Christian David A, Garbuzenko Olga B, Minko Tamara, Discher Dennis E
Department of Chemical & Biomolecular Engineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Macromol Rapid Commun. 2010 Jan 18;31(2):135-41. doi: 10.1002/marc.200900589. Epub 2009 Dec 1.
Polymersomes are block copolymer-based vesicles whose long circulation times or "stealth" in vivo coupled with the loading and controlled release of drugs, siRNA, and other compounds has made them attractive for delivery. A brushy corona of non-ionic polyethylene glycol (PEG) likely contributes stealth, but red blood cells (RBCs) possess a negatively charged glycocalyx and circulate much longer. Polyanionic block copolymers were therefore mixed into polymersomes which were also labeled with a near IR fluorophore to quantify biodistribution in live mice and excised organs. Charge shifts tissue distribution, and high resolution imaging of vesicles in blood capillaries further shows that organ cultures can provide deeper insight into microscale transport within tissue microenvironments.
聚合物囊泡是基于嵌段共聚物的囊泡,其在体内的长循环时间或“隐身”特性,以及药物、小干扰RNA(siRNA)和其他化合物的装载与控释能力,使其成为有吸引力的递送载体。非离子聚乙二醇(PEG)形成的毛刷状冠层可能有助于实现隐身,而红细胞(RBC)具有带负电荷的糖萼且循环时间长得多。因此,将聚阴离子嵌段共聚物混入聚合物囊泡中,这些聚合物囊泡还用近红外荧光团进行标记,以量化在活体小鼠和切除器官中的生物分布。电荷会改变组织分布,对毛细血管中囊泡的高分辨率成像进一步表明,器官培养能够更深入地洞察组织微环境内的微观运输。