Ashok Beena, Arleth Lise, Hjelm Rex P, Rubinstein Israel, Onyüksel Hayat
Department of Biopharmaceutical Sciences, University of Illinois at Chicago, Chicago, IL 60612, USA.
J Pharm Sci. 2004 Oct;93(10):2476-87. doi: 10.1002/jps.20150.
Sterically stabilized micelles (SSM) composed of poly(ethylene glycol-2000)-grafted distearoylphosphatidylethanolamine (DSPE-PEG) and sterically stabilized mixed micelles (SSMM) composed of DSPE-PEG and egg-phosphatidyl choline (PC) have recently been introduced as novel lipid based carriers for water-insoluble drugs. However, factors that affect the solubilization behavior of these phospholipid micelles are not well understood. This study investigates the effect of PEG chain length and PC content on physical properties and solubilization potential of PEGylated phospholipid micelles. Critical micelle concentrations (CMC) determined for DSPE-PEG with different PEG chain lengths (2000, 3000, and 5000) using a fluorescent probe were in the micromolar range (0.5-1.5 microM) with higher CMC for longer PEG chain length. The size of micelles determined by quasi-elastic light scattering (QELS) showed that micellar systems became heterogeneous when PC was added at > or =25% for DSPE-PEG 2000 and > or = 40% for DSPE-PEG 5000, respectively. Above these critical PC ratios a significant increase in aggregation number and formation of rodlike particles were observed by small angle neutron scattering (SANS). Solubilization of diazepam was greater with DSPE-PEG 2000 than DSPE-PEG 5000 simple micelles as determined by RP-HPLC. However, DSPE-PEG 5000 micelles showed greater improvement in solubilization of the water-insoluble drug with an increase in PC content. In conclusion, phospholipid micelle size and solubilization potential varied with PEG chain length and PC content in the mixed micelle. Aggregation number and shape of the micelles did not significantly change until the critical PC concentrations.
由聚乙二醇-2000接枝的二硬脂酰磷脂酰乙醇胺(DSPE-PEG)组成的空间稳定胶束(SSM)以及由DSPE-PEG和蛋黄卵磷脂(PC)组成的空间稳定混合胶束(SSMM),最近已被引入作为水不溶性药物的新型脂质载体。然而,影响这些磷脂胶束增溶行为的因素尚未得到充分了解。本研究考察了PEG链长和PC含量对聚乙二醇化磷脂胶束物理性质和增溶潜力的影响。使用荧光探针测定不同PEG链长(2000、3000和5000)的DSPE-PEG的临界胶束浓度(CMC)在微摩尔范围内(0.5 - 1.5 microM),PEG链长越长CMC越高。通过准弹性光散射(QELS)测定的胶束大小表明,当分别向DSPE-PEG 2000中添加≥25%的PC以及向DSPE-PEG 5000中添加≥40%的PC时,胶束体系变得不均匀。在这些临界PC比例以上,通过小角中子散射(SANS)观察到聚集数显著增加且形成了棒状颗粒。通过反相高效液相色谱(RP-HPLC)测定,地西泮在DSPE-PEG 2000简单胶束中的增溶效果比DSPE-PEG 5000好。然而,随着PC含量的增加,DSPE-PEG 5000胶束在水不溶性药物增溶方面表现出更大的改善。总之,磷脂胶束的大小和增溶潜力随混合胶束中PEG链长和PC含量而变化。在达到临界PC浓度之前,胶束的聚集数和形状没有显著变化。