Nguyen Hoai X, O'Rear Edgar A
a School of Chemical, Biological and Materials Engineering, University of Oklahoma , Norman , OK , USA.
b Institute for Biomedical Engineering, Science and Technology , Norman , OK , USA.
J Microencapsul. 2017 May;34(3):299-307. doi: 10.1080/02652048.2017.1323036. Epub 2017 May 10.
In this study, we describe the synthesis of an amine-modified acetalated dextran polymer, which is combined with heparin (HP) as the basis for a novel controlled release system. Dextran-amine (DEXAM) conjugates, synthesised using reductive amination, were incorporated into DEXAM/HP microspheres. HP binds to positively charged ammonium ions of the DEXAM conjugates, contributing to the structural integrity of the microspheres. Crystal violet (CV) was encapsulated inside DEXAM/HP microspheres as a model drug to test the system. Protamine with a high affinity for HP functioned as a trigger to release CV. DEXAM/HP microspheres were characterised by particle size, encapsulation efficiency, scanning electron microscope images, and in vitro release profile. Release of CV from microspheres varied with primary amine content of DEXAM conjugates, amount of HP, and concentration of protamine added. The system is considered for controlled delivery of agents without the necessity of chemical modification.
在本研究中,我们描述了一种胺修饰的缩醛化葡聚糖聚合物的合成,该聚合物与肝素(HP)结合,作为新型控释系统的基础。使用还原胺化法合成的葡聚糖-胺(DEXAM)缀合物被纳入DEXAM/HP微球中。HP与DEXAM缀合物带正电荷的铵离子结合,有助于微球的结构完整性。结晶紫(CV)作为模型药物被包裹在DEXAM/HP微球内以测试该系统。对HP具有高亲和力的鱼精蛋白用作释放CV的触发剂。通过粒径、包封效率、扫描电子显微镜图像和体外释放曲线对DEXAM/HP微球进行了表征。微球中CV的释放随DEXAM缀合物的伯胺含量、HP的量和添加的鱼精蛋白浓度而变化。该系统被认为可用于无需化学修饰的药物控释。