Optimization of Metformin HCl 500mg Sustained Release Matrix Tablets Using Artificial Neural Network (ANN) Based on Multilayer Perceptrons (MLP) Model

    • MANDAL Uttam
    • Bioequivalence Study Centre, Department of Pharmaceutical Technology Jadavpur University
    • GOWDA Veeran
    • Bioequivalence Study Centre, Department of Pharmaceutical Technology Jadavpur University
    • GHOSH Animesh
    • Bioequivalence Study Centre, Department of Pharmaceutical Technology Jadavpur University
    • BOSE Anirbandeep
    • Bioequivalence Study Centre, Department of Pharmaceutical Technology Jadavpur University

    • BHAUMIK Uttam
    • Bioequivalence Study Centre, Department of Pharmaceutical Technology Jadavpur University
    • PAL Tapan Kumar
    • Bioequivalence Study Centre, Department of Pharmaceutical Technology Jadavpur University

Abstract

The aim of the present study was to apply the simultaneous optimization method incorporating Artificial Neural Network (ANN) using Multi-layer Perceptron (MLP) model to the development of a metformin HCl 500mg sustained release matrix tablets with an optimized in vitro release profile. The amounts of HPMC K15M and PVP K30 at three levels (-1, 0, +1) for each were selected as casual factors. In vitro dissolution time profiles at four different sampling times (1h, 2h, 4h and 8h) were chosen as output variables. 13 kinds of metformin matrix tablets were prepared according to a 2^3 factorial design (central composite) with five extra center points, and their dissolution tests were performed. Commercially available STATISTICA Neural Network software (Stat Soft, Inc., Tulsa, OK, U.S.A.) was used throughout the study. The training process of MLP was completed until a satisfactory value of root square mean (RSM) for the test data was obtained using feed forward back propagation method. The root mean square value for the trained network was 0.000097, which indicated that the optimal MLP model was reached. The optimal tablet formulation based on some predetermined release criteria predicted by MLP was 336mg of HPMC K15M and 130mg of PVP K30. Calculated difference (f_1 2.19) and similarity (f_2 89.79) factors indicated that there was no difference between predicted and experimentally observed drug release profiles for the optimal formulation. This work illustrates the potential for an artificial neural network with MLP, to assist in development of sustained release dosage forms.

Journal

Chemical & pharmaceutical bulletin   [List of Volumes]

Chemical & pharmaceutical bulletin 56(2), 150-155, 2008-02-01  [Table of Contents]

The Pharmaceutical Society of Japan

References:  41

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Codes

  • NII Article ID (NAID) :
    110006570589
  • NII NACSIS-CAT ID (NCID) :
    AA00602100
  • Text Lang :
    ENG
  • Article Type :
    ART
  • ISSN :
    00092363
  • NDL Article ID :
    9351289
  • NDL Source Classification :
    ZS51(科学技術--薬学) // ZP1(科学技術--化学・化学工業)
  • NDL Call No. :
    Z53-D167
  • Databases :
    CJP  NDL  NII-ELS  J-STAGE