Egermann H, Krumphuber A, Frank P
Institute of Pharmaceutical Technology, University of Innsbruck, Austria.
J Pharm Sci. 1992 Aug;81(8):773-6. doi: 10.1002/jps.2600810811.
The validity of an equation developed to determine the quality of binary random mixtures (eq 1) was evaluated with tablets prepared from random mixtures of a coarse constituent A (sucrose) and fine constituent B [microcrystalline cellulose (Avicel PH 101)-talc] with the A:B ratios (w/w) varying from 10:90 to 80:20. With all A:B ratios, superior agreement was established between the random content variations determined with eq 1 and the content variations found in the tablets. The 80:20 ratio, however, was just at the boundary, and random quality was achieved with the 50-mg tablets but not with the 200-mg tablets because of segregation. From percolation theory, this result is a consequence of the small proportion by volume (bv) of B that is almost equal to the precolation threshold (Pcb) of B of 0.3. With bv less than Pcb, the fine constituent B does not form a coherent lattice, and eq 1 is no longer valid. To estimate the volume proportions av and bv from the mass proportions a and b, two methods were established. Method 1 assumed the bulk densities of A and B to be representative and was used when av was higher than the percolation threshold (Pca) of A of 0.3 (a, 0.5). Method 2 used the true particle density of A and was valid with av values of less than 0.1 (a, 0.3), in which case the particles of A were dispersed as individuals in the matrix of B.
用由粗颗粒成分A(蔗糖)和细颗粒成分B[微晶纤维素(Avicel PH 101)-滑石粉]的随机混合物制备的片剂,评估了用于确定二元随机混合物质量的方程(方程1)的有效性,其中A:B的比例(w/w)从10:90变化到80:20。对于所有的A:B比例,方程1所确定的随机含量变化与片剂中发现的含量变化之间都建立了高度一致性。然而,80:20的比例刚好处于边界,50毫克片剂实现了随机质量,但200毫克片剂由于分层未实现随机质量。根据渗流理论,这一结果是由于B的体积比例(bv)较小,几乎等于B的预渗流阈值(Pcb)0.3。当bv小于Pcb时,细颗粒成分B不会形成连贯的晶格,方程1不再有效。为了从质量比例a和b估算体积比例av和bv,建立了两种方法。方法1假设A和B的堆积密度具有代表性,当av高于A的渗流阈值(Pca)0.3(a,0.5)时使用。方法2使用A的真实颗粒密度,当av值小于0.1(a,0.3)时有效,在这种情况下,A的颗粒以单个形式分散在B的基质中。