Evidence map›Paper›PMID 37576585›Full record

ArticleChemistry of materials : a publication of the American Chemical Society2023

Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations.

Talia A Shmool, Laura K Martin, Andreas Jirkas, Richard P Matthews, Anna P Constantinou, Devkee M Vadukul, Theoni K Georgiou, Francesco A Aprile, Jason P Hallett

Abstract read
In one paragraph

Article in Chemistry of materials : a publication of the American Chemical Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Magnetic Ionogel and Its Applications.Gels (Basel, Switzerland) · 2025
    Review
  7. Review
  8. 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

9 authors.

Talia A ShmoolDepartment of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.ORCID https://orcid.org/0000-0002-0415-3050
Laura K MartinDepartment of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ, U.K.
Andreas JirkasDepartment of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.
Richard P MatthewsDepartment of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.ORCID https://orcid.org/0000-0003-3328-4954
Anna P ConstantinouDepartment of Materials, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.ORCID https://orcid.org/0000-0002-1606-8515
Devkee M VadukulDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.
Theoni K GeorgiouDepartment of Materials, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.ORCID https://orcid.org/0000-0003-4474-6931
Francesco A AprileDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.ORCID https://orcid.org/0000-0002-5040-4420
Jason P HallettDepartment of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.ORCID https://orcid.org/0000-0003-3431-2371

Funding

Medical Research Council MR/S033947/1
6 · The paper itself

Abstract

We present an approach for the rational development of stimuli-responsive ionogels which can be formulated for precise control of multiple unique ionogel features and fill niche pharmaceutical applications. Ionogels are captivating materials, exhibiting self-healing characteristics, tunable mechanical and structural properties, high thermal stability, and electroconductivity. However, the majority of ionogels developed require complex chemistry, exhibit high viscosity, poor biocompatibility, and low biodegradability. In our work, we overcome these limitations. We employ a facile production process and strategically integrate silk fibroin, the biocompatible ionic liquids (ILs) choline acetate ([Cho][OAc]), choline dihydrogen phosphate ([Cho][DHP]), and choline chloride ([Cho][Cl]), traditional pharmaceutical excipients, and the model antiepileptic drug phenobarbital. In the absence of ILs, we failed to observe gel formation; yet in the presence of ILs, thermoresponsive ionogels formed. Systems were assessed via visual tests, transmission electron microscopy, confocal reflection microscopy, dynamic light scattering, zeta potential and rheology measurements. We formed diverse ionogels of strengths ranging between 18 and 642 Pa. Under 25 °C storage, formulations containing polyvinylpyrrolidone (PVP) showed an ionogel formation period ranging over 14 days, increasing in the order of [Cho][DHP], [Cho][OAc], and [Cho][Cl]. Formulations lacking PVP showed an ionogel formation period ranging over 32 days, increasing in the order of [Cho][OAc], [Cho][DHP] and [Cho][Cl]. By heating from 25 to 60 °C, immediately following preparation, thermoresponsive ionogels formed below 41 °C in the absence of PVP. Based on our experimental results and density functional theory calculations, we attribute ionogel formation to macromolecular crowding and confinement effects, further enhanced upon PVP inclusion. Holistically, applying our rational development strategy enables the production of ionogels of tunable physicochemical and rheological properties, enhanced drug solubility, and structural and energetic stability. We believe our rational development approach will advance the design of biomaterials and smart platforms for diverse drug delivery applications.

Identifiers

PMID37576585
PMCPMC10413859

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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.