Evidence map›Paper›PMID 32443790›Full record

ArticlePharmaceutics2020

Development and In Vivo Application of a Water-Soluble Anticancer Copper Ionophore System Using a Temperature-Sensitive Liposome Formulation.

Anikó Gaál, Tamás M Garay, Ildikó Horváth, Domokos Máthé, Dávid Szöllősi, Dániel S Veres, Jeremiah Mbuotidem, Tibor Kovács, József Tóvári, Ralf Bergmann and 5 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 17 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

15 authors at 7 institutions in 3 countries.

Anikó GaálBiological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Magyar Tudósok Körútja 2, H-1117 Budapest, Hungary.
Tamás M GarayFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, H-1083 Budapest, Práter utca 50/a, Hungary.
Ildikó HorváthDepartment of Biophysics and Radiation Biology, Semmelweis University, H-1094 Budapest, Hungary.
Domokos MáthéDepartment of Biophysics and Radiation Biology, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0001-7343-0413
Dávid SzöllősiDepartment of Biophysics and Radiation Biology, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0002-3363-3862
Dániel S VeresDepartment of Biophysics and Radiation Biology, Semmelweis University, H-1094 Budapest, Hungary.
Jeremiah MbuotidemInstitute of Translational Medicine, Semmelweis University, H-1094 Budapest, Hungary.
Tibor KovácsInstitute of Radiochemistry and Radioecology, University of Pannonia, H-8200 Veszprém, Hungary.ORCID 0000-0003-2606-0397
József TóváriDepartment of Experimental Pharmacology, National Institute of Oncology, H-1122 Budapest, Hungary.ORCID 0000-0002-5543-3204
Ralf BergmannDepartment of Biophysics and Radiation Biology, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0002-8733-4286
Christina StreliInstitute of Atomic and Subatomic Physics, Atominstitut, TU Wien, A-1020 Vienna, Stadionallee 2, Austria.
Gergely SzakácsInstitute of Enzymology, Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.
Judith MihályBiological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Magyar Tudósok Körútja 2, H-1117 Budapest, Hungary.
Zoltán VargaBiological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Magyar Tudósok Körútja 2, H-1117 Budapest, Hungary.
Norbert SzoboszlaiLaboratory for Environmental Chemistry and Bioanalytics, Institute of Chemistry, Eötvös Loránd University, H-1117 Budapest, Pázmány Péter Stny. 1/A, Hungary.
Semmelweis University · HUInstitute of Materials and Environmental Chemistry · HUEötvös Loránd University · HUInstitute of Molecular Life Sciences · HUNational Institute of Oncology · HUTU Wien · ATUniversity of Pannonia · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liposomes containing copper and the copper ionophore neocuproine were prepared and characterized for in vitro and in vivo anticancer activity. Thermosensitive PEGylated liposomes were prepared with different molar ratios of 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) and hydrogenated soybean phosphatidylcholine (HSPC) in the presence of copper(II) ions. Optimal, temperature dependent drug release was obtained at 70:30 DPPC to HSPC weight ratio. Neocuproine (applied at 0.2 mol to 1 mol phospholipid) was encapsulated through a pH gradient while using unbuffered solution at pH 4.5 inside the liposomes, and 100 mM HEPES buffer pH 7.8 outside the liposomes. Copper ions were present in excess, yielding 0.5 mM copper-(neocuproine)

Indexed as

copper nanotoxinin vivo antitumor effectmild hyperthermiaMRPSneocuproinethemosensitive liposomal formulation

Identifiers

PMID32443790
PMCPMC7284829
OpenAlexW3028015872

What OpenQuestion holds

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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.