Leach W Thomas, Simpson Dale T, Val Tibisay N, Yu Zhongshui, Lim Kwon T, Park Eun J, Williams Robert O, Johnston Keith P
Pharmaceutics Division, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA.
AAPS PharmSciTech. 2005 Dec 6;6(4):E605-17. doi: 10.1208/pt060475.
A new spinning oil film (SOF) solid-in-oil-in-oil emulsion process was developed to produce uniform-sized protein-loaded biodegradable microspheres. A thin SOF on a cylindrical rotor was used to shear droplets from a nozzle tip to control droplet size. The resulting microspheres with low polydispersity (6%) produced a low burst (6%-11%) release even at high loadings (13%-18% encapsulated solids, 8%-12% protein). The SOF process had a high yield and did not require the presence of water, which can cause protein denaturation, or surfactants, which may be unwanted in the final product. Amorphous protein and crystalline excipient solids were encapsulated into 3 different polymers, giving a homogenous drug distribution throughout the microspheres, and an essentially complete protein encapsulation efficiency (average = 99%). In contrast, large burst release was observed for polydisperse microspheres produced by a conventional emulsification technique, particularly for microspheres smaller than 25 mum in diameter, which gave 93% burst at 15% loading. The uniform encapsulation of high loadings of proteins into microspheres with low polydispersity in an anhydrous process is of practical interest in the development of controlled-release protein therapeutics.
开发了一种新的旋转油膜(SOF)油包固油包油乳液工艺,以生产尺寸均匀的载蛋白可生物降解微球。圆柱形转子上的薄SOF用于从喷嘴尖端剪切液滴以控制液滴大小。所得具有低多分散性(6%)的微球即使在高载量(13%-18%包封固体,8%-12%蛋白质)下也具有低突释(6%-11%)。SOF工艺产率高,不需要可能导致蛋白质变性的水或最终产品中可能不需要的表面活性剂的存在。无定形蛋白质和结晶赋形剂固体被包封到3种不同的聚合物中,使药物在整个微球中分布均匀,并且蛋白质包封效率基本完全(平均=99%)。相比之下,通过传统乳化技术生产的多分散微球观察到较大的突释,特别是对于直径小于25μm的微球,在15%载量下突释率为93%。在无水工艺中将高载量蛋白质均匀包封到低多分散性微球中,在控释蛋白质治疗剂的开发中具有实际意义。