Spectrophotometric determination of total proteins in blood plasma with p-benzoquinone
Braz. j. med. biol. res
;
25(6): 549-55, 1992. ilus
Artículo
en Inglés
| LILACS
| ID: lil-109069
RESUMO
In the present study we have documented the use of the reagent p-benzoquinone (PBQ) for the spectrophotometric determination of total protein in blood plasma. Since the products of reaction are stable for several hours at room temperature after the 20-min boiling step, the time at which absorbance is measured is not a critical factor. Common anticoagulants such as EDTYA, citrate, or heparin do not interfere with the PBQ method at concentrations used in clinical laboratories. The products of the reaction between PBQ and either plasma (specific absorbance 2.33 x 10-3 ñ 0.20 x 10-3 ug cm -2) or purified proteins (specific absorbance 2.61 x 10-3 ñ 0.31 x 10-3 ug cm-2) show an absorption band at 350 nm, which follows Beer's law, and therefore can be used for analytical purposes. The PBQ method has a lower limit of detection (4 ug/ml) than that of biuret method (45 yg/ml) for a final reaction mixture of 5.0 and 4.2 ml, respectively
Buscar en Google
Índice:
LILACS (Américas)
Asunto principal:
Espectrofotometría
/
Proteínas
/
Benzoquinonas
/
Anticoagulantes
Idioma:
Inglés
Revista:
Braz. j. med. biol. res
Asunto de la revista:
Biologia
/
Medicina
Año:
1992
Tipo del documento:
Artículo
Similares
MEDLINE
...
LILACS
LIS