首页> 外文期刊>Pharmacognosy Research >The Influence of Pluronic F68 and F127 Nanocarrier on Physicochemical Properties, In vitro Release, and Antiproliferative Activity of Thymoquinone Drug
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The Influence of Pluronic F68 and F127 Nanocarrier on Physicochemical Properties, In vitro Release, and Antiproliferative Activity of Thymoquinone Drug

机译:Pluronic F68和F127纳米载体对胸腺醌药物的理化性质,体外释放和抗增殖活性的影响

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Background: This study reports on hydrophobic drug thymoquinone (TQ), an active compound found in the volatile oil of Nigella sativa that exhibits anticancer activities. Nanoformulation of this drug could potentially increase its bioavailability to specific target cells. Objective: The aim of this study was to formulate TQ into polymer micelle, Pluronic F127 (5.0 wt %) and Pluronic F68 (0.1 wt %), as a drug carrier to enhance its solubility and instability in aqueous media. Materials and Methods: Polymeric micelles encapsulated TQ were prepared by the microwave-assisted solvent evaporation technique. Fourier transform infrared spectroscopy and ultraviolet-visible spectrophotometer were utilized for qualitative confirmation of micelles encapsulation. The surface morphology and mean particle size of the prepared micelles were determined by using transmission electron microscopy (TEM). Cytotoxicity effect was studied using 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt (MTS) assay. Results: Dynamic laser light scattering (DLS) technique showed hydrodynamic size distribution of optimized micelles of 50 nm, which was in close agreement with the mean particle size obtained from TEM of about 51 nm. Drug release study showed the maximum percentage of TQ release at 61% after 72 h, while the entrapment efficiency of TQ obtained was 46% using PF127. The cytotoxic effect of PF127-encapsulated TQ was considerably higher compared to PF68-encapsulated TQ against MCF7 cells, as they exhibited IC50value of 8 μM and 18 μM, respectively. Conclusion: This study suggests higher molecular weight Pluronic polymer micelles (F127) with hydrophilic-hydrophobic segments which could be used as a suitable candidate for sustainable delivery of TQ. However, comprehensive studies should be carried out to establish the suitability of Pluronic F127 as a carrier for other drugs with similar challenges as TQ. SUMMARY There is a rising interest in integrating nanotechnology with medicine, creating a nanomedicine aiming for high efficiency and efficacy of disease diagnosis and treatment. In drug delivery, the term nanomedicine describes the nanometer-sized range (1-1000 nm) of a multi-component drug for disease treatments. As such, liposome-based nanoparticulate delivery vehicles have been approved by the Food and Drug Administration (FDA) for clinical applications. The main purpose of introducing nanoscale drug delivery is to improve the pharmacological and pharmacokinetic profiles of therapeutic molecules. Drug or therapeutic molecules can be either released through the cleavage of a covalent linkage between drug molecules and polymers (conjugation) or through the diffusion from a drug and polymer blended matrix (physical encapsulation). Polymers play an important role in the design of nanocarriers for therapeutic deliveries. In Asia, Nigella sativa seed oil has been used traditionally for its various medicinal benefits. One of its most potent compound which is thymoquinone has been intensively investigated for its anti-cancer effects in colorectal carcinoma, breast adenocarcinoma, osteosarcoma, ovarian carcinoma, myeloblastic leukemia, and pancreatic carcinoma. In addition, it is reported to show anti-inflammatory potential, antidiabetic, antihistaminic effects, as well as the ability to alleviate respiratory diseases, rheumatoid arthritis, multiple sclerosis, and Parkinson's disease. This study aims to formulate and characterize different pluronic-based thymoquinone nanocarrier and investigate its effect against breast cancer cells Abbreviations Used : ATR-IR: Attenuated Total Reflectance-Infrared Spectroscopy, CH3CN: Acetonitrile, DLS: Dynamic Light Scattering, MTS: [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, NPs: Nanoparticles, PF127/TQ: Pluronic F127 encapsulated TQ, PF68/TQ: Pluronic F68 encapsulated TQ, PLGA: Poly-(D,L-lactide-co-glycolide), PVA: Poly-vinylalcohol, TQ: Thymoquinone, UV/VIS: Ultravioletvisible spectrophotometry.
机译:背景:这项研究报道了疏水性药物胸腺醌(TQ),这是一种在鼠尾草挥发油中发现的具有活性的化合物,具有抗癌活性。纳米制剂的这种药物可能会增加其对特定靶细胞的生物利用度。目的:本研究的目的是将TQ制成高分子胶束,Pluronic F127(5.0 wt%)和Pluronic F68(0.1 wt%)作为药物载体,以增强其在水性介质中的溶解度和不稳定性。材料与方法:采用微波辅助溶剂蒸发技术制备了包裹TQ的聚合物胶束。利用傅里叶变换红外光谱和紫外可见分光光度计对胶束的包封进行定性确认。通过使用透射电子显微镜(TEM)确定所制备的胶束的表面形态和平均粒径。使用3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺基苯基)-2H-四唑内盐(MTS)分析研究了细胞毒性作用。结果:动态激光散射(DLS)技术显示了优化的50纳米胶束的流体动力学尺寸分布,这与从TEM获得的平均粒径约51 nm紧密一致。药物释放研究表明,在72小时后,TQ的最大释放百分比为61%,而使用PF127获得的TQ的包封率为46%。与PF68包裹的TQ相比,PF127包裹的TQ对MCF7细胞的细胞毒性作用要高得多,因为它们的IC 50 值分别为8μM和18μM。结论:这项研究表明,具有亲水-疏水链段的较高分子量的Pluronic聚合物胶束(F127)可以用作TQ可持续传递的合适候选者。但是,应该进行综合研究以建立Pluronic F127作为其他与TQ具有类似挑战的药物的载体的适用性。发明内容对将纳米技术与医学结合,产生旨在实现疾病诊断和治疗的高效率和功效的纳米医学的兴趣日益浓厚。在药物输送中,术语“纳米药物”描述了用于疾病治疗的多组分药物的纳米尺寸范围(1-1000 nm)。这样,基于脂质体的纳米颗粒递送载体已被食品和药物管理局(FDA)批准用于临床。引入纳米级药物递送的主要目的是改善治疗分子的药理和药代动力学特性。药物或治疗分子可以通过药物分子与聚合物之间的共价键断裂(结合)或通过药物与聚合物混合基质的扩散(物理包封)来释放。聚合物在用于治疗性递送的纳米载体的设计中起重要作用。在亚洲,传统上已将黑夜蛾种子油用于各种医学用途。其最有效的化合物之一是胸腺醌,因其在结直肠癌,乳腺癌,腺癌,骨肉瘤,卵巢癌,粒细胞性白血病和胰腺癌中的抗癌作用而进行了深入研究。另外,据报道其显示出抗炎潜力,抗糖尿病,抗组胺作用,以及减轻呼吸系统疾病,类风湿性关节炎,多发性硬化症和帕金森氏病的能力。这项研究旨在配制和表征不同的基于普卢尼克的胸腺醌纳米载体,并研究其对乳腺癌细胞的作用。​​使用的缩写:ATR-IR:衰减全反射红外光谱法,CH 3 CN:乙腈,DLS:动态光散射,MTS:[3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺基苯基)-2H-四唑鎓盐,NPs:纳米颗粒,PF127 / TQ:Pluronic F127封装的TQ,PF68 / TQ:Pluronic F68封装的TQ,PLGA:聚(D,L-丙交酯-乙交酯),PVA:聚乙烯醇,TQ:胸醌,UV / VIS:紫外可见分光光度法。

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