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Critical solvent properties affecting the particle formation process and characteristics of celecoxib-loaded PLGA microparticles via spray-drying

机译:通过喷雾干燥影响粒子形成工艺的临界溶剂性能和Celecoxib加载PLGA微粒的特性

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摘要

Purpose: It is imperative to understand the particle formation mechanisms when designing advanced nano/microparticulate drug delivery systems. We investigated how the solvent power and volatility influence the texture and surface chemistry of celecoxib-loaded poly (lactic-co-glycolic acid) (PLGA) microparticles prepared by spray-drying. Methods: Binary mixtures of acetone and methanol at different molar ratios were applied to dissolve celecoxib and PLGA prior to spray-drying. The resulting microparticles were characterized with respect to morphology, texture, surface chemistry, solid state properties and drug release profile. The evaporation profiles of the feed solutions were investigated using thermogravimetric analysis (TGA). Results: Spherical PLGA microparticles were obtained, irrespectively of the solvent composition. The particle size and surface chemistry were highly dependent on the solvent power of the feed solution. An obvious burst release was observed for the microparticles prepared by the feed solutions with the highest amount of poor solvent for PLGA. TGA analysis revealed distinct drying kinetics for the binary mixtures. Conclusions: The particle formation process is mainly governed by the PLGA precipitation rate, which is solvent-dependent, and the migration rate of celecoxib molecules during drying. The texture and surface chemistry of the spray-dried PLGA microparticles can therefore be tailored by adjusting the solvent composition. [Figure not available: see fulltext.]
机译:目的:在设计先进的纳米/微粒药物递送系统时,必须了解粒子形成机制。我们研究了溶剂功率和挥发性如何影响通过喷雾干燥制备的索引荷载的聚(乳酸 - 共乙醇酸)(PLGA)微粒的质地和表面化学。方法:在喷雾干燥之前施加不同摩尔比以不同摩尔比的丙酮和甲醇的二元混合物溶解塞克西布和PLGA。相对于形态,质地,表面化学,固态性质和药物释放曲线表征所得的微粒。使用热重分析(TGA)研究进料溶液的蒸发谱。结果:与溶剂组合物无关,获得球形PLGA微粒。粒度和表面化学高度依赖于进料溶液的溶剂功率。观察到通过饲料溶液制备的微粒的显着爆发释放,所述饲料溶液具有最高量的PLGA差的溶剂。 TGA分析显示二元混合物的不同干燥动力学。结论:颗粒形成过程主要由PLGA沉淀速率控制,该沉淀速率是依赖于溶剂依赖性的,以及在干燥过程中塞克西布分子的迁移率。因此,可以通过调节溶剂组合物来定制喷雾干燥的PLGGA微粒的纹理和表面化学。 [不可用:查看全文。]

著录项

  • 来源
    《Pharmaceutical research》 |2013年第4期|共12页
  • 作者单位

    Department of Pharmacy Faculty of Health and Medical Sciences University of Copenhagen;

    Department of Pharmacy Faculty of Health and Medical Sciences University of Copenhagen;

    Biopharma Application Development Novozymes Biopharma A/S Krogshoejvej 36 2880 Bagsvaerd Denmark;

    Preformulation and Delivery/Oral Protein Delivery Diabetes Research Unit Novo Nordisk A/S M?l?v;

    Department of Pharmacy Faculty of Health and Medical Sciences University of Copenhagen;

    Department of Pharmacy Faculty of Health and Medical Sciences University of Copenhagen;

    Department of Pharmacy Faculty of Health and Medical Sciences University of Copenhagen;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生药学(天然药物学);
  • 关键词

    celecoxib; microparticles; particle formation; poly (lactic-co-glycolic acid); spray drying;

    机译:Celecoxib;微粒;颗粒形成;聚(乳酸 - 共乙醇酸);喷雾干燥;

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