The standardisation of frozen hydrated bulk biological specimens using gelatin standards is described. The relationship between corrected elemental X-ray counts and ionic concentration was found to be linear, and minimum detectable limits for each element are stated. Variations in uncorrected standard curves were found to be due to changes in aluminium coating thickness. There was an inverse relationship between coating thickness and elemental X-ray counts. The factors causing this are discussed. To avoid errors arising from inconsistent aluminium thickness, experimental material should only be compared with standards of similar aluminium net counts. This can be achieved most easily by mounting and analysing specimen and standard together.

Specimens of neoplastic and non-neoplastic human urothelium were rapidly frozen against a copper block immersed in liquid nitrogen, planed in a cryoultramicrotome and then examined by low-temperature scanning electron microscopy (LTSEM) following coating by aluminium. Energy dispersive X-ray microanalysis (XRMA) was performed on the superficial urothelial cells and on gelatin blocks mounted in parallel which had known concentrations of sodium, potassium, chloride, and phosphorus. The neoplastic urothelial cells had significantly less phosphorus (P less than 0.05) than non-neoplastic cells and the ratios K+/P,K+/Na+, and K+/Cl- were significantly higher in neoplastic cells than in non-neoplastic cells (P less than 0.00001). These results are consistent with those expected in cells with a sustained increase in intracellular pH caused by stimulation of Na+/H+ ion membrane exchange.

The appearance of neoplastic human urothelium viewed by low-temperature scanning electron microscopy (LTSEM) and conventional scanning electron microscopy (CSEM) was compared. Fixed, dehydrated neoplastic cells viewed by CSEM had well-defined, often raised cell junctions; no intercellular gaps; and varying degrees of pleomorphic surface microvilli. The frozen hydrated material viewed by LTSEM, however, was quite different. The cells had a flat or dimpled surface, but no microvilli. There were labyrinthine lateral processes which interdigitated with those of adjacent cells and outlined large intercellular gaps. The process of fixation and dehydration will inevitably distort cell contours and on theoretical grounds, the images of frozen hydrated material should more closely resemble the in vivo appearance.