Velasco M V, Ford J L, Rowe P, Rajabi-Siahboomi A R
School of Pharmacy and Chemistry, Liverpool John Moores University, UK.
J Control Release. 1999 Jan 4;57(1):75-85. doi: 10.1016/s0168-3659(98)00110-2.
This study evaluates the relationship and influence of formulation and technological factors such as drug:hydroxypropylmethylcellulose (HPMC) ratio, particle size of the drug, particle size of HPMC and compression force, on drug release from matrices containing HPMC and diclofenac sodium as a model drug. The influence of these variables was assessed by multi-way analysis of variance. The results of the present study point out that the rate and mechanism of diclofenac sodium release from HPMC K15M matrices are mainly controlled by the drug:HPMC ratio. The drug and HPMC particle size also influence the drug release parameters, although to a lesser extent. Finally, the independence of the drug release from matrix tablets with respect to the compression force is reported.
本研究评估了诸如药物与羟丙基甲基纤维素(HPMC)的比例、药物的粒径、HPMC的粒径以及压缩力等制剂和工艺因素对含HPMC和双氯芬酸钠作为模型药物的基质中药物释放的关系和影响。通过多因素方差分析评估了这些变量的影响。本研究结果指出,双氯芬酸钠从HPMC K15M基质中的释放速率和机制主要受药物与HPMC比例的控制。药物和HPMC的粒径也会影响药物释放参数,尽管影响程度较小。最后,报告了基质片剂的药物释放与压缩力无关。