Laboratory of Pharmaceutical Technology, Ghent University, Harelbekestraat 72, Ghent B-9000, Belgium.
Int J Pharm. 2012 Jan 17;422(1-2):310-7. doi: 10.1016/j.ijpharm.2011.11.017. Epub 2011 Nov 11.
A design of experiments (DOE) approach (2-level full factorial design) was used to investigate the effect of several formulation and process variables on the properties of fast disintegrating tablets comprising starch-based pellets and excipient granules and to optimize and validate the design space. The percentage of starch pellets (30-50%, w/w), type of disintegrants (Ac-di-sol, Explotab, Polyplasdone), percentage of external disintegrant (4-8%, w/w) and compression force (5-15 kN) were the evaluated factors (24 runs+9 centre points=33 experiments), while tablet hardness, friability and disintegration time were the studied tablet properties (responses). Starch pellets were prepared by extrusion-spheronisation. Excipient granules containing microcrystalline cellulose, lactose, internal disintegrant (8%) and polyvinylpyrrolidone K-30 (4%) were prepared by wet granulation. Pellets, granules (700-1000 μm) and external disintegrant were mixed and compressed into oblong tablets (17.1mm long, 8.2mm wide). Evaluation of the effects calculated from the DOE results showed that a lower concentration of starch pellets and higher compression force were required to yield tablets with a high hardness, a low friability (<1%) and short disintegration time (<3 min). Polyplasdone granules had the lowest porosity and friability which was reflected in the DOE study, where the Polyplasdone-containing tablets were harder, less friable and disintegrated faster compared to Ac-di-sol and Explotab-containing tablets. Monte carlo simulations at the optimal factor settings (30% starch pellets, 4% Polyplasdone and 10 kN compression force) indicated that a robust system was formed as the probability to exceed the limits was low for all responses. Validation of the design space (at optimal settings) showed that the results predicted via the DOE models correlated well with the observed experimental data.
采用实验设计(DOE)方法(2 水平完全因子设计)来研究包含基于淀粉的丸剂和赋形剂颗粒的速崩片的性质,并优化和验证设计空间。评估因素为淀粉丸剂的百分比(30-50%,w/w)、崩解剂的类型(Ac-di-sol、Explotab、Polyplasdone)、外部崩解剂的百分比(4-8%,w/w)和压缩力(5-15 kN)(24 次运行+9 个中心点=33 次实验),而片剂硬度、脆碎度和崩解时间是研究的片剂性质(响应)。淀粉丸剂通过挤出造粒制备。含微晶纤维素、乳糖、内部崩解剂(8%)和聚乙烯吡咯烷酮 K-30(4%)的赋形剂颗粒通过湿法制粒制备。将丸剂、颗粒(700-1000μm)和外部崩解剂混合并压缩成长方形片剂(17.1mm 长,8.2mm 宽)。从 DOE 结果计算出的影响评估表明,需要较低浓度的淀粉丸剂和较高的压缩力,才能使片剂具有较高的硬度、较低的脆碎度(<1%)和较短的崩解时间(<3 分钟)。Polyplasdone 颗粒具有最低的孔隙率和脆碎度,这在 DOE 研究中得到了反映,其中含有 Polyplasdone 的片剂比含有 Ac-di-sol 和 Explotab 的片剂更硬、更不易脆碎且崩解更快。在最优因子设置(30%淀粉丸剂、4%Polyplasdone 和 10 kN 压缩力)下进行蒙特卡罗模拟表明,由于所有响应的超出限制的概率都较低,因此形成了一个稳健的系统。设计空间的验证(在最优设置下)表明,通过 DOE 模型预测的结果与观察到的实验数据很好地相关。