Evidence map›Paper›PMID 31460049›Full record

ArticleACS omega2019

Molecular Docking-Guided Ungual Drug-Delivery Design for Amelioration of Onychomycosis.

Nazia Hassan, Manvi Singh, Sufiyanu Sulaiman, Pooja Jain, Kalicharan Sharma, Shyamasree Nandy, Mridu Dudeja, Asgar Ali, Zeenat Iqbal

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

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  4. Nanoscale advances · 2024
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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

9 authors at 1 institution in 1 country.

Nazia HassanDepartment of Pharmaceutics, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, and Department of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Manvi SinghDepartment of Pharmaceutics, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, and Department of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Sufiyanu SulaimanDepartment of Pharmaceutics, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, and Department of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Pooja JainDepartment of Pharmaceutics, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, and Department of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Kalicharan SharmaDepartment of Pharmaceutics, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, and Department of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Shyamasree NandyDepartment of Pharmaceutics, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, and Department of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Mridu DudejaDepartment of Pharmaceutics, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, and Department of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Asgar AliDepartment of Pharmaceutics, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, and Department of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Zeenat IqbalDepartment of Pharmaceutics, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, and Department of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Jamia Hamdard · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present work envisaged an adherent luliconazole-loaded bilayer nail lacquer (BNL) with significant transungual activity. The locally applied sustained-release BNL formulation was designed for an improved retention, payload, and final dermatokinetic disposition. A primary step in the fabrication of a BNL included overcoming of physical barriers like α-keratin (also α-keratin), a protein present in human nails, and then allowing the drug molecule to permeate at the site of action. Although luliconazole is an established antifungal agent, has limited clinical exploitation for its use in treating onychomycosis. An in silico study elucidating its interaction with lanosterol-14-α demethylase, an enzyme which is the key region of drug action mechanism, was highly supportive of its imminent clinical potential. Optimization of prepared BNL formulations via response surface modeling (Box-Behnken Design-Expert 10.0.6) logically ascertained the effect of selected independent variables and showcased its effect via dependent responses. Surface morphology of the prepared BNL films was well corroborated for the presence of two distinct polymeric layers through scanning electron microscopy imaging. Nail permeation studies revealed a cumulative drug release of 71.25 ± 0.11% through bovine hooves up to 24 h. Luliconazole while exposing antifungal activity against clinical isolates of

Identifiers

PMID31460049
PMCPMC6648890
OpenAlexW2947344879

What OpenQuestion holds

Textmetadata
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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.