ANTIBODY MAGNETITE NANOPARTICLES - IN-VITRO CHARACTERIZATION OF A POTENTIAL TUMOR-SPECIFIC CONTRAST AGENT FOR MAGNETIC-RESONANCE-IMAGING

被引:126
作者
TIEFENAUER, LX
KUHNE, G
ANDRES, RY
机构
[1] Paul Scherrer Institute
关键词
D O I
10.1021/bc00023a007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Target-specific superparamagnetic contrast agents may allow the localization of specific tissues such as tumors by magnetic resonance imaging (MRI). In this report the preparation and in vitro characterization of tumor-specific superparamagnetic particles (SMP) are described. Particles of uniform size (9.6 +/- 0.8 nm) were prepared from an alkaline solution of ferric and ferrous ions and isolated by differential centrifugation. The resulting nanoparticle suspension is stabilized in buffer using a polypeptide coat to which a monoclonal antibody, specific to carcinoembryonic antigen (CEA), was covalently attached at the hinge region. The resulting anti-CEA SMP have a hydrodynamic radius of less than 50 nm, and specifically bind to CEA in vitro. The visualization of epitopes, present on a cell surface in very low density as expected for tumor antigens or receptors, may be achieved due to the high R2 relaxivity of 300 L mmol-1 s-1 of the contrast agent described here. Furthermore, the polypeptide coat chosen provides an ideal platform for the attachment of biological modifiers needed for the reduction of the antigenicity and blood clearance rate of anti-CEA SMP.
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收藏
页码:347 / 352
页数:6
相关论文
共 36 条
[1]   NEW CLEAVABLE REAGENT FOR CROSS-LINKING AND REVERSIBLE IMMOBILIZATION OF PROTEINS [J].
ABDELLA, PM ;
SMITH, PK ;
ROYER, GP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1979, 87 (03) :734-742
[2]  
ABUCHOWSKI A, 1977, J BIOL CHEM, V252, P3582
[3]   UPTAKE OF LIPOSOMES BY CULTURED MOUSE BONE-MARROW MACROPHAGES - INFLUENCE OF LIPOSOME COMPOSITION AND SIZE [J].
ALLEN, TM ;
AUSTIN, GA ;
CHONN, A ;
LIN, L ;
LEE, KC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1061 (01) :56-64
[4]   LIPOSOMES WITH PROLONGED CIRCULATION TIMES - FACTORS AFFECTING UPTAKE BY RETICULOENDOTHELIAL AND OTHER TISSUES [J].
ALLEN, TM ;
HANSEN, C ;
RUTLEDGE, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 981 (01) :27-35
[5]   IMMUNOSCINTIGRAPHIC LOCALIZATION OF INFLAMMATORY LESIONS - CONCEPT, RADIOLABELLING AND INVITRO TESTING OF A GRANULOCYTE SPECIFIC ANTIBODY [J].
ANDRES, RY ;
SCHUBIGER, PA ;
TIEFENAUER, L ;
SEYBOLD, K ;
LOCHER, JT ;
MACH, JP ;
BUCHEGGER, F .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1988, 13 (11) :582-586
[6]  
ANDRES RY, 1990, 9TH ANN M SOC MAGN R
[7]   ANTIGEN-IMMOBILIZED VERSUS ANTIBODY-IMMOBILIZED ELISA PROCEDURES BASED ON A BIOTINYL-ESTRADIOL CONJUGATE [J].
BODMER, DM ;
TIEFENAUER, LX ;
ANDRES, RY .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1989, 33 (06) :1161-1166
[8]  
BUSKE N, 1984, COLLOID SURFACE, V112, P195
[9]   MONOCLONAL ANTIBODY-COATED MAGNETITE PARTICLES AS CONTRAST AGENTS IN MAGNETIC-RESONANCE IMAGING OF TUMORS [J].
CERDAN, S ;
LOTSCHER, HR ;
KUNNECKE, B ;
SEELIG, J .
MAGNETIC RESONANCE IN MEDICINE, 1989, 12 (02) :151-163
[10]   THE IMMUNE-RESPONSE AGAINST THERAPEUTIC MONOCLONAL-ANTIBODIES [J].
CHATENOUD, L .
IMMUNOLOGY TODAY, 1986, 7 (12) :367-368