Evidence map›Paper›PMID 36551913›Full record

ArticleBiomedicines2022

A Bioengineered Quercetin-Loaded 3D Bio-Polymeric Graft for Tissue Regeneration and Repair.

Archna Dhasmana, Sumira Malik, Anuj Ranjan, Abhishek Chauhan, Hanaa M Tashkandi, Shafiul Haque, Rajaa Al-Raddadi, Steve Harakeh, Gökhan Zengin

Abstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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.

Archna DhasmanaHimalayan School of Biosciences, Swami Rama Himalayan, Jolly Grant, Dehradun 248140, Uttarakhand, India.ORCID 0000-0002-1120-2009
Sumira MalikAmity Institute of Biotechnology, Amity University Jharkhand, Ranchi 834001, Jharkhand, India.ORCID 0000-0001-5077-1493
Anuj RanjanAcademy of Biology and Biotechnology, Southern Federal University, 344006 Rostov-on-Don, Russia.ORCID 0000-0003-2592-9716
Abhishek ChauhanAmity Institute of Environmental Toxicology, Safety and Management, Amity University, Noida 201303, Uttar Pradesh, India.ORCID 0000-0001-6475-1266
Hanaa M TashkandiDepartment of General Surgery, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Shafiul HaqueResearch and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan 45142, Saudi Arabia.ORCID 0000-0002-2989-121X
Rajaa Al-RaddadiCommunity Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia.ORCID 0000-0002-8921-9628
Steve HarakehKing Fahd Medical Research Center, and Yousef Abdullatif Jameel Chair of Prophetic Medicine Application, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Gökhan ZenginDepartment of Biology, Science Faculty, Selcuk University, Konya 42250, Turkey.ORCID 0000-0001-6548-7823

Funding

the Ministry of Education and King Abdulaziz University, Deanship of Scientific Research, Jed-dah, Saudi Arabia. IFPIP:1627-141-1443
6 · The paper itself

Abstract

Phytochemicals extracted from plant sources have potential remedial effects to cure a broad range of acute to severe illnesses and ailments. Quercetin is a flavonoid isolated from different dietary sources such as vegetables and fruits, exhibiting strong anti-inflammatory, anti-oxidative and non-toxic effects on the biological system. However, the direct uptake or administration of quercetin results in loss of functionality, poor activity, and reduced shelf-life of the bioactive component. In this regard, to improve the uptake, potential, and efficiency of natural components with prolonged storage in the host's body after administration, numerous polymer drug delivery systems have been created. In the current study, three-dimensional (3D) porous (porosity: 92%; pore size: 81 µm) bio-polymeric foaming gelatin-alginate (GA) beads were fabricated for the entrapment of quercetin as therapeutic drug molecules-gelatin-alginate-quercetin (GAQ). The GAQ beads showed a significant uptake of quercetin molecules resulting in a reduction of reduced porosity up to 64% and pore size 63 µm with a controlled release profile in the PBS medium, showing ~80% release within 24 h. Subsequently, the GAQ beads showed remarkable antioxidant effects, and 95% anti-inflammatory activities along with remarkable in vitro cell culture growth and the observed proliferation of seeded fibroblast cells. Thus, we can conclude that the consistent release of quercetin showed non-toxic effects on normal cell lines and the bioactive surface of the GAQ beads enhances cell adhesion, proliferation, and differentiation more effectively than control GA polymeric beads and tissue culture plates (TCP). In summary, these findings show that these GAQ beads act as a biocompatible 3D construct with enormous potential in medicinal administration and tissue regeneration for accelerated healing.

Indexed as

biocompatibilitydruggraftherbalquercetinregeneration

Identifiers

PMID36551913
PMCPMC9775630

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.