Blume H, Ali S L, Elze M, Krämer J, Scholz M E
Zentrallaboratorium Deutscher Apotheker, Eschborn.
Arzneimittelforschung. 1996 Oct;46(10):975-80.
Relative Bioavailability Studies on Paracetamol in Suppositories as Compared to Tablets. Relative bioavailabilities of 250 mg paracetamol (CAS 103-90-2) in ben-u-ron 125 mg and ben-u-ron 250 mg suppositories were determined in comparison with that of cut-in-half Benuron tablets 500 mg in an open intraindividual 3-period-changeover-study in 18 healthy volunteers. Plasma concentrations of paracetamol were analyzed by means of a specific and sensitive HPLC-method with UV-detection. For the assessment of the bioavailability AUC, Cmax, tmax and HVD (half value duration) were used as pharmacokinetic characteristics. Relative bioavailability of paracetamol was 102% for 125 mg and 93% for 250 mg suppositories, compared with that of cut-in-half 500 mg tablets. Mean maximum paracetamol plasma concentrations (Cmax) were determined as 2.1 micrograms/ml (CV = 31%; (CV = Coefficient of Variation), 2.0 micrograms/ml (CV = 27%) and 3.5 micrograms/ml (CV = 27%) after administration of 125 mg and 250 mg suppositories and 500 mg cut-in-half tablets, respectively. These maximum concentrations were achieved 2.2 +/- 0.7, 1.8 +/- 0.7 and 0.6 +/- 0.3 h (tmax) after administration of the respective preparations. The corresponding HVD-values were 3.8 +/- 1.0, 3.5 +/- 0.9 and 1.8 +/- 0.8 h, respectively. Extent of bioavailability of paracetamol (dose: 250 mg) following administration of 125 mg as well as 250 mg suppositories in comparison with 500 mg tablets was shown to be equivalent. The results obtained in this study confirm the adequate bioavailability of both suppositories compared with tablets. On the other hand both suppository preparations were assessed as being bioequivalent concerning AUC and Cmax.
对乙酰氨基酚栓剂与片剂的相对生物利用度研究。在18名健康志愿者参与的开放个体内3期交叉研究中,测定了250mg对乙酰氨基酚(CAS 103 - 90 - 2)在125mg贝努龙栓剂和250mg贝努龙栓剂中的相对生物利用度,并与将500mg贝努龙片剂切成两半后的情况进行比较。采用具有紫外检测的特异性灵敏高效液相色谱法分析对乙酰氨基酚的血浆浓度。为评估生物利用度,使用AUC、Cmax、tmax和HVD(半衰期)作为药代动力学特征。与切成两半的500mg片剂相比,125mg栓剂中对乙酰氨基酚的相对生物利用度为102%,250mg栓剂中为93%。分别给予125mg和250mg栓剂以及切成两半的500mg片剂后,对乙酰氨基酚的平均最大血浆浓度(Cmax)分别测定为2.1微克/毫升(CV = 31%;CV =变异系数)、2.0微克/毫升(CV = 27%)和3.5微克/毫升(CV = 27%)。这些最大浓度在分别给予相应制剂后2.2±0.7、1.8±0.7和0.6±0.3小时(tmax)达到。相应的HVD值分别为3.8±1.0、3.5±0.9和1.8±0.8小时。与500mg片剂相比,给予125mg以及250mg栓剂后对乙酰氨基酚(剂量:250mg)的生物利用度范围显示相当。本研究获得的结果证实,与片剂相比,两种栓剂均具有足够的生物利用度。另一方面,两种栓剂制剂在AUC和Cmax方面被评估为生物等效。