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Preparation and In Vitro Evaluation of Glycyrrhetinic Acid-Modified Curcumin-Loaded Nanostructured Lipid Carriers

机译:甘草次酸修饰的姜黄素负载纳米结构脂质载体的制备及体外评价

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摘要

Curcumin, a phenolic antioxidant compound derived from the rhizome of the turmeric plant Curcuma longa, has proven to be a modulator of intracellular signaling pathways that control cancer cell growth, inflammation, invasion and apoptosis, revealing its anticancer potential. In this study, a Glycyrrhetinic Acid-Modified Curcumin-Loaded Nanostructured Lipid Carrier (Cur-GA-PEG-NLC) was prepared by the film ultrasound method to improve the tumor-targeting ability. The drug content was detected by an UV spectrophotometry method. The encapsulation efficiency of curcumin in the nanostructured lipid carriers (NLCs) was determined using a mini-column centrifugation method. The encapsulation efficiency for various Cur-GA-PEG-NLC was within the range of 90.06%–95.31% and particle size was between 123.1 nm and 132.7 nm. An in vitro MTT assay showed that Cur-GA10%-PEG-NLC had significantly high cellular uptake and cytotoxicity against HepG2 cells compared with other groups.
机译:姜黄素是一种源自姜黄植物姜黄的根茎的酚类抗氧化剂化合物,已被证明是控制癌细胞生长,炎症,侵袭和凋亡的细胞内信号通路的调节剂,显示出其抗癌潜力。在这项研究中,通过膜超声方法制备了甘草次酸修饰的姜黄素负载纳米结构脂质载体(Cur-GA-PEG-NLC),以提高肿瘤靶向能力。通过UV分光光度法检测药物含量。姜黄素在纳米结构脂质载体(NLCs)中的包封效率是使用微型柱离心法确定的。各种Cur-GA-PEG-NLC的包封效率在90.06%–95.31%的范围内,粒径在123.1 nm至132.7 nm之间。体外MTT分析显示,与其他组相比,Cur-GA10%-PEG-NLC对HepG2细胞具有明显高的细胞摄取和细胞毒性。

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