Rapoport N Y, Herron J N, Pitt W G, Pitina L
Department of Bioengineering and Center for Biopolymers on Interfaces, University of Utah, Salt Lake City, UT 84112, USA.
J Control Release. 1999 Mar 29;58(2):153-62. doi: 10.1016/s0168-3659(98)00149-7.
The effect of Pluronic P-105 micelle structure and ultrasound on the uptake of two anthracycline drugs, doxorubicin and its paramagnetic analogue, ruboxyl, by HL-60 cells was investigated. Pluronic micellization was studied over the temperature range of 25-42 degrees C using the EPR and fluorescence spectroscopy. In the presence of Pluronic P-105 at concentrations corresponding to unimers (or loose aggregates), drug uptake by HL-60 cells was enhanced, apparently due to the effect of the polymeric surfactant on cell membrane permeability. At Pluronic concentrations corresponding to the formation of dense micelles with hydrophobic cores, drug uptake was substantially decreased. However, insonation with 70 kHz ultrasound enhanced the intracellular uptake of drugs encapsulated in dense Pluronic micelles. These findings may provide for developing a new technique of drug targeting by encapsulating the drug in micelles to prevent unwanted interactions with healthy cells and focusing ultrasound on a tumor to enhance drug uptake at the tumor site.
研究了普朗尼克P - 105胶束结构和超声对HL - 60细胞摄取两种蒽环类药物(阿霉素及其顺磁性类似物鲁博昔尔)的影响。使用电子顺磁共振(EPR)和荧光光谱法,在25 - 42摄氏度的温度范围内研究了普朗尼克的胶束化过程。在与单聚物(或松散聚集体)浓度相当的普朗尼克P - 105存在下,HL - 60细胞对药物的摄取增强,这显然是由于聚合物表面活性剂对细胞膜通透性的影响。在与具有疏水核心的致密胶束形成浓度相当的普朗尼克浓度下,药物摄取显著降低。然而,70 kHz超声的声处理增强了包裹在致密普朗尼克胶束中的药物的细胞内摄取。这些发现可能有助于开发一种新的药物靶向技术,即将药物包裹在胶束中以防止与健康细胞发生不必要的相互作用,并将超声聚焦在肿瘤上以增强肿瘤部位的药物摄取。