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

被引:31
作者
Cao, Meiwen [1 ,2 ]
Zhao, Wenjing [1 ,2 ]
Wang, Lei [1 ,2 ]
Li, Ruiheng [3 ]
Gong, Haoning [3 ]
Zhang, Yu [1 ,2 ]
Xu, Hai [1 ,2 ]
Lu, Jian Ren [3 ]
机构
[1] China Univ Petr East China, Coll Chem Engn, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] China Univ Petr East China, Coll Chem Engn, Ctr Bioengn & Biotechnol, Qingdao 266580, Peoples R China
[3] Univ Manchester, Sch Phys & Astron, Phys Biol Lab, Schuster Bldg,Oxford Rd, Manchester M13 9PL, Lancs, England
基金
英国工程与自然科学研究理事会; 中国国家自然科学基金;
关键词
sustained release; antibacterial peptides; self-assembly; graphene oxide; layer-by-layer; GRAPHITE OXIDE; POLYELECTROLYTE MULTILAYERS; MOLECULAR-MECHANISMS; TRIGGERED RELEASE; CELL SELECTIVITY; DELIVERY; FILMS; DRUG; DOXORUBICIN; SURFACES;
D O I
10.1021/acsami.8b07417
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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.
引用
收藏
页码:24937 / 24946
页数:10
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