Optimizing silk nanoparticle assembly with potassium ions : effects on physicochemical properties and encapsulation efficiency
Roamcharern, Napaporn and Brady, Daniel J. and Parkinson, John A. and Rattray, Zahra and Seib, F. Philipp (2025) Optimizing silk nanoparticle assembly with potassium ions : effects on physicochemical properties and encapsulation efficiency. ACS Applied Bio Materials, 8 (8). pp. 6854-6864. ISSN 2576-6422 (https://doi.org/10.1021/acsabm.5c00598)
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Abstract
Silk fibroin is a promising biomaterial for nanocarrier-based drug delivery due to its biocompatibility, biodegradability, and tunable mechanical properties. In addition, the silk protein is amenable to various processing strategies, offering flexibility for optimizing particle characteristics. Emerging evidence highlights that metal ions can modulate silk conformation and structure in the silk gland, as well as influencing self-assembly, potentially impacting silk nanoparticle fabrication. Our previous study highlighted the potential of Ca in silk nanoparticle fabrication. However, other metal ions in the silk gland influence silk fibroin behavior too. Here, we investigate how potassium ions (K ), with similar abundance to Ca in the silkworm gland, influence silk nanoparticle formation as modulators of self-assembly and material properties, aiming to produce nanoparticles with distinct physicochemical profiles. We show that K enhances silk assembly, increases nanoparticle size, alters surface charge (zeta potential), and boosts production yield, thereby minimizing silk wastage during silk nanoparticle preparation. Potassium ions also significantly improve payload encapsulation efficiency, making K inclusion valuable for a range of drug-loading applications. The resulting silk nanoparticles exhibit reduced toxicity and inflammatory response, highlighting their promise as safe and effective nanocarrier candidates for drug delivery. Our findings establish K as a fundamental yet powerful tool for tuning silk nanoparticle properties to meet pharmaceutical needs.
ORCID iDs
Roamcharern, Napaporn
ORCID: https://orcid.org/0009-0002-2003-1093, Brady, Daniel J., Parkinson, John A.
ORCID: https://orcid.org/0000-0003-4270-6135, Rattray, Zahra
ORCID: https://orcid.org/0000-0002-8371-8549 and Seib, F. Philipp
ORCID: https://orcid.org/0000-0002-1955-1975;
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Item type: Article ID code: 93572 Dates: DateEvent18 August 2025Published7 August 2025Published Online18 July 2025Accepted28 March 2025SubmittedSubjects: Science > Microbiology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences
Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > BionanotechnologyDepositing user: Pure Administrator Date deposited: 24 Jul 2025 13:01 Last modified: 12 Aug 2026 12:56 URI: https://strathprints.strath.ac.uk/id/eprint/93572
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