Hydrophobin-Coated Noisomes as Drug Carriers in Lung Cancer Cells - A Review

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Abstract

Nanoparticles loaded with anti-cancer drugs are designed to selectively target Lung Cancer Cells (LCCs) by interacting with various receptors. Hydrophobin-coated niosomes, a type of carrier system, show lower cytotoxicity in vitro compared to existing anti-cancer drugs. The hydrophobin-coated formulation demonstrates higher cytotoxicity against cancer cells than control cells. Lung cancer can spread to distant organs, posing challenges such as multidrug resistance and recurrence. Traditional chemotherapies may face resistance due to genetic mutations. Convolutional Neural Network (CNN)-based automatic organ segmentation has been validated for radiation treatment planning in lung cancer patients. LCCs-CNN niosomes, similar to liposomes, offer enhanced cellular membrane permeability and high biocompatibility. This carrier system shields the drug molecule from breakdown and deactivation. Hydrophobin-coated niosomes outperform polyethylene glycol-coated ones in various aspects, including size distribution, entrapment efficiency, release profile, biocompatibility, and cancer prevention success.
在肺癌细胞中作为药物载体的亲水素包裹的噪音体--综述
装载抗癌药物的纳米粒子旨在通过与各种受体相互作用,选择性地靶向肺癌细胞(LCC)。与现有的抗癌药物相比,载体系统的一种--涂有疏水性蛋白的niosomes在体外显示出较低的细胞毒性。与对照细胞相比,涂有疏水性蛋白的制剂对癌细胞的细胞毒性更高。肺癌可扩散到远处器官,带来多种药物耐药性和复发等挑战。传统的化疗方法可能会因基因突变而产生抗药性。基于卷积神经网络(CNN)的自动器官分割已在肺癌患者的放射治疗规划中得到验证。LCCs-CNNiosomes 类似于脂质体,具有更强的细胞膜渗透性和高生物相容性。这种载体系统能保护药物分子不被分解和失活。憎水素包裹的niosomes在各方面都优于聚乙二醇包裹的niosomes,包括尺寸分布、夹持效率、释放曲线、生物相容性和防癌效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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