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Solid Dosage, Vol. 3

Price: $199.00
Item Number: PTSZ102
Contents include:
 
Powders
  • Powder Characterization
  • Modeling Pharmaceutical Powder-Flow Performance Using Particle-Size Distribution Data
Excipients
  • Tracking Excipients
  • Excipients in Polymeric Drug Delivery and Formulation
  • Assessing Hisbiscus Rosa-Sinensis Linn as an Excipient in Sustained-Release Tablets
  • Influence of Common Excipients on the Crystal Line Modification of Freeze-Dried Mannitol
  • Development of Orally Disintegrating Tablets Based on a New Excipient
  • A New Hypromellose Excipient for Direct-Compression, Controlled-Release Applications
  • A Novel Preglatinized Starch as a Sustained-Releas Matrix Excipient
  • A New Hypromellose Excipient for Direct-Compression, Controlled-Release Applications
  • A Novel Preglatinized Starch as a Sustained-Release Matrix Excipient
  • Ethyl Lactate as a Pharmaceutical-Grade Excipient
Mixing and Blending
  • Foam Granulation Technology
  • The Effect of Mill Type on Two Dry-Granulated Placebo Formulations
Tableting
  • Improving Tablet Quality with Compression to Equal Force Technology
  • Developments in Tooling Inspections and Technology
  • Effect of Binder Type and Binder Level on the Properties of Agglomerates Containing Lactose and Dibasic Calcium Phosphate Dihydrate
  • Roller Compaction of Anhydrous Lactose and Blends of Anhydrous Lactose with MCC
Coating
  • A Fresh Coat Innovation in Excipients
  • A Risk-Based Approach to Product and Process Quality in Spray Drying
Standards
  • Variability of USP Lot P Prednisone Reference Standard Tablets
  • Orally Disintegrating Tablets-The Effect of Recent FDA Guidance on ODT Technologies and Applications
  • Dimethyl Sulfoxide USP, PHEur in Approved Pharmaceutical Products and Medical Devices
  • An Alternative to the USP Disintegration Test for Orally Disintegrating Tablets
Formulation
  • Formulation Effects on the Thermomechanical Properties and Permeability of Free Films and Coating Films
  • Formulation Development of Taste-Masked Rapidly Dissolving Films of Cetirizine Hydrochloride
  • Influence of Superdisintegrants on the Rate of Drug Dissolution from Oral Solid Dosage Forms
  • Modification and Characterization of Gellan Gum
  • Formulation and Evaluation of Famotindine Floating Matrix Tablets
Testing
  • Raw-Material Authentication Using a Hand Held Raman Spectrometer
  • New Dimensions in Tablet Imaging
  • Developments in Scanning Electron Microscopy for Tablet and Granule Characterization
  • Getting the Truth Out of Dissolution Testing

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