Li Wenji, Ng Ka-yun, Heng Paul Wan Sia
Department of Pharmacy, National University of Singapore.
Biol Pharm Bull. 2014;37(6):926-37. doi: 10.1248/bpb.b13-00864.
The aim of this study was to develop optimized sucrose ester (SE) stabilized oleanolic acid (OA) nanosuspensions (NS) for enhanced delivery via wet ball milling by design of experiments (DOE). In this study, SEOA NS batches were prepared by wet ball milling method. Mean particle sizes and polydispersity indices were determined using a nanosizer. The percent encapsulation efficiency, saturation solubility and in vitro dissolution rate were obtained with analyses using HPLC. Preparation methods were optimized by DOE using the Minitab software. The in vitro bioefficacy was obtained by methyl thiazolyl tetrazolium (MTT) measurements in A549 human non small cell lung cancer cell line. The in vivo pharmacokinetics profile was determined using LC-electrospray ionization (ESI)-MS/MS. The study produced spherical SEOA NS particles (ca. 100 nm in diameter) which were found to be able to increase OA saturation solubility considerably. Optimized SEOA-GBD NS (milled at 600 rpm for 3 h, sucrose monolaurate (SEL) : sucrose monopalmitate (SEP) at 9 : 1, w/w; SE : OA at 1 : 1, w/w) was found to be physically stable over 14 d at 4°C. The NS showed much higher dissolution rate, cytotoxicity and bioavailability when compared with the free drug. Thus, the prepared OA as SE stabilized NS particles by wet ball milling enhanced the saturation solubility, in vitro dissolution rate, bioefficacy and in vivo bioavailability of OA. The use of sugar esters may also be potentially applied to other hydrophobic drugs.
本研究的目的是通过实验设计(DOE)开发优化的蔗糖酯(SE)稳定的齐墩果酸(OA)纳米混悬液(NS),以通过湿球磨法增强药物递送。在本研究中,通过湿球磨法制备了SEOA NS批次。使用纳米粒度仪测定平均粒径和多分散指数。通过高效液相色谱法(HPLC)分析获得包封率、饱和溶解度和体外溶出速率。使用Minitab软件通过DOE优化制备方法。通过在A549人非小细胞肺癌细胞系中进行甲基噻唑基四氮唑(MTT)测量获得体外生物有效性。使用液相色谱-电喷雾电离(ESI)-串联质谱(MS/MS)测定体内药代动力学特征。该研究制备出了球形的SEOA NS颗粒(直径约100 nm),发现其能够显著提高OA的饱和溶解度。优化后的SEOA-GBD NS(在600 rpm下研磨3 h,月桂酸蔗糖酯(SEL)∶棕榈酸蔗糖酯(SEP)为9∶1,w/w;SE∶OA为1∶1,w/w)在4°C下14天内物理性质稳定。与游离药物相比,该纳米混悬液显示出更高的溶出速率、细胞毒性和生物利用度。因此,通过湿球磨法制备的以SE稳定的OA纳米混悬液颗粒提高了OA的饱和溶解度、体外溶出速率、生物有效性和体内生物利用度。糖酯的应用也可能潜在地应用于其他疏水性药物。