Porcine small intestine submucosa does not show antimicrobial properties

被引:25
作者
Holtom, PD
Shinar, Z
Benna, J
Patzakis, MJ
机构
[1] Univ So Calif, Dept Med, Div Infect Dis, Los Angeles, CA USA
[2] Univ So Calif, Dept Orthopaed Surg, Keck Sch Med, Los Angeles, CA USA
关键词
D O I
10.1097/01.blo.0000143573.03645.b4
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The goal of this study is to examine whether porcine small intestine submucosa (SIS) exhibits antimicrobial properties in a standard in vitro system, without pretreatment with acetic acid or extraction of soluble proteins. Previous animal studies suggest that porcine SIS may have inherent antibiotic properties. Using the guidelines for disk diffusion susceptibility testing by Bauer, 17/64-inch diameter disks made of porcine small intestine submucosa and of gortex were compared with standard antibiotic-impregnated disks against six organisms. The zone of inhibition was measured after 24 hours and minimum bacterial concentrations were determined by serial dilutions of a solution in which porcine small intestine submucosa was allowed to elute for 24 hours. Neither porcine SIS or gortex discs caused inhibition of the growth of any organism. The porcine small intestine submucosa discs showed bacterial growth on top of the discs whereas the gortex did not. Neither the dilutional concentrations of the porcine small intestine submucosa eluent nor the gortex eluent inhibited the growth of any organism. These findings suggest that the porcine small intestine submucosa does not have intrinsic antimicrobial properties. The growth of bacteria on top of the porcine small intestine submucosa suggests that porcine small intestine submucosa itself may provide a favorable environment for the growth of bacteria. More research is necessary to decide what role porcine small intestine submucosa plays in the treatment of infected surgical sites.
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页码:18 / 21
页数:4
相关论文
共 18 条
  • [1] ISOLATION OF 3 ANTIBACTERIAL PEPTIDES FROM PIG INTESTINE - GASTRIC-INHIBITORY POLYPEPTIDE(7-42), DIAZEPAM-BINDING INHIBITOR(32-86) AND A NOVEL FACTOR, PEPTIDE-3910
    AGERBERTH, B
    BOMAN, A
    ANDERSSON, M
    JORNVALL, H
    MUTT, V
    BOMAN, HG
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 216 (02): : 623 - 629
  • [2] [Anonymous], M100S11 NCCLS
  • [3] BADYLAK SF, 1993, TISSUE ENGINEERING, P179
  • [4] Small intestinal submucosa: A rapidly resorbed bioscaffold for augmentation cystoplasty in a dog model
    Badylak, SF
    Kropp, B
    McPherson, T
    Liang, H
    Snyder, PW
    [J]. TISSUE ENGINEERING, 1998, 4 (04): : 379 - 387
  • [5] COMPARISON OF THE RESISTANCE TO INFECTION OF INTESTINAL SUBMUCOSA ARTERIAL AUTOGRAFTS VERSUS POLYTETRAFLUOROETHYLENE ARTERIAL PROSTHESES IN A DOG-MODEL
    BADYLAK, SF
    COFFEY, AC
    LANTZ, GC
    TACKER, WA
    GEDDES, LA
    [J]. JOURNAL OF VASCULAR SURGERY, 1994, 19 (03) : 465 - 472
  • [6] MECHANISMS OF ACTION ON ESCHERICHIA-COLI OF CECROPIN-P1 AND PR-39, 2 ANTIBACTERIAL PEPTIDES FROM PIG INTESTINE
    BOMAN, HG
    AGERBERTH, B
    BOMAN, A
    [J]. INFECTION AND IMMUNITY, 1993, 61 (07) : 2978 - 2984
  • [7] Brown-Etris M, 2002, WOUNDS, V14, P150
  • [8] POROSITY OF PORCINE SMALL-INTESTINAL SUBMUCOSA FOR USE AS A VASCULAR GRAFT
    HILES, MC
    BADYLAK, SF
    GEDDES, LA
    KOKINI, K
    MORFF, RJ
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1993, 27 (02): : 139 - 144
  • [9] Hodde J P, 1996, Tissue Eng, V2, P209, DOI 10.1089/ten.1996.2.209
  • [10] KROPP BP, 1989, UROLOGY, V46, P396