Evidence map›Paper›PMID 35011448›Full record

ArticleMolecules (Basel, Switzerland)2021

Panos-Fermented Extract-Mediated Nanoemulsion: Preparation, Characterization, and In Vitro Anti-Inflammatory Effects on RAW 264.7 Cells.

Rui Zhang, Esrat Jahan Rupa, Siwen Zheng, Jinnatun Nahar, Deok Chun Yang, Se Chan Kang, Yingping Wang

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. 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. New Triterpenoids from the Leaves ofMolecules (Basel, Switzerland) · 2024
    Article
  2. 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

7 authors.

Rui ZhangState Local Joint Engineering Research Center of Ginseng Breeding and Application, Jilin Agricultural University, Changchun 130118, China.
Esrat Jahan RupaDepartment of Oriental Medicinal Biotechnology, College of Life Science, Kyung Hee University, Yongin-si 17104, Korea.ORCID 0000-0002-1334-3876
Siwen ZhengState Local Joint Engineering Research Center of Ginseng Breeding and Application, Jilin Agricultural University, Changchun 130118, China.
Jinnatun NaharDepartment of Oriental Medicinal Biotechnology, College of Life Science, Kyung Hee University, Yongin-si 17104, Korea.
Deok Chun YangDepartment of Oriental Medicinal Biotechnology, College of Life Science, Kyung Hee University, Yongin-si 17104, Korea.ORCID 0000-0003-2394-4728
Se Chan KangDepartment of Oriental Medicinal Biotechnology, College of Life Science, Kyung Hee University, Yongin-si 17104, Korea.ORCID 0000-0003-0790-2237
Yingping WangState Local Joint Engineering Research Center of Ginseng Breeding and Application, Jilin Agricultural University, Changchun 130118, China.

Funding

This research was funded by Project for Science and Development plan for Jilin prov-ince (NO: 202110401123YY) NO: 202110401123YY
6 · The paper itself

Abstract

This study focused on developing Panos nanoemulsion (P-NE) and enhancing the anti-inflammatory efficacy for the treatment of inflammation. The effects of P-NE were evaluated in terms of Nitric oxide (NO production) in Lipopolysaccharide (LPS), induced RAW 264.7 cells, Reactive oxygen species (ROS) generation using Human Keratinocyte cells (HaCaT), and quantitative polymerase chain reaction (qPCR) analysis. Sea buckthorn oil, Tween 80, and span 80 were used and optimize the process. Panos extract (P-Ext) was prepared using the fermentation process. Further high-energy ultra-sonication was used for the preparation of P-NE. The developed nanoemulsion (NE) was characterized using different analytical methods. Field emission transmission electron microscopy (FE-TEM) analyzed the spherical shape and morphology. In addition, stability was analyzed by Dynamic light scattering (DLS) analysis, where particle size was analyzed 83 nm, and Zeta potential -28.20 ± 2 (mV). Furthermore, 90 days of stability was tested using different temperatures conditions where excellent stability was observed. P-NE are non-toxic in (HaCaT), and RAW264.7 cells up to 100 µg/mL further showed effects on ROS and NO production of the cells at 50 µg/mL. The qPCR analysis demonstrated the suppression of pro-inflammatory mediators for (Cox 2, IL-6, IL-1β, and TNF-α, NF-κB, Ikkα, and iNOS) gene expression. The prepared NE exhibited anti-inflammatory effects, demonstrating its potential as a safe and non-toxic nanomedicine.

Indexed as

EmulsionsFermentationAnimalsAnti-Inflammatory AgentsBenzodiazepinesCell SurvivalChemical PhenomenaDrug StabilityInflammation MediatorsMiceNitric OxidePlant ExtractsRAW 264.7 CellsReactive Oxygen SpeciesSpectrum AnalysisAnti-Inflammatory AgentsBenzodiazepinesEmulsionsInflammation MediatorsNitric OxidePlant ExtractsReactive Oxygen Speciestetrazepamanti-inflammatorynanoemulsionNO productionpanosROS generationultrasonication

Identifiers

PMID35011448
PMCPMC8746678

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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.