Department of Bioanalytical Sciences, Ramnarain Ruia College, Mumbai, 400019, India.
The Centre for Advanced Materials & Industrial Chemistry, School of Science, RMIT University, Melbourne, 3000, Australia.
Chem Phys Lipids. 2020 Nov;233:104988. doi: 10.1016/j.chemphyslip.2020.104988. Epub 2020 Oct 6.
Nanotechnology has come up as a protean field integrating concepts of alternate drug delivery systems using nanocarriers. The idea of encapsulating a drug molecule into a colloidal carrier like solid lipid nanoparticle has been a promising approach for development of nanomedicines. In this research work, a hydrophobic, natural, and an anticancer bioflavonoid, morin hydrate (MH) was encapsulated into solid lipid nanoparticles to overcome the issues of its poor aqueous solubility and low oral bioavailability. The prepared morin hydrate loaded solid lipid nanoparticles (MSN) were characterized by DLS, FTIR, and DSC analysis. The MSN showed nanoscale size, good steric stability, and release in simulated intestinal fluid. The in-vitro anticancer studies against human cervical cancer cells revealed the higher cytotoxicity of encapsulated MH than free or pure MH. MSN also demonstrated a significant improvement in pharmacokinetics of encapsulated MH.
纳米技术已经成为一个多用途的领域,它整合了使用纳米载体的替代药物传递系统的概念。将药物分子封装到胶体载体(如固体脂质纳米粒)中的想法,是开发纳米药物的一种很有前途的方法。在这项研究工作中,一种疏水的、天然的、具有抗癌作用的生物类黄酮,即密蒙花苷(MH)被封装到固体脂质纳米粒中,以克服其水溶性差和口服生物利用度低的问题。所制备的密蒙花苷负载固体脂质纳米粒(MSN)通过 DLS、FTIR 和 DSC 分析进行了表征。MSN 显示出纳米级尺寸、良好的空间稳定性和在模拟肠液中的释放。对人宫颈癌细胞的体外抗癌研究表明,包封的 MH 的细胞毒性比游离或纯 MH 更高。MSN 还显著改善了包封 MH 的药代动力学。