Evidence map›Paper›PMID 37746316›Full record

ArticleJournal of toxicology2023

Acute Toxicity of Dental Gel Based on

Karakoz Badekova, Gayane Atazhanova, Irina Losseva, Aigul Medeshova, Ailazzat Aitkenova, Anar Brazhanova

Abstract read
In one paragraph

Article in Journal of toxicology, 2023. 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. Identification of compounds fromSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    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.

Karakoz BadekovaInstitute of Life Science, NC JSC "Karaganda Medical University", Karaganda, Kazakhstan.ORCID https://orcid.org/0000-0003-2736-8633
Gayane AtazhanovaInstitute of Life Science, NC JSC "Karaganda Medical University", Karaganda, Kazakhstan.ORCID https://orcid.org/0000-0003-1615-9967
Irina LossevaInstitute of Life Science, NC JSC "Karaganda Medical University", Karaganda, Kazakhstan.ORCID https://orcid.org/0000-0002-6592-228X
Aigul MedeshovaInstitute of Life Science, NC JSC "Karaganda Medical University", Karaganda, Kazakhstan.ORCID https://orcid.org/0000-0002-1447-0850
Ailazzat AitkenovaInstitute of Life Science, NC JSC "Karaganda Medical University", Karaganda, Kazakhstan.ORCID https://orcid.org/0000-0002-0851-866X
Anar BrazhanovaInstitute of Life Science, NC JSC "Karaganda Medical University", Karaganda, Kazakhstan.ORCID https://orcid.org/0000-0002-8683-3630

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: The creation of new herbal medicines for their use in dentistry is relevant. The purpose of this work is to study the acute toxicity of the anticaries dental gel (ACDG3) developed by us based on Results: In case of studying the safety of anticaries dental gel "ACDG3" in animals, that with a single dose of up to 2000 mg/kg, the absence of pathological changes in the behavior of animals was noted. Biochemical studies indicate that the studied doses of dental gel did not lead to significant deviations in the blood parameters of mice and deviations fluctuated within the reference values. According to the results of a morphometric study conducted 15 days after the administration of the drug, no deviations were found. The histological evaluation of organs showed little change in the cardiac architecture in animals treated with ACDG3 at doses of 1000 mg/kg and 2000 mg/kg. On the other hand, no significant changes in the cardiac function were observed in all treated mice. Conclusion: As follows from the results obtained, in case of determining acute toxicity, the studied anticaries gel, ACDG3, showed low toxicity. For mice, LD50 was 2000 mg/kg intragastrically. So, according to the generally accepted classification of the toxicity of substances, ACDG3 can be attributed to the class of low-toxic substances (IV class of toxicity, LD50 > 5000 mg/kg, intragastric administration), that is, to practically nontoxic compounds.

Identifiers

PMID37746316
PMCPMC10513860

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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.