Systematic development of pH-independent controlled release tablets of carvedilol using central composite design and artificial neural networks

被引:12
作者
Aktas, Elcin [1 ]
Eroglu, Hakan [1 ]
Kockan, Umit [2 ]
Oner, Levent [1 ]
机构
[1] Hacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, Turkey
[2] Middle E Tech Univ, Grad Sch Nat & Appl Sci, TR-06531 Ankara, Turkey
关键词
Carvedilol; pH-dependent solubility; pH-independent release; artificial neural network; HPMC K4M; EUDRAGIT L100; WEAKLY BASIC DRUG; MATRIX TABLETS; HYDROPHILIC MATRICES; DELIVERY-SYSTEMS; BETA-BLOCKERS; HYDROCHLORIDE; OPTIMIZATION; FORMULATION; DISSOLUTION; SOLUBILITY;
D O I
10.3109/03639045.2012.705291
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The purpose of this study was to apply the optimization method incorporating artificial neural network (ANN) using pH-independent release of weakly basic drug, carvedilol from HPMC-based matrix formulation. Because of weakly basic nature of carvedilol, drug shows pH-dependent solubility. The enteric polymer EUDRAGIT L100 was added formulations to overcome pH-dependent solubility of carvedilol. Effects of the Hydroxypropylmethyl cellulose (HPMC) K4M and EUDRAGIT L100 amount on drug release were investigated. For this purpose 13 kinds of formulations were prepared at three different levels of each variables. The optimization of the formulation was evaluated by using ANN method. Two formulation parameters, the amounts of HPMC K4M and Eudragit L100 at three levels (-1, 0, 1) were selected as independent/input variables. In-vitro dissolution sampling times at twelve different time points were selected as dependent/output variables. By using experimental dissolution results and amount of HPMC K4M and EUDRAGIT L100, percentage of dissolved carvedilol was predicted by ANN. Similarity factor (f(2)) between predicted and experimentally observed profile was calculated and f(2) value was found 76.33. This value showed that there was no difference between predicted and experimentally observed drug release profile. As a result of these experiments, it was found that ANNs can be successfully used to optimize controlled release drug delivery systems.
引用
收藏
页码:1207 / 1216
页数:10
相关论文
共 27 条
  • [1] Studies on dissolution enhancement and mathematical modeling of drug release of a poorly water-soluble drug using water-soluble carriers
    Ahuja, Naveen
    Katare, Om Prakash
    Singh, Bhupinder
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2007, 65 (01) : 26 - 38
  • [2] Pharmacokinetic/pharmacodynamic modeling of the cardiovascular effects of beta blockers in humans
    Baek, In-hwan
    Yun, Min-hyuk
    Yun, Hwi-yeol
    Kwon, Kwang-il
    [J]. ARCHIVES OF PHARMACAL RESEARCH, 2008, 31 (06) : 814 - 821
  • [3] Validation of chromatographic methods in biomedical analysis - Viewpoint and discussion
    Causon, R
    [J]. JOURNAL OF CHROMATOGRAPHY B, 1997, 689 (01): : 175 - 180
  • [4] New, simple, and validated UV-spectrophotometric method for the estimation of some beta blockers in bulk and formulations
    Golcu, Aysegul
    [J]. JOURNAL OF ANALYTICAL CHEMISTRY, 2008, 63 (06) : 538 - 543
  • [5] Strategies to Overcome pH-Dependent Solubility of Weakly Basic Drugs by Using Different Types of Alginates
    Gutsche, S.
    Krause, M.
    Kranz, H.
    [J]. DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2008, 34 (12) : 1277 - 1284
  • [6] Optimization of pH-independent release of nicardipine hydrochloride extended-release matrix tablets using response surface methodology
    Huang, YB
    Tsai, YH
    Lee, SH
    Chang, JS
    Wu, PC
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 289 (1-2) : 87 - 95
  • [7] Ibric Svetlana, 2003, AAPS PharmSciTech, V4, pE9
  • [8] Formulation and Evaluation of Gastroretentive Drug Delivery System of Propranolol Hydrochloride
    Jagdale, Swati C.
    Agavekar, Amit J.
    Pandya, Sudhir V.
    Kuchekar, Bhanudas S.
    Chabukswar, Aniruddha R.
    [J]. AAPS PHARMSCITECH, 2009, 10 (03): : 1071 - 1079
  • [9] Artificial neural networks (ANNs) and modeling of powder flow
    Kachrimanis, K
    Karamyan, V
    Malamataris, S
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 250 (01) : 13 - 23
  • [10] MECHANISMS OF SOLUTE RELEASE FROM POROUS HYDROPHILIC POLYMERS
    KORSMEYER, RW
    GURNY, R
    DOELKER, E
    BURI, P
    PEPPAS, NA
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1983, 15 (01) : 25 - 35