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相关概念视频

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

Modified-Release Drug Delivery Systems: Site-Targeted

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.
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...
Microbial Corrosion01:24

Microbial Corrosion

Microbiologically Influenced Corrosion (MIC) is a significant form of material degradation caused by the metabolic activities of microorganisms. This phenomenon poses substantial challenges across various industries, including oil and gas, maritime, and water treatment sectors.MIC occurs when microorganisms, such as bacteria, archaea, and fungi, colonize metal surfaces, forming biofilms that alter the local electrochemical environment. These biofilms can lead to the production of corrosive...

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相关实验视频

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Facile Preparation of Internally Self-assembled Lipid Particles Stabilized by Carbon Nanotubes
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使用金属响应的动态纳米载体进行抗菌药物输送.

N G Hasitha Raviranga1, Olof Ramström1,2

  • 1Department of Chemistry, University of Massachusetts Lowell, One University Ave., 01854 Lowell, Massachusetts, United States.

ACS applied bio materials
|July 4, 2024
PubMed
概括

新的生物相容纳米载体载有抗微生物和抗生素,有效地对抗多药耐药性病原体. 这些新材料在治疗耐药细菌引起的感染方面表现有前途,包括生物膜中的细菌.

科学领域:

  • 生物材料科学 生物材料科学
  • 纳米技术 纳米技术
  • 抗菌研究 抗菌研究

背景情况:

  • 越来越多的抗药性 (MDR) 病原体需要超越传统抗生素的新疗法.
  • 药物重新定位,协同组合和先进的输送系统是创新的关键领域.
  • 生物相容的纳米载体为结合抗菌剂提供了一个平台,以提高有效性.

研究的目的:

  • 开发和评估生物相容的纳米载体,包括抗微生物子 (GaIII,InIII) 和抗生素.
  • 评估这些纳米载体对包括生物膜在内的多抗药性病原体的疗效.
  • 研究金属在阴离子递送和抗菌活性中的作用.

主要方法:

  • 用GaIII或InIII协调的基托基纳米载体 (100-200nm) 的制造,有或没有封装的抗生素.
  • 对MDR临床分离物的抗菌活性评估,包括*Pseudomonas aeruginosa*.
  • 对A549和NIH/3T3细胞的生物膜抑制和消除的评估,以及细胞毒性测定.

主要成果:

  • 在营养限制条件下,纳米载体有效抑制了MDR *Pseudomonas aeruginosa*.
  • 带有阴离子和抗生素的纳米模块显示出对格拉姆阴性和格拉姆阳性病原体的有效性.
关键词:
在P. aeruginosa的研究中,P.抗微生物药物是一种抗菌药物.基多酸盐的使用方法(Gallium) 是一种的物质.印度是印度的元素.纳米载体的纳米载体

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  • 含的纳米载体对细菌生物膜,特别是P. aeruginosa和Staphylococcus epidermidis表现出增强的活性.
  • 观察到A549细胞的低细胞毒性,NIH/3T3细胞的可改善值.
  • 结论:

    • 生物相容的纳米载体为对抗多药耐药病原体提供了一个有前途的战略.
    • 基于的纳米载体显示出生物膜消除的特殊潜力.
    • 开发的纳米载体对潜在的治疗应用具有有利的安全性.