Evidence map›Paper›PMID 35416873›Full record

ArticleRevista da Sociedade Brasileira de Medicina Tropical2022

In vitro and in vivo Anti-leishmanial Potential of [Ag (PTA) 4 ]BF 4 and [Ag(HBPz 3 )(PPh 3 )] Silver Complexes.

Pauline de Faria Soldera, Ana Flavia da Silva Chagas, Anny Maisa Vargas Brasil, Claudia Dantas Comandolli-Wyrepkowski, Marina Porchia, Antonia Maria Ramos Franco Pereira

Open access · diamondAbstract read
In one paragraph

Article in Revista da Sociedade Brasileira de Medicina Tropical, 2022. 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
0.4field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

6 authors at 2 institutions in 2 countries.

Pauline de Faria SolderaUniversidade Federal do Amazonas, Programa de Pós-Graduação Stricto Sensu em Inovação Farmacêutica, Manaus, AM, Brasil.ORCID http://orcid.org/0000-0003-1730-0029
Ana Flavia da Silva ChagasUniversidade Federal do Amazonas, Programa de Pós-Graduação Stricto Sensu em Inovação Farmacêutica, Manaus, AM, Brasil.ORCID http://orcid.org/0000-0002-6677-9833
Anny Maisa Vargas BrasilUniversidade Federal do Amazonas, Programa de Pós-Graduação Stricto Sensu em Inovação Farmacêutica, Manaus, AM, Brasil.ORCID http://orcid.org/0000-0001-7191-3999
Claudia Dantas Comandolli-WyrepkowskiInstituto Nacional de Pesquisas da Amazônia, Laboratório de Leishmaniose e Doença de Chagas, Manaus, AM, Brasil.ORCID http://orcid.org/0000-0001-9699-7308
Marina PorchiaIstituto di Chimica della Materia Condensata e di Tecnologie per l'Energia, Pádua, Italy.ORCID http://orcid.org/0000-0003-0435-6576
Antonia Maria Ramos Franco PereiraInstituto Nacional de Pesquisas da Amazônia, Laboratório de Leishmaniose e Doença de Chagas, Manaus, AM, Brasil.ORCID http://orcid.org/0000-0002-4300-5325
Instituto Nacional de Pesquisas da Amazônia · BRInstitute of Condensed Matter Chemistry and Technologies for Energy · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmerican tegumentary leishmaniasis is a parasitic disease known for being difficult to treat; therefore, the search for more effective therapeutic methods is necessary. The objective of this study was to evaluate the in vitro and in vivo antileishmanial activity of silver complexes [Ag(PTA)4]BF4 (Ag1) and [Ag(HBPz3)(PPh3)] (Ag2) against Leishmania (Leishmania) amazonensis [L. (L.) amazonensis] and Leishmania (Viannia) guyanensis.

methodsIn vitro bioassays were performed to evaluate the activity of the complexes against promastigote and amastigote forms and evaluate their cytotoxicity. In vivo experiments were performed with hamsters (Mesocricetus auratus) infected and treated topically with two gels containing each metallic complex.

resultsBoth complexes reduced the number of viable parasites against the promastigote forms of L. (L.) amazonensis. Ag2 was mainly effective against the amastigote forms. The Ag2 complex did not present cellular cytotoxicity, and regarding the selectivity index, both complexes were considered acceptable, with Ag2 having the best selectivity index in murine peritoneal macrophages in relation to L. (L.) amazonensis. Ag2 showed better results in the topical treatment against infections caused by L. (L.) amazonensis, with a small reduction in the lesion volume after the 14th day of treatment and less parasitic load at the lesion site.

conclusionsAg2 was more effective than Ag1 against L. (L.) amazonensis.

Indexed as

Antiprotozoal AgentsLeishmaniaLeishmania guyanensisLeishmaniasis, CutaneousAnimalsCricetinaeMacrophagesMiceMice, Inbred BALB CSilverAntiprotozoal AgentsSilver

Identifiers

PMID35416873
PMCPMC9009886
OpenAlexW4226231319

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.