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Overview of the Manufacturing Methods of Solid Dispersion Technology for Improving the Solubility of Poorly Water-Soluble Drugs and Application to Anticancer Drugs

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Pharmaceutical Dispersion Techniques for Dissolution and Bioavailability Enhancement of Poorly Water-Soluble Drugs

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Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective

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Improvement of Dissolution Rates of Poorly Water Soluble APIs Using Novel Spray Freezing into Liquid Technology

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Emerging Freeze-Drying Process Development and Scale-up Issues

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Pharmaceutical development and preliminary clinical testing of an oral solid dispersion formulation of docetaxel (ModraDoc001)

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Physicochemical properties of tadalafil solid dispersions – Impact of polymer on the apparent solubility and dissolution rate of tadalafil

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Antiretroviral Solid Drug Nanoparticles with Enhanced Oral Bioavailability: Production, Characterization, and In Vitro–In Vivo Correlation

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Process optimization of a novel production method for nanosuspensions using design of experiments (DoE)

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Manufacturing of High-Concentration Monoclonal Antibody Formulations via Spray Drying--the Road to Manufacturing Scale

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Controlled Crystallization of the Lipophilic Drug Fenofibrate During Freeze-Drying: Elucidation of the Mechanism by In-Line Raman Spectroscopy

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Preparation of drug nanocrystals by controlled crystallization: Application of a 3-way nozzle to prevent premature crystallization for large scale production

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Comparison of powder produced by evaporative precipitation into aqueous solution (EPAS) and spray freezing into liquid (SFL) technologies using novel Z-contrast STEM and complimentary techniques

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Enhancement of docetaxel solubility using binary and ternary solid dispersion systems

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Enhancing the Solubility of Curcumin Using a Solid Dispersion System with Hydroxypropyl-β-Cyclodextrin Prepared by Grinding, Freeze-Drying, and Common Solvent Evaporation Methods

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Efficient approach to enhance drug solubility by particle engineering of bovine serum albumin

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An Investigation of Nifedipine Miscibility in Solid Dispersions Using Raman Spectroscopy

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Exploring the feasibility of the use of biopolymers as a carrier in the formulation of amorphous solid dispersions – Part I: Gelatin

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A Retrospective Biopharmaceutical Analysis of >800 Approved Oral Drug Products: Are Drug Properties of Solid Dispersions and Lipid-Based Formulations Distinctive?

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Lyophilized flutamide dispersions with polyols and amino acids: preparation and in vitro evaluation

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Development of solid dispersions of artemisinin for transdermal delivery

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A combined bottom–up/top–down approach to prepare a sterile injectable nanosuspension

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In Vitro and In Vivo Evaluation of Amorphous Solid Dispersions Generated by Different Bench-Scale Processes, Using Griseofulvin as a Model Compound

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Bioavailability Improvement Strategies for Poorly Water-Soluble Drugs Based on the Supersaturation Mechanism: An Update

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A comparative study of spray-dried and freeze-dried hydrocortisone/polyvinyl pyrrolidone solid dispersions

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Preparation of Hydrophobic Drugs Cyclodextrin Complex by Lyophilization Monophase Solution

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Drug nanoparticles by emulsion-freeze-drying via the employment of branched block copolymer nanoparticles

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The Production of a Stable Infliximab Powder: The Evaluation of Spray and Freeze-Drying for Production

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