介质纳米颗粒表面功能修饰对口服胰岛素输送的影响:一篇综述
Jie Zheng1, Long Wan1, Xiaowei Zhang2
1Department of Pharmacy, the First Hospital of China Medical University, 155 Nanjing North Street, Shenyang 110001, Liaoning, China; School of Pharmacy, China Medical University, 77 Puhe Road, Shenyang 110122, Liaoning, China.
International journal of biological macromolecules
|July 5, 2025
概括
口服胰岛素因胃肠道退化而面临挑战. 半孔纳米粒子 (MSN) 是有前途的,但表面修改对于高效的口服胰岛素输送系统至关重要.
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:
- 皮下胰岛素注射是不方便的,并与不良结果相关.
- 口服胰岛素供应是理想的,以使患者能够获得治疗,并减少副作用.
- 胰岛素在胃肠道中的结构不稳定性阻碍了口服.
研究的目的:
- 审查口服胰岛素输送中的挑战.
- 为了总结用于胰岛素加载和保护的半孔纳米颗粒 (MSN).
- 讨论MSNs的表面修改,以提高口服胰岛素的输送.
主要方法:
- 综合方法和MSNs作为药物载体的特性审查.
- 用于输送胰岛素的MSN应用的表面修饰的摘要.
- 对修改后的MSN用于口服胰岛素的优缺点的分析.
主要成果:
- 由于其孔隙结构和生物相容性,MSN提供高效的胰岛素载荷并保护其活性.
- 未经修改的MSN努力克服胃肠道障碍,以有效的胰岛素输送.
- 各种表面修改提高MSN的性能,用于口服胰岛素的输送.
结论:
- 表面修饰的MSN代表了克服口服胰岛素输送障碍的有希望的战略.
- 需要进一步的研究来优化基于MSN的系统用于临床应用.
- 解决局限性和探索未来的前景是推进口服胰岛素配方的关键.
相关概念视频
Factors Affecting Dissolution: Particle Size and Effective Surface Area
1.0K
Dissolution kinetics, an essential aspect of oral drug delivery, is significantly influenced by the drug's particle size. According to the Noyes-Whitney dissolution model, the dissolution rate correlates directly with the drug's surface area. The larger the surface area, the higher the drug's solubility in water, leading to a faster drug dissolution rate. Reducing particle size increases the effective surface area, enhancing the dissolution process. Micronization and nanosizing are...
1.0K
Insulin Formulations: Types and Delivery
275
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...
275
Oral Hypoglycemic Agents: Glinides
269
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...
269
Oral Hypoglycemic Agents: Sulfonylureas
349
Sulfonylureas are oral hypoglycemic agents utilized in treating type 2 diabetes. They are characterized by their unique sulfonylurea chemical structure. The family of sulfonylureas is divided into generations. First-generation sulfonylureas, including tolbutamide (Orinase), chlorpropamide (Diabinese), and tolazamide (Tolinase), trigger insulin release from pancreatic β cells and enhance peripheral tissues' insulin sensitivity. The second-generation members, such as glipizide...
349
Oral Hypoglycemic Agents: Biguanides and Glitazones
309
Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood...
309
Insulin: Dosing Regimen and Adverse Effects
265
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...
265


