Evidence map›Paper›PMID 35986172›Full record

ArticleJournal of molecular modeling2022

Utilization of boron carbide nanosheet in the recognition cathinone drug concentration in the human body.

Huifang Liu, KeWei Wang

Abstract read
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Article in Journal of molecular modeling, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Huifang LiuDepartment of Pharmacology, School of Pharmacy, Qingdao University, Shandong Province, Qingdao, 266021, China.
KeWei WangDepartment of Pharmacology, School of Pharmacy, Qingdao University, Shandong Province, Qingdao, 266021, China. wangkwqduedu@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study adopted density functional theory (DFT) and analyzed the interaction of the conventional cathinone (CA) drug with perfect and defected monolayer nanosheets of boron carbide (BC3). BC3 was found to have poor interactions with CA. Hence, the perfect nanosheets had poor CA sensitivity. The potential of single and double vacancy (SV and DV) defects in the nanosheet to strengthen the nanosheet-drug interaction were assessed. The energy of adsorption of CA adsorption onto SV-BC3 and DV-BC3 was nearly - 23.78 and - 15.32 kcal/mol, respectively. The adsorption substantially altered the work function and bandgap of the defected nanosheets. However, the perfect BC3 experienced a change merely in bandgap during the drug adsorption-the work function change was slight. Thus, the defected nanosheets could be Φ-type and electronic sensors of CA, whereas the perfect nanosheet has the potential to be solely an electronic detector of CA. A larger dielectric constant led to a significant change in the adsorption energy. Furthermore, DV-BC3 considerably changed in magnetic characteristics due to the drug adsorption.

Indexed as

BoronNanostructuresAlkaloidsBoron CompoundsHuman BodyHumansAlkaloidsBoronBoron CompoundscathinoneAdsorptionDefectedDielectricWork function

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.