A novel liposomal drug delivery system for PMMA bone cements

被引:38
作者
Ayre, Wayne Nishio [1 ]
Birchall, James C. [2 ]
Evans, Samuel L. [3 ]
Denyer, Stephen P. [4 ]
机构
[1] Cardiff Univ, Sch Dent, Cardiff CF14 4XY, S Glam, Wales
[2] Cardiff Univ, Sch Pharm & Pharmaceut Sci, Cardiff CF10 3NB, S Glam, Wales
[3] Cardiff Univ, Sch Engn, Cardiff CF24 3AA, S Glam, Wales
[4] Sch Pharm & Biomol Sci, Brighton BN2 4GJ, E Sussex, England
关键词
bone cement; PMMA; acrylic; antimicrobial; controlled release; infection; joint replacement; FATIGUE-CRACK-PROPAGATION; MECHANICAL-PROPERTIES; ANTIBIOTIC RELEASE; RESISTANT STRAINS; LIQUID GENTAMICIN; FORMULATION;
D O I
10.1002/jbm.b.33488
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The population in developed countries is ageing and the number of people experiencing joint-related conditions, such as osteoarthritis, is expected to increase. Joint replacements are currently the most effective treatment for severe joint conditions and although many of these procedures are successful, infection developing after the procedure is still an issue, requiring complex and expensive revisions. Whilst incorporating a powdered antibiotic within the bone cement can reduce infection rates, the powder frequently agglomerates, resulting in poor antibiotic release characteristics and compromised mechanical performance of the cement. To overcome these issues, a novel delivery system consisting of antibiotic-loaded nano-sized liposomes was developed for inclusion into polymethyl methacrylate (PMMA) bone cement. This system was tested in a commercial cement (Palacos R) and consistently delivered a higher percentage (22%) of the incorporated antibiotic when compared to the powdered antibiotic cement (9%), meaning less antibiotic needs to be incorporated than with conventional cement. The novel system resulted in a controlled and gradual release of antibiotic over a longer, 30-day period and enhanced the toughness, bending strength and Vickers hardness of the cement, without altering its polymerization or molecular structure. This new material has the potential to significantly reduce infections in cemented joint replacements leading to enhanced patient quality of life and reduced healthcare costs. (C) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:1510 / 1524
页数:15
相关论文
共 55 条
[1]   Ageing and moisture uptake in polymethyl methacrylate (PMMA) bone cements [J].
Ayre, Wayne Nishio ;
Denyer, Stephen P. ;
Evans, Samuel L. .
JOURNAL OF THE MECHANICAL BEHAVIOR OF BIOMEDICAL MATERIALS, 2014, 32 :76-88
[2]  
Briggs T., 2012, Getting it right first time: improving the quality of orthopaedic care within the national health service in England
[3]  
BUCHHOLZ HW, 1970, CHIRURG, V41, P511
[4]  
Buchholz HW, 1979, RECENT ADV ORTHOPAED, V3, P139
[5]   Clinical development of liposome-based drugs: formulation, characterization, and therapeutic efficacy [J].
Chang, Hsin-I ;
Yeh, Ming-Kung .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2012, 7 :49-60
[6]  
Cherubino Paolo, 2013, Open Orthop J, V7, P190, DOI 10.2174/1874325001307010190
[7]   The effect of interfacial adhesion on toughening behaviour of rubber modified poly(methyl methacrylate) [J].
Cho, KW ;
Yang, JH ;
Park, CE .
POLYMER, 1997, 38 (20) :5161-5167
[8]   Liposomal Formulation Increases Local Delivery of Amphotericin from Bone Cement: A Pilot Study [J].
Cunningham, Brian ;
McLaren, Alex C. ;
Pauken, Christine ;
McLemore, Ryan .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2012, 470 (10) :2671-2676
[9]  
Davis EJR, 2003, HDB MAT MED DEVICES
[10]   In vitro study of the efficacy of acrylic bone cement loaded with supplementary amounts of gentamicin - Effect on mechanical properties, antibiotic release, and biofilm formation [J].
Dunne, Nicholas ;
Hill, Janet ;
McAfeel, Patricia ;
Todd, Katy ;
Kirkpatrick, Rachel ;
Tunney, Michael ;
Patrick, Sheila .
ACTA ORTHOPAEDICA, 2007, 78 (06) :774-785