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Formulation design, preparation, and in vitro and in vivo characterizations of β-Elemene- loaded nanostructured lipid carriers

机译:β-榄香烯负载的纳米结构脂质载体的配方设计,制备以及体外和体内表征

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Abstract: In the present study, nanostructured lipid carriers (NLCs) were prepared and optimized for the intravenous delivery of β-Elemene (β-E). Aqueous dispersions of NLCs were successfully prepared by high-pressure homogenization method using glycerol monostearate as the solid lipid and a mixture of Maisine 35-1 and Labrafil M1944 CS as the liquid lipid. The results revealed that the morphology of the NLCs was spheroidal. The particle size, zeta potential, and entrapment efficiency (EE) for the optimized formulation were observed as 138.9 nm, –20.2 mV, and 82.11%, respectively. X-ray diffraction analysis revealed the formation of less ordered structures in the inner core of the NLC particles. Moreover, the β-E-loaded NLCs were also less irritating and less toxic compared to Elemene injection. In addition, β-E-NLCs showed a significantly higher bioavailability and anti-tumor efficacy than Elemene injection. Taken together, our data indicate that the β-E-NLCs described in this study are well-suited for the intravenous delivery of β-E.
机译:摘要:在本研究中,制备并优化了纳米结构脂质载体(NLC)的β-榄香烯(β-E)的静脉内输送。 NLCs的水分散体是通过高压均质法成功制备的,其中使用单硬脂酸甘油酯作为固体脂质,并将Maisine 35-1和Labrafil M1944 CS的混合物用作液体脂质。结果表明,NLC的形态为球形。优化配方的粒径,ζ电势和截留效率(EE)分别为138.9 nm,–20.2 mV和82.11%。 X射线衍射分析表明在NLC颗粒的内核中形成了较不规则的结构。此外,与榄香烯注射液相比,负载β-E的NLC刺激性也较小,毒性也较小。此外,β-E-NLCs比榄香烯注射液具有更高的生物利用度和抗肿瘤功效。综上所述,我们的数据表明,本研究中描述的β-E-NLC非常适合静脉内输送β-E。

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