Gagliardi Agnese, Voci Silvia, Bonacci Sonia, Iriti Giuseppe, Procopio Antonio, Fresta Massimo, Cosco Donato
Department of Health Sciences, University "Magna Græcia" of Catanzaro, Campus Universitario "S Venuta", I-88100 Catanzaro, Italy.
Department of Health Sciences, University "Magna Græcia" of Catanzaro, Campus Universitario "S Venuta", I-88100 Catanzaro, Italy.
Int J Biol Macromol. 2021 Dec 15;193(Pt A):713-720. doi: 10.1016/j.ijbiomac.2021.10.184. Epub 2021 Oct 27.
Sclareol is a labdane diterpene which carries on a broad range of biological activities. However, its poor water solubility and bioavailability are the foremost drawbacks that limit its application in therapeutics. The purpose of this investigation was to develop a natural nanoformulation made up of a biopolymer i.e. zein and sclareol in order to address this issue and to enhance the pharmacological efficacy of the drug. The sclarein nanoparticles (sclareol-loaded zein nanosystems) showed a typical monomodal pattern, characterized by a mean diameter of ~120 nm, a narrow size distribution and a surface charge of ~-30 mV. The evaluation of the entrapment efficiency and the drug-loading capacity of the nanosystems demonstrated the noteworthy ability of the protein matrix to hold sclareol while allowing a gradual release of the compound over time. The nanosystems increased the cytotoxicity of sclareol at a drug concentration of ≥5 μM with respect to the free compound after just 24 h incubation against various cancer cell lines. Indeed, the interaction of tritiated sclarein formulations with cells showed a time-dependent cell uptake of the nanosystems commencing as early as 1 h from the onset of incubation, favouring a significant decrease of the efficacious concentration of the drug.
香紫苏醇是一种具有广泛生物活性的半日花烷二萜。然而,其较差的水溶性和生物利用度是限制其在治疗领域应用的主要缺点。本研究的目的是开发一种由生物聚合物即玉米醇溶蛋白和香紫苏醇组成的天然纳米制剂,以解决这一问题并提高药物的药理疗效。香紫苏醇纳米颗粒(负载香紫苏醇的玉米醇溶蛋白纳米系统)呈现出典型的单峰模式,其平均直径约为120nm,粒径分布窄,表面电荷约为 -30mV。对纳米系统的包封率和载药量的评估表明,蛋白质基质具有显著的能力来容纳香紫苏醇,同时允许该化合物随时间逐渐释放。在针对各种癌细胞系孵育仅24小时后,纳米系统在药物浓度≥5μM时相对于游离化合物增加了香紫苏醇的细胞毒性。实际上,氚标记的香紫苏醇制剂与细胞的相互作用表明,纳米系统从孵育开始1小时起就呈现出时间依赖性的细胞摄取,有利于显著降低药物的有效浓度。