Department of Chemical Engineering, National Institute of Technology, Tiruchirappalli, 620 015 Tamilnadu, India.
Department of Chemistry, National Institute of Technology, Tiruchirappalli, 620 015 Tamilnadu, India.
Int J Biol Macromol. 2017 Apr;97:513-525. doi: 10.1016/j.ijbiomac.2017.01.036. Epub 2017 Jan 10.
The CaFeO nanoparticles (CFNP) were synthesized using the solution combustion method. The CFNP-chitosan-ampicillin was prepared by the ionic gelation method using tripolyphosphate (TPP). The CFNP, chitosan-CFNP, chitosan-CFNP-ampicillin materials were characterized by XRD, FT-IR and TGA analysis in order to evaluate the particle nature and size, the presence of functional groups and their thermal stability. The FESEM and EDAX analysis were performed to understand the surface morphology of the materials and the presence of CFNP in the material, respectively. The vibrating sample magnetometer (VSM) analysis was performed to analyze the magnetic property of the chitosan-CFNP material. The squareness value of 0.1733 obtained by VSM measurements indicates the super paramagnetic nature of chitosan-CFNP. Taguchi orthogonal array method was applied to identify the significant impacting parameters for maximizing the drug encapsulation of chitosan-CFNP. The drug release studies showed that the drug was released rapidly in acidic medium as compared to the basic or neutral medium. The drug release kinetic data were fitted with different linear kinetic model equations and the best fit was obtained with Korsmeyer-Peppas model. The model drug ampicillin release from chitosan-CFNP was tested against staphylococcus epidermis bacteria through disc diffusion method for checking biocompatibility and antibacterial activity.
采用溶液燃烧法合成了 CaFeO 纳米颗粒(CFNP)。采用三聚磷酸钠(TPP)的离子凝胶化法制备了 CFNP-壳聚糖-氨苄西林。通过 XRD、FT-IR 和 TGA 分析对 CFNP、壳聚糖-CFNP、壳聚糖-CFNP-氨苄西林材料进行了表征,以评估颗粒的性质和大小、官能团的存在及其热稳定性。通过 FESEM 和 EDAX 分析分别了解材料的表面形态和材料中 CFNP 的存在。通过振动样品磁强计(VSM)分析对壳聚糖-CFNP 材料的磁性进行了分析。VSM 测量得到的 0.1733 的方值表明壳聚糖-CFNP 具有超顺磁性。田口正交数组法用于确定影响最大程度地包封药物的壳聚糖-CFNP 的显著影响参数。药物释放研究表明,与碱性或中性介质相比,药物在酸性介质中迅速释放。药物释放动力学数据拟合了不同的线性动力学模型方程,最佳拟合是用 Korsmeyer-Peppas 模型获得的。通过圆盘扩散法测试了模型药物氨苄西林从壳聚糖-CFNP 中的释放,以检查生物相容性和抗菌活性。