Department of Chemical Engineering and California NanoSystems Institute, University of California-Santa Barbara, Santa Barbara, California 93106-6105, USA.
ACS Nano. 2013 Jun 25;7(6):4933-45. doi: 10.1021/nn400243d. Epub 2013 Jun 3.
Nanoparticles have opened new exciting avenues for both diagnostic and therapeutic applications in human disease, and targeted nanoparticles are increasingly used as specific drug delivery vehicles. The precise quantification of nanoparticle internalization is of importance to measure the impact of physical and chemical properties on the uptake of nanoparticles into target cells or into cells responsible for rapid clearance. Internalization of nanoparticles has been measured by various techniques, but comparability of data between different laboratories is impeded by lack of a generally accepted standardized assay. Furthermore, the distinction between associated and internalized particles has been a challenge for many years, although this distinction is critical for most research questions. Previously used methods to verify intracellular location are typically not quantitative and do not lend themselves to high-throughput analysis. Here, we developed a mathematical model which integrates the data from high-throughput flow cytometry measurements with data from quantitative confocal microscopy. The generic method described here will be a useful tool in biomedical nanotechnology studies. The method was then applied to measure the impact of surface coatings of vesosomes on their internalization by cells of the reticuloendothelial system (RES). RES cells are responsible for rapid clearance of nanoparticles, and the resulting fast blood clearance is one of the major challenges in biomedical applications of nanoparticles. Coating of vesosomes with long chain polyethylene glycol showed a trend for lower internalization by RES cells.
纳米颗粒为人类疾病的诊断和治疗应用开辟了新的令人兴奋的途径,靶向纳米颗粒越来越多地被用作特定的药物递送载体。精确量化纳米颗粒的内化对于测量物理和化学性质对纳米颗粒进入靶细胞或负责快速清除的细胞的摄取的影响非常重要。已经使用各种技术来测量纳米颗粒的内化,但由于缺乏普遍接受的标准化测定,不同实验室之间的数据可比性受到阻碍。此外,虽然这种区别对于大多数研究问题至关重要,但多年来一直难以区分相关颗粒和内化颗粒。以前用于验证细胞内位置的方法通常不是定量的,不适合高通量分析。在这里,我们开发了一种数学模型,该模型将高通量流式细胞术测量的数据与定量共聚焦显微镜的数据相结合。这里描述的通用方法将成为生物医学纳米技术研究的有用工具。然后,该方法用于测量囊泡的表面涂层对其被网状内皮系统 (RES) 细胞内化的影响。RES 细胞负责快速清除纳米颗粒,而快速的血液清除是纳米颗粒在生物医学应用中的主要挑战之一。用长链聚乙二醇对囊泡进行涂层显示出 RES 细胞内化程度降低的趋势。