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Synthesis of iron oxide nanoparticles, characterization, applications as nanozyme, and future prospects 氧化铁纳米粒子的合成、表征、作为纳米酶的应用及前景
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2023-01-27 DOI: 10.1680/jbibn.21.00068
Fouzia Tanvir, Nimra Sadar, A. Yaqub, S. A. Ditta
Iron oxide nanoparticles (NPs) have recently attracted wider attention because of their unique properties, such as superparamagnetism, larger surface area, surface-to-volume ratio, and simple manufacturing process. Several chemical, physical, and biological techniques have been employed to synthesize NPs with admissible surface chemistry. This paper summarises the approaches for producing iron oxide NPs, shape, and size management, and inviting properties in bioengineering, pharmaceutical, and modern applications. Iron oxides have significant potential in biology, climate change, and horticulture, among other fields. Surface coatings with organic or inorganic particles are one of a kind. The surface coatings of the IONPs are critical to their performance because they prevent nanoparticle aggregation, reduce the risk of immunogenicity, and limit nonspecific cellular uptake. Chitosan is a biodegradable polymer that is applied to iron oxide nanoparticles to coat them. Chitosan subordinates like O-HTCC (an ammonium-quaternary CS subsidiary) have a long-lasting positive charge that allows them to work in different pH ranges allowing their interactions with cell layers at physiological pH. By reacting epoxy propyl trimethyl ammonium chloride (ETA) with chitosan (CS), the hydro-solvent N-(2-hydroxyl) propyl-3-trimethyl ammonium chitosan chloride (HTCC) is formed. For hyperthermic treatment of patients, NPs can also be coordinated to an organ, tissue, or tumor via an external attractive field. Given the increasing interest in iron NPs, the purpose of this review is to present data from iron oxide nanoparticles specially chitosan-capped iron NPs for different biomedical fields.
氧化铁纳米颗粒(NP)由于其独特的性质,如超顺磁性、更大的表面积、表体积比和简单的制造工艺,近年来引起了人们的广泛关注。已经采用了几种化学、物理和生物技术来合成具有容许表面化学性质的纳米颗粒。本文总结了氧化铁纳米颗粒的生产方法、形状和尺寸管理,以及在生物工程、制药和现代应用中的诱人特性。氧化铁在生物学、气候变化和园艺等领域具有巨大潜力。含有有机或无机颗粒的表面涂层是其中之一。IONP的表面涂层对其性能至关重要,因为它们可以防止纳米颗粒聚集,降低免疫原性风险,并限制非特异性细胞摄取。壳聚糖是一种可生物降解的聚合物,应用于氧化铁纳米颗粒上以包覆它们。壳聚糖的副产物,如O-HTCC(一种季铵CS副产物)具有持久的正电荷,使其能够在不同的pH范围内工作,从而在生理pH下与细胞层相互作用。通过环氧丙基三甲基氯化铵(ETA)与壳聚糖(CS)反应,形成水溶剂N-(2-羟基)丙基-3-三甲基氯化壳聚糖铵(HTCC)。对于患者的热疗,NP也可以通过外部吸引场与器官、组织或肿瘤协调。鉴于人们对铁纳米粒子越来越感兴趣,本综述的目的是提供用于不同生物医学领域的氧化铁纳米粒子(特别是壳聚糖封端的铁纳米粒子)的数据。
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引用次数: 2
In vitro and In vivo evaluation of clarithromycin solid dispersion prepared via spray drying technique 喷雾干燥法制备克拉霉素固体分散体的体外、体内评价
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2023-01-26 DOI: 10.1680/jbibn.21.00065
Sadia Pervez Lali, M. Sher, M. Hussain, A. Fatima, M. Naeem-ul-Hassan, Maqsood Ahmed, S. N. Bukhari
The aim of this study was to develop solid dispersions (SDs) of Clarithromycin (CLA) using hydrophilic polymer hydroxypropyl- methylcellulose (HPMC) and Xanthan Gum (XNG) as drug carrier. The in vitro dissolution study was performed in dissolution media of pH 6.8 and compared with that of standard drugs. In vivo pharmacokinetic studies were carried out on animal model (rabbits).The thermal behavior of each SDs formulation was studied by differential scanning calorimetry (DSC) analysis. The results concluded that crystalline nature of CLA has been transformed to amorphous form in SDs. Pharmacokinetic parameters were observed to be improved in HPMC as well as XNG based SDs than that of standard drugs. Additionally, powder X-ray diffraction (PXRD) analysis also confirmed the phase transition (crystalline to amorphous) of drug present in SDs. The higher values of Cmax, were found in case of HPMC based SDs, whereas, tmax values were prolonged in SDs based on XNG. Additionally, enhanced half-life values predicted that SDs would have potential to achieve once daily dose and improved patient compliance of drugs. Hence, the formulated SDs of poorly soluble drug, based on HPMC and XNG as carriers, exhibited more hydrophilic nature with enhanced aqueous solubility and therefore improved bioavailability as compared to that of standard drug.
本研究的目的是以亲水性聚合物羟丙基甲基纤维素(HPMC)和黄原胶(XNG)为药物载体,制备克拉霉素(CLA)的固体分散体。体外溶出度研究在pH 6.8的溶出介质中进行,并与标准药物的溶出度进行比较。在动物模型(兔)上进行了体内药代动力学研究。通过差示扫描量热法(DSC)分析研究了每种SDs制剂的热行为。结果表明,在SDs中,CLA的结晶性质已转变为无定形形式。观察到HPMC和基于XNG的SD的药代动力学参数比标准药物有所改善。此外,粉末X射线衍射(PXRD)分析也证实了SD中存在的药物的相变(结晶到无定形)。在基于HPMC的SD中发现Cmax值较高,而在基于XNG的SD中,tmax值延长。此外,半衰期值的提高预测了SDs将有可能实现每日一次的剂量,并提高患者的药物依从性。因此,与标准药物相比,基于HPMC和XNG作为载体的难溶性药物的配方SD表现出更亲水的性质,水溶性增强,从而提高了生物利用度。
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引用次数: 0
Microbial synthesis of nano-selenium and nano-titanium dioxide: mechanisms of selenite respiration 微生物合成纳米硒和纳米二氧化钛:亚硒酸盐呼吸机制
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2023-01-04 DOI: 10.1680/jbibn.21.00064
Sabere Nouri, Fatemeh Yousef-Saber, G. Emtiazi, N. Habibi
Background: The unique physicochemical properties of nano-metals compared to non-nano materials has led to many investigations in recent decades. Nano-Titanium dioxide has been chiefly applied in novel implant forms. In addition, the structures of Selenium-containing compounds play a critical role in the biological activity of these elements. According to recent studies, nano-Selenium is not only less toxic but also has higher biological activity than Selenium ions such as Se4+ and Se6+. Methods: Researchers have turned to green nano-structure synthesis due to drawbacks of chemical techniques. This article presents a literature review on recent advances in microbial synthesis methods to produce nano-Selenium and nano-Titanium dioxide. Results: Despite numerous research articles on green nanoparticle production, little information has been provided on the microbial formation of Titanium and Selenium nanoparticles. This review article focuses on the possible mechanism of nano-Selenium production by Selenium respiration. Although there are reports of microbial synthesis of these particles, their production by probiotic bacteria is of great value. Conclusion: Considering the compatibility of probiotic bacteria with the immune system and their tremendous applications in medicine, it is suggested to use them in combination with nano-Titanium dioxide and nano-Selenium for various ends such as implant scaffolds and food additives, respectively.
背景:近几十年来,与非纳米材料相比,纳米金属独特的物理化学性质引起了许多研究。纳米二氧化钛主要应用于新型植入物。此外,含硒化合物的结构在这些元素的生物活性中起着关键作用。根据最近的研究,纳米硒不仅毒性较小,而且比Se4+和Se6+等硒离子具有更高的生物活性。方法:由于化学技术的缺陷,研究人员已转向绿色纳米结构合成。本文综述了近年来微生物合成纳米硒和纳米二氧化钛的研究进展。结果:尽管有许多关于绿色纳米颗粒生产的研究文章,但很少提供关于钛和硒纳米颗粒的微生物形成的信息。本文综述了硒呼吸产生纳米硒的可能机制。尽管有关于这些颗粒的微生物合成的报道,但益生菌生产这些颗粒具有很大的价值。结论:考虑到益生菌与免疫系统的兼容性及其在医学上的巨大应用,建议将其与纳米二氧化钛和纳米硒分别用于植入支架和食品添加剂等不同用途。
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引用次数: 0
A strong system of magnetic nanocatalysts in absorbing and releasing ampicillin along with its antibacterial properties 一个强大的磁性纳米催化剂系统吸收和释放氨苄西林及其抗菌性能
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2022-12-07 DOI: 10.1680/jbibn.21.00066
M. Binandeh
Background: Magnetic nanoparticles are the main source of synthesis and design of magnetic nanocatalysts, which are obtained from iron salts by chemical co-precipitation method. Objective: The main goal of this research is to investigate the absorption, release and antibacterial properties of magnetic nanocatalysts with silica coating and silica/amine linker. Methods: The structure of the obtained nanocatalyst is detected by several analyzes such as SEM, TEM, EDX and IR. Results: Here is reaction between the ampicillin 10 µl (25 µg/ml) and the Fe3O4@SiO2 and Fe3O4@SiO2/NH magnetic nanocatalyst 200 mg (2 mole%), under 25°C and double distilled water. In this way, the amount of absorbed ampicillin on MNPs@silica/amine structure in covalent is more than MNPs@silica structure in non-covalent bonding, i.e. 85 to 65%, but the rate of release in non-covalent is above 90%, but in covalent is less than 80%. Also, the bactericidal properties of nanocatalysts have been tested separately at a temperature of 37 degrees for the non-covalent type are more than 80% compared to Covalance form is 70%. Conclusions: The overall result was that the percentage efficiency of the absorption/release reaction in the non-covalent bonding state was much better and about 10% more release.
背景:磁性纳米颗粒是合成和设计磁性纳米催化剂的主要来源,它是由铁盐通过化学共沉淀法获得的。目的:本研究的主要目的是研究具有二氧化硅涂层和二氧化硅/胺连接体的磁性纳米催化剂的吸收、释放和抗菌性能。方法:采用扫描电镜、透射电镜、能谱仪、红外光谱等分析手段对所得纳米催化剂的结构进行了表征 µl(25 µg/ml)和Fe3O4@SiO2和Fe3O4@SiO2/NH磁性纳米催化剂200 毫克(2 摩尔%),在25°C和双蒸馏水下。通过这种方式,对氨苄青霉素的吸收量MNPs@silica/共价胺结构超过MNPs@silica非共价键中的结构,即85%至65%,但非共价键的释放率在90%以上,但共价键的小于80%。此外,已经在37度的温度下单独测试了纳米催化剂的杀菌性能,与Covalance形式的70%相比,非共价型的杀菌性能超过80%。结论:总的结果是,在非共价键状态下的吸收/释放反应的百分比效率要好得多,释放率高出约10%。
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引用次数: 1
Apoptotic-based topotecan-loaded superparamagnetic drug delivery system: an in vitro study in MCF7 基于凋亡的拓扑替康超顺磁性给药系统:MCF7的体外研究
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2022-11-07 DOI: 10.1680/jbibn.21.00053
Niyousha Yazdanmehr, M. Tajabadi, R. Bigdeli, Hanif Goran Orimi, V. Asgary
Biological barriers could be overcome using nano-biotechnology, which promotes the development of nanomaterial-based delivery systems. The primary objective of the present investigation focuses on superparamagnetic iron oxide nanoparticle (SPION) production for the delivery of topotecan to human breast cancer cells (MCF-7). The XRD results confirm the formation of pure SPION. The FTIR spectra indicate the functional groups related to aminopropyl trimethoxy silane (APTS) as a coating agent and topotecan. Topotecan-loaded magnetite nanoparticles with an IC50 of approximately 156 µg/mL exhibited dose-dependent cytotoxicity. The PCR method also proved that, in the mentioned cell line, topotecan-loaded SPION could increase the Bax/Bcl2 ratio and P53 gene expression. Annexin V/PI detection assay was done in order to detect the induction of apoptosis. According to the results, the nanoparticles inhibitively influence the survival of the MCF-7 breast cancer cells via boosting apoptosis, which helps to slow the growth of tumor cells.
使用纳米生物技术可以克服生物障碍,这促进了基于纳米材料的递送系统的发展。本研究的主要目的集中于超顺磁性氧化铁纳米颗粒(SPION)的生产,用于将拓扑替康递送至人类乳腺癌症细胞(MCF-7)。XRD结果证实了纯SPION的形成。FTIR光谱显示了与氨基丙基三甲氧基硅烷(APTS)作为涂层剂和拓扑替康相关的官能团。拓扑替康负载的磁铁矿纳米颗粒,IC50约为156 µg/mL表现出剂量依赖性细胞毒性。PCR方法还证明,在上述细胞系中,拓扑替康负载的SPION可以提高Bax/Bcl2比率和P53基因的表达。采用膜联蛋白V/PI检测法检测细胞凋亡的诱导作用。根据研究结果,纳米颗粒通过促进细胞凋亡来抑制MCF-7乳腺癌症细胞的存活,这有助于减缓肿瘤细胞的生长。
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引用次数: 0
Biologically inspired innovation: a review on structural materials and manufacturing methods 生物启发的创新:结构材料和制造方法综述
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2022-11-03 DOI: 10.1680/jbibn.22.00027
Melissa Anahí Olvera Carreño, E. N. A. Mireles, E. Rocha-Rangel
Several natural materials have demonstrated excellent mechanical performance by using abundant resources and friendly chemistry. Additionally, these materials have evolved to optimize weight and maximize strength and energy absorption at the macro, micro, and nanostructural level. Likewise, engineers still face challenges regarding the same issues. Therefore, this paper aims to identify current literature on structural materials and their manufacturing methods. In this sense, a review was conducted to assess this extent in local databases through a research question and boolean operators. Results were classified into four main categories: plastic, metals, ceramic-composite materials, and organism-oriented structural materials, and their mechanical properties (energy absorption, fracture toughness, stiffness) were discussed. The results of this study can be generalized and easily comprehended by scientists, innovators, researchers, and the general public. This review contains structural materials where mechanical properties enhancement is of vital importance. Finally, this study illustrates how bio-inspiration provides a powerful tool to tune mechanical properties in diverse materials through structural arrangement and no significant modification to constituent materials composition. Likewise, it addresses trends in manufacturing processing routes and their scalability to drive further innovation within the field.
多种天然材料利用丰富的资源和友好的化学反应表现出优异的力学性能。此外,这些材料已经在宏观、微观和纳米结构水平上优化了重量,最大限度地提高了强度和能量吸收。同样,工程师们仍然面临着同样问题的挑战。因此,本文旨在确定当前的文献结构材料及其制造方法。在这个意义上,通过一个研究问题和布尔运算符,在本地数据库中进行了一次审查,以评估这种程度。将研究结果分为塑料、金属、陶瓷复合材料和生物取向结构材料四大类,并对其力学性能(吸能、断裂韧性、刚度)进行了讨论。这项研究的结果可以被科学家、革新者、研究人员和一般公众概括和容易理解。这篇综述包含了机械性能增强至关重要的结构材料。最后,本研究说明了生物灵感如何通过结构安排而不显着改变组成材料的成分,为调整不同材料的机械性能提供了强大的工具。同样,它解决了制造加工路线的趋势及其可扩展性,以推动该领域的进一步创新。
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引用次数: 1
Increased chemical stabilities of well-dispersed hydroxyapatite (HAp) powders prepared by calcination of HAp-β-cyclodextrin-methylene blue@carbon 煅烧羟基磷灰石-β-环糊精-亚甲基制备的高分散羟基磷灰石(HAp)粉末的化学稳定性blue@carbon
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2022-10-26 DOI: 10.1680/jbibn.21.00011
Kaijie Zhang, Xiangyu Zhang, Haibin Sun, Xiaowei Li, J. Bai, Qingyang Du, Chengfeng Li
Biocompatible hydroxyapatite (HAp) powders have thermodynamically driven tendencies to lower their surface areas due to the formation of irreversible aggregations. To address this challenge, HAp hybrid powders are herein prepared by a traditional wet-precipitation method with subsequent hydrothermal carbonization for surface modification. The crystallite size, crystallite degree and area ratio of the infrared peak assigned to bonding water versus that of free water are determined to investigate the variation of HAp crystallization with processing parameters. The crystallization of HAp is facilitated by enriched water in a stealth layer with water molecules evolved by citrate, N-contained methylene blue (MB), hydrogen groups-rich β-cyclodextrin (CD) and oxygen-contained organic carbon shells. The low surface areas result in fabrication of nano-sized HAp powders with uniform size distribution, well-dispersed morphologies and smooth surfaces through calcination of HAp-CD-MB@C. The pH values of acidic buffers increase slowly during incubation of HAp-CD-MB@C powders with chemical stability and large grain size after calcination at 550°C for 2 h. The present study will shed light on the preparation of nano-sized inorganic powders with uniform size distribution, well-dispersed morphologies and modulated chemical stabilities for their potential applications as carries of small molecular substances and fillers in composite materials.
生物相容性羟基磷灰石(HAp)粉末由于形成不可逆的聚集体而具有降低其表面积的热力学驱动趋势。为了应对这一挑战,本文通过传统的湿法沉淀方法制备了HAp杂化粉末,随后进行水热碳化以进行表面改性。测定了键合水红外峰与游离水红外峰的晶粒尺寸、晶粒度和面积比,以研究HAp结晶随工艺参数的变化。HAp的结晶是由柠檬酸盐、含氮亚甲基蓝(MB)、富含氢基团的β-环糊精(CD)和含氧有机碳壳形成的水分子在隐形层中富集的水促进的。低表面积导致通过煅烧HAp-CD-MB@C.酸性缓冲液的pH值在培养过程中缓慢增加HAp-CD-MB@C在550°C下煅烧2小时后具有化学稳定性和大晶粒度的粉末 h.本研究将阐明具有均匀尺寸分布、良好分散形态和调节化学稳定性的纳米无机粉末的制备,以及它们作为小分子物质载体和填料在复合材料中的潜在应用。
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引用次数: 0
A silver nanoparticle-based chemosensor for optical detection of captopril in pharmaceutical preparations 一种用于药物制剂中卡托普利光学检测的银纳米粒子化学传感器
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2022-09-23 DOI: 10.1680/jbibn.21.00056
F. Bamdad, Farnaz Kazemzadeh
Captopril is an angiotensin-converting enzyme commonly used to treat high blood pressure and to improve survival after a heart attack. Considering the importance of the assay of this drug, we have proposed a simple and cost-effective colorimetric technique for the quantitative determination of it. The detection strategy was based on the redshift of the surface plasmon resonance band of silver nanoparticles (AgNps) induced by the action of captopril molecules. Under optimal experimental conditions, the interaction of AgNPs with captopril molecules in the presence of barium ions motivates the aggregation of AgNPs. The final result of this process is an observable change in the color of the tested solution from pale yellow to light brown. Our experiments showed that there is a linear relationship between the absorbance of AgNps solution and captopril concentration at about 720 nm, thus it is possible to assay the captopril amount just by measuring the absorbance of the examined solution at this wavelength. The calibration curve was linear in the range of 1.0 to 6.0 μM captopril with a detection limit equal to 0.4 μM. The proposed strategy was successfully applied to the determination of captopril in pharmaceutical preparations.
卡托普利是一种血管紧张素转换酶,通常用于治疗高血压和提高心脏病发作后的生存率。考虑到该药物测定的重要性,我们提出了一种简单、经济的比色法定量测定该药物的方法。检测策略是基于卡托普利分子作用下银纳米粒子表面等离子体共振带的红移。在最佳实验条件下,在钡离子存在下AgNPs与卡托普利分子相互作用激发AgNPs聚集。这个过程的最终结果是可观察到被测溶液的颜色从淡黄色变为浅棕色。我们的实验表明,AgNps溶液的吸光度与卡托普利浓度在720 nm左右存在线性关系,因此可以通过测量被测溶液在该波长的吸光度来测定卡托普利的量。卡托普利浓度在1.0 ~ 6.0 μM范围内线性良好,检出限为0.4 μM。该方法成功地应用于药物制剂中卡托普利的含量测定。
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引用次数: 0
Dexamethasone encapsulated PLGA nanoparticles as drug delivery vehicle for the treatment of neuroinflammation 地塞米松包封PLGA纳米颗粒作为给药载体治疗神经炎症
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2022-09-23 DOI: 10.1680/jbibn.21.00059
B. J. Stephen, Ankit Chokriwal, M. Sharma, D. Jain, J. Saxena, Harshdeep Dhaliwal, Vikram Sharma, Rajeev Mishra, Ramandeep Kaur, Abhijeet Singh
Neuroinflammation is a condition that contribute significantly to the pathogenesis and progression of several neurodegenerative disorders. Targeting neuroinflammation is a novel therapeutic approach for the treatment of these disorders. Dexamethasone is a steroidal based anti-inflammatory drug with the potential to treat neuroinflammation. However, in order to maintain the efficacy of the drug, dexamethasone needs to be coupled with an effective drug delivery vehicle to be able to be transported across Central Nervous System. PLGA nanoparticles has been used as drug delivery vehicles for transport of drugs into the central nervous system. The article describes the preparation and encapsulation of dexamethasone loaded PLGA nanoparticles by solvent evaporation method. Statistical Experimental Design approach was performed, wherein Response Surface Methodology was carried out to optimize the parameters associated with synthesis process. Further, kinetic modeling and drug release profile were also determined. The drug encapsulated nanoparticles were validated for its effectiveness in vitro. Toxicity studies revealed the nanodrug to be non-cytotoxic and Griess assay highlighted its ability to lower neuroinflammation. Further, genetic studies revealed the anti-inflammatory properties of the nanodrug was successfully in modulating neuroinflammation.
神经炎症是一种对几种神经退行性疾病的发病和进展起重要作用的疾病。靶向神经炎症是治疗这些疾病的一种新的治疗方法。地塞米松是一种基于甾体的抗炎药,具有治疗神经炎症的潜力。然而,为了保持药物的有效性,地塞米松需要与有效的药物递送载体相结合,以便能够通过中枢神经系统运输。PLGA纳米颗粒已被用作药物递送载体,用于将药物运输到中枢神经系统。采用溶剂蒸发法制备了负载地塞米松的聚乳酸纳米颗粒。采用统计实验设计方法,采用响应面法对合成工艺参数进行优化。此外,动力学建模和药物释放谱也被确定。体外验证了药物包封纳米颗粒的有效性。毒性研究显示纳米药物无细胞毒性,Griess试验强调其降低神经炎症的能力。此外,遗传研究表明,纳米药物的抗炎特性成功地调节了神经炎症。
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引用次数: 0
Investigation of antibacterial activity of new bionanocomposite based on polyvinyl alcohol(PVA)/arabic gum(AG)/MgO nanoparticles by Taguchi design for mouthwash application 田口设计聚乙烯醇(PVA)/阿拉伯胶(AG)/MgO纳米颗粒生物纳米复合材料漱口水抗菌性能研究
4区 工程技术 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2022-08-11 DOI: 10.1680/jbibn.21.00035
Mohammad Salmani Mobarakeh, A. Moghadam
Untreated dental caries is an important word challenge in human life. In this work, we synthesized polyvinyl alcohol-gum arabic-magnesium oxide nanoparticles new bionanocomposite and evaluated the antibacterial properties of its against Streptococcus mutans biofilm in vitro. For optimization of variables to have the maximum antibacterial property, L9 orthogonal array of Taguchi method was used for design of extraction conditions. The nanocomposites were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), X-ray energy diffraction (EDS), Thermogravimetric analysis (TGA) and transmission electron microscopy (TEM) tests. The FESEM images of nanocomposite inhibit that the nanoparticles are entirely surrounded with polymers chains of matrix and nanoparticles are deposited on the its walls, thus a layered nanocomposite is formed. The sheet width and size range of the nanocomposite was determined between 30-40 and 20-90 nm, respectively. The results showed that the synthesized nanocomposite with conditions of 1 mg/ml PVA, 3 mg/ml AG, and 6 mg/ml MgO (experiment 3), had the strongest antibacterial activity against the Streptococcus mutans bacteria’s biofilm. In this condition, the bacterial survival rate was the lowest at 0.21 CFU/ml and under this optimal conditions could inhibit the activity of Streptococcus mutans bacteria at a rate of 0.09 CFU/ml.
未经治疗的龋齿是人类生活中的一个重要挑战。本工作合成了聚乙烯醇-阿拉伯树胶-氧化镁纳米复合材料,并对其对变形链球菌生物膜的体外抗菌性能进行了评价。为了优化具有最大抗菌性能的变量,采用田口法L9正交阵列设计了提取条件。通过X射线衍射(XRD)、场发射扫描电子显微镜(FESEM)、X射线能量衍射(EDS)、热重分析(TGA)和透射电子显微镜(TEM)测试对纳米复合材料进行了表征。纳米复合材料的FESEM图像抑制了纳米颗粒完全被基质的聚合物链包围,纳米颗粒沉积在其壁上,从而形成了层状纳米复合材料。纳米复合材料的片宽和尺寸范围在30-40和20-90之间确定 nm。结果表明,在1 mg/ml PVA,3 mg/ml AG和6 mg/ml MgO(实验3)对变形链球菌的生物膜具有最强的抗菌活性。在这种情况下,细菌存活率最低,为0.21 CFU/ml,在该最佳条件下对变形链球菌的抑制率为0.09 CFU/ml。
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引用次数: 0
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