Evidence map›Paper›PMID 30406460›Full record

ArticlePharmaceutical research2018

Pharmaceutical Potential of a Novel Chitosan Derivative Schiff Base with Special Reference to Antibacterial, Anti-Biofilm, Antioxidant, Anti-Inflammatory, Hemocompatibility and Cytotoxic Activities.

Sameh S Ali, El-Refaie Kenawy, Fatma I Sonbol, Jianzhong Sun, Marwa Al-Etewy, Asmaa Ali, Liu Huizi, Nessma A El-Zawawy

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 84 citations in OpenAlex.

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  18. Journal of traditional and complementary medicine · 2020
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  19. Eco-friendly synthesis of functionalized chitosan-based nanoantibiotic system for potential delivery of linezolid as antimicrobial agents.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2020
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  20. 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

8 authors at 3 institutions in 2 countries.

Sameh S AliBiofuels Institute, School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang, 212013, China. samh_samir@science.tanta.edu.eg.ORCID http://orcid.org/0000-0002-7033-8387
El-Refaie KenawyPolymer Research Group, Department of Chemistry, Faculty of Science, Tanta University, Tanta, 31527, Egypt.
Fatma I SonbolDepartment of Microbiology, Faculty of Pharmacy, Tanta University, Tanta, 31527, Egypt.
Jianzhong SunBiofuels Institute, School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang, 212013, China. jzsun1002@ujs.edu.cn.ORCID http://orcid.org/0000-0002-0857-2842
Marwa Al-EtewyPolymer Research Group, Department of Chemistry, Faculty of Science, Tanta University, Tanta, 31527, Egypt.
Asmaa AliMinistry of Health and Population, Chest Directorate, Abbassia Chest Hospital, Cairo, Egypt.
Liu HuiziBiofuels Institute, School of the Environment and Safety Engineering, Jiangsu University, Zhenjiang, 212013, China.
Nessma A El-ZawawyBotany Department, Faculty of Science, Tanta University, Tanta, 31527, Egypt.
Tanta University · EGJiangsu University · CNMinistry of Health and Population · EG

Funding

Egyptian Ministry of Higher Education & Scientific Research (MHESR); Support of Excellent Students Projects (SESP) Egyptian Ministry of Higher Education & Scientific Research (MHESR); Support of Excellent Students Projects (SESP)National Natural Science Foundation of China NNSF-31772529Priority of Academic Program Development PAPD-4013000011
6 · The paper itself

Abstract

purposeChitosan and its derivatives possess several unique properties relevant in the field of pharmaceutics and medicinal chemistry. This study aimed to evaluate the pharmaceutical performance of an innovative chitosan derivative, methyl acrylate chitosan bearing p-nitrobenzaldehyde (MA*CS*pNBA) Schiff base.

methodsThe antibacterial activity of MA*CS*pNBA was tested against multi-drug resistant (MDR) Gram-negative and Gram-positive bacteria using agar-well diffusion method. Anti-biofilm formation was analyzed using a microtitre plate. Antioxidant assays were performed to assess the scavenging activity of MA*CS*pNBA using DPPH, hydrogen peroxide, superoxide together with its reducing power activity. Anti-inflammatory activity was evaluated by albumin denaturation, membrane stabilization, and proteinase inhibition methods. MA*CS*pNBA was tested for its hemolytic efficiency on human erythrocytes. Cytotoxicity of MA*CS*pNBA was evaluated by MTT assay.

resultsMA*CS*pNBA showed a significant performance as an antibacterial candidate against MDR bacteria, anti-biofilm, antioxidant and anti-inflammatory biomaterial, evidencing hemocompatibility and no cytotoxicity. It exhibited a significant negative correlation with biofilm formation by the MDR-PA-09 strain. Biological activities were found to be significantly concentration-dependent.

conclusionsthe newly chitosan derivative MA*CS*pNBA showed to be promising for pharmaceutical applications, expanding the treatment ways toward skin burn infections since it allied excellent antibacterial, anti-biofilm, antioxidant, anti-inflammatory, hemocompatibility and absence of cytotoxic activities.

Indexed as

AnimalsAnti-Bacterial AgentsAnti-Inflammatory AgentsAntioxidantsBacteriaBiocompatible MaterialsBiofilmsCell LineChitosanHumansMiceSchiff BasesAnti-Bacterial AgentsAnti-Inflammatory AgentsAntioxidantsBiocompatible MaterialsChitosanSchiff Basesantibacterialanti-inflammatoryantioxidantchitosan Schiff basescytotoxicity

Identifiers

PMID30406460
OpenAlexW2899716759

What OpenQuestion holds

Textmetadata
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.