Bacteriostatic properties of biomatrices against common orthopaedic pathogens

被引:124
作者
Carlson, GA
Dragoo, JL
Samimi, B
Bruckner, DA
Bernard, GW
Hedrick, M
Benhaim, P [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Surg, Lab Regenerat Bioengn & Repair, Los Angeles, CA USA
[2] Univ Calif Los Angeles, Sch Med, Dept Orthopaed Surg, Los Angeles, CA USA
[3] Univ Calif Los Angeles, Sch Med, Dept Microbiol, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Sch Med, Dept Oral Biol, Los Angeles, CA 90024 USA
关键词
biomatrices; bacteriostatic; orthopaedic; tissue-engineering; collagen; hydroxyapatite; hyaluronic acid; PLGA;
D O I
10.1016/j.bbrc.2004.06.165
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Tissue-engineered grafts for tissue regeneration include either mature or progenitor cells seeded onto biomatrices that provide shape and support for developing tissue. Popular biomaterials used in orthopaedic surgery include collagen type I, hyaluronic acid, hydroxyapatite, and polylactic polyglycolic acid (PLGA). Biomatrices with bacteriostatic properties may be beneficial in promoting tissue-engineered graft survival in patients susceptible to infection. We evaluated the bacteriostatic effects of these biomaterials on the growth of the four most common orthopaedic bacterial pathogens: Staphylococcus aureus, Staphylococcus epidermidis, beta-hemolytic Streptococcus, and Pseudomonas aeruginosa. Hyaluronic acid demonstrated the largest bacteriostatic effect on these pathogens by inhibiting bacterial growth by an average of 76.8% (p = 0.0005). Hydroxyapatite and collagen inhibited growth on average by 49.7% (p = 0.011) and 37.5% (p = 0.102), respectively. PLGA exhibited the least bacteriostasis with an average inhibition of 9.8% (NS) and actually accelerated the growth of beta-hemolytic Streptococcus and P. aeruginosa. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:472 / 478
页数:7
相关论文
共 34 条
[1]
COURTBROWN CM, 1996, MANAGEMENT OPEN FRAC, P37
[2]
Role of Staphylococcus aureus surface adhesins in orthopaedic device infections: Are results model-dependent? [J].
Darouiche, RO ;
Landon, GC ;
Patti, JM ;
Nguyen, LL ;
Fernau, RC ;
McDevitt, D ;
Greene, C ;
Foster, T ;
Klima, M .
JOURNAL OF MEDICAL MICROBIOLOGY, 1997, 46 (01) :75-79
[3]
Dexter SJ, 2001, J BIOMED MATER RES, V56, P222, DOI 10.1002/1097-4636(200108)56:2<222::AID-JBM1087>3.0.CO
[4]
2-L
[5]
Bone cells and matrices in orthopedic tissue engineering [J].
Fleming, JE ;
Cornell, CN ;
Muschler, GE .
ORTHOPEDIC CLINICS OF NORTH AMERICA, 2000, 31 (03) :357-+
[6]
CELL BIOLOGY AND MOLECULAR MECHANISMS IN ARTIFICIAL DEVICE INFECTIONS [J].
GRISTINA, AG ;
GIRIDHAR, G ;
GABRIEL, BL ;
NAYLOR, PT ;
MYRVIK, QN .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 1993, 16 (11) :755-763
[7]
BIOMATERIAL-CENTERED INFECTION - MICROBIAL ADHESION VERSUS TISSUE INTEGRATION [J].
GRISTINA, AG .
SCIENCE, 1987, 237 (4822) :1588-1595
[8]
ADHERENT BACTERIAL-COLONIZATION IN THE PATHOGENESIS OF OSTEOMYELITIS [J].
GRISTINA, AG ;
OGA, M ;
WEBB, LX ;
HOBGOOD, CD .
SCIENCE, 1985, 228 (4702) :990-993
[9]
A polymer foam conduit seeded with Schwann cells promotes guided peripheral nerve regeneration [J].
Hadlock, T ;
Sundback, C ;
Hunter, D ;
Cheney, M ;
Vacanti, JP .
TISSUE ENGINEERING, 2000, 6 (02) :119-127
[10]
Expression of liver-specific functions by rat hepatocytes seeded in treated poly( lactic-co-glycolic) acid biodegradable foams [J].
Hasirci, V ;
Berthiaume, F ;
Bondre, SP ;
Gresser, JD ;
Trantolo, DJ ;
Toner, M ;
Wise, DL .
TISSUE ENGINEERING, 2001, 7 (04) :385-394