Acoustophoretic separation of infected erythrocytes from blood plasma in a microfluidic platform using biofunctionalized, matched-impedance layers

2017 ◽  
Vol 34 (4) ◽  
pp. e2943 ◽  
Author(s):  
Tamaghna Gupta ◽  
Ritwick Ghosh ◽  
Ranjan Ganguly
Keyword(s):  
Blood Plasma ◽  
Microfluidic Platform ◽  
Matched Impedance

A Circular Gradient-Width Crossflow Microfluidic Platform for High-Efficiency Blood Plasma Separation

2021 ◽  
pp. 131180
Author(s):  
Han Zhang ◽  
Kanjirakat Anoop ◽  
Can Huang ◽  
Reza Sadr ◽  
Rohit Gupte ◽  
...  
Keyword(s):  
Blood Plasma ◽  
High Efficiency ◽  
Microfluidic Platform ◽  
Plasma Separation ◽  
Blood Plasma Separation

Protection from Hg-Inactivation of Factor XIII by Mercaptalbumin

1970 ◽  
Vol 24 (03/04) ◽  
pp. 352-355 ◽  
Author(s):  
P Fantl
Keyword(s):  
Blood Plasma ◽  
Factor Xiii ◽  
Active Component ◽  
Plasma Albumin ◽  
Plasma Factor ◽  
Mercuric Ions

SummaryThe blood plasma factor XIII (fibrin stabilizing factor) is inactivated by mercuric ions and can be reactivated by serum - or plasma albumin of which the active component is mercaptalbumin. A relation between mercaptalbumin concentration and factor XIII activity is pointed out.

Validation of Simvastatin Analysis Methods in Human Blood Plasma (In Vitro) Using HPLC-UV Detector

2018 ◽  
Vol 8 (2) ◽  
Author(s):  
Iyan Sopyan ◽  
Cynthia Jaya ◽  
Driyanti Rahayu
Keyword(s):  
Blood Plasma ◽  
Human Plasma ◽  
Disease Risk ◽  
Protein Precipitation ◽  
Precipitation Method ◽  
Human Blood Plasma ◽  
Analysis Method ◽  
Uv Detector ◽  
Number Of Patients ◽  
System Suitability

The use of simvastatin (SV) increases along with the increasing number of patients with hyperlipidemia and cardiovascular disease risk factors. Consequently, this condition leads to the increasing need of analytical determination of SV in blood plasma. Analysis of SV in human plasma using protein precipitation method and HPLC with UV detector has not been reported. This research was purpose to find out the rapid, accurate, and valid of SV analysis method in human plasma. In this research plasma samples were treated with protein precipitation method. The analyte was then analyzed using HPLC with C18 column 250x4 mm and 5 µm of particle size, the mobile phase contained of phosphate buffer 0.01 M (pH 4.0) and acetonitrile 30:70 v/v with flow rate 1 mL/minute, and detected at 239 nm. The analysis method was validated based on some parameters, such as selectivity, accuracy, precision, repeatability, linearity, LOD, LOQ, and system suitability. The result showed selectivity represented by Rs was 2.870, repeatability by its CV less than 2%, and linearity by its coefficient correlation (r) 0.9992 for concentration range 0.08-0.32 ppm. Based on chromatogram peak area, LOD and LOQ were 0.0132 and 0.0440 ppm respectively, accuracy and precision were 86.25-89.36% and 0.66-1.81% were obtained. The result of system suitability test from retention time and chromatogram peak area showed by its CV less than 2%. The analysis method was proved to be valid for SV analysis in human plasma

The Relationship between the Blood Plasma Vitamin A Levels of Sows and of their Suckling Pigs

1956 ◽  
Vol 15 (2) ◽  
pp. 400-406
Author(s):  
I. R. Sibbald ◽  
J. P. Bowland ◽  
R. T. Berg
Keyword(s):  
Vitamin A ◽  
Blood Plasma ◽  
Plasma Vitamin ◽  
The Relationship
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