de Juan Mora Blanca, Filipe Luís, Forte Andreia, Santos Miguel M, Alves Celso, Teodoro Fernando, Pedrosa Rui, Ribeiro Carrott Manuela, Branco Luís C, Gago Sandra
LAQV-REQUIMTE, Departamento de Química da Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, Campus da Caparica, 2829-516 Caparica, Portugal.
MARE-Marine and Environmental Sciences Centre, Politécnico de Leiria, Avenida Porto de Pesca, 2520-630 Peniche, Portugal.
Pharmaceutics. 2021 Feb 5;13(2):218. doi: 10.3390/pharmaceutics13020218.
Mesoporous silica nanoparticles (MSNs) are very promising nanomaterials for treating bacterial infections when combined with pharmaceutical drugs. Herein, we report the preparation of two nanomaterials based on the immobilization of ciprofloxacin in mesoporous silica nanoparticles, either as the counter-ion of the choline derivative cation (MSN-[Ch][Cip]) or via anchoring on the surface of amino-group modified MSNs via an amide bond (MSN-Cip). Both nanomaterials were characterized by TEM, FTIR and solution H NMR spectroscopies, elemental analysis, XRD and N adsorption at 77 K in order to provide the desired structures. No cytotoxicity from the prepared mesoporous nanoparticles on 3T3 murine fibroblasts was observed. The antimicrobial activity of the nanomaterials was determined against Gram-positive ( and ) and Gram-negative () bacteria and the results were promising against . In the case of , both nanomaterials exhibited higher antimicrobial activity than the precursor [Ch][Cip], and in the case of they exhibited higher activity than neutral ciprofloxacin.
介孔二氧化硅纳米颗粒(MSNs)与药物联合使用时,是治疗细菌感染非常有前景的纳米材料。在此,我们报告了两种基于将环丙沙星固定在介孔二氧化硅纳米颗粒中的纳米材料的制备方法,一种是作为胆碱衍生物阳离子的抗衡离子(MSN-[Ch][Cip]),另一种是通过酰胺键锚定在氨基修饰的MSN表面(MSN-Cip)。通过透射电子显微镜(TEM)、傅里叶变换红外光谱(FTIR)、溶液氢核磁共振光谱(¹H NMR)、元素分析、X射线衍射(XRD)和77 K下的氮吸附对这两种纳米材料进行了表征,以获得所需的结构。未观察到所制备的介孔纳米颗粒对3T3小鼠成纤维细胞有细胞毒性。测定了这些纳米材料对革兰氏阳性菌( 和 )和革兰氏阴性菌( )的抗菌活性,结果对 很有前景。在 的情况下,两种纳米材料均表现出比前体[Ch][Cip]更高的抗菌活性,而在 的情况下,它们表现出比中性环丙沙星更高的活性。