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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 2
2024 pubmed

Engineering poly(dehydroalanine)-based gels <i>via</i> droplet-based microfluidics: from bulk to microspheres.

Mathews. Hannah F HF; &#xc7;eper. Tolga T; Speen. Tobias T; Bastard. C&#xe9;line 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 micro‑sized particles (≈30 ”m or 200 ”m) using droplet‑based microfluidics.
  • Increasing cross‑linker density changes the gel’s composition, permeability, and softness, affecting how much LL‑37 it can load.
  • LL‑37 is adsorbed into the gels and released in a pH‑dependent manner; the gels are biocompatible in cell tests.

Practical Outcomes

  • The study suggests a potential method for creating pH‑responsive, peptide‑loaded microgels that could be used for controlled LL‑37 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, water‑loving gels that can hold and release the antimicrobial peptide LL‑37 depending on the pH. They showed that the size of the gel particles and how tightly they’re cross‑linked 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 LL‑37 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 &#x3bc;m or 200 &#x3bc;m 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

Provider

pubmed

Year

2024

Date

2024-08-07T00:00:00.000Z

DOI

10.1039/d4sm00676c

References

69