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[成人及儿童用头孢唑肟栓剂的基础研究]

[Fundamental study on ceftizoxime suppositories in adults and children].

作者信息

Motohiro T, Aramaki M, Tanaka K, Koga T, Shimada Y, Tomita N, Sakata Y, Fujimoto T, Nishiyama T, Kuda N

出版信息

Jpn J Antibiot. 1985 Oct;38(10):3013-56.

PMID:3866091
Abstract

The pharmacokinetics of newly developed ceftizoxime suppository (CZX-S) was studied in healthy volunteers and in children, compared with that of intramuscular CZX and intravenous CZX: In 8 volunteers (aged 19 to 24 years), each of 500 mg (potency) CZX-S containing 3%, 4% and 5% sodium caprate was compared with 500 mg intramuscular CZX and 500 mg intravenous CZX as a single administration in the cross-over method. In addition each of 500 mg CZX-S containing 4% and 5% sodium caprate was studied in 2 groups of 8 volunteers (aged 22 to 24 years) and of 8 volunteers (aged 19 to 27 years); each CZX-S was given 3 times a day successively for 5 days. The pharmacokinetics of 125 mg and 250 mg CZX-S, which contained 3% sodium caprate, were also evaluated as a single administration in 9 children (aged 6 years 4 months to 12 years 0 month) and in 11 children (aged 7 years 8 months to 12 years 4 months), respectively. The irritabilities of CZX-S were studied in all subjects who participated in this trial. The feeling of foreign body, the feeling of defecation, the burning sensation and the pain were evaluated in volunteers; the feeling of defecation and the pain were evaluated in children. The results were as follows: I. Pharmacokinetics in healthy volunteers 1. Given as a single administration The mean peak concentrations of serum CZX were occurred 30 minutes after 500 mg CZX-S containing 3%, 4% and 5% sodium caprate, which were 10.5 mcg/ml, 12.3 mcg/ml and 12.4 mcg/ml, respectively. These values were 1.35 mcg/ml, 1.60 mcg/ml and 1.69 mcg/ml at the conversion unit of 1 mg dose per 1 kg body weight. The mean peak serum CZX concentration of CZX-S containing 3% sodium caprate was slightly lower than that of CZX-S containing 4% or 5% sodium caprate, but was 1.9 times higher than that of the ABPC suppository. There was no marked difference among 3 preparations of CZX-S in mean Tmax and T1/2. Cmax of CZX-S containing 3% sodium caprate was 1.40 mcg/ml at the conversion unit of 1 mg/kg. AUC of CZX-S containing 3% sodium caprate was slightly smaller than that of CZX-S containing 4% or 5% sodium caprate, but 3.1 times that of the ABPC suppository in healthy volunteers. When 500 mg CZX was intramuscularly administered by one shot to 8 volunteers, Tmax was same as that of CZX-S or was slightly later.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在健康志愿者和儿童中研究了新开发的头孢唑肟栓剂(CZX - S)的药代动力学,并与肌肉注射头孢唑肟(CZX)和静脉注射头孢唑肟进行比较:在8名志愿者(年龄19至24岁)中,采用交叉法将含3%、4%和5%癸酸钠的500mg(效价)CZX - S分别与500mg肌肉注射CZX和500mg静脉注射CZX进行单次给药比较。此外,在两组志愿者中研究了含4%和5%癸酸钠的500mg CZX - S,一组8名志愿者(年龄22至24岁),另一组8名志愿者(年龄19至27岁);每种CZX - S连续5天每天给药3次。还分别在9名儿童(年龄6岁4个月至12岁0个月)和11名儿童(年龄7岁8个月至12岁4个月)中对含3%癸酸钠的125mg和250mg CZX - S进行单次给药评估其药代动力学。在参与本试验的所有受试者中研究了CZX - S的刺激性。在志愿者中评估了异物感、排便感、灼烧感和疼痛;在儿童中评估了排便感和疼痛。结果如下:一、健康志愿者的药代动力学1. 单次给药含3%、4%和5%癸酸钠的500mg CZX - S给药后30分钟出现血清CZX的平均峰值浓度,分别为10.5mcg/ml、12.3mcg/ml和12.4mcg/ml。以每1kg体重1mg剂量的换算单位计,这些值分别为1.35mcg/ml、1.60mcg/ml和1.69mcg/ml。含3%癸酸钠的CZX - S的平均峰值血清CZX浓度略低于含4%或5%癸酸钠的CZX - S,但比ABPC栓剂高1.9倍。三种CZX - S制剂在平均达峰时间(Tmax)和半衰期(T1/2)方面无明显差异。含3%癸酸钠的CZX - S在1mg/kg换算单位下的Cmax为1.40mcg/ml。含3%癸酸钠的CZX - S的曲线下面积(AUC)略小于含4%或5%癸酸钠的CZX - S,但在健康志愿者中是ABPC栓剂的3.1倍。当对8名志愿者单次肌肉注射500mg CZX时,Tmax与CZX - S相同或略晚。(摘要截断于400字)

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