Evidence map›Paper›PMID 35799927›Full record

ArticleRSC advances2022

Click gold quantum dots biosynthesis with conjugation of quercetin for adenocarcinoma exertion.

Amol V Pansare, Priyanka V Pansare, Amol A Shedge, Shubham V Pansare, Vishwanath R Patil, Giovanni P Terrasi, Kamini J Donde

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 2 countries.

Amol V PansareComposite Group, Mechanical Systems Engineering, Swiss Federal Laboratories for Materials Science and Technology-Empa 8600 Dübendorf Switzerland giovanni.terrasi@empa.ch amol.pansare@empa.ch.ORCID https://orcid.org/0000-0001-8133-1685
Priyanka V PansareRamnarain Ruia Autonomous College, University of Mumbai Matunga (E) India kaminidonde@ruiacollege.edu.
Amol A ShedgeDepartment of Chemistry, University of Mumbai Santacruz (E) Mumbai 400098 India vishwanathrpatil03@gmail.com.
Shubham V PansareDepartment of Chemistry, University of Mumbai Santacruz (E) Mumbai 400098 India vishwanathrpatil03@gmail.com.
Vishwanath R PatilDepartment of Chemistry, University of Mumbai Santacruz (E) Mumbai 400098 India vishwanathrpatil03@gmail.com.
Giovanni P TerrasiComposite Group, Mechanical Systems Engineering, Swiss Federal Laboratories for Materials Science and Technology-Empa 8600 Dübendorf Switzerland giovanni.terrasi@empa.ch amol.pansare@empa.ch.
Kamini J DondeRamnarain Ruia Autonomous College, University of Mumbai Matunga (E) India kaminidonde@ruiacollege.edu.
University of Mumbai · INSwiss Federal Laboratories for Materials Science and Technology · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We developed a cost-effective and eco-friendly click biosynthesis of small molecule quercetin-gold quantum dots (QRT-AuQDs) involving quick conjugation using an ultrasonication method at ambient temperature by utilizing QRT and gold ions in the proportion of 0.1 : 1 (molar ratio). A comparatively very short amount of time (60 seconds) was required as compared to conventional procedures. The present biomimetics research relates to the isolation of bioactive QRT by the circularly spread silica gel layer technique (CSSGLT) and characterization (UV-Vis, FTIR, NMR and DSC analysis). Characterization of the synthesized QRT-AuQDs conjugated complex was carried out by UV-Vis, HR-TEM, DLS, zeta potential and X-ray diffraction. The main objective of the present work was to study the comparative anticancer activity of QRT and QRT-AuQDs on human lung cancer HOP-62 and leukemia K-562 cell lines. The results suggested that QRT-AuQDs showed potential for applications in anticancer treatment and were found to be a more cytotoxic agent in comparison to QRT, causing > 50% inhibition of cancer cells at the concentration < 10

Identifiers

PMID35799927
PMCPMC9218964
OpenAlexW4284963131

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.