Development of Novel Biocomposites with Antimicrobial-Activity-Based Magnesium-Doped Hydroxyapatite with Amoxicillin.

IF 4.3 2区 医学 Q1 INFECTIOUS DISEASES
Carmen Cimpeanu, Daniela Predoi, Carmen Steluta Ciobanu, Simona Liliana Iconaru, Krzysztof Rokosz, Mihai Valentin Predoi, Steinar Raaen, Monica Luminita Badea
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引用次数: 0

Abstract

Background/Objectives: A biocomposite based on magnesium-doped hydroxyapatite and enriched with amoxicillin (MgHApOx) was synthesized using the coprecipitation method and is presented here for the first time. Methods: The stability of MgHAp and MgHApOx suspensions was evaluated by ultrasound measurements. The structure of the synthesized MgHAp and MgHApOx was examined with X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The crystalline structure was determined by X-ray diffraction. The FTIR data were collected in the range of 4000-400 cm-1. The morphology of the nanoparticles was evaluated by scanning electron microscopy (SEM). Furthermore, the biocompatible properties of MgHAp, MgHApOx and amoxicillin (Ox) suspensions were assessed using human fetal osteoblastic cells (hFOB 1.19 cell line). The antimicrobial properties of the MgHAp, MgHApOx and Ox suspension nanoparticles were assessed using the standard reference microbial strains Staphylococcus aureus ATCC 25923, Escherichia coli ATCC 25922 and Candida albicans ATCC 10231. Results: X-ray studies have shown that the biocomposite retains the characteristics of HAp and amoxicillin. The SEM assessment exhibited that the apatite contains particles at nanometric scale with acicular flakes morphology. The XRD and SEM results exhibited crystalline nanoparticles. The average crystallite size calculated from XRD analysis increased from 15.31 nm for MgHAp to 17.79 nm in the case of the MgHApOx sample. The energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) analysis highlighted the presence of the constituent elements of MgHAp and amoxicillin. Moreover, XPS confirmed the substitution of Ca2+ ions with Mg2+ and the presence of amoxicillin constituents in the MgHAp lattice. The results of the in vitro antimicrobial assay demonstrated that MgHAp, MgHApOx and Ox suspensions exhibited good antimicrobial activity against the tested microbial strains. The results showed that the antimicrobial activity of the samples was influenced by the presence of the antibiotic and also by the incubation time. Conclusions: The findings from the biological assays indicate that MgHAp and MgHApOx are promising candidates for the development of new biocompatible and antimicrobial agents for biomedical applications.

开发基于阿莫西林的掺镁羟基磷灰石抗菌活性新型生物复合材料
背景/目的:本文首次采用共沉淀法合成了一种基于掺镁羟基磷灰石并富含阿莫西林的生物复合材料(MgHApOx)。方法:通过超声测量评估了 MgHAp 和 MgHApOx 悬浮液的稳定性。用 X 射线衍射 (XRD)、傅立叶变换红外光谱 (FT-IR) 和 X 射线光电子能谱 (XPS) 分析了合成的 MgHAp 和 MgHApOx 的结构。晶体结构是通过 X 射线衍射确定的。傅立叶变换红外光谱数据的采集范围为 4000-400 cm-1。扫描电子显微镜(SEM)对纳米颗粒的形态进行了评估。此外,还利用人体胎儿成骨细胞(hFOB 1.19 细胞系)评估了 MgHAp、MgHApOx 和阿莫西林(Ox)悬浮液的生物相容性。使用标准参考微生物菌株金黄色葡萄球菌 ATCC 25923、大肠杆菌 ATCC 25922 和白色念珠菌 ATCC 10231 评估了 MgHAp、MgHApOx 和 Ox 悬浮纳米粒子的抗菌特性。结果:X 射线研究表明,生物复合材料保留了 HAp 和阿莫西林的特性。扫描电子显微镜评估显示,磷灰石含有纳米级颗粒,形态为针状薄片。X 射线衍射和扫描电镜结果显示出结晶性纳米颗粒。XRD 分析计算出的平均结晶尺寸从 MgHAp 的 15.31 nm 增加到 MgHApOx 样品的 17.79 nm。能量色散 X 射线光谱(EDS)和 X 射线光电子能谱(XPS)分析显示了 MgHAp 和阿莫西林的组成元素。此外,XPS 证实了 MgHAp 晶格中 Ca2+ 离子与 Mg2+ 离子的置换以及阿莫西林成分的存在。体外抗菌试验结果表明,MgHAp、MgHApOx 和 Ox 悬浮液对受试微生物菌株具有良好的抗菌活性。结果表明,样品的抗菌活性受抗生素的存在和培养时间的影响。结论生物检测结果表明,MgHAp 和 MgHApOx 是开发生物医学应用领域新型生物相容性和抗菌剂的理想候选材料。
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来源期刊
Antibiotics-Basel
Antibiotics-Basel Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
7.30
自引率
14.60%
发文量
1547
审稿时长
11 weeks
期刊介绍: Antibiotics (ISSN 2079-6382) is an open access, peer reviewed journal on all aspects of antibiotics. Antibiotics is a multi-disciplinary journal encompassing the general fields of biochemistry, chemistry, genetics, microbiology and pharmacology. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers.
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