Ciofani Gianni, Raffa Vittoria, Menciassi Arianna, Dario Paolo
CRIM Lab-Center for Research in Microengineering, Scuola Superiore Sant'Anna, Piazza Martiri della Libertà, 33, 56127, Pisa, Italy.
Biomed Microdevices. 2008 Apr;10(2):131-40. doi: 10.1007/s10544-007-9118-7.
Drug-carrying microstructures which have a size similar to biological structures are very attractive to encapsulate drugs and protect them during the transit in the human body. This paper describes polymeric (alginate and chitosan) particles (average radius 500 nm) produced by homogenization techniques. In vitro studies performed on cell lines demonstrate the effectiveness of such particles for intracellular drug delivery. Our experiments suggest that cellular up - take increases linearly with particle concentration in the growth medium, and the internalization process has a first order kinetics (characteristic time around 0.5 h(-1)). In addition, the particles degrade within 24 h from the up-take without side effects for cell viability.
尺寸与生物结构相似的载药微结构对于包裹药物并在人体转运过程中保护它们而言极具吸引力。本文描述了通过匀化技术制备的聚合物(海藻酸盐和壳聚糖)颗粒(平均半径500纳米)。对细胞系进行的体外研究证明了此类颗粒用于细胞内药物递送的有效性。我们的实验表明,细胞摄取随生长培养基中颗粒浓度呈线性增加,且内化过程具有一级动力学(特征时间约为0.5 h⁻¹)。此外,颗粒在摄取后24小时内降解,对细胞活力无副作用。
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