Valliammai Alaguvel, Selvaraj Anthonymuthu, Mathumitha Poobalan, Aravindraja Chairmandurai, Pandian Shunmugiah Karutha
Department of Biotechnology, Alagappa University, Science Campus, Karaikudi 630003, Tamil Nadu, India.
Department of Biotechnology, Alagappa University, Science Campus, Karaikudi 630003, Tamil Nadu, India; Department of Periodontology, College of Dentistry, University of Florida, Gainesville, FL, USA.
Mater Sci Eng C Mater Biol Appl. 2021 Feb;121:111863. doi: 10.1016/j.msec.2021.111863. Epub 2021 Jan 7.
Biomaterial associated microbial infections are complicated and mostly lead to revision surgery or removal which are painful to the patients and quite expensive. These infections are difficult to treat with antibiotics as it is often related to biofilm formation. Methicillin resistant Staphylococcus aureus (MRSA) is the leading pathogen in biomaterial associated infections and well known to form biofilm on foreign materials. To reduce the risk of biomaterial associated infections, recent treatment strategies focus on modification of the implant surface to prevent the adhesion of bacteria. Antibiofilm coating is the effective approach than coating with antimicrobials as antibiofilm agents will not create selective pressure thereby excludes possibility of drug resistance. The current study identified and validated the synergistic antibiofilm activity of citral (CIT) and thymol (THY) by crystal violet quantification and microscopic analysis without alteration in growth and metabolic viability of MRSA. Polymeric antibiofilm coating with CIT + THY as active ingredients was formulated and coated on titanium surface by the process of spin coating. Fourier-transform infrared spectroscopy (FTIR) analysis confirmed the effective blending of polymeric formulation and the presence of CIT and THY. Atomic force microscopy (AFM) images revealed the homogenous coating and reduced surface roughness and thickness of the coating was measured by surface profilometer. Antibiofilm coating released CIT and THY in a sustained manner for 60 days. Antibiofilm coating effectively inhibited MRSA adherence in vitro and antibiofilm activity of coating was not affected by plasma conditioning. In addition, antibiofilm coating was non-hemolytic and non-toxic to PBMC. Thus, the current study demonstrated the effectual strategy to prevent biomaterial associated infections and proposes the prospective role of antibiofilm coating in clinical applications.
生物材料相关的微生物感染情况复杂,大多会导致翻修手术或移除,这对患者来说很痛苦且费用高昂。这些感染难以用抗生素治疗,因为其通常与生物膜形成有关。耐甲氧西林金黄色葡萄球菌(MRSA)是生物材料相关感染中的主要病原体,并且众所周知它会在异物上形成生物膜。为降低生物材料相关感染的风险,近期的治疗策略集中在对植入物表面进行改性以防止细菌黏附。抗生物膜涂层是比抗菌涂层更有效的方法,因为抗生物膜剂不会产生选择压力,从而排除了耐药性的可能性。本研究通过结晶紫定量和显微镜分析鉴定并验证了柠檬醛(CIT)和百里香酚(THY)的协同抗生物膜活性,且未改变MRSA的生长和代谢活力。以CIT + THY作为活性成分制备了聚合物抗生物膜涂层,并通过旋涂工艺涂覆在钛表面。傅里叶变换红外光谱(FTIR)分析证实了聚合物配方的有效混合以及CIT和THY的存在。原子力显微镜(AFM)图像显示涂层均匀,表面轮廓仪测量了涂层的表面粗糙度降低且涂层厚度减小。抗生物膜涂层持续60天释放CIT和THY。抗生物膜涂层在体外有效抑制MRSA黏附,且涂层的抗生物膜活性不受等离子体处理的影响。此外,抗生物膜涂层对PBMC无溶血和无毒作用。因此,本研究证明了预防生物材料相关感染的有效策略,并提出了抗生物膜涂层在临床应用中的潜在作用。