Evidence map›Paper›PMID 30013324›Full record

ArticleDrug design, development and therapy2018

Self-nanomicellizing solid dispersion of edaravone: part I - oral bioavailability improvement.

Ankit Parikh, Krishna Kathawala, Chun Chuan Tan, Sanjay Garg, Xin-Fu Zhou

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 30 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

5 authors at 1 institution in 1 country.

Ankit ParikhSchool of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia, xin-fu.zhou@unisa.edu.au; sanjay.garg@unisa.edu.au.
Krishna KathawalaSchool of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia, xin-fu.zhou@unisa.edu.au; sanjay.garg@unisa.edu.au.
Chun Chuan TanSchool of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia, xin-fu.zhou@unisa.edu.au; sanjay.garg@unisa.edu.au.
Sanjay GargSchool of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia, xin-fu.zhou@unisa.edu.au; sanjay.garg@unisa.edu.au.
Xin-Fu ZhouSchool of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia, xin-fu.zhou@unisa.edu.au; sanjay.garg@unisa.edu.au.
University of South Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEdaravone (EDR) is known for its free radical scavenging, antiapoptotic, antinecrotic, and anticytokine effects in neurological and non-neurological diseases. It is currently available clinically as Radicava MATERIALS AND

methodsThe selection of a suitable carrier for the development of NEF was performed based on the miscibility study. The optimization of EDR-to-carrier ratio was conducted via kinetic solubility study after preparing SNMSDs using solvent evaporation technique. The drug-polymer carrier interaction and self-nanomicellizing properties of NEF were investigated with advanced characterization studies. In vitro permeation, metabolism, and dissolution study was carried out to examine the effect of the presence of a carrier on physico-chemical properties of EDR. Additionally, the dose-dependent pharmacokinetic study of NEF was conducted and compared with the EDR suspension.

resultsSoluplus

conclusionThe results demonstrated that SNMSD strategy could serve as a promising way to enhance EDR oral BA and NEF could be a potential candidate for the treatment of diseases in which oxidative stress plays a key role in their pathogenesis.

Indexed as

Administration, OralBiological AvailabilityDose-Response Relationship, DrugDrug CarriersDrug CompoundingEdaravoneFree Radical ScavengersHumansKineticsPolymersSolubilityDrug CarriersEdaravoneFree Radical ScavengersPolymersedaravonemetabolismnanotechnologyoral bioavailabilitypermeabilitySoluplus®

Identifiers

PMID30013324
PMCPMC6038876
OpenAlexW2810767862

What OpenQuestion holds

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LicenceCC BY-NC
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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.