Release of antimicrobial peptide Dhvar-5 from polymethylmethacrylate beads

被引:33
作者
Faber, C [1 ]
Stallmann, HP
Lyaruu, DM
de Blieck, JMA
Bervoets, TJM
van Nieuw Amerongen, A
Wuisman, PIJM
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Orthopaed Surg, Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Acad Ctr Dent Amsterdam, Dept Oral Cell Biol, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Acad Ctr Dent Amsterdam, Dept Oral Biochem, Amsterdam, Netherlands
关键词
antimicrobial peptides; Dhvar-5; PMMA beads; release kinetics;
D O I
10.1093/jac/dkg258
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Osteomyelitis is still a major cause of morbidity and remains a difficult complication to treat in orthopaedic surgery. The treatment of choice is a combination of systemic and local antibiotics. The insertion of gentamicin-loaded polymethylmethacrylate (PMMA) beads into the bone results in high local concentrations of gentamicin and low systemic concentrations. However, the effectiveness of this treatment is being hampered by the emergence of antimicrobial resistance. New antimicrobial agents are therefore needed. One new class of promising antibiotics is antimicrobial peptides (AMP). Derived from natural human peptides, these have a low tendency to induce antimicrobial resistance. Dhvar-5 is an antimicrobial peptide based on histatin-5, which is found in human saliva and consists of 14 amino acids. It has demonstrated bactericidal activity in vitro. In order to develop a new local treatment using Dhvar-5 for osteomyelitis, we investigated its release from PMMA beads and its antimicrobial activity against a clinical isolate of methicillin-resistant Staphylococcus aureus (MRSA) before and after release from PMMA beads. Specific amounts of Dhvar-5 were incorporated into PMMA mini beads, containing 120, 600 and 1200 mug of Dhvar-5, respectively. Dhvar-5 was released from the beads in all three groups. Total release from the 120 mug beads was 9 mug per bead after 7 days. However, the release per bead in the 600 and 1200 mug beads was far more, respectively, 416 and 1091 mug over a 28 day period. After release, the Dhvar-5 also retained its antimicrobial activity against MRSA. On the basis of these data we conclude that the amount of Dhvar-5 release from PMMA beads is not proportionate to the amount incorporated; instead, it demonstrated an exponential relationship to the amount of total peptide released. Furthermore, the released peptide remained biologically active against a clinical isolate of MRSA.
引用
收藏
页码:1359 / 1364
页数:6
相关论文
共 32 条
[1]  
BUCHHOLZ HW, 1970, CHIRURG, V41, P511
[2]   MANAGEMENT OF DEEP INFECTION OF TOTAL HIP-REPLACEMENT [J].
BUCHHOLZ, HW ;
ELSON, RA ;
ENGELBRECHT, E ;
LODENKAMPER, H ;
ROTTGER, J ;
SIEGEL, A .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1981, 63 (03) :342-353
[3]   Emergence of vancomycin-intermediate Staphylococcus aureus in a Belgian hospital:: microbiological and clinical features [J].
Denis, O ;
Nonhoff, C ;
Byl, B ;
Knoop, C ;
Bobin-Dubreux, S ;
Struelens, MJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (03) :383-391
[4]   Bactericidal/permeability-increasing protein -: Lessons learned from the phase III, randomized, clinical trial of rBPI21 for adjunctive treatment of children with severe meningococcemia [J].
Giroir, BP ;
Scannon, PJ ;
Levin, M .
CRITICAL CARE MEDICINE, 2001, 29 (07) :S130-S135
[5]   Preliminary evaluation of recombinant amino-terminal fragment of human bactericidal/permeability-increasing protein in children with severe meningococcal sepsis [J].
Giroir, BP ;
Quint, PA ;
Barton, P ;
Kirsch, EA ;
Kitchen, L ;
Goldstein, B ;
Nelson, BJ ;
Wedel, NI ;
Carroll, SF ;
Scannon, PJ .
LANCET, 1997, 350 (9089) :1439-1443
[6]   Peptide antibiotics [J].
Hancock, REW .
LANCET, 1997, 349 (9049) :418-422
[7]  
HARLE A, 1980, CHIRURG, V51, P693
[8]   The cellular target of histatin 5 on Candida albicans is the energized mitochondrion [J].
Helmerhorst, EJ ;
Breeuwer, P ;
van't Hof, W ;
Walgreen-Weterings, E ;
Oomen, LCJM ;
Veerman, ECI ;
Amerongen, AVN ;
Abee, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (11) :7286-7291
[9]   Synthetic histatin analogues with broad-spectrum antimicrobial activity [J].
Helmerhorst, EJ ;
VantHof, W ;
Veerman, ECI ;
SimoonsSmit, I ;
Amerongen, AVN .
BIOCHEMICAL JOURNAL, 1997, 326 :39-45
[10]   A critical comparison of the hemolytic and fungicidal activities of cationic antimicrobial peptides [J].
Helmerhorst, EJ ;
Reijnders, IM ;
van't Hof, W ;
Veerman, ECI ;
Amerongen, AVN .
FEBS LETTERS, 1999, 449 (2-3) :105-110