Evidence map›Paper›PMID 30823653›Full record

ArticleMolecules (Basel, Switzerland)2019

Engineering Peptide-Based Polyelectrolyte Complexes with Increased Hydrophobicity.

Sara Tabandeh, Lorraine Leon

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Exploring the effects of excipients on complex coacervation.Journal of colloid and interface science · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Self-Assembling Polypeptides in Complex Coacervation.Accounts of chemical research · 2024
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Peptide-based coacervates in therapeutic applications.Frontiers in bioengineering and biotechnology · 2022
    Review
  18. Article
  19. Article
  20. 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

2 authors.

Sara TabandehDepartment of Materials Science and Engineering, University of Central Florida, Orlando, FL 32816, USA. sara.tabandeh@Knights.ucf.edu.
Lorraine LeonDepartment of Materials Science and Engineering, University of Central Florida, Orlando, FL 32816, USA. lorraine.leon@ucf.edu.ORCID 0000-0002-8957-9148

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyelectrolyte complexation is a versatile platform for the design of self-assembled materials. Here we use rational design to create ionic hydrophobically-patterned peptides that allow us to precisely explore the role of hydrophobicity on electrostatic self-assembly. Polycations and polyanions were designed and synthesized with an alternating sequence of d- and l-chiral patterns of lysine or glutamic acid with either glycine, alanine or leucine due to their increasing hydrophobicity index, respectively. Two motifs were considered for the oppositely charged patterned peptides; one with equal residues of charged and uncharged amino acids and the other with increased charge density. Mass spectroscopy, circular dichroism, H- and F-NMR spectroscopy were used to characterize the polypeptides. Polyelectrolyte complexes (PECs) formed using the sequences were characterized using turbidity measurements, optical microscopy and infrared spectroscopy. Our results show that the critical salt concentration, a key measure of PEC stability, increased with both increasing charge density as well as hydrophobicity. Furthermore, by increasing the hydrophobicity, the amount of PEC formed increased with temperature, contrary to purely ionic PECs. Lastly, we assessed the encapsulation behavior of these materials using a hydrophobic dye. Concluding that encapsulation efficiency increased with hydrophobic content of the complexes providing insight for future work on the application of these materials for drug delivery.

Indexed as

Drug Delivery SystemsProtein EngineeringCircular DichroismGlutamic AcidHumansHydrophobic and Hydrophilic InteractionsLysineMass SpectrometryPeptidesPolyaminesPolyelectrolytesPolymersStatic ElectricityGlutamic AcidLysinePeptidesPolyaminesPolyelectrolytesPolymerschiralitycoacervatesencapsulationhydrophobicitypolyelectrolyte complexespolypeptidesself-assembly

Identifiers

PMID30823653
PMCPMC6429441

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Registered trials

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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.