5277818 Albumin preparation and process for preparing the same

1994 ◽  
Vol 12 (3) ◽  
pp. 582
Keyword(s):  
2021 ◽  
Vol 65 (6) ◽  
pp. 38-46
Author(s):  
A Lunev ◽  
O. Klement'eva ◽  
A Zverev

The article is written about studying of radiation safety of 188Re-labeled microspheres of albumin preparation (hand mode) for treatment of resistant synovitis. The study material was a radiopharmaceutical based on albumin microspheres 5 –10 µm with rhenium-188 for treatment of resistant synovitis. The studying has led to conclusion the number of radiopharmaceutical portions prepared by one operator should not exceed 70 times a year, which will ensure that the main limits of equivalent doses to hands and skin with a reserve factor of 2 (250 μSv/h) are not exceeded. Protective equipment should be used to reduce doses to hands, as the most critical to operator's body part irradiation.


1949 ◽  
Vol 47 (4) ◽  
pp. 360-383
Author(s):  
G. R. E. Naylor

1. The reaction horse serum and a pool of rabbit antihorse serum exhibiting four α procedure optima has been investigated with a view to analysing the antigens involved in the production of the multiple zones.2. The following conclusions have been reached regarding the antigenic constitution of horse serum, a horse serum-albumin preparation and a horse serum-globulin preparation: Horse serum consists of at least five antigens. The horse serum-albumin preparation contains three antigens, two of which are probably impurities, one of these being a globulin. The horse serum-globulin preparation consists of three antigens and evidence was obtained of a fourth. Electrophoretic analysis of these protein preparations gave concordant result.3. Multiple zones of rapid particulation in the precipitation reaction are due to the independent activity of multiple antigens and their homologous antibodies.4. The absorption of precipitin from a mixture of antibodies by a mixture of antigens at a single α procedure optimum is both a useful and a practicable procedures.5. Attention is drawn to the fact that the method of antigenic analysis used in the present series of experiments, involving the correlation of α; procedure optima occurring in the parallel titrations of a single antiserum against a mixed antigen and equivalent concentrations of physically or chemically prepared fractions of it supplemented by absorption of precipitins at individual and multiple α precedure optima and retitration of the absorbed sera, could be applied to the identification and nomenclature of proteins occurring in natural mixtures, and also to the quantitative and qualitative appraisal of the purity of proteins prepared by physical or chemical means. The method does not rely on the preparation of highly purified protein samples containing a single antigen.


1977 ◽  
Vol 164 (3) ◽  
pp. 607-616 ◽  
Author(s):  
A T Moore ◽  
K E Williams ◽  
J B Lloyd

Portions of a 125I-iodinated bovine serum albumin preparation were exposed to freezing, acetic acid (pH 3.5, 3.0 or 2.5), urea or formaldehyde, and the effect of these treatments on the rates of pinocytic uptake by yolk sacs from 17.5-day-pregnant rats cultured in vitro and of clearance from the rat bloodstream were studied. Uptake of albumin by the yolk sac was followed by rapid release of [125I]iodo-L-tyrosine into the culture medium. Similarly clearance of albumin in vivo was accompanied by the appearance of trichloroacetic acid-soluble radioactivity in the bloodstream. In both systems the rates of uptake of modified albumin preparations formed a series: formaldehyde or urea greater than acetic acid greater than freezing. The increased rates of uptake of modified albumin preparations could not be ascribed to the formation of aggregates nor, in the yolk-sac system, to an increase in the rate of pinosome formation. It is concluded that the various treatments to which the albumin was subjected increase to varying degrees the affinity of the albumin molecule for binding sites on that region of the plasma membrane from which pinocytic vesicles are formed. Some comparable experiments with native and desialylated human orosomucoid indicate that the rat yolk-sac epithelial cells do not possess the recognition system for uptake of asialoglycoproteins that exists on the surface of hepatic parenchymal cells.


1959 ◽  
Vol 19 (3) ◽  
pp. 221-231 ◽  
Author(s):  
K. W. TAYLOR ◽  
P. J. RANDLE

SUMMARY The uptake of glucose by isolated rat diaphragm is increased in vitro by serum from normal oxen and diabetic patients treated with ox insulin; by slower moving albumin, β- and γ-globulin fractions of serum from normal oxen; by slower moving albumin, α2-, β- and γ-globulin fractions of serum from treated diabetics (prepared by zone electrophoresis on columns of treated cellulose). More rapidly moving albumins from both types of serum did not stimulate glucose uptake. The effect of serum or protein fractions of serum was absent or markedly reduced in the presence of antiserum to ox insulin prepared in guinea-pigs. It is concluded that the stimulating effect of serum and protein fractions of serum on uptake of glucose by diaphragm is due to circulating insulin. The effect of insulin on uptake of glucose by diaphragm is shown to be potentiated by the presence of corticotrophin, prolactin, normal guinea-pig serum and an albumin preparation from the serum of hypophysectomized rats. The significance of these results in relation to the detection and assay of insulin in blood with isolated diaphragm and to the transport of insulin in blood is discussed.


Redox Biology ◽  
2018 ◽  
Vol 14 ◽  
pp. 354-360 ◽  
Author(s):  
Mayumi Ikeda ◽  
Yu Ishima ◽  
Ryo Kinoshita ◽  
Victor T.G. Chuang ◽  
Nanami Tasaka ◽  
...  

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