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Improvement of Nanoprecipitation Technique for Preparation of Gelatin Nanoparticles and Potential Macromolecular Drug Loading

机译:明胶纳米颗粒制备中纳米沉淀技术的改进及潜在的大分子载药量

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摘要

An optimum nanoprecipitation technique for gelatin nanoparticles is established, based on aqueous gelatin solution and ethanolic solution containing stabilizer. Crosslinking with glutaraldehyde results in stable gelatine nanoparticles. Several factors such as the surfactant concentration, type of surfactant, type of nonsolvent and gelatin concentration are evaluated. Gelatin nanoparticles with 200–300nm can be produced using 20–30mgmL~(-1) of gelatin and a minimum of 7% w/v stabilizer (Poloxamer 407 or 188). Furthermore, methanol and ethanol are good nonsolvents, whereas other nonsolvents such as acetone, isopropyl alcohol, and acetonitrile, result in phase separation and visible precipitates. The entrapment efficiency of fluorescein-isothiocyanate (FITC)-dextran as model drug was determined to 50% with no substantial effect on particle size. 80% of the drug is only released after enzymatic digestion.
机译:基于明胶水溶液和含稳定剂的乙醇溶液,建立了明胶纳米颗粒的最佳纳米沉淀技术。与戊二醛交联产生稳定的明胶纳米颗粒。评价了一些因素,例如表面活性剂浓度,表面活性剂类型,非溶剂类型和明胶浓度。使用20–30mgmL〜(-1)的明胶和最少7%w / v的稳定剂(Poloxamer 407或188)可以生产200-300nm的明胶纳米颗粒。此外,甲醇和乙醇是良好的非溶剂,而其他非溶剂(如丙酮,异丙醇和乙腈)导致相分离和可见的沉淀。荧光素-异硫氰酸酯(FITC)-右旋糖酐作为模型药物的包封效率确定为50%,对粒径没有实质影响。仅在酶消化后才释放80%的药物。

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