4.8 Article

Graphene Oxide-Assisted Accumulation and Layer-by-Layer Assembly of Antibacterial Peptide for Sustained Release Applications

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 10, Issue 29, Pages 24937-24946

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b07417

Keywords

sustained release; antibacterial peptides; self-assembly; graphene oxide; layer-by-layer

Funding

  1. National Natural Science Foundation of China [21473255, 21003160]
  2. Fundamental Research Funds for the Central Universities [17CX02050]
  3. Key Laboratory of Applied Surface and Colloid Chemistry (Shaanxi Normal University)
  4. U.K. Physical Sciences and Engineering Research Council (EPSRC) [EP/F062966/1]
  5. Innovate U.K. [KTP008143, KTP009043]
  6. Graphene Grand Challenges by the University of Manchester
  7. EPSRC [EP/F062966/1] Funding Source: UKRI

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Fabrication of antibacterial materials with sustained release of active components is of great importance for long-term antibacterial applications. Graphene oxide (GO) has been found to be an excellent carrier for accumulating the antibacterial peptide of G(IIKK)(4)I-NH2 and mediating its loading into the layer-by-layer (LBL) films for sustained release applications. G(IIKK)(4)I-NH2 takes random coiled conformation in monomeric state below 0.17 mM but self-assembles into supramolecular aggregates with alpha-helical secondary structure at higher concentrations. It can bind onto GO surface in both monomeric and aggregate states to form stable GO@G(IIKK)(4)I-NH2 composites. Upon binding, the local amphiphilic environment of GO surface induces a conformational transition of G(IIKK)(4)I-NH2 monomers from random coils to alpha-helix. The aggregate binding enhances the loading amount greatly. GO (1 mg) can load as high as 1.7 mg of peptide at saturation. This enables the GO@G(IIKK)(4)I-NH2 composites to serve as reservoirs for sustained release of active G(IIKK)(4)I-NH(2 )monomers. Moreover, G(IIKK)(4)I-NH2 itself shows low efficiency in LBL assembly, whereas the GO@G(IIKK)(4)I-NH2 composites are ideal LBL assembling units with highly enhanced loading efficiency of G(IIKK)(4)I-NH2. The LBL films involving degradable poly(beta-amino esters) can realize sustained release of G(IIKK)(4)I-NH2 for bacteria killing in a well-controlled manner. This study demonstrates an efficient strategy for fabrication of long-durable antibacterial materials and surface coatings by using GO as the carrier for drug accumulation and loading.

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