超分子德克斯/聚胺酸纳米囊具有智能响应性,用于治疗药物的封装
Aharon Steffè1, Francesca Milano1, Santiago Giménez Reyes2
1Department of Chemistry 'Ugo Schiff', University of Florence, via della Lastruccia 3-13, 50019 Sesto Fiorentino (FI), Italy.
Journal of colloid and interface science
|December 20, 2024
概括
研究人员开发了新的德克斯功能化聚亚胺化物 (PAH:DEX) 纳米囊. 这些pH响应组件可以封装和释放蛋白质,显示有针对性的药物输送应用的潜力.
科学领域:
- 材料科学 材料科学 材料科学
- 聚合物化学 聚合物化学
- 纳米技术纳米技术
背景情况:
- 聚氨酸化物 (PAH) 是一种合成聚合物,在药物输送中具有潜在的应用.
- 德克斯 (DEX) 是一种生物相容的多糖,可以增强聚合物特性.
- 使用DEX功能化PAH可以创建具有改进特性的新型纳米载体.
研究的目的:
- 为了合成和表征PAH:DEX聚合物具有不同的德克斯结合.
- 研究超分子组件的形成和特性,特别是纳米囊 (NCs).
- 评估这些新型NC的pH响应和蛋白质传递能力.
主要方法:
- 对于PAH-DEX结合的还原性氨化.
- 动态光散射 (DLS),z电位,冷电子显微镜和小角度X射线散射 (SAXS) 用于表征.
- 光相关谱学 (FCS) 和循环二极化 (CD) 用于蛋白质释放和形状研究.
主要成果:
- PAH:DEX聚合物形成了pH响应的超分子组件,包括1:1比例的纳米囊.
- 在pH<6下拆解并在pH6-9重新组装的NCs,证明了pH的灵敏度.
- 牛血清白蛋白 (BSA) 的成功封装和pH触发释放得到实现.
结论:
- 新型PAH:DEX纳米囊成功合成和表征.
- 这些纳米囊表现出适合控制释放应用的pH响应性行为.
- 这些发现表明,在治疗性蛋白质和酶的内体体传递中,有潜在的应用.
相关概念视频
Bioavailability Enhancement: Drug Stability Enhancement and GI Retention
Improving a drug's stability in the gastrointestinal (GI) tract is paramount for enhancing its bioavailability and therapeutic effectiveness. Various strategies are employed to protect the drug from the harsh gastric milieu and to ensure its release and absorption at the desired site within the GI tract.Polymer coatings are one such method used to shield drugs from the stomach's acidic environment. By preventing premature drug release, these coatings improve the bioavailability of unstable...
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: 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-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...


