A novel strategy affords high-yield coupling of antibody to extremities of liposomal surface-grafted PEG chains

被引:42
作者
Mercadal, M
Domingo, JC
Petriz, J
Garcia, J
de Madariaga, MA
机构
[1] Univ Barcelona, Fac Chem, Dept Biochem & Mol Biol, E-08028 Barcelona, Spain
[2] Oncol Res Inst, Dept Cryobiol & Celullar Therapy, Barcelona 08907, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 1999年 / 1418卷 / 01期
关键词
immunoliposome; sterically stabilized immunoliposome; CD34; antigen; stem cell;
D O I
10.1016/S0005-2736(99)00033-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several methodologies for the preparation of polyethylene glycol-grafted immunoliposomes have been developed by attaching antibodies to the terminus of the polymer. Unilamellar liposomes were prepared containing a combination of a functionalized polyethylene glycol(3400) and an inert polyethylene glycol(2000) phosphatidylethanolamine derivate up to 5 mol%. The greater length of the functionalized polyethylene glycol derivate did not alter the liposomal sterical stability or the remote loading of doxorubicin. Anti-CD34 immunoliposomes were prepared by the reaction of maleimide-derivatized My10 antibody with generated thiol groups at the periphery of the liposomes and efficiencies of nearly 100% were obtained. The greater accessibility of the reactive group makes this strategy more efficient than others described. The immunoliposomes prepared bound specifically to CD34+ cells, (C) 1999 Elsevier Science B.V, All rights reserved.
引用
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页码:232 / 238
页数:7
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