Evidence map›Paper›PMID 35628233›Full record

ArticleInternational journal of molecular sciences2022

Green Synthesis of Silymarin-Chitosan Nanoparticles as a New Nano Formulation with Enhanced Anti-Fibrotic Effects against Liver Fibrosis.

Abdullah Saad Abdullah, Ibrahim El Tantawy El Sayed, Abdel Moneim A El-Torgoman, Abul Kalam, S Wageh, Maher A Kamel

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

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  14. Formulation of silymarin surface modified vesicles: In vitro characterization to cell viability assessment.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 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

6 authors at 5 institutions in 3 countries.

Abdullah Saad AbdullahDepartment of Chemistry, Faculty of Science, Menoufia University, Shebin El Koom 13829, Egypt.
Ibrahim El Tantawy El SayedDepartment of Chemistry, Faculty of Science, Menoufia University, Shebin El Koom 13829, Egypt.
Abdel Moneim A El-TorgomanDepartment of Chemistry, Faculty of Science, Menoufia University, Shebin El Koom 13829, Egypt.
Abul KalamResearch Center for Advanced Materials Science (RCAMS), King Khalid University, P.O. Box 9004, Abha 61413, Saudi Arabia.
S WagehDepartment of Physics, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0002-9494-4568
Maher A KamelDepartment of Biochemistry, Medical Research Institute, Alexandria University, Alexandria 21516, Egypt.ORCID 0000-0002-6791-9850
Menoufia University · EGAlexandria University · EGKing Abdulaziz University · SAKing Khalid University · SAThamar University · YE

Funding

King Khalid University rgrant no: RCAMS/KKU/0010/21.
6 · The paper itself

Abstract

backgroundSilymarin (SIL) has long been utilized to treat a variety of liver illnesses, but due to its poor water solubility and low membrane permeability, it has a low oral bioavailability, limiting its therapeutic potential.

aimDesign and evaluate hepatic-targeted delivery of safe biocompatible formulated SIL-loaded chitosan nanoparticles (SCNPs) to enhance SIL's anti-fibrotic effectiveness in rats with CCl

methodsThe SCNPs and chitosan nanoparticles (CNPs) were prepared by ionotropic gelation technique and are characterized by physicochemical parameters such as particle size, morphology, zeta potential, and in vitro release studies. The therapeutic efficacy of successfully formulated SCNPs and CNPs were subjected to in vivo evaluation studies. Rats were daily administered SIL, SCNPs, and CNPs orally for 30 days.

resultsThe in vivo study revealed that the synthesized SCNPs demonstrated a significant antifibrotic therapeutic action against CCl

conclusionsAccording to the above results, SCNPs might be the best suitable carrier to target liver cells in the treatment of liver fibrosis.

Indexed as

ChitosanMicroRNAsNanoparticlesSilymarinAnimalsLiver CirrhosisRatsChitosanMicroRNAsMIRN22 microRNA, ratSilymarinchitosan nanoparticlesepigeneticsliver fibrosismicroRNAsoxidative stresssilymarin

Identifiers

PMID35628233
PMCPMC9141191
OpenAlexW4280495451

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.