Engineering poly(dehydroalanine)-based gels <i>via</i> droplet-based microfluidics: from bulk to microspheres.
Mathews. Hannah F HF; Çeper. Tolga T; Speen. Tobias T; Bastard. Céline C; Bulut. Selin S; Pieper. Maria I MI; Schacher. Felix H FH; De Laporte. Laura L; Pich. Andrij A
Key Findings
- Poly(dehydroalanine) gels can be produced in bulk or as microâsized particles (â30âŻÂ”m or 200âŻÂ”m) using dropletâbased microfluidics.
- Increasing crossâlinker density changes the gelâs composition, permeability, and softness, affecting how much LLâ37 it can load.
- LLâ37 is adsorbed into the gels and released in a pHâdependent manner; the gels are biocompatible in cell tests.
Practical Outcomes
- The study suggests a potential method for creating pHâresponsive, peptideâloaded microgels that could be used for controlled LLâ37 delivery. It does not provide dosage recommendations, safety data for human use, or a DIY protocol, so its immediate usefulness for biohackers is limited.
Summary
Scientists made tiny, waterâloving gels that can hold and release the antimicrobial peptide LLâ37 depending on the pH. They showed that the size of the gel particles and how tightly theyâre crossâlinked change how much peptide they can carry, and the gels are safe for cells. However, the work is about the material itself, not about how to take LLâ37 for health benefits.
Abstract
Biomedical applications such as drug delivery, tissue engineering, and functional surface coating rely on switchable adsorption and desorption of specialized guest molecules. Poly(dehydroalanine), a polyzwitterion containing pH-dependent positive and negative charges, shows promise for such reversible loading, especially when integrated into a gel network. Herein, we present the fabrication of poly(dehydroalanine)-derived gels of different size scales and evaluate them with respect to their practical use in biomedicine. Already existing protocols for bulk gelation were remodeled to derive suitable reaction conditions for droplet-based microfluidic synthesis. Depending on the layout of the microfluidic chip, microgels with a size of approximately 30 μm or 200 μm were obtained, whose crosslinking density can be increased by implementing a multi-arm crosslinker. We analyzed the effects of the crosslinker species on composition, permeability, and softness and show that the microgels exhibit advantageous properties inherent to zwitterionic polymer systems, including high hydrophilicity as well as pH- and ionic strength-sensitivity. We demonstrate pH-regulated uptake and release of fluorescent model dyes before testing the adsorption of a small antimicrobial peptide, LL-37. Quantification of the peptide accommodated within the microgels reveals the impact of size and crosslinking density of the microgels. Biocompatibility of the microgels was validated by cell tests.
Study Information
pubmed
2024
2024-08-07T00:00:00.000Z
10.1039/d4sm00676c
69