Andrea Campostrini , Elena Ghedini , Teresa Botrè , Sabrina Manente , Alessia Giordana , Giuseppina Cerrato , Giuseppe Cruciani , Alex W. Robertson , Michela Signoretto , Federica Menegazzo
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Specifically, the silica nanoparticles were modified with sulphonic groups to functionalize the silica structure and its interaction with the antimicrobial compound, thereby aiming to regulate its release. Microbiological tests were conducted to determine Biotin T ® antimicrobial activity at low concentrations. The nanomaterials were characterized by N<sub>2</sub> physisorption, XRD, TPO, TG/TDA, Raman IR/ATR spectroscopy, SEM, EDS, and HR-TEM, whereas Biotin T ® release was studied through UV spectroscopy. The functionalized silica nanoparticle-based matrix can encapsulate and gradually release the commercial biocidal. 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引用次数: 0
摘要
虽然科学界日益认识到保护具有重要文化意义的材料的重要性,但它仍然与传统 做法和小型手工艺公司的经验知识密切相关。这些程序通常非常有效,但是,尤其是在处理生物降解现象时,它们往往跟不上最新的科学创新,因此并不总是考虑到其使用对环境的影响。MCM-41 硅基纳米粒子被用作纳米容器,用于封装并在随后释放抗菌剂生物素 T ®。具体来说,用磺酸基团对二氧化硅纳米颗粒进行改性,使二氧化硅结构功能化,并使其与抗菌剂化合物相互作用,从而达到调节其释放的目的。为了确定生物素 T ® 在低浓度下的抗菌活性,对其进行了微生物测试。纳米材料的表征方法包括 N2 物理吸附、XRD、TPO、TG/TDA、拉曼 IR/ATR 光谱、SEM、EDS 和 HR-TEM,而生物素 T ® 的释放则通过紫外光谱进行研究。基于功能化二氧化硅纳米颗粒的基质可以封装并逐渐释放商用杀菌剂。其中两种基质(MCM-41 和 MCM-SO3H)在功能化后表现出不同的特性,两者都保持了原有结构,但与抗菌产品的相互作用更强。
Engineered silica NPs to hold and release the antimicrobial product Biotin T ®
While the preservation of culturally significant materials is increasingly recognized as important within the scientific community, it remains closely tied to traditional practices and the empiric knowledge of small handicraft companies. These procedures are usually highly effective, but, especially when dealing with biological degradation phenomena, they are often not updated to the latest scientific innovations and hence do not always consider the impact of their use on the environment. MCM-41 silica-based nanoparticles were employed as nanocontainers to encapsulate and later release the antimicrobial agent Biotin T ®. Specifically, the silica nanoparticles were modified with sulphonic groups to functionalize the silica structure and its interaction with the antimicrobial compound, thereby aiming to regulate its release. Microbiological tests were conducted to determine Biotin T ® antimicrobial activity at low concentrations. The nanomaterials were characterized by N2 physisorption, XRD, TPO, TG/TDA, Raman IR/ATR spectroscopy, SEM, EDS, and HR-TEM, whereas Biotin T ® release was studied through UV spectroscopy. The functionalized silica nanoparticle-based matrix can encapsulate and gradually release the commercial biocidal. Two of the matrices, MCM-41 and MCM-SO3H, exhibited different properties after functionalization, with both maintaining the original structure but leading to a higher interaction with the antimicrobial product.