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In vitroandin vivoassessment of the bioavailability of potassium from a potassium tartrate tablet

机译:体外用药剂对酒石酸钾片中钾的生物利用度进行体内评估

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AbstractThe bioavailability of potassium from orally administered potassium tartrate was evaluated in 20 normal subjects under metabolic balance conditions. Subjects were given 34 mmol potassium (5 tablets of Cal‐K®) as a divided dose on each of 2 consecutive days. Urinary excretion of potassium, as determined from 24‐h urinary collections on the 3 days preceding dosage totalled 192·6 ± 50·9 mmol (mean ± S.D.,n= 20). It increased significantly (p<0·05) to 258·7 ± 54·2 mmol for the 2 days of dosage and the following day. The difference of 66.1 mmol representing absorbed potassium was close to the 68 mmol potassium given and indicated a bioavailability of potassium in excess of 97 per cent; after correction for creatinine excretion, potassium recovery rose to 99·9 per cent. The dissolution characteristics of the Cal‐K® tablets were also determined. After dissolution in simulated gastric juice (pH 1·2), 84·4 ± 10·6 per cent (mean ± S.D., 6 experiments) was dissolved; after adjustment to pH 7·3, dissolved potassium increased to 91·3·8·5 per cent. No precipitation or residue formed as a result of the pH change. Both sets of results indicate that potassium from these potassium tartrate tablets is in a
机译:摘要在代谢平衡条件下,在20例正常受试者中评估了口服酒石酸钾钾的生物利用度。受试者在连续 2 天的每一天分别给予 34 mmol 钾(5 片 Cal-K®)作为分次剂量。根据给药前 3 天 24 小时的尿液收集确定的钾尿排泄总计为 192·6 ± 50·9 mmol(平均 ± S.D.,n= 20)。在给药2天和次日,它显着增加(p<0·05)至258·7±54·2 mmol。代表吸收钾的66.1 mmol的差异接近所给予的68 mmol钾,表明钾的生物利用度超过97%;在对肌酐排泄进行校正后,钾回收率上升到99.9%。还测定了Cal-K®片剂的溶出特性。在模拟胃液(pH 1·2)中溶解后,溶解了84·4%±10·6%(平均±S.D.,6个实验);调节pH值至7·3后,溶解钾增至91·3·8·5%。不会因pH值变化而形成沉淀或残留物。两组结果都表明,这些酒石酸钾片中的钾存在于

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