Evidence map›Paper›PMID 28671589›Full record

ArticleInternational journal of molecular sciences2017

Theranostic Liposome-Nanoparticle Hybrids for Drug Delivery and Bioimaging.

Muharrem Seleci, Didem Ag Seleci, Thomas Scheper, Frank Stahl

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 79 citations in OpenAlex.

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  13. Toxicity of metal-based nanoparticles: Challenges in the nano era.Frontiers in bioengineering and biotechnology · 2022
    Review
  14. Review
  15. Article
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  17. Vitamin C and Cardiovascular Disease: An Update.Antioxidants (Basel, Switzerland) · 2020
    Review
  18. 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

4 authors at 1 institution in 1 country.

Muharrem SeleciInstitute of Technical Chemistry, Leibniz University of Hanover, Callinstr. 5, 30167 Hanover, Germany. muharremseleci@hotmail.com.
Didem Ag SeleciInstitute of Technical Chemistry, Leibniz University of Hanover, Callinstr. 5, 30167 Hanover, Germany. didemag@hotmail.com.
Thomas ScheperInstitute of Technical Chemistry, Leibniz University of Hanover, Callinstr. 5, 30167 Hanover, Germany. scheper@iftc.uni-hannover.de.
Frank StahlInstitute of Technical Chemistry, Leibniz University of Hanover, Callinstr. 5, 30167 Hanover, Germany. stahl@iftc.uni-hannover.de.
Leibniz University Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced theranostic nanomedicine is a multifunctional approach which combines the diagnosis and effective therapy of diseased tissues. Here, we investigated the preparation, characterization and in vitro evaluation of theranostic liposomes. As is known, liposome-quantum dot (L-QD) hybrid vesicles are promising nanoconstructs for cell imaging and liposomal-topotecan (L-TPT) enhances the efficiency of TPT by providing protection against systemic clearance and allowing extended time for it to accumulate in tumors. In the present study, hydrophobic CdSe/ZnS QD and TPT were located in the bilayer membrane and inner core of liposomes, respectively. Dynamic light scattering (DLS), zeta potential (ζ) measurements and fluorescence/absorption spectroscopy were performed to determine the vesicle size, charge and spectroscopic properties of the liposomes. Moreover, drug release was studied under neutral and acidic pH conditions. Fluorescence microscopy and flow cytometry analysis were used to examine the cellular uptake and intracellular distribution of the TPT-loaded L-QD formulation. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was utilized to investigate the in vitro cytotoxicity of the formulations on HeLa cells. According to the results, the TPT-loaded L-QD hybrid has adequate physicochemical properties and is a promising multifunctional delivery vehicle which is capable of a simultaneous co-delivery of therapeutic and diagnostic agents.

Indexed as

Diagnostic ImagingDrug Delivery SystemsLiposomesNanoparticlesTheranostic NanomedicineAnimalsCell SurvivalDrug CompoundingDrug LiberationHeLa CellsHumansHydrophobic and Hydrophilic InteractionsParticle SizeQuantum DotsLiposomesbioimagingdrug deliveryquantum dotstheranostic liposomes

Identifiers

PMID28671589
PMCPMC5535907
OpenAlexW2731912524

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.