State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, People's Republic of China.
J Biomed Mater Res B Appl Biomater. 2012 Jul;100(5):1397-403. doi: 10.1002/jbm.b.32711. Epub 2012 May 7.
Hollow mesoporous silica nanoparticles (HMSNs) are considered a potential drug delivery system owing to their recognized advantages in drug loading and releasing. However, whether HMSN could be degraded inside the cells remains unknown. In this study, based on the observations by transmission electron microscopy, fluorescence staining, enzymatic proteolysis, and inductively coupled plasma atomic emission spectroscopy, HMSNs were proved to be degradable in human umbilical vein endothelial cells. The degradation first took place in cytoplasm and lysosomes, and secondly in lysosomes only. The Si content in culture medium increased as the time increases, suggesting that the degradation product inside the cells could be excreted into the culture medium. The degrading rate is fast in the first 2 days and slow after 2 days. The present results provided a clue to further research on the metabolic way and cytotoxicity of silica nanoparticles.
介孔中空硅纳米颗粒(HMSNs)由于其在药物负载和释放方面的公认优势,被认为是一种有潜力的药物传递系统。然而,HMSN 是否能在细胞内降解仍然未知。在这项研究中,基于透射电子显微镜观察、荧光染色、酶蛋白水解和电感耦合等离子体原子发射光谱,证明 HMSN 在人脐静脉内皮细胞中是可降解的。降解首先发生在细胞质和溶酶体中,其次仅发生在溶酶体中。培养基中的 Si 含量随着时间的增加而增加,这表明细胞内的降解产物可能被分泌到培养基中。在最初的 2 天内,降解速度较快,之后速度较慢。本研究结果为进一步研究硅纳米颗粒的代谢途径和细胞毒性提供了线索。