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皮下注射胰岛素的药代动力学。在便携式泵治疗中的应用(1)

[Pharmacokinetics of insulin administered subcutaneously. Application to treatment by portable pump (1)].

作者信息

Scheen A J

机构信息

Département de Médecine, Centre Hospitalier Universitaire de Liège, Belgique.

出版信息

Diabete Metab. 1989 May-Jun;15(3):128-38.

PMID:2668053
Abstract

Continuous subcutaneous insulin infusion is characterized by a basal insulin delivery rate to which insulin boluses are added. The basal delivery rate maintains a small insulin reserve in the local subcutaneous depot. This reserve averages 2 to 5 times the hourly basal rate at the steady-state which is reached after about 7 hours but depends on numerous factors: subcutaneous blood flow, skinfold thickness, insulin concentration, etc. It explains the pharmacokinetics time-lag of the system, more particularly the similar effects of a basal rate delivered in either a pulsatile/intermittent or a continuous manner, the lack of deleterious effect of a 1-h pump arrest, the 2-h delay before significant metabolic deterioration during a more prolonged interruption of the infusion, the delayed plasma insulin changes when the basal insulin delivery rate is doubled or reduced by half, etc. Insulin boluses pharmacokinetics is not fundamentally different from that of soluble insulin injection in conventional therapy. As an example, insulin boluses should ideally be given 30 min before the meals in order to better prevent post-prandial hyperglycaemia. However, the absence of intermediate zinc-insulin in the system may result in an earlier increase of plasma free insulin levels, which for instance allows a rapid correction of the metabolic alterations induced by a prolonged interruption of the basal infusion rate. This kinetics does not seem to be significantly altered by insulin concentration nor by the profile of the bolus but is affected by the insulin content of the subcutaneous depot at the time the bolus is delivered.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

持续皮下胰岛素输注的特点是有基础胰岛素输注速率,并在此基础上追加胰岛素大剂量注射。基础输注速率可在局部皮下储库中维持少量胰岛素储备。在约7小时后达到稳态时,该储备量平均为每小时基础输注速率的2至5倍,但这取决于众多因素:皮下血流量、皮褶厚度、胰岛素浓度等。这解释了该系统的药代动力学时滞,尤其是以脉冲式/间歇式或连续方式输注基础胰岛素速率时产生的相似效果、1小时泵停止工作无有害影响、在更长时间的输注中断期间,2小时后才会出现明显的代谢恶化、基础胰岛素输注速率加倍或减半时血浆胰岛素变化延迟等情况。胰岛素大剂量注射的药代动力学与传统疗法中可溶性胰岛素注射的药代动力学并无根本差异。例如,为更好地预防餐后高血糖,理想情况下应在餐前30分钟注射胰岛素大剂量。然而,该系统中不存在中效锌胰岛素可能导致血浆游离胰岛素水平更早升高,例如这使得能够快速纠正因基础输注速率长时间中断引起的代谢改变。这种动力学似乎不受胰岛素浓度或大剂量注射模式的显著影响,但会受到注射大剂量胰岛素时皮下储库中胰岛素含量的影响。(摘要截选至250字)

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