Ogungbesan Shephrah Olubusola, Zhou Chao, Kalulu Mulenga, Anselm Oluwaseun Hannah, Ogunneye Adeyemi Lawrence, Adedokun Rosemary Anwuli, Díaz Díaz David, Fu Guodong
School of Chemistry and Chemical Engineering, Southeast University, 2 Southeast University Road, Nanjing, 211189, P. R. China.
Institute of Biomedical Engineering and Health Sciences, Changzhou University, Changzhou, 213164, Jiangsu, China.
Chemphyschem. 2025 Jun 23;26(12):e202400987. doi: 10.1002/cphc.202400987. Epub 2025 Apr 10.
Despite the known nontoxicity, stability, and efficiency of WO and MoO against microbes as a result of their catalytic activities, these oxides are not effective photocatalysts because the O absorbed cannot be reduced by the photogenerated electrons in their conduction band, which leads to the rebinding of electrons and holes on the surface. The doping of these two n-type semiconductor metal oxides and incorporation of a biocompatible, biodegradable, and bioavailable polymer (such as chitosan) to form a film, to a large extent, affects the surface area interaction and multipurpose applicability of the film as a therapeutic, controlled delivery, and dual sensitive material. The WO-NP and WOMoO nanocomposites are synthesized via a deep eutectic solvent-assisted hydrothermal-based method, which afford fine-sized nanoparticles and nanocomposites, which are further incorporated into a chitosan matrix to form nanohybrid films via the solvent casting method. The structural, optical, and morphological characterization of the materials is carried out via X-ray diffraction (XRD), Fourier transform infrared (FT-IR), UV, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and dynamic light scattering. XRD and FT-IR analyses reveal that WOMoO nanocomposites are successfully formed and incorporated into the chitosan matrix. The nanohybrid film shows antimicrobial activity with a minimum inhibitory concentration of 100 μg mL. Furthermore, the nanohybrid film shows no significant toxicity.
尽管由于其催化活性,氧化钨(WO)和氧化钼(MoO)对微生物具有已知的无毒、稳定和高效性,但这些氧化物并不是有效的光催化剂,因为所吸附的氧不能被其导带中的光生电子还原,这导致电子和空穴在表面重新结合。对这两种n型半导体金属氧化物进行掺杂,并加入生物相容性、可生物降解和生物可利用的聚合物(如壳聚糖)以形成薄膜,在很大程度上影响了薄膜作为治疗、控释和双敏感材料的表面积相互作用和多用途适用性。通过基于深共熔溶剂辅助水热法合成了WO纳米颗粒(WO-NP)和WO-MoO纳米复合材料,得到了尺寸精细的纳米颗粒和纳米复合材料,然后通过溶液浇铸法将其进一步掺入壳聚糖基质中以形成纳米杂化膜。通过X射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)、紫外光谱、X射线光电子能谱、扫描电子显微镜、透射电子显微镜、能量色散X射线光谱和动态光散射对材料进行结构、光学和形态表征。XRD和FT-IR分析表明,成功形成了WO-MoO纳米复合材料并将其掺入壳聚糖基质中。该纳米杂化膜具有抗菌活性,最低抑菌浓度为100μg/mL。此外,该纳米杂化膜没有明显的毒性。