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首页> 外文期刊>Current Pharmaceutical Biotechnology >Development of Formulation Methods and Physical Characterization of Injectable Sodium Selenite Nanoparticles for the Delivery of Sorafenib tosylate
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Development of Formulation Methods and Physical Characterization of Injectable Sodium Selenite Nanoparticles for the Delivery of Sorafenib tosylate

机译:制剂的制剂方法和物理表征可注射钠硒纳米粒子递送Sorafenib甲磺酸盐

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Background: Sorafenib is the fast oral therapeutic agent to show the activity against human hepatocellular carcinoma. Sorafenib leads to severe toxicity due to the multiple-dose regimen. Reducing the overall dose of sorafenib through injectable dosage form to release sustainably is of therapeutically more important to combat drug-induced toxicity.Objective: The purpose of this study was to formulate and evaluate the physical parameters of sorafenib-loaded Sodium Selenite Nanoparticles (SSSNP).Methods: Two different methods: chemical crosslinking and solvent evaporation were applied for the formulation of nanoparticles using various crosslinkers such as formaldehyde, magnesium sulfate, tripolyphosphate, dextran sulfate, and aluminum hydroxide. Physical characterization was performed with zeta potential analysis, polydispersity index, particle size and scanning electron microscopic studies for morphological analysis for all the formulated nanoparticles developed using the chemical crosslinking technique based ionic interaction.Results: Tripolyphosphate was selected as an ideal crosslinker and used for nanoparticle formulation with the solvent evaporation technique. Based on the physical characterization, SSSNP was formulated successfully with the solvent evaporation technique using tripolyphosphate as a cross-linker. The zeta potential of SSSNP was -37.5 mV, PDI was approximately 0.3 to 0.4, and the observed size (diameter) was in the range of 208 nm to 0.2 mu m. Furthermore, the particles were smooth in morphology and appeared as crystals.Conclusion: The novel injectable sorafenib loaded sodium selenite nanoparticle dosage form will serve better than conventional oral dosage form to elicit a safe therapeutic effect.
机译:背景:Sorafenib是快速口服治疗剂,以显示针对人肝细胞癌的活性。由于多剂量方案,索拉非尼导致严重的毒性。通过可食用性剂型减少索拉非尼的总剂量是可持续的治疗性更重要的是对抗药物诱导的毒性更为重要。目的:本研究的目的是制定和评估索拉非尼钠硒矿石纳米粒子的物理参数(SSSNP) 。方法:两种不同的方法:使用各种交联剂如甲醛,硫酸镁,三聚磷酸磷,葡聚糖和氢氧化铝,应用化学交联和溶剂蒸发,用于配制纳米颗粒。用Zeta电位分析,多分散性指数,粒度和扫描电子显微镜进行物理表征,用于使用基于化学交联技术的离子互动产生的所有配方纳米颗粒的形态分析。结果:选择三聚磷酸盐作为理想的交联剂并用于纳米颗粒用溶剂蒸发技术配制。基于物理表征,使用三聚磷酸盐作为交联剂成功配制了SSSNP。 SSSNP的Zeta电位为-37.5mV,PDI约为0.3至0.4,观察到的尺寸(直径)在208nm至0.2μm的范围内。此外,颗粒在形态学中平滑,出现为晶体。结论:新型注射索拉非尼酸钠纳米粒子剂型将优于常规口服剂型以引发安全治疗效果。

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