Development, characterization and in vitro cytotoxicity of kaempferol-loaded nanostructured lipid carriers in glioblastoma multiforme cells

山奈酚 细胞毒性 胶质母细胞瘤 生物利用度 化学 药物输送 药理学 体外 Zeta电位 癌细胞 类黄酮 纳米技术 癌症研究 生物化学 抗氧化剂 材料科学 生物 癌症 有机化学 纳米颗粒 遗传学
作者
Luisa Ribeiro Nicoleti,Leonardo Delello Di Filippo,Jonatas Lobato Duarte,Marcela Tavares Luiz,Rafael Miguel Sábio,Marlus Chorilli
出处
期刊:Colloids and Surfaces B: Biointerfaces [Elsevier BV]
卷期号:226: 113309-113309 被引量:28
标识
DOI:10.1016/j.colsurfb.2023.113309
摘要

Glioblastoma multiforme is the most common and most aggressive human brain cancer. GBM treatment is still a challenge because many drugs are not able to cross the blood-brain barrier, in addition to the increasing resistance to currently available chemotherapy. New therapeutic alternatives are emerging, and, in this context, we highlight kaempferol, a flavonoid with remarkable anti-tumor activity but with limited bioavailability due to its strong lipophilic property. A promising tool to improve the biopharmaceutical properties of molecules such as kaempferol is the use of drug-delivery nanosystems, such as nanostructured lipid carriers (NLC), which can facilitate the dispersion and delivery of highly lipophilic molecules. The present work aimed at the development and characterization of kaempferol-loaded NLC (K-NLC) and the evaluation of its biological properties using in vitro models. The K-NLC showed an average size of 120 nm, zeta potential of - 21 mV, and polydispersity index of 0.099. The K-NLC presented high kaempferol encapsulation efficiency (93%), a drug loading of 3.58%, and a sustained kaempferol release profile for up to 48 h. In addition to presenting a 7-fold increase in kaempferol cytotoxicity, its encapsulation in NLC promoted a cellular uptake of 75%, which corroborates with increased cytotoxicity in U-87MG cells, as observed. Together, these data reinforce the promising antineoplastic properties of kaempferol in addition to the key role of NLC as a platform for the efficient delivery of lipophilic drugs to neoplastic cells, which improved their uptake and therapeutic efficacy in glioblastoma multiforme cells.
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