The application of biomacromolecule systems in medical implants for the localized release of therapeutic agents is advancing rapidly. This progress is largely fueled by the rising global demand for sophisticated medical devices, particularly in the context of an aging population (). Implants such as catheters, stents, and prosthetic joints are indispensable in modern healthcare, serving to replace, support, or enhance biological structures. Yet, surgical implantation is inherently associated with risks, including infection, impaired healing, and complications that may be worsened by immunosuppression linked to conditions such as AIDS, cancer, or diabetes. In this regard, biomacromolecules—large biomolecules including proteins, nucleic acids, and polysaccharides—have shown remarkable potential as carriers for controlled therapeutic delivery. These systems not only reduce postoperative risks but also improve therapeutic outcomes by enabling localized and sustained release of bioactive molecules (; ). Nevertheless, significant challenges remain. Optimizing biocompatibility, ensuring long-term stability, and fine-tuning release kinetics are essential to fully unlock the clinical potential of these strategies.
Over the past decade, biomacromolecule delivery has evolved from classical polysaccharide and protein carriers into modular and hybrid platforms that merge biological recognition with materials engineering. Emerging modalities include peptide–polymer conjugates and amphiphilic peptides with antimicrobial or pro-regenerative functions; nucleic acid systems (siRNA/miRNA/DNA) condensed by cationic biopolymers for gene-level modulation; and protein–polymer hybrid depots that enable spatiotemporally controlled release of growth factors (). In parallel, bioinspired coatings and layer-by-layer assemblies on metallic and polymeric implants integrate polysaccharides (e.g., chitosan, hyaluronan), proteins, and catechol-functionalized polymers to improve adhesion, provide on-demand drug elution, and inhibit biofilm formation (). Triggered release mechanisms—responsive to pH, enzymes, redox conditions, or mild external stimuli—are now routine, while translational efforts increasingly focus on hemocompatibility, biofilm prevention, reproducibility, sterilization, and scalable manufacturing. Together, these developments position biomacromolecule systems as versatile interfaces capable of transforming passive devices into active therapeutic platforms.
The field continues to diversify. Hybrid peptide–polymer carriers are being designed for antimicrobial and immunomodulatory applications, coupling intrinsic bioactivity with enhanced stability (). Self-assembling nanosystems—such as peptide amphiphiles, polypeptide micelles, and bioinspired films—are directly integrated onto implant surfaces to achieve contact killing, disrupt quorum sensing, and provide sustained drug release. Nucleic acid payloads (e.g., siRNA, CRISPR guides) are increasingly incorporated into polysaccharide and protein matrices to locally modulate inflammation and fibrosis (). These strategies underscore the convergence of biomacromolecule science with surface and polymer engineering, defining a broad and dynamic landscape that frames this Research Topic.
Within this context, the present Research Topic features seven contributions that highlight both experimental and conceptual advances in biomacromolecule-assisted biomedical implants. The original research articles include those by Almuhayawi et al., González et al., and Pulido et al., complemented by reviews from Du et al., Sánchez-Trasviña et al., Calais et al., and Chen et al.. Collectively, these works illustrate strategies spanning drug-eluting coatings, antimicrobial macromolecules, bio–nano interfaces, and metallic implant surface engineering.
Altogether, this Research Topic emphasizes the transformative potential of biomacromolecule-based delivery systems in medical implants. By bridging fundamental science with clinical translation, the contributions presented here point to innovative approaches that may redefine the therapeutic role of implants in modern biomedicine. Beyond the specific examples covered, the scope also embraces peptide–polymer hybrids, self-assembled biointerfaces, and nucleic acid-enabled platforms that are shaping the next-generation of therapeutic implants.
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Author contributions
JL: Writing – review and editing. NT: Writing – review and editing. JH-M: Writing – original draft, Writing – review and editing.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. This work was partly supported by Fondecyt Regular–Chile (Grant Number 1230553).
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The editors appreciate the contributions of all authors to this Research Topic, the constructive comments of all the reviewers, and the editorial support from Frontiers throughout the publication process.
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Summary
Keywords
biomacromolecule, therapeutic delivery, localized delivery, medical implants, drug delievery
Citation
Lopes JH, Tabary N and Hernandez-Montelongo J (2025) Editorial: Biomacromolecule systems for enhanced therapeutic delivery in medical implants. Front. Bioeng. Biotechnol. 13:1700914. doi: 10.3389/fbioe.2025.1700914
Received
07 September 2025
Accepted
07 October 2025
Published
13 October 2025
Volume
13 - 2025
Edited and reviewed by
Candan Tamerler, University of Kansas, United States
Updates
Copyright
© 2025 Lopes, Tabary and Hernandez-Montelongo.
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*Correspondence: Jacobo Hernandez-Montelongo, jacobo.hernandez@uct.cl
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.