Department of Conservative Dentistry, Jena University Hospital, Friedrich-Schiller-Universität Jena, Germany.
Dent Mater. 2012 Feb;28(2):179-88. doi: 10.1016/j.dental.2011.12.006. Epub 2012 Jan 4.
We aimed to achieve detailed biomaterials characterization of a drug delivery system for local periodontitis treatment based on electrospun metronidazole-loaded resorbable polylactide (PLA) fibers.
PLA fibers loaded with 0.1-40% (w/w) MNA were electrospun and were characterized by SEM and DSC. HPLC techniques were used to analyze the release profiles of metronidazole (MNA) from these fibers. The antibacterial efficacy was determined by measuring inhibition zones of drug-containing aliquots from the same electrospun fiber mats in an agar diffusion test. Three pathogenic periodontal bacterial strains: Fusobacterium nucleatum, Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis were studied. Cytotoxicity testing was performed with human gingival fibroblasts by: (i) counting viable cells via live/dead staining methods and (ii) by exposing cells directly onto the surface of MNA-loaded fibers.
MNA concentration influenced fiber diameters and thus w/w surface areas: diameter being minimal and area maximal at 20% MNA. HPLC showed that these 20% MNA fibers had the fastest initial MNA release. From the third day, MNA release was slower and nearly linear with time. All fiber mats released 32-48% of their total drug content within the first 7 days. Aliquots of media taken from the fiber mats inhibited the growth of all three bacterial strains. MNA released up to the 28th day from fiber mats containing 40% MNA significantly decreased the viability of F. nucleatum and P. gingivalis and up to the 2nd day also for the resistant A. actinomycetemcomitans. All of the investigated fibers and aliquots showed excellent cytocompatibility.
This study shows that MNA-loaded electrospun fiber mats represent an interesting class of resorbable drug delivery systems. Sustained drug release properties and cytocompatibility suggest their potential clinical applicability for the treatment of periodontal diseases.
我们旨在对局部牙周炎治疗用载药可吸收聚乳酸(PLA)纤维进行详细的生物材料特性分析,该载药系统基于米诺环素(MNA)的电纺。
载有 0.1-40%(w/w)MNA 的 PLA 纤维进行电纺,通过 SEM 和 DSC 进行表征。HPLC 技术用于分析这些纤维中米诺环素(MNA)的释放曲线。通过琼脂扩散试验,测量来自同一电纺纤维垫的含药部分的抑菌圈,来确定抗菌功效。研究了三种牙周病致病菌:产黑色素普氏菌、伴放线放线杆菌和牙龈卟啉单胞菌。通过:(i)通过活/死染色方法对细胞进行计数和(ii)直接将细胞暴露在载 MNA 纤维表面,对人牙龈成纤维细胞进行细胞毒性测试。
MNA 浓度影响纤维直径,从而影响 w/w 表面积:在 20% MNA 时,直径最小,面积最大。HPLC 显示,这些 20% MNA 纤维具有最快的初始 MNA 释放速度。从第三天开始,MNA 释放速度较慢,几乎呈线性随时间变化。所有纤维垫在最初的 7 天内释放了 32-48%的总药物含量。从纤维垫中取出的介质部分抑制了所有三种细菌的生长。在含有 40%MNA 的纤维垫中,MNA 释放到第 28 天显著降低了产黑色素普氏菌和牙龈卟啉单胞菌的活力,并且在第 2 天,也显著降低了耐药伴放线放线杆菌的活力。所有研究的纤维和介质部分均表现出良好的细胞相容性。
本研究表明,载 MNA 的电纺纤维垫代表了一类有前途的可吸收药物输送系统。持续的药物释放特性和细胞相容性表明,它们在牙周病治疗方面具有潜在的临床应用价值。