Advances in antimicrobial orthopaedic devices and FDA regulatory challenges

被引:3
作者
Kazemzadeh-Narbat, Mehdi [1 ]
Memic, Asija [2 ]
McGowan, Kevin B. [1 ]
Memic, Adnan [3 ,4 ]
Tamayol, Ali [4 ]
机构
[1] MCRA LLC, 803 7th St NW, Washington, DC 20001 USA
[2] Wayne State Univ, Coll Nursing, Detroit, MI 48202 USA
[3] King Abdulaziz Univ, Ctr Nanotechnol, Jeddah 21589, Saudi Arabia
[4] Univ Connecticut Hlth Ctr, Dept Biomed Engn, Farmington, CT 06030 USA
来源
PROGRESS IN BIOMEDICAL ENGINEERING | 2024年 / 6卷 / 03期
关键词
antimicrobial; antibacterial; orthopaedic implant; FDA; regulatory processes; BACTERICIDAL ACTIVITY; GECKO SKIN; SURFACES; SILVER; WETTABILITY; INFECTION; TITANIUM; BIOFILM; RELEASE; LEAVES;
D O I
10.1088/2516-1091/ad5cb1
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Implant-associated infections, caused by the formation of biofilms especially antibiotic resistant organisms, are among the leading causes of orthopaedic implant failure. Current strategies to combat infection and biofilm focus on either inhibiting bacterial growth or preventing bacterial adherence that could lead to biofilm creation. Despite research on developing numerous antimicrobial orthopaedic devices, to date, no robust solution has been translated to the clinic. One of the key bottlenecks is the disconnect between researchers and regulatory agencies. In this review, we outline recent strategies for minimizing orthopaedic implant-associated infections. In addition, we discuss the relevant Food and Drug Administration regulatory perspectives, challenges. We also highlight emerging technologies and the directions the field that is expected to expand. We discuss in depth challenges that include identifying strategies that render implants antibacterial permanently or for a long period of time without the use of antimicrobial compounds that could generate resistance in pathogens and negatively impact osseointegration.
引用
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页数:18
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