Study of the critical points and the role of the pores and viscosity in carbamazepine hydrophilic matrix tablets

被引:21
作者
Aguilar-de-Leyva, Angela [1 ]
Cifuentes, Celia [1 ]
Rajabi-Siahboomi, Ali R. [2 ]
Caraballo, Isidoro [1 ]
机构
[1] Univ Seville, Dept Pharm & Pharmaceut Technol, E-41012 Seville, Spain
[2] Colorcon Inc, Global Headquarters, Harleysville, PA USA
关键词
Hydroxypropylmethyl cellulose; Hydrophilic matrices; Carbamazepine; Tablet porosity; Percolation threshold extended release; CONTROLLED DRUG-DELIVERY; PERCOLATION THEORY; PARTICLE-SIZE; SOLUTE RELEASE; HPMC; SYSTEMS; THRESHOLDS; MECHANISMS; DIFFUSION; RATIO;
D O I
10.1016/j.ejpb.2011.09.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Percolation theory has been applied to estimate the Hypromellose (HPMC) percolation thresholds and the influence of the polymer viscosity and the initial porosity on these thresholds in carbamazepine multicomponent matrix formulations. Different batches containing two viscosity grades of HPMC as hydrophilic matrix forming polymer. MCC and lactose as fillers, and a lubricant mixture have been manufactured varying the compression pressure in order to obtain matrices with three levels of initial porosity. The results suggested the existence of an excipient percolation threshold between 13 and 15% v/v of HPMC for the different batches prepared. It has been found that the percolation threshold for this polymer is independent on the formulation factors studied in this paper: polymer viscosity and initial porosity of the matrices. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 142
页数:7
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