改善内生物聚合物药物输送系统:一个体内研究
Stefania Goncalves1, Torin Thielhelm1, Devon Pawley2,3
1Department of Otolaryngology - Head and Neck Surgery, University of Miami Ear Institute, University of Miami, Miller School of Medicine, Miami, FL, USA.
Acta oto-laryngologica
|November 10, 2024
概括
这项研究表明,用德克萨米他 (DXM) 输入的微针是生物相容的,并防止听力损失在动物模型的耳毒性损伤. 这种新的药物输送方法为治疗听力损失提供了潜力.
科学领域:
- 汽车技术 汽车技术
- 药物输送系统 药物输送系统
- 再生医学是一种再生医学.
背景情况:
- 由于耳解剖学,内耳药物输送是复杂的.
- 对于听力损失的治疗,需要最小的侵入性耳内耳道器件.
- 目前的方法在向药物输送方面面临挑战.
研究的目的:
- 评估用于内耳药物输送的用德克萨米他 (DXM) 输入的PLGA微针.
- 为了测试DXM微针在毒性损伤的*in vivo*模型中的有效性.
- 为了评估内微针的生物相容性.
主要方法:
- 在一项随机对照研究中,使用了24只老鼠.
- 毒性损伤是使用乙烯酸和kanamycin诱导的.
- 动物接受了DXM微针,普通微针或没有治疗.
- 听觉脑干响应测试监测了28天的听力功能.
主要成果:
- 耳内微针是生物相容的,在对照组中没有显示任何不良影响.
- 用DXM注入的微针显著防止了暴露于耳毒剂的动物的听力恶化.
- 这项研究证明了微针装置的成功*in vivo*应用.
结论:
- 装有DXM的微针是一种可行的,生物相容的技术,用于内药物输送.
- 这种方法在预防或治疗因耳毒性引起的听力损失方面表现有前途.
- 最少侵入性的微针技术为内耳治疗提供了一个新的策略.
相关概念视频
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: Bioavailability
Modified-release (MR) dosage forms are designed to extend drug release over time, thereby maintaining stable plasma concentrations and reducing dosing frequency. However, their bioavailability is typically below 100% due to incomplete drug release and presystemic metabolism, and limitations in drug permeability across the gastrointestinal epithelium, all of which can restrict the fraction of the drug reaching systemic circulation. Consequently, studying the in vivo bioavailability of MR...
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-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-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 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...


