Evidence map›Paper›PMID 25734967›Full record

ArticleColloids and surfaces. B, Biointerfaces2015

S-layer fusion protein as a tool functionalizing emulsomes and CurcuEmulsomes for antibody binding and targeting.

Mehmet H Ucisik, Seta Küpcü, Andreas Breitwieser, Nicola Gelbmann, Bernhard Schuster, Uwe B Sleytr

Open access · hybridAbstract read
In one paragraph

Article in Colloids and surfaces. B, Biointerfaces, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

16 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Microencapsulation of Omeprazole byIranian journal of pharmaceutical research : IJPR · 2020
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
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 at 3 institutions in 2 countries.

Mehmet H UcisikInstitute for Synthetic Bioarchitectures, Department of Nanobiotechnology, University of Natural Resources and Life Sciences (BOKU) Vienna, Muthgasse 11, 1190 Vienna, Austria; Department of Biomedical Engineering, School of Engineering and Natural Sciences, Istanbul Medipol University, Ekinciler Cad. No. 19 Kavacık Kavşağı, Beykoz 34810, Istanbul, Turkey. Electronic address: m.h.ucisik@gmail.com.
Seta KüpcüInstitute for Synthetic Bioarchitectures, Department of Nanobiotechnology, University of Natural Resources and Life Sciences (BOKU) Vienna, Muthgasse 11, 1190 Vienna, Austria.
Andreas BreitwieserInstitute for Biophysics, Department of Nanobiotechnology, University of Natural Resources and Life Sciences (BOKU) Vienna, Muthgasse 11, 1190 Vienna, Austria.
Nicola GelbmannOctapharma GmbH, Oberlaaer Straße 235, 1100 Vienna, Austria.
Bernhard SchusterInstitute for Synthetic Bioarchitectures, Department of Nanobiotechnology, University of Natural Resources and Life Sciences (BOKU) Vienna, Muthgasse 11, 1190 Vienna, Austria.
Uwe B SleytrInstitute for Biophysics, Department of Nanobiotechnology, University of Natural Resources and Life Sciences (BOKU) Vienna, Muthgasse 11, 1190 Vienna, Austria.
BOKU University · ATIstanbul Medipol University · TROctapharma (Austria) · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Selective targeting of tumor cells by nanoparticle-based drug delivery systems is highly desirable because it maximizes the drug concentration at the desired target while simultaneously protecting the surrounding healthy tissues. Here, we show a design for smart nanocarriers based on a biomimetic approach that utilizes the building principle of virus envelope structures. Emulsomes and CurcuEmulsomes comprising a tripalmitin solid core surrounded by phospholipid layers are modified by S-layer proteins that self-assemble into a two-dimensional array to form a surface layer. One significant advantage of this nanoformulation is that it increases the solubility of the lipophilic anti-cancer agent curcumin in the CurcuEmulsomes by a factor of 2700. In order to make the emulsomes specific for IgG, the S-layer protein is fused with two protein G domains. This S-layer fusion protein preserves its recrystallization characteristics, forming an ordered surface layer (square lattice with 13 nm unit-by-unit distance). The GG domains are presented in a predicted orientation and exhibit a selective binding affinity for IgG.

Indexed as

Drug Delivery SystemsAntineoplastic Agents, PhytogenicBacillaceaeBacterial ProteinsBiomimetic MaterialsCurcuminDrug CompoundingEmulsionsEscherichia coliGene ExpressionHumansHydrophobic and Hydrophilic InteractionsImmunoconjugatesImmunoglobulin GLiposomesMembrane GlycoproteinsAntineoplastic Agents, PhytogenicBacterial ProteinsCurcuminEmulsionsImmunoconjugatesImmunoglobulin GLiposomesMembrane GlycoproteinsMonosaccharide Transport ProteinsRecombinant Fusion ProteinsSbpA protein, bacteriaS-layer proteinsTriglyceridestripalmitinActive drug deliveryCurcuminEmulsomesImmunoglobulin G (IgG) TargetingS-layer (fusion) proteins

Identifiers

PMID25734967
PMCPMC4406452
OpenAlexW1968794732

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.