通过在生理水平上使用分分钟压力,从宏封装小岛增强治疗性胰岛素输送
bioRxiv : the preprint server for biology
|January 3, 2024
概括
施加生理压力可以增强胰岛素从缩小岛的输送,用于1型糖尿病治疗. 这一突破可以实现按需胰岛素的输送,并实现胰岛素独立.
科学领域:
- 生物医学工程 生物医学工程
- 内分泌学 在内分泌学.
- 再生医学是一种再生医学.
背景情况:
- 1型糖尿病治疗面临的挑战是免疫相容性和实现生理血糖控制.
- 目前依赖于扩散进行胰岛素输送的宏封装方法尚未实现胰岛素独立性.
- 扩散有限的胰岛素运输阻碍了自封装小岛的恒温,按需的输送.
研究的目的:
- 调查施加生理压力是否可以增强来自宏观封装小岛的胰岛素运输.
- 为了证明在1型糖尿病中实现按需胰岛素输送和葡萄糖调节的潜在解决方案.
主要方法:
- 通过免疫隔离膜进行压力驱动的胰岛素传输的理论建模和实验验证.
- 将增压系统与基于的外血管装置相结合.
- 在糖尿病动物模型中进行测试,以评估降糖功效和治疗效果.
主要成果:
- 施加类似于透缩血压的压力,使胰岛素流量增加了近三倍.
- 实现了精确的,分分钟调节玻尿酸和基础胰岛素的输送.
- 在糖尿病动物中显示出快速降低葡萄糖水平,模仿皮下胰岛素效应.
结论:
- 压力驱动的胰岛素运输显著克服了宏封装中的扩散限制.
- 这种技术提供了一种可行的策略,可以从封装的小岛提供按需的胰岛素.
- 为1型糖尿病患者实现胰岛素独立提供了潜在的途径.
更多相关视频
09:31Sustained Administration of β-cell Mitogens to Intact Mouse Islets Ex Vivo Using Biodegradable Poly(lactic-co-glycolic acid) Microspheres
Published on: November 5, 2016
7.3K
08:04Author Spotlight: Investigating Islet Abnormalities and Function with a Pseudoislet Protocol
Published on: November 3, 2023
2.0K
相关概念视频
Insulin Formulations: Types and Delivery
197
Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
Short-acting insulins are divided into...
Short-acting insulins are divided into...
197
Glucose Homeostasis: Pancreatic Islets and Insulin Secretion
1.3K
The pancreatic islets comprising only 1%-2% of the volume are highly vascularized and innervated mini-organs. They contain five endocrine cell types, including β cells that secrete insulin, which is synthesized as a single polypeptide chain, preproinsulin, processed to proinsulin, and finally to insulin and C-peptide. This process is complex and regulated, involving the Golgi complex, the endoplasmic reticulum, and the secretory granules of the β cell.
Insulin and C-peptide are...
Insulin and C-peptide are...
1.3K
Insulin Secretory Vesicles
5.0K
Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
5.0K
Insulin: Biosynthesis, Chemistry, and Preparation
384
The endoplasmic reticulum (ER) of pancreatic β-cells synthesizes preproinsulin, which consists of a signal peptide, A and B chains, and a C-peptide. Preproinsulin is then cleaved and folded into proinsulin, which translocates to the Golgi apparatus for sorting and packaging into secretory granules. In these granules, enzymatic clipping generates insulin and C-peptide.
Damage or functional impairment of β-cells inhibits insulin production, leading to diabetes. Diabetes treatment...
Damage or functional impairment of β-cells inhibits insulin production, leading to diabetes. Diabetes treatment...
384
Insulin: Dosing Regimen and Adverse Effects
176
Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
176
