Evidence map›Paper›PMID 30478403›Full record

ArticleScientific reports2018

A biophysical study on the mechanism of interactions of DOX or PTX with α-lactalbumin as a delivery carrier.

Behdad Delavari, Fatemeh Mamashli, Bahareh Bigdeli, Atefeh Poursoleiman, Leila Karami, Zahra Zolmajd-Haghighi, Atiyeh Ghasemi, Samaneh Samaei-Daryan, Morteza Hosseini, Thomas Haertlé and 6 more

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-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

6 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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    Article
  3. Article
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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

16 authors at 7 institutions in 5 countries.

Behdad DelavariInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran.
Fatemeh MamashliInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran.
Bahareh BigdeliInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran.
Atefeh PoursoleimanInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran.
Leila KaramiDepartment of Cell and Molecular Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.
Zahra Zolmajd-HaghighiInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran.
Atiyeh GhasemiInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran.
Samaneh Samaei-DaryanInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran.
Morteza HosseiniDepartment of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.
Thomas HaertléPoznań University of Life Sciences, Department of Animal Nutrition and Feed Management, Poznań, Poland.
Vladimir I MuronetzBelozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119234, Moscow, Russia.
Øyvind HalskauDepartment of Molecular Biology, University of Bergen, PB 7803, N-5020, Bergen, Norway.
Ali Akbar Moosavi-MovahediInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran.
Bahram GoliaeiInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran.
Ali Hossein RezayanDepartment of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.
Ali Akbar SabouryInstitute of Biochemistry and Biophysics, University of Tehran, Mailbox, 13145-1384, Tehran, Iran. saboury@ut.ac.ir.
Institute of Biochemistry and Biophysics, Polish Academy of Sciences · PLUniversity of Tehran · IRStem Cell Technology Research Center · IRKharazmi University · IRLomonosov Moscow State University · RUUniversity of Bergen · NOUniversity of Life Sciences in Poznań · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Doxorubicin and paclitaxel, two hydrophobic chemotherapeutic agents, are used in cancer therapies. Presence of hydrophobic patches and a flexible fold could probably make α-Lactalbumin a suitable carrier for hydrophobic drugs. In the present study, a variety of thermodynamic, spectroscopic, computational, and cellular techniques were applied to assess α-lactalbumin potential as a carrier for doxorubicin and paclitaxel. According to isothermal titration calorimetry data, the interaction between α-lactalbumin and doxorubicin or paclitaxel is spontaneous and the K (M

Indexed as

CalorimetryCalorimetry, Differential ScanningCell Line, TumorCell ProliferationCircular DichroismDoxorubicinDrug CarriersDrug Delivery SystemsDrug LiberationFluorescence PolarizationHumansHydrogen BondingLactalbuminMolecular Docking SimulationPaclitaxelProtein StabilityDoxorubicinDrug CarriersLactalbuminPaclitaxel

Identifiers

PMID30478403
PMCPMC6255783
OpenAlexW2900548468

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.