Lukyanov Anatoly N, Elbayoumi Tamer A, Chakilam Ananthsrinivas R, Torchilin Vladimir P
Department of Pharmaceutical Sciences, Bouve College of Health Sciences, Northeastern University, Mugar Bldg 312, 360 Huntington Aveneu, Boston, MA 02115, USA.
J Control Release. 2004 Nov 5;100(1):135-44. doi: 10.1016/j.jconrel.2004.08.007.
Commercially available doxorubicin-loaded long-circulating liposomes (Doxil, Alza Pharmaceuticals) were modified with the monoclonal nucleosome (NS)-specific 2C5 antibody (mAb 2C5) that recognizes a broad variety of tumors via the tumor cell surface-bound NSs. For incorporation into liposomes, mAb 2C5 was modified with poly(ethylene glycol)-phosphatidyl ethanolamine conjugate (PEG-PE) with the free PEG terminus activated with the p-nitrophenylcarbonyl group (pNP-PEG-PE). Derivatives of mAb 2C5 containing a variable number of PEG-PE residues (10-32) per protein molecule were prepared with a reasonably good preservation of the antibody specific activity even at the highest degree of modification. PEG-PE-modified antibody quantitatively incorporated into the liposomal membrane of doxorubicin-loaded liposomes with a loss of not more than 20% of the encapsulated doxorubicin. 2C5-targeted Doxil liposomes acquired the ability to recognize NSs and specifically bind to various tumor cells. Doxorubicin-loaded long-circulating liposomes modified with the mAb 2C5 kill various tumor cells in vitro with the efficiency higher than non-targeted doxorubicin-loaded liposomes.
市售的载有多柔比星的长循环脂质体(多美素,阿尔扎制药公司)用单克隆核小体(NS)特异性2C5抗体(单克隆抗体2C5)进行修饰,该抗体通过肿瘤细胞表面结合的核小体识别多种肿瘤。为了掺入脂质体中,用聚乙二醇 - 磷脂酰乙醇胺缀合物(PEG-PE)修饰单克隆抗体2C5,其中游离的PEG末端用对硝基苯基羰基(pNP-PEG-PE)活化。制备了每个蛋白质分子含有可变数量(10 - 32个)PEG-PE残基的单克隆抗体2C5衍生物,即使在最高修饰程度下,抗体的特异性活性也能得到较好的保留。PEG-PE修饰的抗体定量掺入载有多柔比星的脂质体的脂质体膜中,包封的多柔比星损失不超过20%。2C5靶向的多美素脂质体获得了识别核小体并特异性结合各种肿瘤细胞的能力。用单克隆抗体2C5修饰的载有多柔比星的长循环脂质体在体外杀死各种肿瘤细胞,其效率高于非靶向的载有多柔比星的脂质体。