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首页> 外文期刊>Journal of drug delivery science and technology >Magnetic assisted curcumin drug delivery using folate receptor targeted hybrid casein-calcium ferrite nanocarrier
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Magnetic assisted curcumin drug delivery using folate receptor targeted hybrid casein-calcium ferrite nanocarrier

机译:磁辅助姜黄素药物递送使用叶酸受体靶向杂交酪蛋白 - 钙铁氧体纳米载体

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摘要

Receptor targeted nanocarriers in the multimodal delivery of cancer therapeutics with minimal side effects are being intensively researched. In this study, folate receptor targeted hybrid protein inorganic nanocarrier was investigated for magnetic-assisted curcumin drug delivery. The protein carrier, casein was hybridized with su-perparamagnetic calcium ferrite nanoparticles (CFNP) in which the anti-cancer drug, curcumin (Cur) was encapsulated. Finally, folic acid (FA) was conjugated to enable receptor-mediated endocytosis. The synthesized materials were characterized using XRD, FTIR, SEM, VSM and DLS analysis confirming their formulation. The drug loading parameters were optimized by Taguchi technique. Curcumin release from the carrier was studied under the influence of pH, initial drug concentrations and magnetic field. Drug release rate was higher in acidic conditions, increased drug concentrations and under the influence of magnetic field. The drug release mechanism from the carrier were proposed using different kinetic models. Biocompatibility and cytotoxicity tests were performed for the synthesized drug carrier systems using L929 murine fibroblast and MCF-7 breast cancer cells, respectively. The IC_(50) value reduced nearly six fold for MCF-7 cells, for casein-Cur with FA conjugation in comparison to the carrier without FA. The study clearly demonstrated casein-CFNP-Cur-FA as a novel potential formulation for targeted drug delivery.
机译:受到密集副作用的癌症治疗剂的多式式递送中的受体靶向纳米载体。在该研究中,研究了叶酸受体靶向杂交蛋白无机纳米载体用于磁辅助姜黄素药物递送。蛋白质载体,酪蛋白与抗癌药物,抗癌药物,姜黄素(CUR)杂交杂交。最后,叶酸(Fa)缀合,以使受体介导的内吞作用。使用XRD,FTIR,SEM,VSM和DLS分析表征合成材料,确认其配方。通过Taguchi技术优化了药物负载参数。在pH,初始药物浓度和磁场的影响下研究来自载体的姜黄素释放。酸性条件下药物释放率较高,药物浓度增加,磁场的影响下。使用不同的动力学模型提出了来自载体的药物释放机制。使用L929鼠成纤维细胞和MCF-7乳腺癌细胞的合成药物载体系统进行生物相容性和细胞毒性试验。对于MCF-7细胞的IC_(50)值减少了近6倍,对于与FA的载体相比,与FA缀合的酪蛋白CUR。该研究清楚地证明了酪蛋白-CFNP-Cur-Fa作为针对靶向药物递送的新型潜在制剂。

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