Literature DB >> 12716782

Release of antimicrobial peptide Dhvar-5 from polymethylmethacrylate beads.

C Faber1, H P Stallmann, D M Lyaruu, J M A de Blieck, Th J M Bervoets, A van Nieuw Amerongen, P I J M Wuisman.   

Abstract

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 microg of Dhvar-5, respectively. Dhvar-5 was released from the beads in all three groups. Total release from the 120 microg beads was 9 microg per bead after 7 days. However, the release per bead in the 600 and 1200 microg beads was far more, respectively, 416 and 1091 microg 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.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12716782     DOI: 10.1093/jac/dkg258

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  5 in total

1.  Ultrashort peptide bioconjugates are exclusively antifungal agents and synergize with cyclodextrin and amphotericin B.

Authors:  Christopher J Arnusch; Hannah Ulm; Michaele Josten; Yana Shadkchan; Nir Osherov; Hans-Georg Sahl; Yechiel Shai
Journal:  Antimicrob Agents Chemother       Date:  2011-10-17       Impact factor: 5.191

2.  Antimicrobial peptide in polymethylmethacrylate bone cement as a prophylaxis of infectious complications in orthopedics-an experiment in a murine model.

Authors:  Pavel Melicherčík; Karel Kotaška; David Jahoda; Ivan Landor; Václav Čeřovský
Journal:  Folia Microbiol (Praha)       Date:  2022-05-25       Impact factor: 2.629

3.  In vitro gentamicin release from commercially available calcium-phosphate bone substitutes influence of carrier type on duration of the release profile.

Authors:  Hein P Stallmann; Chris Faber; Antonius L J J Bronckers; Arie V Nieuw Amerongen; Paul I J M Wuisman
Journal:  BMC Musculoskelet Disord       Date:  2006-02-26       Impact factor: 2.362

4.  Antimicrobial Peptides for Topical Treatment of Osteomyelitis and Implant-Related Infections: Study in the Spongy Bone.

Authors:  Pavel Melicherčík; Ondřej Nešuta; Václav Čeřovský
Journal:  Pharmaceuticals (Basel)       Date:  2018-02-16

5.  An In Vitro Comparison of PMMA and Calcium Sulfate as Carriers for the Local Delivery of Gallium(III) Nitrate to Staphylococcal Infected Surgical Sites.

Authors:  Rebecca A Garcia; David J Tennent; David Chang; Joseph C Wenke; Carlos J Sanchez
Journal:  Biomed Res Int       Date:  2016-01-17       Impact factor: 3.411

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.