A novel liposomal drug delivery system for PMMA bone cements

被引:36
|
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 50 条
  • [41] Bioactivity in glass/PMMA composites used as drug delivery system
    Arcos, D
    Ragel, CV
    Vallet-Regí, M
    BIOMATERIALS, 2001, 22 (07) : 701 - 708
  • [42] Novel drug delivery systems for ocular therapy: With special reference to liposomal ocular delivery
    Bhattacharjee, Arpita
    Das, Pranab J.
    Adhikari, Piya
    Marbaniang, Daphisha
    Pal, Paulami
    Ray, Subhabrata
    Mazumder, Bhaskar
    EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2019, 29 (01) : 113 - 126
  • [43] Calcium phosphate bone cements reinforced with biodegradable polymer fibres for drug delivery
    Irbe, Zilgma
    Loca, Dagnija
    Bistrova, Ivita
    Berzina-Cimdina, Liga
    ENGINEERING MATERIALS & TRIBOLOGY XXII, 2014, 604 : 184 - 187
  • [44] A novel, quorum sensor-infused liposomal drug delivery system suppresses Candida albicans biofilms
    Bandara, H. M. H. N.
    Hewavitharana, A. K.
    Shaw, P. N.
    Smyth, H. D. C.
    Samaranayake, L. P.
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2020, 578
  • [45] Pulmonary Drug Delivery System: A Novel Approach for Drug Delivery
    Singh, Anupama
    Malviya, Rishabha
    Sharma, Pramod K.
    CURRENT DRUG THERAPY, 2011, 6 (02) : 137 - 151
  • [47] A novel peptide for a drug delivery system to preferentially target bone formation sites
    Wu, Heng
    Zhang, Ge
    Guo, Bao Sheng
    Tao, Tang
    Li, Gang
    Lee, Kwong Man
    Hung, Leung Kim
    Qin, Ling
    BONE, 2010, 47 : S413 - S414
  • [48] BONE CEMENTS FOR LOCAL GENTAMICIN DELIVERY
    Tracuma, Eliza
    Loca, Dagnija
    Skrinda, Marite
    Locs, Janis
    TISSUE ENGINEERING PART A, 2022, 28 : S203 - S203
  • [49] Ionomer cements for drug delivery.
    Roos, AM
    Luttikhedde, HJG
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1998, 216 : U879 - U879
  • [50] LIPOSOMAL OPHTHALMIC DRUG DELIVERY SYSTEM .2. DIHYDROSTREPTOMYCIN SULFATE
    SINGH, K
    MEZEI, M
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1984, 19 (03) : 263 - 269