Data mining of solubility parameters for computational prediction of drug–excipient miscibility

Method to study the effect of blend flowability on the homogeneity of acetaminophen

(2012) Marcos Llusá et al.   DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY

Prediction of acetaminophen’s solubility in poly(ethylene oxide) at room temperature using the Flory–Huggins theory

(2012) Min Yang et al.   DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY

Influence of lactose carrier particle size on the aerosol performance of budesonide from a dry powder inhaler

(2012) Waseem Kaialy et al.   POWDER TECHNOLOGY

Solubility Behavior and Solution Chemistry of Indomethacin Cocrystals in Organic Solvents

(2011) Amjad Alhalaweh et al.   CRYSTAL GROWTH & DESIGN

Modelling formulations using gene expression programming – A comparative analysis with artificial neural networks

(2011) E.A. Colbourn et al.   EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES

Hansen solubility parameter as a tool to predict cocrystal formation

(2011) Mohammad Amin Mohammad et al.   INTERNATIONAL JOURNAL OF PHARMACEUTICS

Application of Hansen solubility parameters for understanding and prediction of drug distribution in microspheres

(2011) Kerstin Vay et al.   INTERNATIONAL JOURNAL OF PHARMACEUTICS

TowardIn SilicoPrediction of Glass-Forming Ability from Molecular Structure Alone: A Screening Tool in Early Drug Development

(2011) Denny Mahlin et al.   MOLECULAR PHARMACEUTICS

Increasing availability of industrial systems through data stream mining

(2010) Ahmad Alzghoul et al.   COMPUTERS & INDUSTRIAL ENGINEERING

Formation of Cocrystals from Stoichiometric Solutions of Incongruently Saturating Systems by Spray Drying

(2010) Amjad Alhalaweh et al.   CRYSTAL GROWTH & DESIGN

Data clustering: 50 years beyond K-means

(2009) Anil K. Jain   PATTERN RECOGNITION LETTERS

Drugs release from hydrodynamically balanced systems analyzed with data-mining procedures by artificial neural networks

(2008) Aleksander Mendyk et al.   EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES

Estimation of Drug–Polymer Miscibility and Solubility in Amorphous Solid Dispersions Using Experimentally Determined Interaction Parameters

(2008) Patrick J. Marsac et al.   PHARMACEUTICAL RESEARCH