Antibacterial Analysis of a Zinc-based Glass Polyalkenoate Cement

被引:11
作者
Clarkin, Owen [2 ]
Wren, Anthony [1 ]
Thornton, Roibeard [3 ]
Cooney, Jakki [3 ]
Towler, Mark [1 ]
机构
[1] Alfred Univ, Inamori Sch Engn, Alfred, NY 14802 USA
[2] Univ Limerick, Mat & Surface Sci Inst, Limerick, Ireland
[3] Univ Limerick, Dept Life Sci, Limerick, Ireland
关键词
glass polyalkenoate cement; antibacterial; zinc; tobramycin; bone cement; ACRYLIC BONE-CEMENT; IONOMER CEMENTS; MEDICAL DEVICES; NEWBORN RATS; TOBRAMYCIN; RELEASE; ALUMINUM; GENTAMICIN; OXIDE; ARTHROPLASTY;
D O I
10.1177/0885328210364430
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Infection following surgery can result in significant pain and morbidity for patients undergoing vertebroplasty/kyphoplasty, and often results in revision surgery. This study focuses on the development of Al-free glass polyalkenoate cements (GPCs) based on 0.04SrO-0.12CaO-0.36ZnO-0.48SiO(2) glass, with the intent of optimizing their antibacterial efficacy by incorporating low-molecular-weight polyacrylic acids (PAA) and trisodium citrate (TSC), and evaluating the resultant GPCs against bacteria relevant to spinal infections, P. aeruginosa and E. coli. Ion-release profiles were determined for the GPC formulation containing E6 PAA (Cement A) and E7 PAA (Cement B), and Zn, Na, and Sr release was recorded over 1, 7, and 30 days. Inhibition was found in E. coli at each time period (0-30 days) and this generally decreased with exposure time in water. The largest GPC inhibition zones were produced by Cement A (6 mm); however the control material Simplex P + tobramycin produced much higher inhibition zones (11 mm). When testing the GPC against P. aeruginosa, inhibition was only present at the 0-day time period. Simplex P + tobramycin was found to produce inhibition at each time frame. Analysis of the agar from the inhibition zone of the E. coli test revealed that there is a significant change in Zn concentration as compared to a control agar specimen, which suggests that Zn release is responsible for the antibacterial effect of the GPCs.
引用
收藏
页码:277 / 292
页数:16
相关论文
共 50 条
  • [1] Bacterial contaminants and antibiotic prophylaxis in total hip arthroplasty
    Al-Maiyah, M
    Hill, D
    Bajwa, A
    Slater, S
    Patil, P
    Port, A
    Gregg, PJ
    [J]. JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2005, 87B (09): : 1256 - 1258
  • [2] Amerongen Willem E., 1996, J PUB HLTH DENT, V56, P150
  • [3] RELEASE OF GENTAMICIN FROM ACRYLIC BONE-CEMENT - ELUTION AND DIFFUSION STUDIES
    BAKER, AS
    GREENHAM, LW
    [J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1988, 70A (10) : 1551 - 1557
  • [4] ACID TOLERANCE, PROTON PERMEABILITIES, AND MEMBRANE ATPASES OF ORAL STREPTOCOCCI
    BENDER, GR
    SUTTON, SVW
    MARQUIS, RE
    [J]. INFECTION AND IMMUNITY, 1986, 53 (02) : 331 - 338
  • [5] Zinc-based glass polyalkenoate cements with improved setting times and mechanical properties
    Boyd, D.
    Clarkin, O. M.
    Wren, A. W.
    Towler, M. R.
    [J]. ACTA BIOMATERIALIA, 2008, 4 (02) : 425 - 431
  • [6] The antibacterial effects of zinc ion migration from zinc-based glass polyalkenoate cements
    Boyd, D.
    Li, H.
    Tanner, D. A.
    Towler, M. R.
    Wall, J. G.
    [J]. JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2006, 17 (06) : 489 - 494
  • [7] COMPARATIVE ACTIVITY OF NETILMICIN, GENTAMICIN, AMIKACIN, AND TOBRAMYCIN AGAINST PSEUDOMONAS-AERUGINOSA AND ENTEROBACTERIACEAE
    BRIEDIS, DJ
    ROBSON, HG
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1976, 10 (04) : 592 - 597
  • [8] Bush A., 2004, ALZHEIMERS AUSTR, V5, P1
  • [9] An investigation into the pathogenic properties of Escherichia coli strains BLR, BL21, DH5α and EQ1
    Chart, H
    Smith, HR
    La Ragione, RM
    Woodward, MJ
    [J]. JOURNAL OF APPLIED MICROBIOLOGY, 2000, 89 (06) : 1048 - 1058
  • [10] Antibacterial coatings for medical devices based on glass polyalkenoate cement chemistry
    Coughlan, A.
    Boyd, D.
    Douglas, C. W. I.
    Towler, M. R.
    [J]. JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2008, 19 (12) : 3555 - 3560