Antimicrobial PMMA Bone Cement Containing Long Releasing Multi-Walled Carbon Nanotubes

被引:17
作者
Al Thaher, Yazan [1 ]
Khalil, Raida [2 ]
Abdelghany, Sharif [3 ]
Salem, Mutaz S. [1 ,4 ]
机构
[1] Philadelphia Univ, Fac Pharm, Amman 19392, Jordan
[2] Philadelphia Univ, Fac Sci, Dept Biotechnol & Genet Engn, Amman 19392, Jordan
[3] Univ Jordan, Sch Pharm, Amman 11942, Jordan
[4] Jordan Univ Sci & Technol, Fac Pharm, Irbid 22110, Jordan
关键词
PMMA; bone cement; carbon nanotubes; gentamicin; antimicrobial; cytotoxicity; compression strength; JOINT INFECTION; TOTAL HIP; IN-VITRO; GENTAMICIN; BIOCOMPATIBILITY; COMBINATION; COMPOSITES; DIAGNOSIS;
D O I
10.3390/nano12081381
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Prosthetic joint infections (PJIs) ensued from total joint replacement (TJR) pose a severe threat to patients that involve poor health outcomes, severe pain, death (in severe cases), and negative influence patients' quality of life. Antibiotic-loaded bone cement (ALBC) is frequently used for the prevention and treatment of PJI. This work aims to study gentamicin release from carbon nanotubes (CNTs) incorporated in polymethyl methacrylate (PMMA) bone cement to prolong release over several weeks to provide prophylaxis from PJIs after surgery. Different CNT concentrations were tested with the presence of gentamicin as a powder or preloaded onto carboxyl functionalized CNTs. The different types of bone cement were tested for drug release, mechanical properties, water uptake, antimicrobial properties, and cytocompatibility with human osteoblast cells (MTT, LDH, alizarin red, and morphology). Results showed prolonged release of gentamicin from CNT-loaded bone cements over several weeks compared to gentamicin-containing bone cement. Additionally, the presence of CNT enhanced the percentage of gentamicin released without adversely affecting the nanocomposite mechanical and antimicrobial properties needed for performance. Cytotoxicity testing showed non-inferior performance of the CNT-containing bone cement to the equivalent powder containing cement. Therefore, the developed nanocomposites may serve as a novel PMMA bone cement to prevent PJIs.
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页数:19
相关论文
共 54 条
[1]   Health-Related Quality of Life and Outcome after Total Knee Replacement: Results from a Cross-Sectional Survey in Jordan [J].
Al Thaher, Yazan ;
Alfuqaha, Othman A. ;
Dweidari, Ahmed .
ADVANCES IN ORTHOPEDICS, 2021, 2021
[2]   PMMA bone cement containing long releasing silica-based chlorhexidine nanocarriers [J].
Al Thaher, Yazan ;
Alotaibi, Hadil Faris ;
Yang, Lirong ;
Prokopovich, Polina .
PLOS ONE, 2021, 16 (09)
[3]   Tailored gentamicin release from silica nanocarriers coated with polyelectrolyte multilayers [J].
Al Thaher, Yazan .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2021, 614
[4]   LbL-assembled gentamicin delivery system for PMMA bone cements to prolong antimicrobial activity [J].
Al Thaher, Yazan ;
Yang, Lirong ;
Jones, Steve A. ;
Perni, Stefano ;
Prokopovich, Polina .
PLOS ONE, 2018, 13 (12)
[5]   Nano-carrier based drug delivery systems for sustained antimicrobial agent release from orthopaedic cementous material [J].
Al Thaher, Yazan ;
Perni, Stefano ;
Prokopovich, Polina .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2017, 249 :234-247
[6]  
Anagnostakos Konstantinos, 2017, J Bone Jt Infect, V2, P29, DOI 10.7150/jbji.16067
[7]  
[Anonymous], ISO 58332002 IMPLANT
[8]   Effects of environment on the creep properties of a poly(ethylmethacrylate) based bone cement [J].
Arnold, JC ;
Venditti, NP .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2001, 12 (08) :707-717
[9]   A novel liposomal drug delivery system for PMMA bone cements [J].
Ayre, Wayne Nishio ;
Birchall, James C. ;
Evans, Samuel L. ;
Denyer, Stephen P. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2016, 104 (08) :1510-1524
[10]   A new method for screening anti-infective biomaterials [J].
Bechert, T ;
Steinrücke, P ;
Guggenbichler, JP .
NATURE MEDICINE, 2000, 6 (09) :1053-1056