Rehydration of air-dried smears with normal saline. Application in fluid cytology.

Ninety fluid specimens (30 each of urine, ascitic and pleural fluid) were studied by preparing three comparable smears. One was air dried for Giemsa stain, one wet fixed in 95% ethanol and one dried on a hot plate at 37 degrees C, rehydrated in normal saline for 30 seconds and fixed in ethanol. The latter two were stained with Papanicolaou stain, and a comparison was made of the (1) retention of red blood cells, (2) retention of epithelial or mesothelial cells, and (3) cytologic preservation. The Giemsa-stained smear was used as a control for (1) and (2). Complete lysis of red blood cells was noted in the rehydration smears as compared with 70% red blood cell retention in the wet-fixed smears (P < .01). The rehydration smears retained 78% urothelial cells as compared with 55% in the wet-fixed smears (P < .01). For ascitic and pleural fluid the cell retention did not differ significantly. The wet-fixed smears scored better for overall cytologic preservation, but the difference was not significant. The rehydration smears showed a decrease in the chromaticity of staining, more flattened cell clusters and slight cell enlargement. The rehydration method was beneficial for urine and blood-stained body cavity fluids.

A physiological and system analysis hybrid pharmacokinetic model to characterize carbon tetrachloride blood concentrations following administration in different oral vehicles.

Oral absorption of chemicals can be influenced significantly by the administration vehicle or diluent. It has been observed that the oral absorption of carbon tetrachloride (CCl4) and other volatile organic chemicals is markedly affected by the dosing vehicle, with administration in oils producing erratic blood concentration-time profiles with multiple peaks. Analysis of this type of data by a compartmental modeling approach can be difficult, and requires numerous assumptions about the absorption processes. Alternatively, a system analysis method with few assumptions may provide a more accurate description of the observed data. In the current investigations, a nonlinear system analysis approach was applied to blood CCl4 concentration-time data obtained following iv and oral administration. The oral regimens consisted of 25 mg CCl4/kg body wt given as an aqueous emulsion, in water, as pure chemicals, and in corn oil. The system analysis procedure, based upon a disposition decomposition method, provided an absorption input rate function, F, for each regimen. A physiological pharmacokinetic model, based primarily on parameters available in the literature, and the F input functions, formed a hybrid model that adequately described the observed blood CCl4 concentration-time data. The same physiological pharmacokinetic model, employing conventional first-order absorption input schemes, did not predict the data as well. Overall, the system analysis approach allowed the oral absorption of CCl4 to be characterized accurately, regardless of the vehicle. Though system analysis is based on general mathematical properties of a system's behavior rather than on its causal mechanisms, this work demonstrates that it can be a useful adjunct to physiological pharmacokinetic models.

Development of DNA probes for Candida albicans.

An attempt was made to produce DNA probes that could be used as a rapid and efficient means of detecting candidiasis (invasive Candida infection) in immunocompromised patients. Whole DNA from Candida albicans was digested with restriction endonuclease, and the resulting fragments were randomly cloned into a plasmid vector. Several recombinant plasmids were evaluated for cross-hybridization to various other Candida species, other fungal DNAs, and to nonfungal DNAs. Cross reactions were observed between the probes and different yeasts, but none with unrelated DNAs. Some recombinants were genus-specific, and two of these were applied to the analysis of C. albicans growth curves. It became evident that, although both 32P- and biotin-labelled probes could be made quite sensitive, a possible limitation in their diagnostic potential was the poor liberation of Candida DNA from cells. Thus, better methods of treatment of clinical specimens will be required before such probes will be useful in routine diagnosis.