Shweqa Nada S, El-Naggar Noura El-Ahmady, Abdelmigid Hala M, Alyamani Amal A, Elshafey Naglaa, El-Shall Hadeel, Heikal Yasmin M, Soliman Hoda M
Botany Department, Faculty of Science, Mansoura University, Mansoura 35516, Egypt.
Department of Bioprocess Development, Genetic Engineering and Biotechnology Research Institute (GEBRI), City of Scientific Research and Technological Applications (SRTA-City), New Borg El Arab City 21934, Egypt.
J Funct Biomater. 2024 Nov 21;15(12):354. doi: 10.3390/jfb15120354.
Nanotechnological methods for creating multifunctional fabrics are attracting global interest. The incorporation of nanoparticles in the field of textiles enables the creation of multifunctional textiles exhibiting UV irradiation protection, antimicrobial properties, self-cleaning properties and photocatalytic. Nanomaterials-loaded textiles have many innovative applications in pharmaceuticals, sports, military the textile industry etc. This study details the biosynthesis and characterization of silver nanoparticles (AgNPs) using the aqueous mycelial-free filtrate of . The formation of AgNPs was indicated by a brown color in the extracellular filtrate and confirmed by UV-Vis spectroscopy with a peak at 426 nm. The Box-Behnken design (BBD) is used to optimize the physicochemical parameters affecting AgNPs biosynthesis. The desirability function was employed to theoretically predict the optimal conditions for the biosynthesis of AgNPs, which were subsequently experimentally validated. Through the desirability function, the optimal conditions for the maximum predicted value for the biosynthesized AgNPs (235.72 µg/mL) have been identified as follows: incubation time (58.12 h), initial pH (7.99), AgNO concentration (4.84 mM/mL), and temperature (34.84 °C). Under these conditions, the highest experimental value of AgNPs biosynthesis was 247.53 µg/mL. Model validation confirmed the great accuracy of the model predictions. Scanning electron microscopy (SEM) revealed spherical AgNPs measuring 8.93-19.11 nm, which was confirmed by transmission electron microscopy (TEM). Zeta potential analysis indicated a positive surface charge (+1.69 mV), implying good stability. X-ray diffraction (XRD) confirmed the crystalline nature, while energy-dispersive X-ray spectroscopy (EDX) verified elemental silver (49.61%). FTIR findings indicate the presence of phenols, proteins, alkanes, alkenes, aliphatic and aromatic amines, and alkyl groups which play significant roles in the reduction, capping, and stabilization of AgNPs. Cotton fabrics embedded with AgNPs biosynthesized using the aqueous mycelial-free filtrate of showed strong antimicrobial activity. The disc diffusion method revealed inhibition zones of 15, 12, and 17 mm against (Gram-negative), (Gram-positive), and (yeast), respectively. These fabrics have potential applications in protective clothing, packaging, and medical care. In silico modeling suggested that the predicted compound derived from AgNPs on cotton fabric could inhibit Penicillin-binding proteins (PBPs) and Lanosterol 14-alpha-demethylase (L-14α-DM), with binding energies of -4.7 and -5.2 Kcal/mol, respectively. Pharmacokinetic analysis and sensitizer prediction indicated that this compound merits further investigation.
用于制造多功能织物的纳米技术方法正引起全球关注。在纺织品领域引入纳米颗粒能够制造出具有紫外线辐射防护、抗菌性能、自清洁性能和光催化性能的多功能纺织品。负载纳米材料的纺织品在制药、体育、军事和纺织工业等领域有许多创新应用。本研究详细阐述了使用[具体菌种]的无菌丝体水相滤液生物合成和表征银纳米颗粒(AgNPs)的过程。细胞外滤液中出现棕色表明形成了AgNPs,并通过紫外可见光谱在426nm处有峰值得以确认。采用Box-Behnken设计(BBD)来优化影响AgNPs生物合成的物理化学参数。使用期望函数从理论上预测AgNPs生物合成的最佳条件,随后进行实验验证。通过期望函数,已确定生物合成AgNPs最大预测值(235.72μg/mL)的最佳条件如下:孵育时间(58.12小时)、初始pH(7.99)、AgNO浓度(4.84mM/mL)和温度(34.84°C)。在这些条件下,AgNPs生物合成的最高实验值为247.53μg/mL。模型验证证实了模型预测的高度准确性。扫描电子显微镜(SEM)显示球形AgNPs尺寸为8.93 - 19.11nm,透射电子显微镜(TEM)也证实了这一点。zeta电位分析表明表面带正电荷(+1.69mV),意味着稳定性良好。X射线衍射(XRD)证实了其晶体性质,而能量色散X射线光谱(EDX)验证了元素银的存在(49.61%)。傅里叶变换红外光谱(FTIR)结果表明存在酚类、蛋白质、烷烃、烯烃、脂肪族和芳香族胺以及烷基,它们在AgNPs的还原、封端和稳定化过程中发挥着重要作用。用[具体菌种]的无菌丝体水相滤液生物合成的AgNPs嵌入的棉织物表现出很强的抗菌活性。纸片扩散法显示对[革兰氏阴性菌名称]、[革兰氏阳性菌名称]和[酵母菌名称]的抑菌圈分别为15、12和17mm。这些织物在防护服、包装和医疗护理方面有潜在应用。计算机模拟表明,棉织物上源自AgNPs的预测化合物可抑制青霉素结合蛋白(PBPs)和羊毛甾醇14-α-脱甲基酶(L-14α-DM),结合能分别为-4.7和-5.2千卡/摩尔。药代动力学分析和致敏剂预测表明该化合物值得进一步研究。