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采用实验设计(DoE)优化非诺贝特双螺杆熔融制粒工艺。

Process optimization of twin-screw melt granulation of fenofibrate using design of experiment (DoE).

机构信息

College of Pharmacy and Health Sciences, St. John's University, Queens, NY, USA.

College of Pharmacy and Health Sciences, St. John's University, Queens, NY, USA; SE Tylose USA Inc., Pharmaceutical Application Laboratory, 140 Commerce Way, Totowa, NJ, USA.

出版信息

Int J Pharm. 2021 Jan 25;593:120101. doi: 10.1016/j.ijpharm.2020.120101. Epub 2020 Dec 10.

Abstract

The purpose of this study was to optimize the melt granulation process of fenofibrate using twin-screw granulator. Initial screening was performed to select the excipients required for melt granulation process. A 3 × 3 factorial design was used to optimize the processing conditions using the % drug loading (X) and screw speed (X) as the independent parameters and granule friability (Y) % yield (Y) as the dependent parameters. The effect of the independent parameters on the dependent parameters was determined using response surface plots and contour plots. A linear relationship was observed between % drug loading (X) and % friability (Y) and a quadratic relationship was observed between the independent parameters (X and X) and % yield (Y). The processing conditions for optimum granules were determined using numerical and graphical optimization and it was found that 15% drug loading at 50 rpm results in maximum % yield of 82.38% and minimum friability of 7.88%. The solid-state characterization of the optimized granules showed that the drug turned from crystalline state to amorphous state during melt granulation process. The optimized granules were compressed into tablets using Purolite® as the super disintegrating agent. The optimized formulation showed >85% drug release in 0.75% SLS solution within 60 min.

摘要

本研究旨在使用双螺杆造粒机优化非诺贝特的熔融制粒工艺。首先进行了初步筛选,以选择熔融制粒过程所需的赋形剂。采用 3×3 析因设计,以药物负载量(X)和螺杆转速(X)为独立参数,颗粒脆碎度(Y)%和产率(Y)为依赖参数,优化加工条件。使用响应面图和等高线图确定独立参数对依赖参数的影响。药物负载量(X)与脆碎度(Y)呈线性关系,独立参数(X 和 X)与产率(Y)呈二次关系。通过数值和图形优化确定最佳颗粒的加工条件,发现 15%的药物负载量在 50rpm 下可获得最大产率 82.38%和最小脆碎度 7.88%。优化颗粒的固态特性表明,药物在熔融制粒过程中从结晶态转变为无定形态。使用 Purolite®作为超级崩解剂将优化的颗粒压制成片剂。优化的配方在 60 分钟内,在 0.75% SLS 溶液中释放超过 85%的药物。

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