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相关概念视频

Site-Targeted Drug Delivery Systems: Polymeric Carriers01:24

Site-Targeted Drug Delivery Systems: Polymeric Carriers

132
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...
132
Modified-Release Drug Delivery Systems: Site-Targeted01:24

Modified-Release Drug Delivery Systems: Site-Targeted

144
Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.
144
Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

108
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...
108
Modified-Release Drug Delivery Systems: Rate-Programmed I01:22

Modified-Release Drug Delivery Systems: Rate-Programmed I

144
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,...
144
Modified-Release Drug Delivery Systems: Classification01:23

Modified-Release Drug Delivery Systems: Classification

289
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...
289
Determination of Multiple Dosing Parameters: Loading and Maintenance Doses01:25

Determination of Multiple Dosing Parameters: Loading and Maintenance Doses

380
A loading dose is an essential pharmacological strategy to rapidly achieve the target plasma drug concentration necessary for an immediate therapeutic effect. This approach is especially critical for drugs characterized by slow absorption or extended half-lives, where delaying therapeutic plasma levels could compromise treatment outcomes. By administering a loading dose, clinicians ensure a prompt onset of drug action, even for agents with complex pharmacokinetic profiles.Achieving steady-state...
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Formulation of Diblock Polymeric Nanoparticles through Nanoprecipitation Technique
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模态药物聚合纳米粒子具有异常高的药物负载和定量负载效率.

Kaimin Cai1, Xi He1,2, Ziyuan Song1

  • 1†Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.

Journal of the American Chemical Society
|March 6, 2015
PubMed
概括

研究人员开发了一种创新的策略,用于创建具有50%以上药物负载和定量效率的聚合物纳米粒子 (NP). 这一突破利用了二维药物合核来增强药物输送系统.

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科学领域:

  • 聚合物化学 聚合物化学
  • 纳米技术 纳米技术
  • 药物运输 药物运输 药物运输

背景情况:

  • 聚合物纳米粒子 (NP) 广泛用于小分子药物封装.
  • 目前的方法往往受到低药物负载和效率的影响.
  • 需要先进的NP配方,提高药物有效载荷能力.

研究的目的:

  • 开发一种新的策略,用于制备具有异常高药物负载和定量负载效率的聚合物NP.
  • 设计一个二维药物合物作为NP的核心构造单元.
  • 调查开发的NP的稳定性和释放特性.

主要方法:

  • 一种二度药物联结物和甲氧多聚 (乙烯基醇) - 阻断聚酸 (mPEG-PLA) 的同时沉.
  • 形成具有二维药物核心和聚合物外的NP.
  • 评估药物加载,加载效率,在生理条件下的稳定性和触发的药物释放.

主要成果:

  • 实现了异常高的药物负载 (>50%) 和定量负载效率.
  • 在生理条件下 (PBS溶液) 证明了NP的良好稳定性.
  • 展示了在外部触发时真正的药物形式的受控释放,没有过早释放.

结论:

  • 开发的战略使得可以制备具有显著增强药物载荷能力的聚合物NP.
  • 二维药物联核心策略为稳定和可控的药物输送系统提供了一个有前途的方法.
  • 这些高药载荷的NP适用于需要高效和触发治疗剂释放的应用.