Next Article in Journal
Linking TLR-7 Signaling to Downregulation of Placental P-Glycoprotein: Implications for Fetal Drug Exposure
Previous Article in Journal
89Zr-Radiolabelling of p-NCS-Bz-DFO-Anti-HER2 Affibody Immunoconjugate: Characterization and Assessment of In Vitro Potential in HER2-Positive Breast Cancer Imaging
Previous Article in Special Issue
Scalability of API-Loaded Multifilament Yarn Production by Hot-Melt Extrusion and Evaluation of Fiber-Based Dosage Forms
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

Fiber-Based Scaffolds as Drug Carriers: Recent Advances

by
Helena P. Felgueiras
Centre for Textile Science and Technology (2C2T), University of Minho, Campus de Azurém, 4800-058 Guimarães, Portugal
Pharmaceutics 2025, 17(6), 740; https://doi.org/10.3390/pharmaceutics17060740
Submission received: 1 April 2025 / Accepted: 17 April 2025 / Published: 5 June 2025
(This article belongs to the Special Issue Fiber-Based Scaffolds as Drug Carriers: Recent Advances)
In recent years, fiber-based materials have been widely explored for their use in biomedical applications, ranging from wound dressings and bone tissue engineering to drug-controlled release and delivery platforms. The increasing prevalence of these materials is attributed to their biocompatibility, biodegradability, and mechanical resilience/resistance, which have made them indispensable in advanced healthcare solutions [1,2]. Among the various biopolymers used, cellulose and its derivatives, along with chitosan and other naturally derived polymers, have played a pivotal role in developing sophisticated drug delivery platforms and tissue engineering scaffolds (Contributions 1 and 2).
The organization and structure of fibers within scaffolds are crucial in determining their efficacy in specific biomedical applications. Different fiber-producing techniques such as electrospinning, wet-spinning, and 3D printing have been explored to optimize these materials for biomedical use (Contributions 1 and 3). Electrospinning, for instance, has emerged as a preferred method for generating fibrous scaffolds that mimic the extracellular matrix (ECM) of human tissues, thereby enhancing cell recognition, adhesion, and proliferation (Contribution 4) [3].
Drug delivery systems have particularly benefited from fiber-based scaffolds. Electrospun nanofibers, with their high surface area and tunable porosity, enable controlled and sustained drug release, reducing systemic side effects and improving therapeutic outcomes (Contribution 2). Studies have demonstrated the efficiency of therapeutic agent-loaded fibrous scaffolds in delivering drugs precisely to target sites, minimizing systemic toxicity and maximizing efficacy (Contribution 1).
Wound healing is one of the key biomedical applications where fiber-based materials have demonstrated significant potential. Due to their ability to promote hemostasis, provide antibacterial protection, and regulate moisture, nanofiber scaffolds are being investigated by many as alternatives to traditional wound dressings (Contribution 2). Moreover, incorporating bioactive agents into these scaffolds has enhanced their healing capabilities, leading to faster tissue regeneration and reduced infection risks. A recent study highlighted the antibacterial and anti-inflammatory properties of electrospun shellac fibers loaded with herbal extracts, showing their potential as advanced wound dressings (Contribution 5) [1]. Additionally, fiber-based scaffolds with embedded nanoparticles, such as zinc oxide (ZnO), have exhibited enhanced antimicrobial activity, making them suitable for treating chronic wounds and diabetic ulcers (Contribution 6). Beyond wound healing, fibrous scaffolds are extensively used in tissue engineering, particularly for tendon, ligament, and bone regeneration. Wet-spun polymeric fibers, for instance, have been identified as potential scaffolds for tendon and ligament repair due to their ability to mimic the native tissue architecture (Contribution 3). Incorporating functional elements such as growth factors has further improved the utility of these scaffolds. For example, scaffolds functionalized with human placental growth factor (PLGF) have demonstrated enhanced osteoplastic material compatibility, paving the way for more effective bone grafting techniques (Contribution 7). Similarly, electrospun polylactic-co-glycolic acid (PLGA) scaffolds modified with antibacterial coatings have shown promising results in preventing infections while promoting cell adhesion (Contribution 4). The development of drug-loaded fibrous scaffolds has revolutionized targeted drug delivery. One of the most promising techniques is hot-melt extrusion, which can be used to embed active pharmaceutical ingredients within multifilament yarns (Contribution 8). This method has enabled the scalable production of fiber-based dosage forms, expanding the potential of fibers in pharmaceutical applications beyond traditional drug delivery systems. Additionally, electrospinning techniques have been refined to facilitate the controlled release of bioactive molecules, including proteins, peptides, and antimicrobial agents. These advances not only enhance drug stability but also allow for the development of patient-specific therapeutic solutions, such as those targeting bacterial activity in diabetic ulcers (Contribution 9).
As research in fiber-based scaffolds continues to evolve, the integration of smart materials, bioactive molecules, and advanced fabrication techniques will drive the next generation of biomedical innovations. The use of biodegradable and biocompatible polymers such as cellulose, chitosan, and PLGA in combination with nanotechnology will further perfect drug delivery mechanisms and tissue engineering applications (Contributions 1 and 2). With ongoing advancements in biomaterials and fiber engineering, fiber-based scaffolds are set to redefine the landscape of regenerative medicine and drug delivery. Future studies should focus on optimizing scaffold design, improving drug-loading efficiencies, and enhancing biocompatibility to maximize their clinical impact. As these materials progress from experimental research to widespread clinical application, they hold promise in significantly improving the outcomes and quality of life of patients [1,2,3].

Acknowledgments

This work was funded by the European Regional Development Fund through the Operational Competitiveness Program and the National Foundation for Science and Technology of Portugal (FCT) under the projects UID/CTM/00264/2020 of 2C2T with its components Base (https://doi.org/10.54499/UIDB/00264/2020) and Programmatic (https://doi.org/10.54499/UIDP/00264/2020). H.P.F. also acknowledges the FCT for auxiliary researcher contract 2021.02720.CEEIND.

Conflicts of Interest

The author declares no conflicts of interest.

List of Contributions

  • Park, D.; Lee, S.J.; Choi, D.K.; Park, J.-W. Therapeutic Agent-Loaded Fibrous Scaffolds for Biomedical Applications. Pharmaceutics 2023, 15, 1522.
  • Jiang, Z.; Zheng, Z.; Yu, S.; Gao, Y.; Ma, J.; Huang, L.; Yang, L. Nanofiber Scaffolds as Drug Delivery Systems Promoting Wound Healing. Pharmaceutics 2023, 15, 1829.
  • Rocha, J.; Araújo, J.C.; Fangueiro, R.; Ferreira, D.P. Wetspun Polymeric Fibrous Systems as Potential Scaffolds for Tendon and Ligament Repair, Healing and Regeneration. Pharmaceutics 2022, 14, 2526.
  • Badaraev, A.D.; Lerner, M.I.; Bakina, O.V.; Sidelev, D.V.; Tran, T.-H.; Krinitcyn, M.G.; Malashicheva, A.B.; Cherempey, E.G.; Slepchenko, G.B.; Kozelskaya, A.I.; et al. Antibacterial Activity and Cytocompatibility of Electrospun PLGA Scaffolds Surface-Modified by Pulsed DC Magnetron Co-Sputtering of Copper and Titanium. Pharmaceutics 2023, 15, 939.
  • Krongrawa, W.; Limmatvapirat, S.; Vollrath, M.K.; Kittakoop, P.; Saibua, S.; Limmatvapirat, C. Fabrication, Optimization, and Characterization of Antibacterial Electrospun Shellac Fibers Loaded with Kaempferia parviflora Extract. Pharmaceutics 2023, 15, 123.
  • Grande-Tovar, C.D.; Castro, J.I.; Valencia Llano, C.H.; Tenorio, D.L.; Saavedra, M.; Zapata, P.A.; Chaur, M.N. Polycaprolactone (PCL)-Polylactic Acid (PLA)-Glycerol (Gly) Composites Incorporated with Zinc Oxide Nanoparticles (ZnO-NPs) and Tea Tree Essential Oil (TTEO) for Tissue Engineering Applications. Pharmaceutics 2023, 15, 43.
  • Aleynik, D.Y.; Bokov, A.E.; Charykova, I.N.; Rubtsova, Y.P.; Linkova, D.D.; Farafontova, E.A.; Egorikhina, M.N. Functionalization of Osteoplastic Material with Human Placental Growth Factor and Assessment of Biocompatibility of the Resulting Material In Vitro. Pharmaceutics 2024, 16, 85.
  • Rosenbaum, C.; Gerds, N.; Hack, L.; Weitschies, W. Scalability of API-Loaded Multifilament Yarn Production by Hot-Melt Extrusion and Evaluation of Fiber-Based Dosage Forms. Pharmaceutics 2024, 16, 1103.
  • Ribeiro, A.R.M.; Miranda, C.S.; Silva, A.F.G.; Mendes, F.D.P.; Silva, B.M.; Oliveira, B.A.S.; Paiva, E.D.; Gonçalves, S.P.; Pereira-Lima, S.M.M.A.; Costa, S.P.G. et al. Inhibition of Enzyme and Bacteria Activities in Diabetic Ulcer-like Scenarios via WAAPV-Loaded Electrospun Fibers. Pharmaceutics 2024, 16, 911.

References

  1. Venugopal, D.; Vishwakarma, S.; Kaur, I.; Samavedi, S. Electrospun fiber-based strategies for controlling early innate immune cell responses: Towards immunomodulatory mesh designs that facilitate robust tissue repair. Acta Biomater. 2023, 163, 228. [Google Scholar] [CrossRef] [PubMed]
  2. Mu, J.; Luo, D.; Li, W.; Ding, Y. Multiscale polymeric fibers for drug delivery and tissue engineering. Biomed. Technol. 2024, 5, 60. [Google Scholar] [CrossRef]
  3. Wal, P.; Wal, A.; Saxena, B.; Mishra, S.; Elossaily, G.M.; Arora, R.; Singh, C.; Sachdeva, M.; Answer, M.K.; Gulati, M.; et al. Insights into the innovative approaches in fiber technology for drug delivery and pharmaceuticals. J. Drug Deliv. Sci. Technol. 2023, 87, 104877. [Google Scholar] [CrossRef]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Felgueiras, H.P. Fiber-Based Scaffolds as Drug Carriers: Recent Advances. Pharmaceutics 2025, 17, 740. https://doi.org/10.3390/pharmaceutics17060740

AMA Style

Felgueiras HP. Fiber-Based Scaffolds as Drug Carriers: Recent Advances. Pharmaceutics. 2025; 17(6):740. https://doi.org/10.3390/pharmaceutics17060740

Chicago/Turabian Style

Felgueiras, Helena P. 2025. "Fiber-Based Scaffolds as Drug Carriers: Recent Advances" Pharmaceutics 17, no. 6: 740. https://doi.org/10.3390/pharmaceutics17060740

APA Style

Felgueiras, H. P. (2025). Fiber-Based Scaffolds as Drug Carriers: Recent Advances. Pharmaceutics, 17(6), 740. https://doi.org/10.3390/pharmaceutics17060740

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop