基于细胞透的宏分子药物的输送:开发,策略和进展
Zhe Sun1, Jinhai Huang1, Zvi Fishelson2
1School of Life Sciences, Tianjin University, Tianjin 300072, China.
Biomedicines
|July 29, 2023
概括
细胞透 (CPPs) 提供了卓越的药物递送性能. 本综述详细介绍了CPP开发,输送系统,吸收机制和宏分子药物的优化策略,强调了成功临床应用的条件.
科学领域:
- 生物技术是生物技术.
- 药理学 药理学是指药理学的学科.
- 药物输送系统 药物输送系统
背景情况:
- 细胞透 (CPPs) 已经研究了30多年,因为它们的药物递送能力.
- 作为各种治疗剂的输送工具,CPP显著有前途,其性能优于其他系统.
- 广泛的研究继续探索和完善CPP,以增强治疗应用.
研究的目的:
- 审查CPP在药物输送中的历史发展和当前状态.
- 总结基于CPP的传递系统,包括组成,分类和细胞吸收机制.
- 概述CPP介导的宏分子药物输送的优化策略,重点关注稳定性,向性和临床成功因素.
主要方法:
- 关于CPP开发和应用的综合文献综述.
- 基于CPP的输送系统,细胞吸收途径和生物障碍的分析.
- 对稳定性,向性和内体细胞逃逸的优化路径的数据综合.
- 对基于CPP的药物输送系统的临床试验结果的评估.
主要成果:
- CPPs表现出多样化的组成和分类,具有既定的细胞吸收机制.
- 已经确定了影响CPP交付和生物障碍的关键因素.
- 优化策略显著提高了CPP稳定性,准效率和内体体逃生.
- 成功的临床试验取决于基于CPP的系统所确定的特定条件.
结论:
- CPPs代表了宏分子药物递送的强大平台,并且正在不断进步.
- 优化的CPP策略对于提高药物递送效率和治疗结果至关重要.
- 本综述为基于CPP的药物输送系统的成功临床转化提供了一个全面的框架和洞察力.
相关概念视频
Cellular Membranes and Drug Transport
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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.
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Mechanisms of Drug Absorption: Paracellular, Transcellular, and Vesicular Transport
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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...
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Drug Delivery: Overview
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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.
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Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the...
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Carrier-Mediated Transport
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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...
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Pore Transport and Ion-Pair Transport
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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...
515


