Advances in Organogelators: Preparation, Properties, and Applications

A special issue of Gels (ISSN 2310-2861). This special issue belongs to the section "Gel Analysis and Characterization".

Deadline for manuscript submissions: 30 September 2025 | Viewed by 899

Special Issue Editor


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Guest Editor
Biologie Tissulaire et Ingénierie Thérapeutique UMR 5305–Vecteurs Colloïdaux et Transport Tissulaire, Institut des Sciences Pharmaceutiques et Biologiques, Université de Lyon (UCBL), 8 Avenue Rockefeller, CEDEX 08, 69373 Lyon, France
Interests: organogels; pharmaceutical formulation; controlled drug delivery; pharmaceutics and pharmaceutical technology; drug formulation; formulation development of pharmaceuticals; pharmaceutical development; pharmaceutics; pharmaceutical research and development; polymers; rheology
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Special Issue Information

Dear Colleagues,

The design of gel-based materials, obtained from gelator molecules self-assembled into 3D network structures and entrapping various solvents, has gained research interest. Different low-molecular-weight organogelators (LMOG) or polymeric organogelators (POG) have been used to form in situ injectable gel materials. These systems are usually prepared by dissolving the gelator in a solvent medium and then cooling the solution below its characteristic gelation transition temperature (Tgel). Most hydrogel or organogel materials are physical gels and, unlike chemical gels (cross-linked polymers), are thermally sensitive and thermally reversible. In solution, gelators self-assemble via non-covalent interactions to form fibrous structures responsible for the gelation phenomena. One promising avenue for these gel materials used as depot formulations lies in the administration of hydrophilic and lipophilic drugs, such as cholinesterase inhibitors, vaccine adjuvants, contraceptive steroids, and anti-inflammatory and chemotherapeutic agents. They are also engineered to interact with biological systems for biomedical applications. Furthermore, another axis of research is developing a bio-inspired approach involving a bottom-up strategy for synthesizing supramolecular gels to generate novel biomaterial candidates. All these demonstrations show the importance of examining these materials and their derivatives for the preparation of new formulations or smart materials for pharmaceutical and medicinal applications.

The purpose of this Special Issue is to summarize the progress achieved regarding advanced organogelators and to encourage the discovery of new organogelators for different applications.

Dr. Plamen Kirilov
Guest Editor

Manuscript Submission Information

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Keywords

  • organogels
  • drug delivery
  • biomaterials
  • device development
  • pharmaceutics
  • drug reservoirs
  • smart delivery systems
  • smart formulations

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Published Papers (1 paper)

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Research

20 pages, 8396 KiB  
Article
Columnar Mesophases and Organogels Formed by H-Bound Dimers Based on 3,6-Terminally Difunctionalized Triphenylenes
by Nahir Vadra, Lisandro J. Giovanetti, Pablo H. Di Chenna and Fabio D. Cukiernik
Gels 2025, 11(1), 9; https://doi.org/10.3390/gels11010009 - 27 Dec 2024
Viewed by 593
Abstract
A series of triphenylene (TP) compounds—denoted 3,6-THTP-DiCnOH—bearing four hexyloxy ancillary chains and two variable-length alkoxy chains terminally functionalized with hydroxyl groups have been synthesized and characterized. The shorter homologs revealed mesogenic characteristics, giving rise to thermotropic mesophases in which π-stacked columns [...] Read more.
A series of triphenylene (TP) compounds—denoted 3,6-THTP-DiCnOH—bearing four hexyloxy ancillary chains and two variable-length alkoxy chains terminally functionalized with hydroxyl groups have been synthesized and characterized. The shorter homologs revealed mesogenic characteristics, giving rise to thermotropic mesophases in which π-stacked columns of H-bound dimers self-organize yielding superstructures. Molecular-scale models are proposed to account for their structural features. The three studied compounds yielded supramolecular gels in methanol; their ability to gelify higher alcohols was found to be enhanced by the presence of water. The intermediate homolog also gelled n-hexane. Compared to their isomeric 2,7-THTP-DiCnOH analogs, the 3,6-derivatives showed a higher tendency to give rise to LC phases (wider thermal ranges) and a lower organogelling ability (variety of gelled solvents, lower gels stabilities). The overall results are analyzed in terms of different kinds of competing H-bonds: intramolecular, face-to-face dimeric, lateral polymeric, and solvent–TP interactions. Full article
(This article belongs to the Special Issue Advances in Organogelators: Preparation, Properties, and Applications)
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