Qin Jing, Chen DaWei, Hu Haiyang, Qiao MingXi, Zhao XiuLi, Chen Baoyu
Department of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning, PR China.
Yakugaku Zasshi. 2007 Sep;127(9):1497-501. doi: 10.1248/yakushi.127.1497.
RGD conjugation liposomes (RGD-liposomes) were evaluated for brain-targeting drug delivery. The flow cytometric in vitro study demonstrated that RGD-liposomes could bind to monocytes and neutrophils effectively. Ferulic acid (4-hydroxy-3-methoxycinnamic, FA) was loaded into liposomes. Rats were subjected to intrastriatal microinjections of 100 units of human recombinant IL-1beta to produce brain inflammation and caudal vein injection of three formulations (FA solution, FA liposome and RGD-coated FA liposome). Animals were sacrificed 15, 30, 60 and 120 min after administration to study the body distribution of the FA in the three formulations. HPLC was used to determine the concentration of FA in vivo with salicylic acid as internal standard. The results of body distribution indicated that RGD-coated liposomes could be mediated into the brain with a 6-fold FA concentration compared to FA solution and 3-fold in comparison to uncoated liposome. Brain targeted delivery was achieved and a reduction in dosage might be allowed.
对RGD偶联脂质体(RGD-脂质体)进行了脑靶向给药评估。体外流式细胞术研究表明,RGD-脂质体可有效结合单核细胞和中性粒细胞。将阿魏酸(4-羟基-3-甲氧基肉桂酸,FA)载入脂质体。给大鼠纹状体内微注射100单位人重组白细胞介素-1β以引发脑部炎症,并经尾静脉注射三种制剂(FA溶液、FA脂质体和RGD包被的FA脂质体)。给药后15、30、60和120分钟处死动物,以研究三种制剂中FA在体内的分布情况。采用高效液相色谱法,以水杨酸为内标物测定体内FA浓度。体内分布结果表明,与FA溶液相比,RGD包被的脂质体介导进入脑内的FA浓度高6倍,与未包被的脂质体相比高3倍。实现了脑靶向给药,且可能允许减少剂量。