Literature DB >> 16354004

Generalization of a prototype intelligent hybrid system for hard gelatin capsule formulation development.

Wendy I Wilson1, Yun Peng, Larry L Augsburger.   

Abstract

The aim of this project was to expand a previously developed prototype expert network for use in the analysis of multiple biopharmaceutics classification system (BCS) class II drugs. The model drugs used were carbamazepine, chlorpropamide, diazepam, ibuprofen, ketoprofen, naproxen, and piroxicam. Recommended formulations were manufactured and tested for dissolution performance. A comprehensive training data set for the model drugs was developed and used to retrain the artificial neural network. The training and the system were validated based on the comparison of predicted and observed performance of the recommended formulations. The initial test of the system resulted in high error values, indicating poor prediction capabilities for drugs other than piroxicam. A new data set, containing 182 batches, was used for retraining. Ten percent of the test batches were used for cross-validation, resulting in models with R2 > or = 70%. The comparison of observed performance to the predicted performance found that the system predicted successfully. The hybrid network was generally able to predict the amount of drug dissolved within 5% for the model drugs. Through validation, the system was proven to be capable of designing formulations that met specific drug performance criteria. By including parameters to address wettability and the intrinsic dissolution characteristics of the drugs, the hybrid system was shown to be suitable for analysis of multiple BCS class II drugs.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16354004      PMCID: PMC2750390          DOI: 10.1208/pt060356

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  16 in total

1.  The use of artificial neural networks for the selection of the most appropriate formulation and processing variables in order to predict the in vitro dissolution of sustained release minitablets.

Authors:  Michael M Leane; Iain Cumming; Owen I Corrigan
Journal:  AAPS PharmSciTech       Date:  2003       Impact factor: 3.246

2.  RXPERT: a prototype expert system for formulary decision making.

Authors:  M L Greer
Journal:  Ann Pharmacother       Date:  1992-02       Impact factor: 3.154

Review 3.  Artificial neural network as a novel method to optimize pharmaceutical formulations.

Authors:  K Takayama; M Fujikawa; T Nagai
Journal:  Pharm Res       Date:  1999-01       Impact factor: 4.200

4.  Artificial neural networks applied to the in vitro-in vivo correlation of an extended-release formulation: initial trials and experience.

Authors:  J A Dowell; A Hussain; J Devane; D Young
Journal:  J Pharm Sci       Date:  1999-01       Impact factor: 3.534

5.  Pharmaceutical granulation and tablet formulation using neural networks.

Authors:  J G Kesavan; G E Peck
Journal:  Pharm Dev Technol       Date:  1996-12       Impact factor: 3.133

6.  Relating formulation variables to in vitro dissolution using an artificial neural network.

Authors:  N K Ebube; T McCall; Y Chen; M C Meyer
Journal:  Pharm Dev Technol       Date:  1997-08       Impact factor: 3.133

7.  Application of artificial neural networks (ANN) in the development of solid dosage forms.

Authors:  J Bourquin; H Schmidli; P van Hoogevest; H Leuenberger
Journal:  Pharm Dev Technol       Date:  1997-05       Impact factor: 3.133

8.  Neural network modeling for estimation of the aqueous solubility of structurally related drugs.

Authors:  J Huuskonen; M Salo; J Taskinen
Journal:  J Pharm Sci       Date:  1997-04       Impact factor: 3.534

9.  Use of artificial neural networks to predict drug dissolution profiles and evaluation of network performance using similarity factor.

Authors:  K K Peh; C P Lim; S S Quek; K H Khoh
Journal:  Pharm Res       Date:  2000-11       Impact factor: 4.200

10.  A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability.

Authors:  G L Amidon; H Lennernäs; V P Shah; J R Crison
Journal:  Pharm Res       Date:  1995-03       Impact factor: 4.200

View more
  3 in total

Review 1.  The use of modeling tools to drive efficient oral product design.

Authors:  Neil R Mathias; John Crison
Journal:  AAPS J       Date:  2012-05-30       Impact factor: 4.009

2.  Summary workshop report: Facilitating oral product development and reducing regulatory burden through novel approaches to assess bioavailability/bioequivalence.

Authors:  James E Polli; Jack A Cook; Barbara M Davit; Paul A Dickinson; Domenick Argenti; Nancy Barbour; Alfredo García-Arieta; Jean-Marie Geoffroy; Kerry Hartauer; Shoufeng Li; Amitava Mitra; Francis X Muller; Vivek Purohit; Manuel Sanchez-Felix; John W Skoug; Kin Tang
Journal:  AAPS J       Date:  2012-06-09       Impact factor: 4.009

3.  Crystal structure transformations and dissolution studies of cimetidine-piroxicam coprecipitates and physical mixtures.

Authors:  Vimon Tantishaiyakul; Sarunyoo Songkro; Krit Suknuntha; Pattakarn Permkum; Pattawee Pipatwarakul
Journal:  AAPS PharmSciTech       Date:  2009-06-12       Impact factor: 3.246

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.