相关实验视频
Updated: Jun 18, 2025

09:03
Manufacture and Drug Delivery Applications of Silk Nanoparticles
Published on: October 8, 2016
15.8K
蛋白质药物与智能EnteroPatho纳米颗粒的平细胞传递
Isabela Ramirez-Velez1, Aditya A Namjoshi1, Unyime M Effiong1
1McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
ACS nano
|August 3, 2024
概括
研究人员开发出智能纳米粒子,可以暂时在肠道中打开通道. 这一突破使得蛋白质药物的有效口服输送成为可能,改善了患者的获取并降低了医疗保健成本.
科学领域:
- 生物材料科学 生物材料科学
- 胃肠病学 胃肠病学
- 药物输送系统 药物输送系统
背景情况:
- 口服生物药物由于胃肠道环境而面临挑战.
- 纳米材料具有保护药物的潜力,并使其在小肠中得到控制释放.
- 穿过肠道粘膜的传输,特别是通过细胞通道的传输,是口服蛋白质输送的关键瓶.
研究的目的:
- 开发一种智能纳米粒子系统,用于增强生物制品的口服输送.
- 为了克服小肠上皮质紧接点 (TJs) 构成的障碍.
- 创建一个安全有效的蛋白质药物口服安全和有效的通用平台.
主要方法:
- 工程"智能"纳米粒子 (EnteroPatho NPs) 灵感来自肠病原性细菌.
- 设计用于附着在上皮质葡萄糖和释放TJ调节器的纳米粒子.
- 由肠道环境触发的TJ调节器的pH响应释放.
- 在体外/体内对TJ干扰和细胞蛋白递送的评估.
主要成果:
- EnteroPatho NPs成功地附着在肠道上皮上.
- 这些纳米颗粒暂时破坏了上皮质紧密结.
- 通过肠道屏障证明了蛋白质的增强型细胞外递.
- 建立了一个用于口服生物药物递送的新平台.
结论:
- 智能纳米粒子可以被设计为调节肠道上皮质紧密结.
- 这种方法促进了细胞外传输,克服了口服生物药物输送中的一个主要障碍.
- 开发的系统代表了一个有前途的整体平台,可以彻底改变口服蛋白质药物管理.
相关概念视频
Mechanisms of Drug Absorption: Paracellular, Transcellular, and Vesicular Transport
489
Drugs need to permeate cell membranes to reach their target sites after administration. Orally administered drugs must transcend intestinal epithelial membrane barriers to infiltrate the systemic circulation. Drugs with a molecular weight of less than 500 Daltons diffuse through gaps between neighboring cells, called paracellular pathways.
However, most drugs use the transcellular route, traversing directly through the cell membranes via two mechanisms: passive and active transport. Passive...
However, most drugs use the transcellular route, traversing directly through the cell membranes via two mechanisms: passive and active transport. Passive...
489
Carrier-Mediated Transport
318
Carrier-mediated transport is a pivotal process in drug absorption, particularly for lipid-insoluble drugs, and encompasses facilitated diffusion and active transport. Facilitated diffusion allows drugs to move along their concentration gradient without energy expenditure, while active transport utilizes ATP to drive drug movement against this gradient.
Active transport involves two types of membrane-spanning transporters: uptake and efflux. Uptake transporters are expressed in the small...
Active transport involves two types of membrane-spanning transporters: uptake and efflux. Uptake transporters are expressed in the small...
318
Cellular Membranes and Drug Transport
378
Drugs must traverse multiple biological barriers, such as multi-layered skin, single-layered intestinal epithelium, and the plasma membrane, to reach their target sites within the body. The plasma membrane, a highly structured composite of phospholipids, carbohydrates, and proteins, is the cell's protective boundary, facilitating selective substance exchange.
Phospholipids arrange themselves into a bilayer, with hydrophilic heads oriented outward and hydrophobic tails facing inward.
Phospholipids arrange themselves into a bilayer, with hydrophilic heads oriented outward and hydrophobic tails facing inward.
378
Drug Delivery: Overview
279
The selection of a drug's delivery route depends upon its physicochemical properties, including lipid or water solubility and ionization, as well as the therapeutic requirement, such as immediate or sustained effect. These routes can be divided into three primary categories: enteral, parenteral, and topical.
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the...
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the...
279
Drug Delivery: Enteral Route
406
The enteral drug administration involves three primary routes: oral, sublingual, and buccal. Oral ingestion is the most prevalent, safe, economical, and convenient method for drug administration. However, it has certain drawbacks, including limited absorption due to the drug's low water solubility or poor membrane permeability, possible emesis from GI mucosa irritation, destruction of drugs by digestive enzymes or low gastric pH, and irregular absorption along with food or other drugs.
406
Pore Transport and Ion-Pair Transport
406
Pore transport and ion-pair formation are critical mechanisms for the absorption and distribution of drugs in the body.
Pore transport, also known as convective transport, is a process where small molecules like urea, water, and sugars rapidly cross cell membranes as though there were channels or pores in the membrane. Although direct microscopic evidence is limited but the concept of pores or channels is widely accepted based on physiological evidence. Despite the lack of direct...
Pore transport, also known as convective transport, is a process where small molecules like urea, water, and sugars rapidly cross cell membranes as though there were channels or pores in the membrane. Although direct microscopic evidence is limited but the concept of pores or channels is widely accepted based on physiological evidence. Despite the lack of direct...
406

