首页> 外国专利> INSULIN FORMULATIONS FOR INSULIN RELEASE AS A FUNCTION OF TISSUE GLUCOSE LEVELS

INSULIN FORMULATIONS FOR INSULIN RELEASE AS A FUNCTION OF TISSUE GLUCOSE LEVELS

机译:胰岛素释放作为组织葡萄糖水平的功能的胰岛素制剂

摘要

Injectable insulin formulations that are capable of modifying the amount of insulin released based on the patient's tissue glucose levels, methods for making and using these formulations are described herein. The formulation may be administered via subcutaneous, intradermal or intramuscular administration. In one preferred embodiment, the formulations are administered via subcutaneous injection. The formulations contain insulin, an oxidizing agent or enzyme and a reducing agent or enzyme, a diluent and optionally one or more thickening agents. If a thickening agent is present in the formulation, the thickening agent increases the viscosity of the formulation following administration. Preferably the formulation contains an insulin, a diluent, glucose oxidase and peroxidase. Following administration to a patient, the insulin is released from the formulations as a function of the patient's tissue glucose level, which in turn maintains the patient's blood glucose level within an optimum range. The formulation is often referred to as a "smart" formulation since it modifies its release rate of insulin according to the patient's needs at a particular time. In a preferred embodiment, the formulation is designed to release insulin into the systemic circulation over time with a basal release profile following injection in a patient. In another embodiment, the formulation is designed to release insulin into the systemic circulation over time with a non-basal release profile following injection in a patient, such as a regular human insulin release profile or a prandial release profile.
机译:本文描述了能够基于患者的组织葡萄糖水平改变释放的胰岛素的量的可注射胰岛素制剂,制备和使用这些制剂的方法。所述制剂可以通过皮下,皮内或肌内施用来施用。在一个优选的实施方案中,所述制剂通过皮下注射给药。该制剂包含胰岛素,氧化剂或酶和还原剂或酶,稀释剂以及任选的一种或多种增稠剂。如果制剂中存在增稠剂,则增稠剂在给药后会增加制剂的粘度。优选地,所述制剂包含胰岛素,稀释剂,葡萄糖氧化酶和过氧化物酶。向患者给药后,根据患者的组织葡萄糖水平从制剂中释放胰岛素,这反过来又将患者的血糖水平维持在最佳范围内。该制剂通常被称为“智能”制剂,因为它根据特定时间患者的需求改变其胰岛素释放速率。在一个优选的实施方案中,该制剂被设计为在注射到患者体内后随时间以基础释放曲线将胰岛素释放到全身循环中。在另一个实施方案中,该制剂被设计为随着时间的推移将胰岛素释放到全身循环中,具有非基础释放特征,例如常规人胰岛素释放特征或餐后释放特征。

著录项

  • 公开/公告号EP2234644B1

    专利类型

  • 公开/公告日2013-07-31

    原文格式PDF

  • 申请/专利权人 BIODEL INC.;

    申请/专利号EP20090700220

  • 申请日2009-01-05

  • 分类号A61K47/46;A61K38/28;

  • 国家 EP

  • 入库时间 2022-08-21 16:34:02

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