A new parameter for characterization of tablet friability based on a systematical study of five excipients

被引:20
作者
Zhao, Haiyue [1 ]
Yu, Yating [2 ,3 ]
Ni, Ni [1 ]
Zhao, Lijie [2 ]
Lin, Xiao [1 ]
Wang, Youjie [2 ]
Du, Ruofei [2 ]
Shen, Lan [1 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Sch Pharm, 1200 Cai Lun Rd, Shanghai 201203, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Engn Res Ctr Modern Preparat Technol Tradit Chine, Minist Educ, 1200 Cai Lun Rd, Shanghai 201203, Peoples R China
[3] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Dept Pharm, Sch Med, Shanghai 200011, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
Friability; Stress; Strain; Mechanical properties; Tablet; DESIGN; QUALITIES;
D O I
10.1016/j.ijpharm.2021.121339
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this paper, a new parameter highly relevant to tablet friability is proposed based on a systematical study of the tablet quality attributes and texture performances of five different direct compression excipients, including microcrystalline cellulose, starch, lactose, mannitol, and dicalcium phosphate anhydrous. The new parameter, named Strain/Stress Max, could indicate the tablet's ability against external force to maintain integrity. It was directly obtained from the diametrical breaking test which is extensively used to assess tablet mechanical strength, and thus no extra work is required. The values varied significantly among the tablets formed by materials with different mechanical properties under the same compression pressure. A design space was developed to achieve <1% tablet friability at various combinations of Strain/Stress Max and tensile strength. Additionally, data from binary mixture tablets validated the availability of the constructed design space. And the upper limit of Strain/Stress Max value was advisable for 1.5 MPa-1 for pharmaceutical tablets. In conclusion, the new parameter and design space are available for fast identification of the tablets with acceptable friability to facilitate the development of tablet formulation using as few active pharmaceutic ingredients as possible.
引用
收藏
页数:11
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