Analysis of serum proteins adsorbed to a hemodialysis membrane of hollowfiber type by thermal lens microscopy

被引:6
作者
Kimura, H [1 ]
Kojima, H
Mukaida, M
Kitamori, T
Sawada, T
机构
[1] Juntendo Univ, Sch Med, Dept Forens Med, Tokyo 1138421, Japan
[2] Asahi Chem Ind Co Ltd, Analyt Res Lab, Analyt & Computat Sci Lab, Shizuoka 4168501, Japan
[3] Natl Def Med Coll, Dept Forens Med, Tokorozawa, Saitama 3598513, Japan
[4] Univ Tokyo, Fac Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, Japan
关键词
protein-analysis; hemodialysis membrane; immunostaining; colloidal gold; thermal-lens microscopy;
D O I
10.2116/analsci.15.1101
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
To analyze serum proteins adsorbed to a hemodialysis membrane. immunostaining with colloidal gold and thermal-lens microscopy were employed. A total of 14 types of hemodialysis membranes were tested. The cross sections of the membranes were stained with fluorescent antibodies. Observations of these specimens using a laser microscope revealed that serum proteins, such as albumin and immune globulins, tended to adsorb into the inner wall of these membranes. The degree of adsorption of serum proteins varied according to various conditions, such as what materials the membranes were made of or what proteins were adsorbed. For a better quantitative analysis of these proteins. the membranes were stained with immunogold and were observed by a thermal lens microscope. Colloidal gold coated with various anti-human serum proteins was used for the staining. and the quantity of colloidal gold was measured with a thermal-lens microscope. The quantity of colloidal gold, coated with anti-human sera antibody, gradiently decreased from the inner to the outer wall of the membrane. Probably, proteins with larger molecules were adsorbed to the inner parts, and those with smaller molecules were adsorbed to the outer parts of the membrane wall. High-resolution thermal-lens microscopy makes possible the sensitive detection of localized proteins adsorbed to a membrane without extracting it. Thus, the analysis of adsorbed proteins should serve to determine the adaptability of medical appliances to the human body and should also be helpful to a retrospective analysis of substances like drugs which are conjugated to the serum proteins.
引用
收藏
页码:1101 / 1107
页数:7
相关论文
共 21 条
[1]   Immunohistochemical localization of N-methyl-D-aspartate and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor subunits in the substantia nigra pars compacta of the rat [J].
Albers, DS ;
Weiss, SW ;
Iadarola, MJ ;
Standaert, DG .
NEUROSCIENCE, 1999, 89 (01) :209-220
[2]  
Barozzi C, 1985, Life Support Syst, V3 Suppl 1, P490
[3]  
Bohler J, 1996, J AM SOC NEPHROL, V7, P234
[4]   SYNTHESIS OF BETA(2)-MICROGLOBULIN IN LYMPHOCYTE CULTURE - ROLE OF HEMODIALYSIS, DIALYSIS MEMBRANES, DIALYSIS-AMYLOIDOSIS, AND LYMPHOKINES [J].
CAMPISTOL, JM ;
MOLINA, R ;
BERNARD, DB ;
RODRIGUEZ, R ;
MIRAPEIX, E ;
MUNOZGOMEZ, JM ;
REVERT, L .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1993, 22 (05) :691-699
[5]  
CHUANG HYK, 1982, J LAB CLIN MED, V92, P483
[6]   PLASMA-PROTEIN ADSORPTION TO HIGHLY PERMEABLE HEMODIALYSIS MEMBRANES [J].
CLARK, WR ;
MACIAS, WL ;
MOLITORIS, BA ;
WANG, NHL .
KIDNEY INTERNATIONAL, 1995, 48 (02) :481-488
[7]  
Drueke T, 1995, Adv Ren Replace Ther, V2, P24
[8]  
FRANCOISE GAM, 1991, J BIOMAT SCI-POLYM E, V2, P263
[9]   Adsorption of complement, cytokines, and proteins by different dialysis membrane materials: Evaluation by confocal laser scanning fluorescence microscopy [J].
Fujimori, A ;
Naito, H ;
Miyazaki, T .
ARTIFICIAL ORGANS, 1998, 22 (12) :1014-1017
[10]   PHOTOTHERMAL MICROSCOPY WITH EXCITATION AND PROBE BEAMS COAXIAL UNDER THE MICROSCOPE AND ITS APPLICATION TO MICROPARTICLE ANALYSIS [J].
HARADA, M ;
IWAMOTO, K ;
KITAMORI, T ;
SAWADA, T .
ANALYTICAL CHEMISTRY, 1993, 65 (20) :2938-2940