Renata Freitas de Araújo-Calumby, Robert L Copeland, Henrique Rodrigues Marcelino, Deise Souza Vilas-Bôas

Abstract readReview
In one paragraph

Review in Discover nano, 2024. 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. Article
  2. 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

6 authors.

Miguel de Jesus Oliveira SantosLaboratory of Immunopathology and Molecular Biology, Department of Biomorfology, Health Sciences Institute, Federal University of Bahia, Salvador Av. Reitor Miguel Calmon, S/N, Salvador, Bahia, CEP 40110-100, Brazil.ORCID http://orcid.org/0000-0002-0448-4407
Jéssica Teles-SouzaLaboratory of Immunopathology and Molecular Biology, Department of Biomorfology, Health Sciences Institute, Federal University of Bahia, Salvador Av. Reitor Miguel Calmon, S/N, Salvador, Bahia, CEP 40110-100, Brazil.ORCID http://orcid.org/0000-0002-9688-2794
Renata Freitas de Araújo-CalumbyLaboratory of Immunopathology and Molecular Biology, Department of Biomorfology, Health Sciences Institute, Federal University of Bahia, Salvador Av. Reitor Miguel Calmon, S/N, Salvador, Bahia, CEP 40110-100, Brazil.ORCID http://orcid.org/0000-0003-2475-5953
Robert L CopelandDepartment of Pharmacology, College of Medicine and Howard University Cancer Center, Howard University, Washington, D.C., 20059, USA.ORCID http://orcid.org/0000-0002-9760-6548
Henrique Rodrigues MarcelinoPost-Graduate Program in Pharmacy, College of Pharmacy, Federal University of Bahia, Salvador, BA, 40170-115, Brazil.ORCID http://orcid.org/0000-0002-3625-7786
Deise Souza Vilas-BôasLaboratory of Immunopathology and Molecular Biology, Department of Biomorfology, Health Sciences Institute, Federal University of Bahia, Salvador Av. Reitor Miguel Calmon, S/N, Salvador, Bahia, CEP 40110-100, Brazil. vilasboasdeise@gmail.com.ORCID http://orcid.org/0000-0002-6557-5417

Funding

CNPq - National Council for Scientific and Technological Development (BR) 424854/20163Dean of Research/Pro Rectory of Research and Postgraduate Studies (PRPPG)/Federal University of Bahia - UFBA (BR) PROPCI/PROPG 004/2016 - 11347FAPESB - Bahia State Research Funding Institution (BR) JCB0048/2013
6 · The paper itself

Abstract

Cancer is highlighted as a major global health challenge in the XXI century. The cyclooxygenase-2 (COX-2) enzyme rises as a widespread tumor progression marker. Celecoxib (CXB) is a selective COX-2 inhibitor used in adjuvant cancer therapy, but high concentrations are required in humans. In this sense, the development of nanocarriers has been proposed once they can improve the biopharmaceutical, pharmacokinetic and pharmacological properties of drugs. In this context, this article reviews the progress in the development of CXB-loaded nanocarriers over the past decade and their prospects. Recent advances in the field of CXB-loaded nanocarriers demonstrate the use of complex formulations and the increasing importance of in vivo studies. The types of CXB-loaded nanocarriers that have been developed are heterogeneous and based on polymers and lipids together or separately. It was found that the work on CXB-loaded nanocarriers is carried out using established techniques and raw materials, such as poly (lactic-co-glicolic acid), cholesterol, phospholipids and poly(ethyleneglycol). The main improvements that have been achieved are the use of cell surface ligands, the simultaneous delivery of different synergistic agents, and the presence of materials that can provide imaging properties and other advanced features. The combination of CXB with other anti-inflammatory drugs and/or apoptosis inducers appears to hold effective pharmacological promise. The greatest advance to date from a clinical perspective is the ability of CXB to enhance the cytotoxic effects of established chemotherapeutic agents.

Indexed as

CancerCelecoxibCOX-2Drug delivery systemsNanocarriersNanoparticles

Identifiers

PMID39240502
PMCPMC11379842

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.