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与传统制剂相比,新型口服缓释单硝酸异山梨酯的药代动力学。

Pharmacokinetics of isosorbide mononitrate in a new sustained release oral form in comparison with a conventional formulation.

作者信息

Gandini R, Cunietti E, Assereto R, Castoldi D, Tofanetti O, Baggio E

机构信息

Medical Department, Buzzi Hospital, Milan, Italy.

出版信息

Arzneimittelforschung. 1987 Jul;37(7):836-9.

PMID:3675680
Abstract

40 mg of isosorbide mononitrate (isosorbide-5-mononitrate, IS5MN) in conventional (Ismo 20) and sustained release formulations (Ismo Diffutab) were administered to 5 male healthy volunteers. The administration of the sustained release formulation was repeated for seven days in order to evaluate the possible occurrence of accumulation. Pharmacokinetic data showed that the sustained release formulation reached significantly lower and delayed mean peak plasma levels compared with the conventional formulation, respectively 452.8 +/- 67.8 ng/ml and 706.7 +/- 57.3 (mean +/- SE) (p less than 0.05). Peak times were 4.6 +/- 0.2 and 2.4 +/- 0.2 (p less than 0.005) h, respectively. A longer plasma half-life together with larger AUC for the sustained release formulation was also observed. The pharmacokinetic parameters of the sustained release formulation are consistent with a therapeutic usefulness and suggest further clinical evaluation.

摘要

将常规剂型(Ismo 20)和缓释剂型(Ismo Diffutab)中的40毫克单硝酸异山梨酯(异山梨醇-5-单硝酸酯,IS5MN)给予5名男性健康志愿者。为评估蓄积的可能发生情况,缓释剂型连续给药7天。药代动力学数据显示,与常规剂型相比,缓释剂型的平均血浆峰浓度显著更低且出现延迟,分别为452.8±67.8纳克/毫升和706.7±57.3(平均值±标准误)(p<0.05)。达峰时间分别为4.6±0.2小时和2.4±0.2小时(p<0.005)。还观察到缓释剂型的血浆半衰期更长且曲线下面积更大。缓释剂型的药代动力学参数与治疗有效性相符,提示需进一步进行临床评估。

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