Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Drug Delivery: Overview01:16

Drug Delivery: Overview

321
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...
321
Biopharmaceutics and Pharmacokinetics: Overview01:28

Biopharmaceutics and Pharmacokinetics: Overview

2.1K
Understanding drugs, drug products, and their performance in pharmaceutical science is pivotal. Drugs, whether simple molecules or complex compounds, are designed to interact with the body's biological systems to diagnose, treat, or prevent diseases. Drug products include various delivery systems such as tablets, capsules, injections, and inhalers. The performance of these drug products is gauged by their ability to deliver the active ingredient to the desired site of action at the...
2.1K
Drug Delivery: Miscellaneous Routes01:22

Drug Delivery: Miscellaneous Routes

380
Drug delivery methods like oral inhalation, nasal sprays, transdermal patches, eye drops, intravitreal injection,  and rectal administration provide localized effects with reduced toxicity.
Oral inhalation and nasal sprays swiftly transfer drugs across the respiratory epithelium's mucosal layer. Inhaled glucocorticoids and bronchodilators directly target lung conditions such as asthma, while fluticasone nasal spray mitigates allergic rhinitis.
Transdermal patches transport drugs...
380
Routes of Drug Administration: Overview01:22

Routes of Drug Administration: Overview

6.3K
Drug administration involves delivering drugs to the body through various routes, such as enteral, parenteral, and topical.
Enteral administration refers to drugs absorbed through the gastrointestinal tract. They can be swallowed (perorally), placed under the tongue (sublingually), or on the inner lining of the cheeks (buccally). Perorally administered drugs take time to be absorbed and have a slower onset of action. The rectal route is another form of enteral administration, which allows for...
6.3K
Mechanisms of Drug Absorption: Paracellular, Transcellular, and Vesicular Transport01:23

Mechanisms of Drug Absorption: Paracellular, Transcellular, and Vesicular Transport

587
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...
587
Non-Oral Extravascular Drug Absorption Routes01:15

Non-Oral Extravascular Drug Absorption Routes

239
Non-oral extravascular routes, which encompass sublingual, buccal, topical, intramuscular, and inhalation methods, primarily utilize passive diffusion to transport drugs into the systemic circulation. The absorption rates and effectiveness of these routes depend on the drug's physicochemical properties, as well as the patient's anatomical and pathophysiological state.
Lipophilic drugs that are stable at salivary pH (6) and exhibit minimal binding to the oral mucosa are absorbed more...
239

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Depleting S100A4 in Cancer-Associated Fibroblasts Reverses Cisplatin Resistance in Esophageal Cancer.

ACS applied bio materials·2026
Same author

FAP-Synergistic Organ-Targeted mRNA-LNP for Overcoming Delivery Barriers in Hepatic and Pulmonary Fibrosis.

Journal of the American Chemical Society·2026
Same author

Transferrin-phosphatidylserine liposomes target TDP-43 and neuroinflammation in male mice with neuropathic pain.

Nature communications·2025
Same author

Engineering of mRNA vaccine platform with reduced lipids and enhanced efficacy.

Nature communications·2025
Same author

Rational Design of Morphology Transformable Oligopeptide Self-Assembly for Specifically Inducing Lysosomal Membrane Permeabilization of Tumor Cell.

ACS applied materials & interfaces·2025
Same author

Fabrication of a Whitlockite/PLGA Scaffold with Hierarchical Porosity for Bone Repair.

Nano letters·2025
Same journal

Nanocapsules as smart natural product drug delivery systems: recent advances and future directions.

Nanoscale horizons·2026
Same journal

Geometry scaling of thermal boundary resistance in plasmonic nanostructures.

Nanoscale horizons·2026
Same journal

Outstanding Reviewers for <i>Nanoscale Horizons</i> in 2025.

Nanoscale horizons·2026
Same journal

The Fe sites in non-precious metal nanocatalysts toward efficient water oxidation.

Nanoscale horizons·2026
Same journal

Bimetallic Cu/Ni-doped porous carbon fibers as high-performance adsorbents for organic dyes.

Nanoscale horizons·2026
Same journal

Anomalous Hall effect in room-temperature two-dimensional van der Waals ferromagnets.

Nanoscale horizons·2026
查看所有相关文章

相关实验视频

Updated: Jul 19, 2025

Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles
07:32

Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles

Published on: August 28, 2015

11.4K

基于特定相互作用的药物加载策略.

Haoqi Yu1,2, Shuhui Zhang1, Huiru Yang1

  • 1CAS Key Laboratory for Biomedical Effects of Nanomaterials & Nanosafety, CAS Center of Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, 100190, China. jitj@nanoctr.cn.

Nanoscale horizons
|August 18, 2023
PubMed
概括
此摘要是机器生成的。

开发新的药物载体和加载策略对于有效地输送超级水友性药物,如神经毒素至关重要,同时最大限度地降低过量风险和代谢负担. 本综述探讨了改善药物输送的基于相互作用的特定方法.

更多相关视频

Experimental Quantification of Interactions Between Drug Delivery Systems and Cells In Vitro: A Guide for Preclinical Nanomedicine Evaluation
08:47

Experimental Quantification of Interactions Between Drug Delivery Systems and Cells In Vitro: A Guide for Preclinical Nanomedicine Evaluation

Published on: September 28, 2022

1.9K
Biosensor-based High Throughput Biopanning and Bioinformatics Analysis Strategy for the Global Validation of Drug-protein Interactions
08:31

Biosensor-based High Throughput Biopanning and Bioinformatics Analysis Strategy for the Global Validation of Drug-protein Interactions

Published on: December 1, 2020

5.1K

相关实验视频

Last Updated: Jul 19, 2025

Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles
07:32

Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles

Published on: August 28, 2015

11.4K
Experimental Quantification of Interactions Between Drug Delivery Systems and Cells In Vitro: A Guide for Preclinical Nanomedicine Evaluation
08:47

Experimental Quantification of Interactions Between Drug Delivery Systems and Cells In Vitro: A Guide for Preclinical Nanomedicine Evaluation

Published on: September 28, 2022

1.9K
Biosensor-based High Throughput Biopanning and Bioinformatics Analysis Strategy for the Global Validation of Drug-protein Interactions
08:31

Biosensor-based High Throughput Biopanning and Bioinformatics Analysis Strategy for the Global Validation of Drug-protein Interactions

Published on: December 1, 2020

5.1K

科学领域:

  • 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
  • 生物医学工程 生物医学工程

背景情况:

  • 药物载体被广泛用于控制释放,提高疗效和减少副作用.
  • 具有狭窄治疗指数的超性药物 (例如神经毒素) 的高负载效率仍然是一个重大挑战.
  • 目前的方法,如增加载体比例的风险过量由于突发释放和增加代谢负担.

研究的目的:

  • 根据特定的药物载体相互作用,审查和讨论药物加载策略.
  • 突出水友药物开发先进药物输送系统的挑战和未来前景.
  • 为克服当前药物封装技术的局限性提供见解.

主要方法:

  • 对现有药物加载策略的文献综述.
  • 分析药物和载体之间的特定相互作用机制.
  • 讨论水友性药物递送的挑战和潜在解决方案.

主要成果:

  • 具体的相互作用为提高药物加载效率提供了一个有希望的途径.
  • 战略必须解决突发释放和载体诱导的代谢负担.
  • 需要进一步的研究来开发创新的运输和装载技术.

结论:

  • 专注于特定相互作用的新型药物加载策略对于有效的水友性药物递送至关重要.
  • 克服突发释放和代谢负载等挑战是推动神经毒素和类似药物应用的关键.
  • 这一综述为针对性和高效的药物输送系统的未来研究提供了基础.