Evidence map›Paper›PMID 35547672›Full record

ArticleRSC advances2018

Formulation, characterization and evaluation of morusin loaded niosomes for potentiation of anticancer therapy.

Srishti Agarwal, M Sheikh Mohamed, Sreejith Raveendran, Ankit K Rochani, Toru Maekawa, D Sakthi Kumar

Abstract read
In one paragraph

Article in RSC advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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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

6 authors.

Srishti AgarwalBio Nano Electronics Research Center, Graduate School of Interdisciplinary New Science, Toyo University Kawagoe Saitama 350-8585 Japan sakthi@toyo.jp +81-366-77-1140 +81-492-39-1636/1375/1640.
M Sheikh MohamedBio Nano Electronics Research Center, Graduate School of Interdisciplinary New Science, Toyo University Kawagoe Saitama 350-8585 Japan sakthi@toyo.jp +81-366-77-1140 +81-492-39-1636/1375/1640.
Sreejith RaveendranSchool of Pharmacy and Biomolecular Sciences, University of Brighton Moulsecoomb Brighton BN2 4GJ UK.
Ankit K RochaniJefferson College of Pharmacy, Department of Pharmaceutical Science, Thomas Jefferson University 1020 Locust Street Philadelphia PA-19107 USA.
Toru MaekawaBio Nano Electronics Research Center, Graduate School of Interdisciplinary New Science, Toyo University Kawagoe Saitama 350-8585 Japan sakthi@toyo.jp +81-366-77-1140 +81-492-39-1636/1375/1640.
D Sakthi KumarBio Nano Electronics Research Center, Graduate School of Interdisciplinary New Science, Toyo University Kawagoe Saitama 350-8585 Japan sakthi@toyo.jp +81-366-77-1140 +81-492-39-1636/1375/1640.ORCID https://orcid.org/0000-0003-4819-2032

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Morusin, a water-insoluble prenylated flavonoid is known for its numerous medicinal properties. It manifests its anticancer potential by suppression of genes involved in tumor progression. However, poor solubility of the drug results in low bioavailability and rapid degradation thus hindering its clinical utilization. In order to overcome this, we have synthesized a niosome system composed of non-ionic surfactant span 60 and cholesterol using a thin-layer evaporation technique to improve the aqueous-phase solubility of the drug. Highly cytocompatible niosomes of 479 nm average size with smooth and uniform spherical morphology were synthesized in a facile manner. Unlike free morusin, nanomorusin was found to be freely dispersible in aqueous media. Having an extremely high drug entrapment efficiency (97%), controlled and sustained release of morusin resulting in enhanced therapeutic efficacy was observed in cancer cell lines of 4 different lineages. The results demonstrate that the morusin-niosome system is a promising strategy for enhanced anti-cancer activity against multiple cancer types and could be an indispensable tool for future targeted chemotherapeutic strategies.

Identifiers

PMID35547672
PMCPMC9086195

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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.