Reduced Albumin Binding Promotes the Stability and Activity of Topotecan in Human Blood

Biochemistry ◽  
1995 ◽  
Vol 34 (42) ◽  
pp. 13722-13728 ◽  
Author(s):  
Zihou Mi ◽  
Henryk Malak ◽  
Thomas G. Burke
1970 ◽  
Vol 24 (03/04) ◽  
pp. 334-337 ◽  
Author(s):  
R Honorato

Summary1. A technique to obtain human serum rich in factor V is described.2. Calcium increases the stability of factor V in the serum.


Cosmetics ◽  
2020 ◽  
Vol 7 (2) ◽  
pp. 28 ◽  
Author(s):  
Ekaterina N. Maevskaia ◽  
Oksana P. Kirichuk ◽  
Sergei I. Kuznetzov ◽  
Elena N. Dresvyanina ◽  
Vladimir V. Yudin ◽  
...  

Composite chitosan fibers filled with chitin nanofibrils (CNF) were obtained by the wet spinning method. The paper discusses the mechanical properties of such type fibers and their hemocompatibility, as well as the possibility of optimizing these properties by adding chitin nanofibrils. It was shown that low CNF concentration (about 0.5%) leads to an increase in fiber tensile strength due to the additional orientation of chitosan macromolecules. At the same time, with an increase in the content of CNF, the stability of the mechanical properties of composite fibers in a humid medium increases. All chitosan fibers, except 0.5% CNF, showed good hemocompatibility, even on prolonged contact with human blood. The addition of chitin nanofibers leads to decrease in hemoglobin molecules sorption due to the decline in optical density at wavelengths of 414 nm and 540 nm. Nevertheless, the hemolysis of fibers was comparable or even lesser that carbon hemosorbent, which is actively used in clinical practice.


1985 ◽  
Vol 9 (2) ◽  
pp. 85-88 ◽  
Author(s):  
Stephen T. Wang ◽  
Frank Peter
Keyword(s):  

2007 ◽  
Vol 375 (1-2) ◽  
pp. 169-170 ◽  
Author(s):  
Angelo Mancinelli ◽  
Emerenziana Iannoni ◽  
Marinus Duran ◽  
Menotti Calvani

Bone ◽  
2009 ◽  
Vol 44 ◽  
pp. S364
Author(s):  
S. við Streym Thomsen⁎ ◽  
L. Rejnmark ◽  
P. Vestergaard ◽  
L. Heickendorff ◽  
L. Mosekilde

2018 ◽  
Vol 485 ◽  
pp. 1-6 ◽  
Author(s):  
Denise S. Tevis ◽  
Jeffery M. Jarrett ◽  
Deanna R. Jones ◽  
Po-Yung Cheng ◽  
Melanie Franklin ◽  
...  
Keyword(s):  
Total Hg ◽  

1961 ◽  
Vol 05 (03) ◽  
pp. 559-565 ◽  
Author(s):  
R Honorato ◽  
G Schindler

Summary1. The influence of 0.025 M, 0.1 M, 0.2 M sodium oxalate and of 0.2 M sodium citrate on the stability of human blood platelets was studied.2. A diminution of the resistance of platelets to glass in the 0.025 M and 0.1.M sodium oxalate blood samples was observed.3. This effect of oxalate was not observed when red blood cells were not present.


1988 ◽  
Vol 117 (1) ◽  
pp. 139-145 ◽  
Author(s):  
A. Tsatsoulis ◽  
K. Mavroudis ◽  
J. Frost ◽  
A. Lambert ◽  
S. M. Shalet ◽  
...  

ABSTRACT The degree of stability in vitro of bioactive and immunoreactive LH in human blood, plasma and serum was examined. Bioactivity and immunoreactivity of LH were assayed by the dispersed mouse Leydig cell assay and by standard radioimmunoassay respectively, using the same reference preparation (first international reference preparation for human pituitary LH 68/40 for immunoassay). Bioactive and immunoreactive LH were stable in blood and plasma at 22 °C for up to 4 and 24 h respectively, and in blood at 4 °C for up to 24 h. There was no loss of biological or immunological LH activity in plasma which had been either snap-frozen and stored at −70 °C, allowed to freeze at −20 °C and stored at that temperature or kept at 4 °C for 24 h and then stored at − 70 °C. Likewise, the levels of LH in plasma and serum which had been stored at either − 20 or − 70 °C and then thawed and refrozen up to four times remained unchanged. In addition, the biological and immunological activity of LH was not affected after vortexing samples of plasma or serum for up to 60 s. Bioactive LH was also stable in plasma samples after prolonged storage (up to 9 months) at either −70 or −20 °C. We conclude that LH bioactivity and immunoreactivity are stable in blood and plasma following a variety of treatments commonly experienced during normal handling of a blood sample after venepuncture. J. Endocr. (1988) 117, 139–145


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