Evidence map›Paper›PMID 31255656›Full record

ArticleEBioMedicine2019

Pre-clinical study of iron oxide nanoparticles fortified artesunate for efficient targeting of malarial parasite.

Deepika Kannan, Nisha Yadav, Shakeel Ahmad, Pragya Namdev, Souvik Bhattacharjee, Bimlesh Lochab, Shailja Singh

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
7.3field-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

24 citing papers in PubMed, 76 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Deepika KannanDepartment of Life Sciences, School of Natural Sciences, Shiv Nadar University, Gautam Buddha Nagar, India.
Nisha YadavDepartment of Chemistry, School of Natural Sciences, Shiv Nadar University, Gautam Buddha Nagar, India.
Shakeel AhmadSpecial Center for Molecular Medicine, Jawaharlal Nehru University, New Mehrauli Road, New Delhi, India.
Pragya NamdevSpecial Center for Molecular Medicine, Jawaharlal Nehru University, New Mehrauli Road, New Delhi, India.
Souvik BhattacharjeeSpecial Center for Molecular Medicine, Jawaharlal Nehru University, New Mehrauli Road, New Delhi, India.
Bimlesh LochabDepartment of Chemistry, School of Natural Sciences, Shiv Nadar University, Gautam Buddha Nagar, India. Electronic address: bimlesh.lochab@snu.edu.in.
Shailja SinghSpecial Center for Molecular Medicine, Jawaharlal Nehru University, New Mehrauli Road, New Delhi, India. Electronic address: shailjasingh@mail.jnu.ac.in.
Jawaharlal Nehru University · INShiv Nadar University · IN

Funding

Using Next-Generation Genomics to Study Antimalarial Drug Resistance in IndiaU19AI089676 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CARLTON, JANE M · 2010 to 2023
$22.6M
NIAID NIH HHS U19 AI089676
6 · The paper itself

Abstract

backgroundArtesunate the most potent antimalarial is widely used for the treatment of multidrug-resistant malaria. The antimalarial cytotoxicity of artesunate has been mainly attributed to its selective, irreversible and iron- radical-mediated damage of parasite biomolecules. In the present research, iron oxide nanoparticle fortified artesunate was tested in P. falciparum and in an experimental malaria mouse model for enhancement in the selectivity and toxicity of artesunate towards parasite. Artesunate was fortified with nontoxic biocompatible surface modified iron oxide nanoparticle which is specially designed and synthesized for the sustained pH-dependent release of Fe

methodsAntimalarial efficacy of Iron oxide nanoparticle fortified artesunate was evaluated in wild type and artemisinin-resistant Plasmodium falciparum (R539T) grown in O + ve human blood and in Plasmodium berghei ANKA infected swiss albino mice. Internalization of nanoparticles, the pH-dependent release of Fe

resultsThe nanoparticle fortified artesunate was highly efficient in the 1/8th concentration of artesunate IC

interpretationSurface coated iron-oxide nanoparticle fortified artesunate can be developed into a potent therapeutic agent towards multidrug-resistant and artemisinin-resistant malaria in humans. FUND: This study is supported by the Centre for Study of Complex Malaria in India funded by the National Institute of Health, USA.

Indexed as

AnimalsAntimalarialsArtesunateFerric CompoundsHumansMalaria, FalciparumMetal NanoparticlesMicePlasmodium falciparumAntimalarialsArtesunateFerric Compoundsferric oxideArtemisinin-resistant malariaArtesunateDNA damageIron oxide nanoparticleMalariaMulti-drug resistant malariaOxidative stressProtein carbonylationRing survival assay

Identifiers

PMID31255656
PMCPMC6642363
OpenAlexW2953847488

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.