MKC253 is glucagon-like peptide 1 (GLP-1, 7-36 amide) adsorbed onto Technosphere microparticles for oral inhalation. The pharmacokinetics of inhaled GLP-1 and the pharmacokinetic-pharmacodynamic (PK-PD) relationship between inhaled GLP-1 and insulin were analyzed in two trials, one in healthy normal volunteers and the other in patients with type 2 diabetes. Inhaled GLP-1 was absorbed quickly, with peak concentrations occurring within 5 min, and levels returned to baseline within 30 min. Inhaled GLP-1 appeared to produce plasma levels of GLP-1 comparable to those of parenteral administration and sufficient to induce insulin secretion resulting in attenuation of postmeal glucose excursions in subjects with type 2 diabetes. An E(max) (maximum effect) model described the relationship between GLP-1 concentration and insulin release. The variability in the E(max) may be due to differences in baseline glucose levels, differences resulting from genetic polymorphisms in GLP-1 receptors (GLP-1Rs), or the stage of diabetes of the patient.

译文

MKC253是胰高血糖素样肽1 (GLP-1,7-36酰胺) 吸附在用于口服吸入的technsphere微粒上。在两项试验中分析了吸入GLP-1的药代动力学以及吸入GLP-1与胰岛素之间的药代动力学-药效学 (pk-pd) 关系,一项在健康正常志愿者中,另一项在2型糖尿病患者中。吸入的GLP-1被迅速吸收,峰值浓度在5分钟内出现,水平在30分钟内恢复到基线。吸入的GLP-1似乎产生的血浆GLP-1水平与肠胃外给药相当,足以诱导胰岛素分泌,导致2型糖尿病患者餐后葡萄糖漂移减弱。E(max) (最大效应) 模型描述了GLP-1浓度与胰岛素释放之间的关系。E(max) 的变异性可能是由于基线葡萄糖水平的差异,由GLP-1受体 (GLP-1Rs) 的遗传多态性引起的差异或患者的糖尿病阶段。

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