Assessment of disintegrant efficacy with fractal dimensions from real-time MRI

被引:20
作者
Quodbach, Julian [1 ]
Moussavi, Amir [2 ]
Tammer, Roland [2 ,3 ]
Frahmb, Jens [2 ,3 ]
Kleinebudde, Peter [1 ]
机构
[1] Univ Dusseldorf, Inst Pharmaceut & Biopharmaceut, D-40225 Dusseldorf, Germany
[2] Biomed NMR Forsch GmbH, Max Planck Inst Biophys Chem, D-37070 Gottingen, Germany
[3] Ctr Nanoscale Microscopy & Mol Physiol Brain CNMP, D-37070 Gottingen, Germany
关键词
Formulation; Polymers; Visualization; Superdisintegrants; Tablet disintegration; TABLET DISINTEGRATION; DISSOLUTION; RESOLUTION; STARCH;
D O I
10.1016/j.ijpharm.2014.09.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
An efficient disintegrant is capable of breaking up a tablet in the smallest possible particles in the shortest time. Until now, comparative data on the efficacy of different disintegrants is based on dissolution studies or the disintegration time. Extending these approaches, this study introduces a method, which defines the evolution of fractal dimensions of tablets as surrogate parameter for the available surface area. Fractal dimensions are a measure for the tortuosity of a line, in this case the upper surface of a disintegrating tablet. High-resolution real-time MRI was used to record videos of disintegrating tablets. The acquired video images were processed to depict the upper surface of the tablets and a box-counting algorithm was used to estimate the fractal dimensions. The influence of six different disintegrants, of different relative tablet density, and increasing disintegrant concentration was investigated to evaluate the performance of the novel method. Changing relative densities hardly affect the progression of fractal dimensions, whereas an increase in disintegrant concentration causes increasing fractal dimensions during disintegration, which are also reached quicker. Different disintegrants display only minor differences in the maximal fractal dimension, yet the kinetic in which the maximum is reached allows a differentiation and classification of disintegrants. (C) 2014 Elsevier B. V. All rights reserved.
引用
收藏
页码:605 / 612
页数:8
相关论文
共 25 条
  • [1] Block K., 2011, 19 ANN M ISMRM MONTR
  • [2] Caramella C, 1990, PHARM TECHNOL INT, V2, P30
  • [3] Chen CR, 1997, CHEM PHARM BULL, V45, P509
  • [4] Commission E.P., 2014, DISINTEGRATION TABLE, P285
  • [5] A COMPARATIVE-EVALUATION OF THE PROPERTIES OF SOME TABLET DISINTEGRANTS
    GISSINGER, D
    STAMM, A
    [J]. DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1980, 6 (05) : 511 - 536
  • [6] THE EFFECT OF AGING ON DISINTEGRANT EFFICIENCY IN DIRECT COMPRESSION TABLETS WITH VARIED SOLUBILITY AND HYGROSCOPICITY, IN TERMS OF DISSOLUTION
    GORDON, MS
    CHOWHAN, ZT
    [J]. DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1990, 16 (03) : 437 - 447
  • [7] Hancock B.C., 2003, Pharm. Technol., V27, P64
  • [8] CAN THE FRACTAL DIMENSION OF IMAGES BE MEASURED
    HUANG, Q
    LORCH, JR
    DUBES, RC
    [J]. PATTERN RECOGNITION, 1994, 27 (03) : 339 - 349
  • [9] An easy-to-use approach for determining the disintegration ability of disintegrants by analysis of available surface area
    Iwao, Yasunori
    Tanaka, Shoko
    Uchimoto, Takeaki
    Noguchi, Shuji
    Itai, Shigeru
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 448 (01) : 1 - 8
  • [10] Jyothi G, 2011, ACTA PHARM SCI, V53, P35