Evidence map›Paper›PMID 38530607›Full record

ArticleDrug delivery and translational research2024

Polyelectrolyte complexes based on a novel and sustainable hemicellulose-rich lignosulphonate for drug delivery applications.

Ioannis Dogaris, Ievgen Pylypchuk, Gunnar Henriksson, Anna Abbadessa

Abstract read
In one paragraph

Article in Drug delivery and translational research, 2024. 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
–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

10 citing papers in PubMed.

  1. Article
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  3. Review
  4. Article
  5. 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.

Ioannis DogarisDepartment of Fiber and Polymer Technology, School of Engineering Sciences in Chemistry, Biotechnology, and Health, Royal Institute of Technology, Teknikringen 56-58, Stockholm, SE-100 44, Sweden.
Ievgen PylypchukDepartment of Fiber and Polymer Technology, School of Engineering Sciences in Chemistry, Biotechnology, and Health, Royal Institute of Technology, Teknikringen 56-58, Stockholm, SE-100 44, Sweden.
Gunnar HenrikssonDepartment of Fiber and Polymer Technology, School of Engineering Sciences in Chemistry, Biotechnology, and Health, Royal Institute of Technology, Teknikringen 56-58, Stockholm, SE-100 44, Sweden.
Anna AbbadessaDepartment of Fiber and Polymer Technology, School of Engineering Sciences in Chemistry, Biotechnology, and Health, Royal Institute of Technology, Teknikringen 56-58, Stockholm, SE-100 44, Sweden. anna.abbadessa@usc.es.ORCID 0000-0003-3095-4086

Funding

'la Caixa' Foundation LCF/BQ/PR22/11920003Nordforsk Nordic Green Growth Research and Innovation Program (project name: "High-Value Products from Lignin")
6 · The paper itself

Abstract

Polyelectrolyte complexes (PECs) are polymeric structures formed by the self-assembly of oppositely charged polymers. Novel biomaterials based on PECs are currently under investigation as drug delivery systems, among other applications. This strategy leverages the ability of PECs to entrap drugs under mild conditions and control their release. In this study, we combined a novel and sustainably produced hemicellulose-rich lignosulphonate polymer (EH, negatively charged) with polyethyleneimine (PEI) or chitosan (CH, positively charged) and agar for the development of drug-releasing PECs. A preliminary screening demonstrated the effect of several parameters (polyelectrolyte ratio, temperature, and type of polycation) on PECs formation. From this, selected formulations were further characterized in terms of thermal properties, surface morphology at the microscale, stability, and ability to load and release methylene blue (MB) as a model drug. EH/PEI complexes had a more pronounced gel-like behaviour compared to the EH/CH complexes. Differential scanning calorimetry (DSC) results supported the establishment of polymeric interactions during complexation. Overall, PECs' stability was positively affected by low pH, ratios close to 1:1, and the addition of agar. PECs with higher EH content showed a higher MB loading, likely promoted by stronger electrostatic interactions. The EH/CH formulation enriched with agar showed the best sustained release profile of MB during the first 30 h in a pH-dependent environment simulating the gastrointestinal tract. Overall, we defined the conditions to formulate novel PECs based on a sustainable hemicellulose-rich lignosulphonate for potential applications in drug delivery, which promotes the valuable synergy between sustainability and the biomedical field.

Indexed as

ChitosanDrug LiberationPolysaccharidesAgarDrug Delivery SystemsHydrogen-Ion ConcentrationLigninMethylene BluePolyelectrolytesPolyethyleneimineAgarChitosanhemicelluloseLigninlignosulfuric acidMethylene BluePolyelectrolytesPolyethyleneiminePolysaccharidesChitosanControlled drug deliveryLigninPolyelectrolyte complexationPolyethylenimineSustainability

Identifiers

PMID38530607
PMCPMC11499397

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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.