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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 2
2013 pubmed

Using electrospun poly(ethylene-oxide) nanofibers for improved retention and efficacy of bacteriolytic antibiotics.

Gatti. John W JW; Smithgall. Marie C MC; Paranjape. Shruti M SM; Rolfes. Ronda J RJ; Paranjape. Makarand M

Key Findings

  • Electrospinning does not destroy LL‑37’s antimicrobial activity.
  • PEO nanofibers (100‑500 nm) can incorporate LL‑37 and release it consistently.
  • In lab tests, LL‑37‑loaded fibers produced a measurable zone of bacterial inhibition and filtered bacteria effectively.

Practical Outcomes

  • For DIY biohackers, this suggests that creating polymer‑based patches or dressings that slowly release LL‑37 is technically possible, but the study stops short of providing a ready‑to‑use recipe or safety data for humans. More work is needed to translate the method into a safe, at‑home protocol.

Summary

Scientists showed that the antimicrobial peptide LL‑37 can be mixed into ultra‑thin fibers made from a polymer (PEO) using a process called electrospinning, and it still works to kill bacteria. The fibers slowly release the peptide, creating a small antibacterial zone in lab tests.

Abstract

The aim of this study was to demonstrate targeted delivery of protein-based bactericidal antibiotics using electrospun polymer nanofibers. Previous studies have utilized electrospinning to create nanofibers for the localized delivery of therapeutic agents, including non-steroidal anti-inflammatory drugs (NSAIDs) and low molecular weight heparin. By employing established electrospinning techniques, nanofibers of varying diameters (100-500 nm) were generated from a 0.05 % solution of poly(ethylene-oxide) (PEO) and the antimicrobial peptide, LL-37 was incorporated into the nanofiber meshwork. Initial experiments determined that the strong electric fields caused by electrospinning do not disrupt the antimicrobial properties of LL-37, thus justifying the application of LL-37 as an electrospun component. Disk diffusion assays and especially bacterial filtration studies with E. coli were conducted to quantify the drug delivery potential of the nanofibers. Disk diffusion revealed a small zone of inhibition of about 1 mm around the LL-37-incorporated nanofiber disk. Filtration tests demonstrated that electrospun PEO fibers were capable of delivering LL-37 consistently while still maintaining their antimicrobial abilities.

Study Information

Provider

pubmed

Year

2013

Date

2013-06-14T00:00:00.000Z

DOI

10.1007/s10544-013-9777-5