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
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;
celecoxib; microparticles; particle formation; poly (lactic-co-glycolic acid); spray drying;
机译:关键的溶剂性质会影响颗粒形成过程和通过喷雾干燥负载塞来昔布的PLGA微粒的特性
机译:使用电喷雾在不同溶剂中制备的载有塞来昔布的聚乳酸-乙醇酸共聚物微粒的颗粒形成和特性
机译:通过喷雾干燥水乳液,通过喷雾干燥的高免疫球蛋白G负载水平和缓释性质的研制进行PLGA微粒
机译:在原位微粒乳液形成期间将来自聚(丙交酯 - 共乙酰化)(PLGA)溶液(PLGA)溶液的溶剂扩散速率的比较
机译:用于动脉粥样硬化磁共振成像的可靶向PLGA微粒和纳米颗粒。
机译:超临界反溶剂法制备可吸入的利福平-聚(l-丙交酯)微粒
机译:通过喷雾干燥水乳液,通过喷雾干燥的高免疫球蛋白G负载水平和缓释性质的研制进行PLGA微粒