首页> 外文期刊>Journal of Microencapsulation: Microcapsules Liposomes Nanoparticles Microcells Microspheres >Physico-chemical characterisation, cytotoxic activity, and biocompatibility studies of tamoxifen-loaded solid lipid nanoparticles prepared via a temperature-modulated solidification method
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Physico-chemical characterisation, cytotoxic activity, and biocompatibility studies of tamoxifen-loaded solid lipid nanoparticles prepared via a temperature-modulated solidification method

机译:通过温度调节凝固方法制备的载有他莫昔芬的固体脂质纳米颗粒的理化特性,细胞毒性活性和生物相容性研究

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Context: Solid lipid nanoparticles (SLNs) can efficiently and efficaciously incorporate anti-cancer agents. Objective: To prepare and characterise tamoxifen (TAM)-loaded SLNs. Materials and methods: Glyceryl monostearate, Tween-80, and trehalose were used in SLNs. SLNs were tested via dynamic light scattering (DLS), transmission electron microscopy (TEM), differential scanning calorimetry (DSC), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). Results: Characterisation studies revealed SLNs of about 540 nm with a negative surface charge and confirmed the entrapment of TAM in the SLNs. The entrapment efficiency was estimated to be 60%. Discussion: The in vitro drug release profile demonstrated a gradual increase followed by a release plateau for several days. A drug concentration-dependent increase in cytotoxic activity was observed when the SLNs were evaluated in cell cultures. Conclusion: Biocompatible and stable lyophilised SLNs were successfully prepared and found to possess properties that may be utilised in an anti-cancer drug delivery system.
机译:背景:固体脂质纳米颗粒(SLN)可以有效地掺入抗癌药。目的:制备并表征他莫昔芬(TAM)负载的SLN。材料和方法:单硬脂酸甘油酯,Tween-80和海藻糖用于SLN。通过动态光散射(DLS),透射电子显微镜(TEM),差示扫描量热法(DSC),X射线衍射(XRD)和傅里叶变换红外光谱(FTIR)对SLN进行了测试。结果:表征研究显示约540 nm的SLN具有负表面电荷,并证实TAM滞留在SLN中。截留效率估计为60%。讨论:体外药物释放曲线显示逐渐增加,随后为几天的释放平台。当在细胞培养物中评估SLN时,观察到药物浓度依赖性的细胞毒性活性增加。结论:成功地制备了生物相容性和稳定的冻干SLN,并发现它们具有可用于抗癌药物递送系统的特性。

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