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相关概念视频

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

Modified-Release Drug Delivery Systems: Rate-Programmed II

137
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...
137
Modified-Release Drug Delivery Systems: Rate-Programmed I01:22

Modified-Release Drug Delivery Systems: Rate-Programmed I

172
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,...
172
Modified-Release Drug Delivery Systems: Stimuli-Activated01:30

Modified-Release Drug Delivery Systems: Stimuli-Activated

177
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...
177
Modified-Release Drug Delivery Systems: Site-Targeted01:24

Modified-Release Drug Delivery Systems: Site-Targeted

164
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.
164
Site-Targeted Drug Delivery Systems: Polymeric Carriers01:24

Site-Targeted Drug Delivery Systems: Polymeric Carriers

160
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...
160
Oral Drug Delivery Systems: Delayed-Release Systems01:11

Oral Drug Delivery Systems: Delayed-Release Systems

222
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...
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相关实验视频

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Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release
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从Cur-LPs装载的自适应注射式自我愈合水凝中持续释放黄素.

Caixia Wu1, Xiaoqun Ning2, Qunfeng Liu3

  • 1National Engineering Research Center for Healthcare Devices, Guangdong Provincial Key Laboratory of Medical Electronic Instruments and Materials, Institute of Biological and Medical Engineering, Guangdong Academy of Sciences, Guangzhou 510316, China.

Polymers
|January 8, 2025
PubMed
概括

一种新型的可注射水凝,由改性氨酸,甘醇基托和瓜尔合成,有效地修复不规则的组织缺陷. 它提供快速凝,自我愈合和持续的黄素释放,用于抗氧化和抗炎组织修复.

关键词:
它具有抗氧化和抗炎作用.可注射粘合剂自愈水凝修复生物组织缺陷的修复.库尔库的可持续释放

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科学领域:

  • 生物材料科学 生物材料科学
  • 组织工程是组织工程.
  • 药物运输 药物运输 药物运输

背景情况:

  • 生物组织缺陷由于不规则的形状,炎症和氧化应激会带来挑战.
  • 开发可注射,可适应的材料来填补缺陷并促进维修至关重要.

研究的目的:

  • 合成和描述一种用于组织缺陷修复的新型注射液凝.
  • 评估水凝的可注射性,组织粘附性,自我愈合性,抗氧化和抗炎性质.
  • 评估黄素持续释放的治疗效果,以提高治疗效果.

主要方法:

  • 合成酸改性氧化氨酸 (OHAPBA) 的合成.
  • 动态交叉连接与catechol组修饰的甘醇基托 (GCHCA) 和瓜尔 (GG).
  • 用黄素脂质体 (Cur-LPs) 加载和水凝性质的表征,包括凝时间,可注射性,粘附性,自我愈合性,生物相容性和药物释放动力学.

主要成果:

  • 水凝表现出快速凝 (30秒内),优异的注射性,组织粘附性和自我愈合能力.
  • 已证明具有良好的生物相容性和显著的DPPH基因清除活性.
  • 达到持续释放黄素长达10天,改善其生物可用性.

结论:

  • 开发出来的水凝有效地填充和粘附不规则的组织缺陷.
  • 它的抗氧化和持续的抗炎性质,通过黄素的释放,促进组织修复.
  • 这种可注射的水凝显示出在组织缺陷修复中应用的巨大潜力.