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Bovine serum albumin as a nanocarrier for the efficient delivery of ginsenoside compound K: preparation, physicochemical characterizations and in vitro biological studies

机译:牛血清白蛋白作为人参皂苷K高效递送的纳米载体:制备,理化性质和体外生物学研究

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Ginsenosides are triterpenoids that are found in P. ginseng; they have numerous important structural, functional and pharmacological properties. In this work, a desolvation method was used to entrap ginsenoside CK within bovine serum albumin (BSA) to form BSA–CK nanoparticles (NPs), which enhance its aqueous solubility and stability. Following purification, the BSA–CK NPs were characterized by several physico-chemical techniques, including high pressure liquid chromatography (HPLC), electrophoresis, 1H NMR spectroscopy, Fourier transform infrared spectroscopy (FT-IR), field emission transmission electron microscopy (FE-TEM), zeta potential, particle size analysis by dynamic light scattering (DLS), and thermogravimetric analysis (TGA); the results confirm that the as-prepared BSA–CK NPs are spherical, highly monodispersed and stable in aqueous systems. In addition, the time-dependent and pH stabilities of the BSA–CK NPs were analyzed over a period of 8 days; the results suggest that the nanoparticles are stable in physiological buffer (pH 7.4), whereas they are readily degraded under acidic conditions (pH 5.0) which mimic intracellular pH conditions. Furthermore, comparative water solubility analysis of the BSA–CK NPs and standard CK showed that the BSA carrier enhances the water solubility of ginsenoside CK. In vitro cytotoxicity assays of the BSA–CK NPs and standard CK revealed that the BSA–CK NPs demonstrate greater in vitro therapeutic efficacy in the HaCaT skin cell line, the A549 lung cancer cell line, the HepG2 liver carcinoma cell line and the HT29 colon cancer cell line in comparison with standard CK. Moreover, RAW264.7 cells treated with BSA–CK NPs exhibited decreased lipopolysaccharide-induced NO production. Collectively, these results suggest that the BSA–CK NPs may be useful as a delivery vehicle in cancer cell lines and may also possess anti-inflammatory effects.
机译:人参皂甙是在 P中发现的三萜类化合物。人参;它们具有许多重要的结构,功能和药理特性。在这项工作中,使用去溶剂化方法将人参皂苷CK包埋在牛血清白蛋白(BSA)中以形成BSA–CK纳米颗粒(NPs),从而增强了其水溶性和稳定性。纯化后,BSA–CK NPs通过几种物理化学技术进行表征,包括高压液相色谱(HPLC),电泳, 1 H NMR光谱,傅立叶变换红外光谱光谱(FT-IR),场发射透射电子显微镜(FE-TEM),ζ电位,通过动态光散射(DLS)进行的粒度分析和热重分析(TGA);结果证实,所制备的BSA–CK NP为球形,高度单分散,在水性体系中稳定。此外,在8天的时间内分析了BSA-CK NP的时间依赖性和pH稳定性。结果表明,纳米颗粒在生理缓冲液(pH 7.4)中稳定,而在模拟细胞内pH条件的酸性条件(pH 5.0)下容易降解。此外,对BSA–CK NP和标准CK的水溶性比较分析表明,BSA载体增强了人参皂苷CK的水溶性。对BSA–CK NP和标准CK的体外细胞毒性试验表明,BSA–CK NP在HaCaT皮肤细胞系A549肺中显示出更高的体外疗效。癌细胞系,HepG2肝癌细胞系和HT29结肠癌细胞系与标准CK相比。此外,用BSA–CK NP处理的RAW264.7细胞表现出降低的脂多糖诱导的NO生成。总的来说,这些结果表明,BSA–CK NPs可以用作癌细胞系中的传递载体,并且还具有抗炎作用。

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