l-Arginine labeled with carbon-14 at the guanido group was injected into rabbits, and the ratio of the rates of entry of radioactivity into the protein and urea was determined. This ratio, multiplied by the rate of arginine utilization in urea synthesis and by the ratio of protein to protein arginine weights, gives the rate of protein synthesis. The method applies to albumin and should apply to any plasma protein synthesized in those liver cells which also synthesize urea.

Summary A direct immunofluorescent technique with fluorescein-labeledantigens was used to examine the jejunal mucosa for specific antibody production in 23 children aged 2-25 months referred for diagnostic biopsy. Plasma cells containing antibodies to p-lactoglobulin (PLG) or bovine serum albumin (BSA) were present in I1 of 16 biopsies from patients with cow's milk protein intolerance (CMPI) but only one of eight controls, all on a diet containing cow's milk. Antibody-containing cells (ACC) constituted approximately 0.5-5% of the total (IgA + IgM) plasma cell population. In children with CMPI there may be gastrointestinal symptoms only, or these may be combined with other allergic manifestations such as eczema or asthma. In many CMPI children diagnostic tests for allergy-skin prick tests or RAST-are negative and the serum IgE is not raised (7, 11,20). This is especially so in those children with only gastrointestinal symptoms. But challenge with cow's milk often produces profound changes in the small intestinal mucosa, including villous atrophy of varying degree (9,10,12,34) and increased numbers of eosinophils (41) intra-epithelial lymphocytes (40) and plasma cells (10,21,33,34). It has not been established whether the increase in plasma cells is just part of a generalized, non-specific response of the immune system to antigenic stimulation (23, 37) or whether it represents a specific response to milk-protein antigens at the point of entry.In order to study the mucosal immune response to bovine milk proteins we have developed a simple direct immunofluorescent technique for the presence of plasma cells containing specific antibody to two bovine milk proteins, PLG and BSA. Brief, preliminary reports of this work have been published (16,27). MATERIALS AND METHODSPatients. Twenty-three children, aged 2-25 months, had been routinely referred to us for diagnostic jejunal biopsy. Informed consent to carry out this procedure was obtained from the parents.In 15 children a diagnosis of CMPI was made, based on a history of vomiting, diarrhoea, and weight loss (or exacerbation of eczema in atopic children) when on CM and improvement when on a CM-free diet. Details of presenting symptoms, dietary history, and results of challenges are given in Table 1. Four of these fifteen patients had additional allergies: to eggs (Nos. 6, 13, and 15), chicken, fish, and antibiotics (No. 11). Five of the fifteen had atopic symptoms such as eczema (Nos. 2, 8 and 13), asthma (NO. 13), and urticaria (No. 6). Five patients (Nos. 4, 5, 9, 10 and 11) were challenged with CM at the time of investigation, and had pre-and postchallenge biopsies as previously described (34); patient No. 4 had a second challenge at age 18 months. In this group a total of 23 biopsies were performed, 16 while the patient was taking CM and 7 while the patient was on a CM-free diet.Eight children whose symptoms could not be related to consumption of CM served as the control group. (Table 2). All were receiving CM at the time of jejunal biopsy.Biopsy specimens. Upper jej...

SUMMARY Twenty-one children aged between 2 and 54 months, 14 with eczema and 7 with allergies in first-degree relatives, were referred for diagnostic jejunal mucosal biopsy for a variety of symptoms. A partial villous atrophy was found in 19 of the 21 biopsies obtained; the other 2 were normal. We report a highly significant (P

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A simple and rapid method for the analysis of carbohydrates in heroin samples by capillary electrophoresis utilizing a borate complexation method is described. Separations were performed using an uncoated fused silica capillary, 50 cm × 50 μm I.D. × 360μm O.D. with an effective separation length of 9 cm. The system was run at 60°C with an applied voltage of −8 kilovolts. Injection of each sample was for 1 sec at −50 mbar. UV detection was employed with the wavelength set at 195 nm. The background electrolyte consisted of 65 mM borate, pH 12.0. Samples and standards were prepared in the run buffer containing 2 mg/mL of mannose as an internal standard. Under these conditions a test mixture containing glucose, sucrose, lactose, mannitol and mannose as an internal standard was resolved within 5 min. The method was used to determine the concentration of carbohydrates in heroin seizure samples and synthetic heroin samples. The results were in good agreement with the reported values.

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