Department of Chemistry, University of Florence, via U Schiff 6, 50519 Sesto Fiorentino, Florence, Italy.
Department of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Viale Pieraccini 6, 50139, Italy.
Eur J Pharm Sci. 2022 Feb 1;169:106090. doi: 10.1016/j.ejps.2021.106090. Epub 2021 Dec 3.
Thymoquinone (TQ) is a natural compound present in the essential oil and in the fixed oil of Nigella sativa L. Like many natural substances, it is characterized by poor aqueous solubility and low stability which limit its bioavailability. Soluplus®-Solutol® HS15 polymeric micelles (TQ-MP) were developed to increase the permeability of TQ with particular attention to overcoming intestinal barrier and the blood brain barrier, for possible oral and parenteral administration. The optimized micelles have dimensions < 100 nm and PdI < 0.2 indicating that the formulation was homogeneous as confirmed also by TEM experiments. EE% was 92.4 ± 0.3%. Stability studies showed a stable formulation following subsequent dilutions and in the gastric-intestinal media. In vitro studies have revealed that the carrier enhances the permeability of TQ in the intestine and in the blood-brain barrier using Parallel Artificial Membrane Permeability Assay (PAMPA) assay and cellular tests with Caco-2 cells and hCMEC/D3 monolayer cells. Up-take study, cell viability and cytotoxicity studies were also conducted. Fluorescent micelles (FITC-MP), were also optimized to perform in vitro up-take study in Caco-2 cells and to study their toxicity in Zebrafish model. The toxicity was evaluated on three lines of Zebrafish: wild type, transgenic line Tg(Myl7:EGFP) in which cardiomyocytes are marked with green fluorescence protein and Tg(flk1-GFP) line which expresses GFP under the control of the vascular endothelial growth factor receptor 2 (vegfr2) promoter.
姜酮(TQ)是一种天然化合物,存在于黑种草籽油和固定油中。像许多天然物质一样,它的水溶性差,稳定性低,限制了它的生物利用度。Soluplus®-Solutol® HS15 聚合物胶束(TQ-MP)的开发是为了提高 TQ 的通透性,特别关注克服肠道屏障和血脑屏障,以实现可能的口服和肠胃外给药。优化后的胶束尺寸<100nm,PdI<0.2,表明制剂是均匀的,这也通过 TEM 实验得到证实。EE%为 92.4±0.3%。稳定性研究表明,制剂在随后的稀释和胃肠介质中稳定。体外研究表明,该载体通过平行人工膜渗透性测定(PAMPA)测定和用 Caco-2 细胞和 hCMEC/D3 单层细胞进行的细胞试验,增强了 TQ 在肠道和血脑屏障中的通透性。摄取研究、细胞活力和细胞毒性研究也进行了。荧光胶束(FITC-MP)也进行了优化,以在 Caco-2 细胞中进行体外摄取研究,并在斑马鱼模型中研究其毒性。毒性评估在三个斑马鱼品系上进行:野生型、心肌细胞用绿色荧光蛋白标记的转基因品系 Tg(Myl7:EGFP)和在血管内皮生长因子受体 2(vegfr2)启动子控制下表达 GFP 的 Tg(flk1-GFP)品系。