Evidence map›Paper›PMID 33578857›Full record

ArticlePharmaceutics2021

Anti-Tumor Efficiency of Perillylalcohol/β-Cyclodextrin Inclusion Complexes in a Sarcoma S180-Induced Mice Model.

Allan A Rezende, Rafael S Santos, Luciana N Andrade, Ricardo G Amaral, Matheus M Pereira, Cristiane Bani, Mo Chen, Ronny Priefer, Classius F da Silva, Ricardo L C de Albuquerque Júnior and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. The Antiviral Potential ofMolecules (Basel, Switzerland) · 2024
    Pooled it
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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

12 authors at 8 institutions in 4 countries.

Allan A RezendeUniversity of Tiradentes (Unit), Postgraduate Program Industrial Biotechnology, and Health and Enviroment. Av. Murilo Dantas, 300, 49010-390 Aracaju, Brazil.ORCID 0000-0003-1402-9608
Rafael S SantosUniversity of Tiradentes (Unit), Postgraduate Program Industrial Biotechnology, and Health and Enviroment. Av. Murilo Dantas, 300, 49010-390 Aracaju, Brazil.ORCID 0000-0002-6458-4661
Luciana N AndradeDepartment of Physiology, Federal University of Sergipe, São Cristovão, 49100-000 Sergipe, Brazil.ORCID 0000-0002-5481-4355
Ricardo G AmaralDepartment of Physiology, Federal University of Sergipe, São Cristovão, 49100-000 Sergipe, Brazil.
Matheus M PereiraCICECO, Aveiro Institute of Materials, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal.ORCID 0000-0003-3524-6900
Cristiane BaniDepartment of Physiology, Federal University of Sergipe, São Cristovão, 49100-000 Sergipe, Brazil.
Mo ChenDepartment of Gynecology, Obstetrics & Gynecology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai 200011, China.
Ronny PrieferSchool of Pharmacy, Massachusetts College of Pharmacy and Health Sciences, 179 Longwood Avenue, Boston, MA 02115, USA.ORCID 0000-0002-4586-0405
Classius F da SilvaInstitute of Environmental, Chemical and Pharmaceutical Sciences, Federal University of São Paulo, 09972-270 Diadema, São Paulo, Brazil.ORCID 0000-0001-9937-5598
Ricardo L C de Albuquerque JúniorUniversity of Tiradentes (Unit), Postgraduate Program Industrial Biotechnology, and Health and Enviroment. Av. Murilo Dantas, 300, 49010-390 Aracaju, Brazil.ORCID 0000-0003-4444-7632
Eliana B SoutoFaculty of Pharmacy, University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, Portugal.ORCID 0000-0002-9737-6017
Patrícia SeverinoUniversity of Tiradentes (Unit), Postgraduate Program Industrial Biotechnology, and Health and Enviroment. Av. Murilo Dantas, 300, 49010-390 Aracaju, Brazil.ORCID 0000-0001-6527-6612
Universidade Federal de Sergipe · BRUniversidade Tiradentes · BRBrigham and Women's Hospital · USMassachusetts College of Pharmacy and Health Sciences · USObstetrics and Gynecology Hospital of Fudan University · CNUniversidade Federal de São Paulo · BRUniversity of Aveiro · PTUniversity of Coimbra · PT

Funding

Banco do Nordeste (grant FUNDECI/2016.0015), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Fundação de Apoio à Pesquisa e à Inovação Tecnológica do Estado de Sergipe (Fapitec) and Coordenação de Aperfeiçoamento de Pessoal de Nível grant FUNDECI/2016.0015Portuguese Science and Technology Foundation (FCT/MCT) and from European Funds (PRODER/COMPETE) for the project UIDB/04469/2020 (strategic fund), co-financed by FEDER, under the Partnership Agreement PT2020 UIDB/04469/2020 (strategic fund)
6 · The paper itself

Abstract

The low solubility and high volatility of perillyl alcohol (POH) compromise its bioavailability and potential use as chemotherapeutic drug. In this work, we have evaluated the anticancer activity of POH complexed with β-cyclodextrin (β-CD) using three complexation approaches. Molecular docking suggests the hydrogen-bond between POH and β-cyclodextrin in molar proportion was 1:1. Thermal analysis and Fourier-transform infrared spectroscopy (FTIR) confirmed that the POH was enclosed in the β-CD cavity. Also, there was a significant reduction of particle size thereof, indicating a modification of the β-cyclodextrin crystals. The complexes were tested against human L929 fibroblasts after 24 h of incubation showing no signs of cytotoxicity. Concerning the histopathological results, the treatment with POH/β-CD at a dose of 50 mg/kg promoted approximately 60% inhibition of tumor growth in a sarcoma S180-induced mice model and the reduction of nuclear immunoexpression of the Ki67 antigen compared to the control group. Obtained data suggest a significant reduction of cycling cells and tumor proliferation. Our results confirm that complexation of POH/β-CD not only solves the problem related to the volatility of the monoterpene but also increases its efficiency as an antitumor agent.

Indexed as

anti-cancercyclodextrininclusion complexperillyl alcoholsarcoma

Identifiers

PMID33578857
PMCPMC7916601
OpenAlexW3128563057

What OpenQuestion 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 OpenQuestion graph.