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

Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

Rate-programmed drug delivery systems release drugs in a controlled manner to maintain therapeutic levels. Three main designs include reservoir, matrix, and hybrid systems.Reservoir systems consist of a drug core enclosed within a membrane that controls drug release. In non-swelling reservoir systems, polymers like ethyl cellulose or polymethacrylates are used. These do not hydrate in aqueous media and control release through membrane thickness, porosity, or insolubility. This type includes...
Modified-Release Drug Delivery Systems: Classification01:23

Modified-Release Drug Delivery Systems: Classification

Modified-release drug delivery systems improve drug efficacy and minimize side effects by controlling the rate and location of drug release. These systems fall into three categories: rate-programmed, stimuli-activated, and site-targeted.Rate-programmed systems release drugs at a predetermined rate, maintaining consistent therapeutic levels and reducing fluctuations that could lead to toxicity or subtherapeutic effects. These systems use polymeric matrices, reservoir-based designs, or osmotic...
Modified-Release Drug Delivery Systems: Rate-Programmed I01:22

Modified-Release Drug Delivery Systems: Rate-Programmed I

Rate-programmed drug delivery systems (DDS) are designed to release drugs at specific, controlled rates to maintain consistent therapeutic levels. These systems are categorized based on their release mechanisms, including dissolution-controlled DDS, diffusion-controlled DDS, and combined dissolution-diffusion-controlled DDS.In dissolution-controlled DDS, the release rate depends on the slow dissolution of the drug itself or the surrounding matrix. Drugs with inherently slow dissolution rates,...
Modified-Release Drug Delivery Systems: Stimuli-Activated01:30

Modified-Release Drug Delivery Systems: Stimuli-Activated

Stimuli-activated drug delivery systems are designed to release drugs in response to specific physical, chemical, or biological stimuli. These systems often utilize hydrogels—three-dimensional, hydrophilic polymer networks capable of swelling in aqueous environments and retaining significant fluid volumes. Upon exposure to particular stimuli, these hydrogels undergo structural transitions that allow the embedded drug to be released. Due to this adaptive behavior, such systems are also called...
Site-Targeted Drug Delivery Systems: Polymeric Carriers01:24

Site-Targeted Drug Delivery Systems: Polymeric Carriers

Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
Oral Drug Delivery Systems: Delayed-Release Systems01:11

Oral Drug Delivery Systems: Delayed-Release Systems

Delayed-release drug delivery systems are specialized pharmaceutical formulations designed to postpone the release of active compounds until the drug reaches a specific region of the gastrointestinal (GI) tract, typically the intestine. These systems are essential for drugs that may cause gastric irritation, are unstable in acidic environments, or need to exert therapeutic effects locally in the intestinal or colonic regions.The core feature of delayed-release systems is the use of enteric...

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

Transport of Molecular Iodine From Antiseptic Iodophors across Hydrophilic-lipophilic Interfaces: Influence of Phospholipids.

ACS omega·2025
Same author

Fungal quorum sensing molecules as potential drugs in the treatment of chronic wounds and their delivery.

Expert opinion on drug delivery·2025
Same author

Efficacy of a New Alcohol-Free Organic Acid-Based Hand Sanitizer against Foodborne Pathogens.

Toxics·2023
Same author

Ciprofloxacin-Loaded Polyvinylpyrrolidone Foils for the Topical Treatment of Wound Infections with Methicillin-Resistant <i>Staphylococcus aureus</i> (MRSA).

Pharmaceutics·2023
Same author

MEMS-Based Tactile Sensors: Materials, Processes and Applications in Robotics.

Micromachines·2022
Same author

Advances in Fibrin-Based Materials in Wound Repair: A Review.

Molecules (Basel, Switzerland)·2022

相关实验视频

Updated: Jun 23, 2026

Combinatorial Synthesis of and High-throughput Protein Release from Polymer Film and Nanoparticle Libraries
10:58

Combinatorial Synthesis of and High-throughput Protein Release from Polymer Film and Nanoparticle Libraries

Published on: September 6, 2012

10.4K

从纳米工程聚糖中控制药物释放.

Ilker S Bayer1

  • 1Smart Materials, Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova, Italy.

Pharmaceutics
|May 27, 2023
PubMed
概括

本次审查强调了数学建模对于理解纳米工程聚糖的持续药物释放的重要性. 分析药物释放动力学可确保这些生物相容材料的高效开发和应用.

科学领域:

  • 生物医学科学 生物医学科学
  • 纳米技术 纳米技术
  • 材料科学 材料科学 材料科学

背景情况:

  • 多糖是多功能生物聚合物,具有用于药物输送的有价值特性.
  • 它们的生物相容性和生物降解性使得它们非常适合纳米级药物封装和释放.
  • 纳米工程聚糖在药物输送系统中提供了先进的解决方案.

研究的目的:

  • 审查从纳米级多糖中持续释放的药物.
  • 强调药物释放动力学和数学建模的关键作用.
  • 引导基于多糖的药物输送系统的开发和应用.

主要方法:

  • 在药物输送中应用多糖的文献综述.
  • 讨论聚糖的制药过程 (凝,稳定等). ) 的情况.
  • 对纳米聚糖 (水凝,纳米纤维,纳米颗粒) 应用的药物释放模型的分析.

主要成果:

  • 从纳米聚糖中持续释放药物涉及复杂的机制,如扩散,降解,侵蚀,胀和相互作用.
  • 数学建模对于预测释放行为和优化实验设计至关重要.
  • 由于并行机制,可能需要多个模型来准确描述释放配置文件.
关键词:
有控制释放的释放.药物释放释放药物释放药物释放的时间运动学的动力学.这些纳米纤维是纳米纤维.纳米颗粒是一种纳米粒子.聚糖是一种多糖.

更多相关视频

Injectable Supramolecular Polymer-Nanoparticle Hydrogels for Cell and Drug Delivery Applications
09:39

Injectable Supramolecular Polymer-Nanoparticle Hydrogels for Cell and Drug Delivery Applications

Published on: February 7, 2021

8.0K
Synthesis of Stimuli-responsive Nanogels using Aqueous One-step Crosslinking and Co-nanopolymerization
06:26

Synthesis of Stimuli-responsive Nanogels using Aqueous One-step Crosslinking and Co-nanopolymerization

Published on: January 24, 2025

1.1K

相关实验视频

Last Updated: Jun 23, 2026

Combinatorial Synthesis of and High-throughput Protein Release from Polymer Film and Nanoparticle Libraries
10:58

Combinatorial Synthesis of and High-throughput Protein Release from Polymer Film and Nanoparticle Libraries

Published on: September 6, 2012

10.4K
Injectable Supramolecular Polymer-Nanoparticle Hydrogels for Cell and Drug Delivery Applications
09:39

Injectable Supramolecular Polymer-Nanoparticle Hydrogels for Cell and Drug Delivery Applications

Published on: February 7, 2021

8.0K
Synthesis of Stimuli-responsive Nanogels using Aqueous One-step Crosslinking and Co-nanopolymerization
06:26

Synthesis of Stimuli-responsive Nanogels using Aqueous One-step Crosslinking and Co-nanopolymerization

Published on: January 24, 2025

1.1K

结论:

  • 详细的运动分析和建模对于研究纳米多糖的持续释放是必不可少的.
  • 有效的建模助力将体外发现转化为体外应用.
  • 纳米工程聚糖对未来的灵敏应用具有重大前景.