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Praziquantel-Solid Lipid Nanoparticles Produced by Supercritical Carbon Dioxide Extraction: Physicochemical Characterization Release Profile and Cytotoxicity

机译:超临界二氧化碳萃取制备的吡喹酮-固体脂质纳米颗粒:物理化学特征释放曲线和细胞毒性

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摘要

Solid lipid nanoparticles (SLNs) can be produced by various methods, but most of them are difficult to scale up. Supercritical fluid (SCF) is an important tool to produce microanoparticles with a narrow size distribution and high encapsulation efficiency. The aim of this work was to produce cetyl palmitate SLNs using SCF to be loaded with praziquantel (PZQ) as an insoluble model drug. The mean particle size (nm), polydispersity index (PdI), zeta potential, and encapsulation efficiency (EE) were determined on the freshly prepared samples, which were also subject of Differential Scanning Calorimetry (DSC), Fourier-Transform Infrared Spectroscopy (FTIR), drug release profile, and in vitro cytotoxicity analyses. PZQ-SLN exhibited a mean size of ~25 nm, PdI ~ 0.5, zeta potential ~−28 mV, and EE 88.37%. The DSC analysis demonstrated that SCF reduced the crystallinity of cetyl palmitate and favored the loading of PZQ into the lipid matrices. No chemical interaction between the PZQ and cetyl palmitate was revealed by FTIR analysis, while the release or PZQ from SLN followed the Weibull model. PZQ-SLN showed low cytotoxicity against fibroblasts cell lines. This study demonstrates that SCF may be a suitable scale-up procedure for the production of SLN, which have shown to be an appropriate carrier for PZQ.
机译:固体脂质纳米颗粒(SLNs)可以通过多种方法生产,但是大多数都难以扩大规模。超临界流体(SCF)是生产具有窄尺寸分布和高封装效率的微米/纳米颗粒的重要工具。这项工作的目的是使用SCF生产棕榈酸十六烷基酯SLN,并装载吡喹酮(PZQ)作为不溶性模型药物。在新鲜制备的样品上确​​定平均粒径(nm),多分散指数(PdI),ζ电位和包封效率(EE),这些样品也应采用差示扫描量热法(DSC),傅里叶变换红外光谱(FTIR) ),药物释放曲线和体外细胞毒性分析。 PZQ-SLN的平均大小约为25 nm,PdI约为0.5,ζ电位约为-28 mV,EE值为88.37%。 DSC分析表明,SCF降低了棕榈酸十六烷基酯的结晶度,并有利于将PZQ装载到脂质基质中。 FTIR分析未显示PZQ和棕榈酸十六烷基酯之间的化学相互作用,而SLN的释放或PZQ遵循Weibull模型。 PZQ-SLN对成纤维细胞细胞系显示出低细胞毒性。这项研究表明,SCF可能是生产SLN的合适的按比例放大程序,已经证明它是PZQ的合适载体。

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