一种新型ZnO纳米颗粒作为药物纳米载体在治疗中的应用:动力学模型和误差分析

S. Karakuş
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引用次数: 4

摘要

纳米技术为医药工业中的几种生物医学和制药应用提供了有希望的可能性。纳米结构在适合新型药物应用的最新技术策略中发挥着重要作用。在这项工作中,使用声化学技术在室温下合成了克林霉素磷酸(CliP)(局部抗炎药),黄原胶(XaG)(生物聚合物)和氧化锌(纳米颗粒)纳米结构。利用傅里叶变换红外(FTIR)和x射线衍射(XRD)对克林霉素磷酸黄原胶/ZnO (CliP-XaG/ZnO)纳米结构进行了表征。光谱学实验阐明了不同pH(1.2和7.4)介质下给药系统的体外机制。本研究采用紫外-可见光谱法对溶液中的药物浓度进行了分析,并计算了几种动力学模型和误差分析,以证明与结果有联系。Higuchi模型的相关参数最好。在XaG (pH值为1.2)和XaG/ZnO (pH值为1.2)溶液中溶胀率分别达到105%和190%,在XaG (pH值为7.4)溶液中溶胀率分别达到530%和655%。结果表明,XaG / ZnO的容量可以作为一种新的局部抗炎药物载体。
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A Novel ZnO Nanoparticle as Drug Nanocarrier in Therapeutic applications: Kinetic Models and Error Analysis
Nanotechnology provides promising possibilities for several biomedical and pharmaceutical  applications in the medicine industry. Nanostructures play a major role in the recent strategies of  technology suitable for novel drug applications. In this work, clindamycin phosphate (CliP) (topical anti-inflammatory drug), xanthan gum (XaG) (biopolymer) and ZnO (zinc oxide) (nanoparticle) nanostructures were synthesised using the sonochemical technique at room temperature. The characterization of the clindamycin phosphate- xanthan gum/ZnO (CliP-XaG/ZnO) nanostructure has been carried out by Fourier transform infrared (FTIR) and X-ray diffraction (XRD). The spectroscopic experiments elucidated in vitro the mechanism of drug delivery system at different pH media (1.2 and 7.4). In this study, the concentration of drug in the solution was analyzed by UV–vis spectroscopy method and several kinetic models and error analysis were calculated to prove a connection with results. The Higuchi model had the best correlation parameters. The percentage of swelling ratio (%) reached up 105% in XaG (pH 1.2) and 190% in XaG/ZnO (pH 1.2) And the swelling ratio (%) reached up 530% within in XaG (pH 7.4) and 655% within in XaG/ZnO (pH 7.4). The results show that the capacity of XaG / ZnO can be preferred as a novel topical anti-inflammatory drug carrier.
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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
81
审稿时长
5 weeks
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