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1.
Eur J Clin Chem Clin Biochem ; 34(3): 171-91, 1996 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-8721405

RESUMEN

The determination of salivary drug concentrations is one of the major domains for the application of saliva in laboratory medicine. Its usefulness, however, has been criticized for many drugs because of the variability of the saliva/plasma concentration ratio (saliva/plasma ratio). Considering saliva as a model for transmembrane transport, drugs can be divided into 4 groups. The first group is characterized by a saliva/plasma ratio less than 1.0. In extreme cases a drug with negligible transport is either not detectable in saliva or is found in very low concentrations which are hard to measure or difficult to interpret. A second group leads to saliva/plasma ratios which are approximately constant and about 1.0 under most of the conditions studied. This group is ideal for monitoring salivary drug concentrations. A third group is sufficiently transferred into saliva, but the saliva/plasma ratio varies under different conditions. The reason for this variation is that the transport is influenced by several factors including an active transport mechanism. The varying influence of these factors on the saliva/plasma ratio largely depends on the physico-chemical characteristics of the particular substance. In a fourth group very high saliva/plasma ratios are observed primarily due to the degree of ionization of weak bases. A representative of each group is presented with its saliva/plasma ratio and its physico-chemical properties: ceftazidim, ethanol, digoxin and prilocain. In all cases the salivary concentration probably reflects the intracellular concentration in target tissues. All examples confirm saliva as an ideal in vivo model for the study of transmembrane transport in the human organism.


Asunto(s)
Anestésicos Locales/farmacocinética , Antibacterianos/farmacocinética , Digoxina/farmacocinética , Inhibidores Enzimáticos/farmacocinética , Drogas Ilícitas/farmacocinética , Saliva/química , Anestésicos Locales/sangre , Anestésicos Locales/metabolismo , Antibacterianos/sangre , Antibacterianos/metabolismo , Transporte Biológico Activo , Permeabilidad de la Membrana Celular , Digoxina/sangre , Digoxina/metabolismo , Relación Dosis-Respuesta a Droga , Monitoreo de Drogas , Inhibidores Enzimáticos/sangre , Inhibidores Enzimáticos/metabolismo , Humanos , Concentración de Iones de Hidrógeno , Drogas Ilícitas/sangre , Drogas Ilícitas/metabolismo , Unión Proteica , Saliva/metabolismo
2.
Ann Biol Clin (Paris) ; 51(10-11): 903-10, 1993.
Artículo en Inglés | MEDLINE | ID: mdl-8210068

RESUMEN

Despite anatomical and biochemical similarities, salivary, sweat and lacrimal glandulas differ in their physiological functions. Salivary and tear fluid are required for the proper function of the epithelial layer from which they are secreted. The physiological function of sweat is the elimination of excess heat. The products of the three glandulas can be used to measure indicators either of glandula or of non-glandular diseases. In the latter case the indicator must be transported from the particular organ to the glandula where it is then secreted. In sweat, only one example has reached well accepted clinical importance. The measurement of electrolyte concentrations is the classical laboratory test for cystic fibrosis. The use of tears for diagnostic purposes has been proposed for drug monitoring, to verify the dry eye syndrome (Schirmer test), to detect lysosomal storage diseases (eg Morbus Gaucher) and hyperglycemia. The major domains for the application of saliva are hormone analyses (especially of steroids) and drug monitoring. Furthermore, the application of saliva has been proposed for the detection of several other analytes (eg secretory IgA, peptide hormones, HIV antibodies).


Asunto(s)
Saliva/química , Sudor/química , Lágrimas/química , Enfermedades de las Glándulas Suprarrenales/diagnóstico , Fibrosis Quística/diagnóstico , Electrólitos/análisis , Humanos , Enfermedades por Almacenamiento Lisosomal/diagnóstico
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