scholarly journals Rapid Simultaneous Determination of Paraquat and Creatinine in Human Serum Using a Piece of Paper

Micromachines ◽  
2018 ◽  
Vol 9 (11) ◽  
pp. 586 ◽  
Author(s):  
Tsui-Hsuan Chang ◽  
Kuo-Hao Tung ◽  
Po-Wen Gu ◽  
Tzung-Hai Yen ◽  
Chao-Min Cheng
Keyword(s):  
Human Serum ◽  
Curve Fitting ◽  
Colorimetric Assay ◽  
Sodium Dithionite ◽  
Normal Human Serum ◽  
The Other ◽  
Chang Gung Memorial Hospital ◽  
Blue Color ◽  
Normal Human ◽  
Analytical Device

Paraquat intoxication is characterized by acute kidney injury and multi-organ failure, causing substantial mortality and morbidity. This study aims to develop a 2-in-1 paper-based analytical device to detect the concentrations of paraquat and creatinine in human serum, which can help clinicians diagnose patients with paraquat poisoning in a more rapid and geographically unrestricted manner. The procedure involves fabrication of a paper-based analytical device, i.e., printing of design on a filter paper, heating of wax-printed micro zone plates so as molten wax diffusing into and completely through the paper to the other side, forming hydrophobic boundaries that could act as detection zones for the paraquat colorimetric assay, and finally analysis using ImageJ software. The paper employed a colorimetric sodium dithionite assay to indicate the paraquat level in a buffer or human serum system in less than 10 min. In this study, colorimetric changes into blue color could be observed by the naked eye. By curve fitting models of sodium dithionite in normal human serum, we evaluated the serum paraquat levels for five paraquat patients. In the sodium dithionate assay, the measured serum paraquat concentrations in patients 1–5 were 22.59, 5.99, 26.52, 35.19 and 25.00 ppm, respectively. On the other hand, by curve fitting models of the creatinine assay in normal human serum, the measured serum creatinine concentrations were 16.10, 12.92, 13.82, 13.58 and 12.20 ppm, respectively. We found that the analytical performance of this device can compete with the standard of Clinical Laboratory of Chang Gung Memorial Hospital, with a less complicated sample preparation process and more rapid results. In conclusion, this 2-in-1 paper-based analytical device has the advantage of being simple and cheap, enabling rapid detection of paraquat intoxication as well as assessment of renal prognosis.

scholarly journals The inhibitory action upon subsequent Phagocytosis, exerted on active normal serum by inactive normal serum through which Bacilli have been passed

1907 ◽  
Vol 79 (534) ◽  
pp. 482-484 ◽  
Keyword(s):  
Human Serum ◽  
Salt Solution ◽  
Inhibitory Action ◽  
Normal Serum ◽  
Normal Human Serum ◽  
The Other ◽  
Supernatant Fluid ◽  
Other Hand ◽  
Difference Of Opinion ◽  
Normal Human

Considerable difference of opinion still prevails regarding the nature of the opsonic substances present in normal serum. Wright, Bulloch and Atkin, etc., uphold the view that the opsonin of normal serum is a simple thermolabile body. Muir, on the other hand, regards the opsonin as a body which behaves like complement, while Dean holds that it is essentially thermostable and in all probability co-operates in its action with a thermolabile complement. The demonstration of anti-bodies by complement-deviation experiments (Bordet, Gengou, Pfeiffer and Friedberger, etc.) has recently proved fruitful in connection with the bacteriolysins, hæmolysins, precipitins of immune sera, and the following experiments were designed to test whether, by a similar method applied to phagocytosis, the presence in normal serum of opsonic amboceptors could be demonstrated :─ Experiment I. Normal human serum was heated for 30 mins. at 60° C. (denoted “ A ”). A very thick emulsion of tubercle bacilli in 1 : 1000 salt solution was added in equal volumes to “ A ” and kept in contact therewith for 1 hr. 30 mins. at 37° C. The mixture was then centrifugalised (7000 revolutions per minute) for 1 hr., and the supernatant fluid pipetted off (denoted “ B ”).

Evaluation of a commercially available radioimmunoassay kit for measurement of doxorubicin in plasma.

1982 ◽  
Vol 28 (1) ◽  
pp. 119-121 ◽  
Author(s):  
E Piall ◽  
G W Aherne ◽  
V Marks
Keyword(s):  
Human Serum ◽  
Normal Human Serum ◽  
Nonspecific Effects ◽  
Normal Human ◽  
Doxorubicin Concentration

Abstract We evaluated a commercially available (Diagnostic Biochemistry Inc.) doxorubicin 125I radioimmunoassay kit. This kit gave a high apparent doxorubicin concentration (greater than 12 micrograms/L), which was not linearly related to dilution, for two pools of normal human serum and plasma and also for samples collected from patients before they received the drug. In contrast, a doxorubicin 3H radioimmunoassay developed by us gave a low blank (2 micrograms/L), which was linearly related to dilution, for the same pools and patients' samples. Doxorubicin concentrations in the plasma of patients receiving the drug were compared by the two methods; the kit gave results five- to 10-fold those obtained with our assay. High nonspecific interference by serum and plasma as measured by the 125I radioimmunoassay must therefore be borne in mind by users of the kit, and we suggest that results should be corrected for these nonspecific effects.

The Presence of Two Forms of Insulin in Normal Human Serum

Biochemistry ◽  
1963 ◽  
Vol 2 (2) ◽  
pp. 286-289 ◽  
Author(s):  
Walter N. Shaw ◽  
Eldon W. Shuey
Keyword(s):  
Human Serum ◽  
Normal Human Serum ◽  
Normal Human

scholarly journals Simple Method To Distinguish between Primary and Secondary C3 Deficiencies

2003 ◽  
Vol 10 (2) ◽  
pp. 216-220
Author(s):  
Marlene Pereira de Carvalho Florido ◽  
Patrícia Ferreira de Paula ◽  
Lourdes Isaac
Keyword(s):  
Human Serum ◽  
Complement System ◽  
Factor H ◽  
Normal Human Serum ◽  
Alternative Complement Pathway ◽  
Complement Pathway ◽  
Factor B ◽  
Alternative Complement ◽  
Normal Human ◽  
The Complement System

ABSTRACT Due to the increasing numbers of reported clinical cases of complement deficiency in medical centers, clinicians are now more aware of the role of the complement system in the protection against infections caused by microorganisms. Therefore, clinical laboratories are now prepared to perform a number of diagnostic tests of the complement system other than the standard 50% hemolytic component assay. Deficiencies of alternative complement pathway proteins are related to severe and recurrent infections; and the application of easy, reliable, and low-cost methods for their detection and distinction are always welcome, notably in developing countries. When activation of the alternative complement pathway is evaluated in hemolytic agarose plates, some but not all human sera cross-react to form a late linear lysis. Since the formation of this linear lysis is dependent on C3 and factor B, it is possible to use late linear lysis to routinely screen for the presence of deficiencies of alternative human complement pathway proteins such as factor B. Furthermore, since linear lysis is observed between normal human serum and primary C3-deficient serum but not between normal human serum and secondary C3-deficient serum caused by the lack of factor H or factor I, this assay may also be used to discriminate between primary and secondary C3 deficiencies.

Sign in / Sign up

Export Citation Format

Share Document