有效的口服胰岛素输送通过酸三甲基基托-移植β-环极素纳米颗粒
Lizhen Yu1,2, Fengge Wang2, Shuyun Bao2
1Anhui Provincial Key Laboratory for Conservation and Exploitation of Biological Resources, School of Life Science, Anhui Normal University, Wuhu 241000, China.
Pharmaceutics
|January 28, 2026
概括
一种新型的纳米药物输送系统使用化三甲基基托移植β-环极 (NCT) 纳米颗粒可增强口服胰岛素的输送. 这个平台可以提高胰岛素的稳定性和生物可用性,为糖尿病管理提供了一个有前途的替代方案.
科学领域:
- 生物材料科学 生物材料科学
- 纳米技术 纳米技术
- 制药科学 制药科学
背景情况:
- 与注射相比,口服胰岛素可以改善患者的服药性.
- 不稳定性和不良的胃肠道透性限制了当前的口服胰岛素配方.
- 对于有效的口服胰岛素输送,需要一种新的阴离子多糖化纳米药物输送平台.
研究的目的:
- 设计和合成一种新的纳米药物输送平台,以有效地输送口服胰岛素.
- 评估开发的纳米载体的物理化学性质和治疗疗效.
- 为了克服口服胰岛素不稳定性和不良透性的局限性.
主要方法:
- 编的三甲基基托桑植入的β-环极 (NCT) 纳米颗粒的合成.
- 关于NCT纳米粒子物理化学性质的表征.
- 在动物模型中进行体内评价,用于链子素诱导的糖尿病动物模型.
主要成果:
- NCT纳米粒子表现出粘液粘附性,透性和pH敏感性,以控制释放.
- 在体内研究表明,胰岛素在小肠中的保留时间延长.
- 5小时后血糖水平下降了39%,胰岛素生物可用性增加了12.58%.
结论:
- NCT纳米颗粒保护胰岛素免受胃肠道的降解.
- 该平台有效地克服了肠道障碍,改善了口服输送.
- 这代表了口服输送胰岛素等生物分子的有希望的策略.
相关概念视频
Insulin Formulations: Types and Delivery
717
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...
717
Oral Cavity
3.1K
The oral cavity, or the mouth, is a complex structure in humans that plays a vital role in our day-to-day lives. Its role is not only in chewing and swallowing food; it also plays a role in speech and facial expressions.
Teeth: The teeth are the hardest structures in our bodies. Humans have two sets of teeth throughout their lifetime: deciduous (baby) teeth and permanent teeth. Each tooth consists of several parts: the crown (visible part), the root (embedded in the jaw), enamel (hard outer...
Teeth: The teeth are the hardest structures in our bodies. Humans have two sets of teeth throughout their lifetime: deciduous (baby) teeth and permanent teeth. Each tooth consists of several parts: the crown (visible part), the root (embedded in the jaw), enamel (hard outer...
3.1K
Insulin Secretory Vesicles
6.8K
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...
6.8K
Insulin: The Receptor and Signaling Pathways
3.0K
Insulin action is mediated through a receptor tyrosine kinase, akin to the IGF-1 receptor. The number of receptors per cell varies significantly, from 40 on erythrocytes to 300,000 on adipocytes and hepatocytes. The insulin receptor consists of linked α/β subunit dimers, forming a heterotetramer glycoprotein with two extracellular α subunits and two β subunits spanning the membrane. The α subunits inhibit the inherent tyrosine kinase activity of the β subunits, but...
3.0K
Insulin: Biosynthesis, Chemistry, and Preparation
1.3K
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...
1.3K
Oral Hypoglycemic Agents: Glinides
643
Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively...
643


