| Authors | سرور بخشی سیچانی,محمد رضا منصور نیا |
| Journal | Journal of Nanostructures |
| Page number | 756 |
| Volume number | 16 |
| IF | ثبت نشده |
| Paper Type | Full Paper |
| Published At | 2026-01-01 |
| Journal Grade | Scientific - research |
| Journal Type | Electronic |
| Journal Country | Iran, Islamic Republic Of |
| Journal Index | ISC ,JCR ,SCOPUS |
| Keywords | Ciprofloxacin, Drug release, Layered double hydroxide, Nanohybrid |
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Abstract
This research exhibits a novel approach to constructing the ZnAl layered double hydroxide (ZnAl-LDH) as a shell on the core of Fe3O4 nanoparticles, followed by the intercalation process of an antibiotic drug, ciprofloxacin (cip). Also, the advantages of the synthetic Fe3O4@ZnAl-LDH as a delivery agent model are investigated. The obtained biocompatible nanostructures were characterized by a range of techniques such as FT-IR, XRD, EDX, FE-SEM, and TGA. Based on the X-ray diffraction results, the increase in the interlayer space indicated successfully intercalation of cip (ZnAl-LDH-cip 95.87 % and Fe3O4@ZnAl-LDH-cip 94.48 %,). The surface morphology, examined by the scanning electron microscopy imaging, displayed the stacked sheets of LDH. In addition, the drug release properties, studied in PBS buffer (pH=7.4) at 37 °C, illustrated a sustained release profile. The great rates of 81.27 % and 82.43 %, were found after 24 h for ZnAl-LDH-cip and Fe3O4@ZnAl-LDH-cip, respectively. The studies showed that the as-synthesized Fe3O4@ZnAl-LDH can be used as an efficient nanocarrier in the targeted and controlled drug release systems.