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健康受试者皮下注射后,五种“短效”和“中效”(NPH)胰岛素预混组合的药代动力学。

The pharmacokinetics of five pre-mixed combinations of 'short-' and 'intermediate-acting' (NPH) insulins in healthy subjects following subcutaneous administration.

作者信息

Owens D R, Jones A L, Dolben J, Dean J D, Petocz P, Coates P A, Luzio S D

机构信息

Diabetes Research Unit, University of Wales College of Medicine, Heath Park, Cardiff, UK.

出版信息

Diabetes Res. 1993;22(2):77-86.

PMID:8205740
Abstract

The pharmacokinetics of five pre-mixed insulin preparations in the ratio of soluble to NPH insulin of 10:90, 20:80, 30:70, 40:60 and 50:50, were examined in a two part study in fasting healthy subjects. Each received by bolus subcutaneous injection into the anterior abdominal wall, on separate occasions one to two weeks apart, 20U of each of three pre-mixed insulin preparations in random order. In Part 1, nine subjects received Penmix 10:90, Penmix 20:80 and Penmix 30:70 and were observed over a period of 24 hours. In Part 2, eight subjects received Penmix 30:70, Penmix 40:60 and Penmix 50:50 and were observed over an 8 hr post-injection period. Three subjects were common to both parts of the study. Plasma glucose, C-peptide and insulin levels were measured frequently throughout both study periods. Increasing soluble insulin content in the pre-mixtures was reflected in increasing peak plasma insulin concentrations and a greater hypoglycaemic response. There were highly significant differences between the five premixtures and preparations in the 0-4 and 0-8 hours area under the curve (AUC) values for plasma glucose, C-peptide and immunoreactive insulin concentration (p < 0.01). Whereas a gradual difference between the premixtures was seen no two adjacent ones were significantly different, however an overall highly significant difference between the five preparations tested was observed.

摘要

在一项针对空腹健康受试者的两部分研究中,检测了可溶性胰岛素与中效胰岛素比例分别为10:90、20:80、30:70、40:60和50:50的五种预混胰岛素制剂的药代动力学。每位受试者在腹部前壁进行皮下大剂量注射,在相隔一至两周的不同时间,以随机顺序分别注射三种预混胰岛素制剂中的每种20U。在第一部分中,九名受试者接受了10:90预混胰岛素、20:80预混胰岛素和30:70预混胰岛素,并观察24小时。在第二部分中,八名受试者接受了30:70预混胰岛素、40:60预混胰岛素和50:50预混胰岛素,并在注射后8小时内进行观察。有三名受试者参与了研究的两个部分。在整个研究期间频繁测量血浆葡萄糖、C肽和胰岛素水平。预混制剂中可溶性胰岛素含量的增加反映在血浆胰岛素峰值浓度的增加和更大的降糖反应上。在0至4小时和0至8小时期间,五种预混制剂和制剂在血浆葡萄糖、C肽和免疫反应性胰岛素浓度的曲线下面积(AUC)值之间存在高度显著差异(p < 0.01)。虽然预混制剂之间存在逐渐差异,但相邻的两种制剂之间没有显著差异,然而,在所测试的五种制剂之间观察到总体高度显著差异。

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