Folate Targeted Galactomannan Coated Iron Oxide Nanoparticles as a Nanocarrier for Targeted Drug Delivery of Capecitabine

V. Subha, S. Kirubanandan, S. Renganathan
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引用次数: 4

Abstract

Iron oxide nanoparticle is the most promising nanoparticles (NPs) capable in Drug Delivery and targeting. Iron oxide nanoparticles were synthesized by green synthesis. Galactomannan, when attached to the surface of the nanoparticles, increases the biocompatibility of the nanoparticles. Folic acid (FA) is used as the ligand to target folate receptors, which are found abundant in cancer cells. FeNPs-GM-FA could target cancer cells when used as drug carriers. The synthesized iron oxide nanoparticles using Mimosa pudica root extract was synthesized for targeted delivery of the anticancer drug, Capecitabine, by grafting folic acid (FA) onto the iron oxide nanoparticles coated with galactomannan (GM), a polysaccharide present in fenugreek gum. The cytotoxicity profile of the nanoparticles on human epithelial type 2 (HEp-2) cells as measured by standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay showed that the particles were nontoxic and may be useful for various in vivo and in vitro biomedical applications. The surface modification by galactomannan and folic acid grafting was confirmed by UV-visible spectroscopy and fourier transforms infrared (FTIR) spectroscopy. The in vitro release profile of capecitabine from FeNPs-GM-FA was characterized by an initial fast release followed by a sustained release phase. The histological investigation evidences the formation of improved liver cell architecture indicating the therapeutic nature of functionalized iron nanoparticles with Capecitabine, confirming a potential option for drug delivery and targeting tumor tissues.
叶酸靶向半乳甘露聚糖包覆氧化铁纳米粒子作为卡培他滨靶向给药的纳米载体
氧化铁纳米颗粒是最有前途的药物递送和靶向纳米颗粒。采用绿色合成法合成了氧化铁纳米粒子。半乳甘露聚糖附着在纳米颗粒表面时,可提高纳米颗粒的生物相容性。叶酸(FA)被用作靶向叶酸受体的配体,叶酸受体在癌症细胞中含量丰富。当用作药物载体时,FeNPs-GM-FA可以靶向癌症细胞。使用含羞草根提取物合成的氧化铁纳米颗粒用于靶向递送抗癌药物卡培他滨,方法是将叶酸(FA)接枝到包有半乳甘露聚糖(GM)的氧化铁纳米微粒上,半乳甘露聚糖是胡芦巴胶中的一种多糖。通过标准的3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物测定法测量的纳米颗粒对人2型上皮细胞(HEp-2)的细胞毒性特征表明,该颗粒无毒,可用于各种体内和体外生物医学应用。通过紫外-可见光谱和傅立叶变换红外光谱证实了半乳甘露聚糖和叶酸接枝的表面改性。卡培他滨从FeNPs GM FA的体外释放特征为初始快速释放,然后是持续释放阶段。组织学研究证明,肝细胞结构的改善表明了卡培他滨功能化铁纳米颗粒的治疗性质,证实了药物递送和靶向肿瘤组织的潜在选择。
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