控制的pH稳定性和可调节的混合电荷纳米粒子的细胞吸收
Pramod P Pillai1, Sabil Huda, Bartlomiej Kowalczyk
1Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, USA.
Journal of the American Chemical Society
|March 27, 2013
概括
在纳米颗粒上混合自组装单层 (m-SAM) 提供可调节的pH依赖沉. 调整连接物比率或粒子大小可以控制沉的pH值,并影响细胞吸收,即使是负电荷粒子.
科学领域:
- 材料科学 材料科学 材料科学
- 纳米技术纳米技术
- 表面化学 表面化学
背景情况:
- 用混合自组装单层 (m-SAM) 功能化的纳米粒子具有pH依赖的稳定性.
- 沉点 (pH(prec)) 对于纳米粒子的应用和处理至关重要.
研究的目的:
- 为了研究m-SAM组成,粒子大小和pH依赖降水之间的关系.
- 探索这些因素如何影响纳米粒子细胞吸收.
主要方法:
- 用混合自组装单层 (m-SAM) 功能化纳米粒子的合成,其中含有不同比例的带电硫醇.
- 纳米粒子稳定性和降水pH (pH(prec)) 在一系列pH值的表征.
- 评估不同表面电荷和组成的功能化纳米粒子的细胞吸收.
主要成果:
- 含有m-SAM的纳米粒子在低和高pH时稳定,但在pH时沉,电荷平衡.
- 通过改变m-SAM连接物比率或粒子大小,可以精确调整pH在约4到7之间.
- 纳米粒子表面电荷和m-SAM组成显著影响细胞吸收效率.
- 在m-SAM中具有正电荷的醇促进细胞吸收,即使是净负电荷的纳米粒子.
结论:
- 混合自组装单层为控制纳米粒子沉pH提供了一个多功能平台.
- 纳米颗粒的可调的表面化学影响它们与生物系统的相互作用,包括细胞吸收.
- 对m-SAM的战略设计可以克服与纳米粒子交付有关的电荷障碍.
相关概念视频
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...
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.
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...


