An MRI analysis of the dissolution of a soluble drug incorporated within an insoluble polymer tablet

被引:8
作者
Karakosta, E. [1 ]
McDonald, P. J. [1 ]
机构
[1] Univ Surrey, Sch Elect & Phys Sci, Dept Phys, Guildford GU2 7XH, Surrey, England
关键词
D O I
10.1007/s00723-007-0001-8
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Magnetic resonance imaging is used to map the ingress of water into a nominally non-swelling polymer-matrix slow-release drug delivery device comprising a compact of particulate Eudragit polymer and Diltiazern Hydrochloride drug. It is shown that the water ingresses with the square root of time: that is, it is "Fickian-like"; and that the release depends only weakly on the particulate size. A dissolution-diffusion model specifically incorporating the drug particulate size is developed to describe the release mechanism. The experimental results are in accord with the model. It is further shown theoretically that the release should become "non-Fickian-like" and particle size dependent if the drug dissolution constant were to be reduced substantially, an observation explained using a dimensionless scaling argument that compares the dissolution and diffusion rates. It has, however, not been possible to perform experiments in this different regime with the same materials.
引用
收藏
页码:75 / 91
页数:17
相关论文
共 30 条
  • [11] The influence of thermal treatment and type of insoluble poly(meth)acrylates on dissolution behavior of very soluble drug from hypromellose matrix tablets evaluated by multivariate data analysis
    Kubova, Katerina
    Pecek, Daniel
    Hasserova, Kristyna
    Dolezel, Petr
    Pavelkova, Miroslava
    Vyslouzil, Jakub
    Muselik, Jan
    Vetchy, David
    PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2017, 22 (02) : 206 - 217
  • [12] Control of poorly soluble drug dissolution in conditions simulating the gastrointestinal tract flow .1. Effect of tablet geometry in buffered medium
    Chakrabarti, S
    Southard, MZ
    JOURNAL OF PHARMACEUTICAL SCIENCES, 1996, 85 (03) : 313 - 319
  • [13] Solidification of meloxicam self-nano emulsifying drug delivery system formulation incorporated into soluble and insoluble carriers using freeze drying method
    Kuncahyo, I.
    Choiri, S.
    Fudholi, A.
    INTERNATIONAL CONFERENCE ON ADVANCED MATERIALS FOR BETTER FUTURE 2018, 2019, 578
  • [14] Correlation between drug dissolution and polymer hydration: A study using texture analysis
    Li, Hongtao
    Gu, Xiaochen
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 342 (1-2) : 18 - 25
  • [15] Use of compressed gas precipitation to enhance the dissolution behavior of a poorly water-soluble drug: Generation of drug microparticles and drug-polymer solid dispersions
    Muhrer, G
    Meier, U
    Fusaro, F
    Albano, S
    Mazzotti, M
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 308 (1-2) : 69 - 83
  • [16] Improvement of dissolution rate of poorly water-soluble drug by wet grinding with bio-compatible phospholipid polymer
    Watano, Satoru
    Matsuo, Mika
    Nakamura, Hideya
    Miyazaki, Tsuyoshi
    CHEMICAL ENGINEERING SCIENCE, 2015, 125 : 25 - 31
  • [17] Investigating the Influence of Tablet Location Inside Dissolution Test Apparatus on Polymer Erosion and Drug Release of a Surface-Erodible Sustained-Release Tablet Using Computational Simulation Methods
    Lou, Hao
    Hageman, Michael J.
    AAPS PHARMSCITECH, 2021, 22 (03)
  • [18] Investigating the Influence of Tablet Location Inside Dissolution Test Apparatus on Polymer Erosion and Drug Release of a Surface-Erodible Sustained-Release Tablet Using Computational Simulation Methods
    Hao Lou
    Michael J. Hageman
    AAPS PharmSciTech, 22
  • [19] High-performance liquid chromatographic analysis of verapamil and its application to determination in tablet dosage forms and to drug dissolution studies
    Özkan, Y
    Yilmaz, N
    Özkan, SA
    Biryol, I
    FARMACO, 2000, 55 (05): : 376 - 382
  • [20] In-situ freeze-drying - forming amorphous solids directly within capsules: An investigation of dissolution enhancement for a poorly soluble drug
    Alqurshi, Abdulmalik
    Chan, K. L. Andrew
    Royall, Paul G.
    SCIENTIFIC REPORTS, 2017, 7