共 28 条
Protein-Based Nanoparticles for the Delivery of Enzymes with Antibacterial Activity
被引:17
作者:

Steiert, Elena
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机构:
Johannes Gutenberg Univ Mainz, Inst Pharm & Biochem, Staudingerweg 5, D-55128 Mainz, Germany Johannes Gutenberg Univ Mainz, Inst Pharm & Biochem, Staudingerweg 5, D-55128 Mainz, Germany

Radi, Lydia
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h-index: 0
机构:
Johannes Gutenberg Univ Mainz, Inst Pharm & Biochem, Staudingerweg 5, D-55128 Mainz, Germany Johannes Gutenberg Univ Mainz, Inst Pharm & Biochem, Staudingerweg 5, D-55128 Mainz, Germany

Fach, Matthias
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机构:
Tech Univ Denmark, Dept Micro & Nanotechnol, Produktionstorvet Bldg 423, DK-2800 Lyngby, Denmark Johannes Gutenberg Univ Mainz, Inst Pharm & Biochem, Staudingerweg 5, D-55128 Mainz, Germany

Wich, Peter R.
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Johannes Gutenberg Univ Mainz, Inst Pharm & Biochem, Staudingerweg 5, D-55128 Mainz, Germany Johannes Gutenberg Univ Mainz, Inst Pharm & Biochem, Staudingerweg 5, D-55128 Mainz, Germany
机构:
[1] Johannes Gutenberg Univ Mainz, Inst Pharm & Biochem, Staudingerweg 5, D-55128 Mainz, Germany
[2] Tech Univ Denmark, Dept Micro & Nanotechnol, Produktionstorvet Bldg 423, DK-2800 Lyngby, Denmark
关键词:
antibacterial activity;
biopolymers;
double emulsion;
lysozyme;
nanoparticles;
BIOPOLYMER;
PARTICLES;
ALBUMIN;
DEXTRAN;
D O I:
10.1002/marc.201800186
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
Proteins represent a versatile biopolymer material for the preparation of nanoparticles due to their biocompatibility, biodegradability, and low immunogenicity. This study presents a protein-based nanoparticle system consisting of high surface PEGylated lysozyme polyethylene glycol-modified lysozyme (LYZ(mPEG)). This protein modification leads to a solubility switch, which allows a nanoparticle preparation using a mild double emulsion method without the need of surfactants. The method allows the encapsulation of large hydrophilic payloads inside of the protein-based nanoparticle system. Native lysozyme (LYZ) was chosen as payload because of its innate activity as natural antibiotic. The mild particle preparation procedure retains the structure and activity of the enzyme which was successfully tested against the gram-positive bacteria strain M. Luteus. In comparison, the particle system shows no toxicity to human cells. This first report of a full protein-based particle material for the transport of large hydrophilic payloads opens up new therapeutic applications for biopolymer-based delivery systems.
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