Evidence map›Paper›PMID 30297791›Full record

ArticleScientific reports2018

A reference document on Permissible Limits for solvents and buffers during in vitro antimalarial screening.

Renugah Naidu, Gowtham Subramanian, Ying Bena Lim, Chwee Teck Lim, Rajesh Chandramohanadas

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Antimalarial Activity of Aqueous Extracts of Nasturtium (Molecules (Basel, Switzerland) · 2024
    Article
  2. Article
  3. Article
  4. 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

5 authors at 2 institutions in 1 country.

Renugah NaiduPillar of Engineering Product Development (EPD), Singapore University of Technology and Design (SUTD), Singapore, 487372, Singapore.ORCID http://orcid.org/0000-0003-4141-9791
Gowtham SubramanianPillar of Engineering Product Development (EPD), Singapore University of Technology and Design (SUTD), Singapore, 487372, Singapore.ORCID http://orcid.org/0000-0003-1044-6770
Ying Bena LimDepartment of Biomedical Engineering, National University of Singapore, Singapore, 117583, Singapore.
Chwee Teck LimDepartment of Biomedical Engineering, National University of Singapore, Singapore, 117583, Singapore.
Rajesh ChandramohanadasPillar of Engineering Product Development (EPD), Singapore University of Technology and Design (SUTD), Singapore, 487372, Singapore. rajesh@sutd.edu.sg.ORCID http://orcid.org/0000-0002-8760-0396
Singapore University of Technology and Design · SGNational University of Singapore · SG

Funding

Agency for Science, Technology and Research (A*STAR) RGAST1503Singapore University of Technology and Design (SUTD) T1MOE1506
6 · The paper itself

Abstract

Antimalarial drug discovery expands on targeted and phenotype-based screening of potential inhibitory molecules to ascertain overall efficacy, phenotypic characteristics and toxicity, prior to exploring pharmacological optimizations. Candidate inhibitors may have varying chemical properties, thereby requiring specific reconstitution conditions to ensure solubility, stability or bioavailability. Hence, a variety of solvents, buffers, detergents and stabilizers become part of antimalarial efficacy assays, all of which, above certain threshold could interfere with parasite viability, invasion or red blood cell properties leading to misinterpretation of the results. Despite their routine use across malaria research laboratories, there is no documentation on non-toxic range for common constituents including DMSO, glycerol, ethanol and methanol. We herein constructed a compatibility reference guide for 14 such chemicals and estimated their Permissible Limit against P. falciparum asexual stages at which viability and replication of parasites are not compromised. We also demonstrate that at the estimated Permissible Limit, red blood cells remain healthy and viable for infection by merozoites. Taken together, this dataset provides a valuable reference tool for the acceptable concentration range for common chemicals during in vitro antimalarial tests.

Indexed as

AntimalarialsBuffersDetergentsDrug DiscoveryDrug Evaluation, PreclinicalErythrocytesExcipientsHumansMalariaPlasmodium falciparumSolventsAntimalarialsBuffersDetergentsExcipientsSolvents

Identifiers

PMID30297791
PMCPMC6175914
OpenAlexW2894638422

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.