We are improving our search experience. To check which content you have full access to, or for advanced search, go back to the old search.

Search

Please fill in this field.
Filters applied:

Search Results

Showing 1-20 of 65 results
  1. Dissolution Kinetics of Nifedipine—Ionizable Polymer Amorphous Solid Dispersion: Comparison Between Bicarbonate and Phosphate Buffers

    Purpose

    The intestinal fluid pH is maintained by the bicarbonate buffer system that shows unique properties regarding drug dissolution. Nevertheless,...

    Aoi Sakamoto, Kiyohiko Sugano in Pharmaceutical Research
    Article 20 December 2021
  2. Impact of Processing Methods on the Physico-chemical Properties of Posaconazole Amorphous Solid Dispersions

    Background & Purpose

    Different methods have been exploited to generate amorphous solid dispersions (ASDs) of poorly water-soluble drugs. However, the...

    Ru He, Matthew S. Lamm, ... Yongjun Li in Pharmaceutical Research
    Article 01 December 2023
  3. ASD Formation Prior to Material Characterization as Key Parameter for Accurate Measurements and Subsequent Process Simulation for Hot-Melt Extrusion

    Process simulation facilitates scale-up of hot-melt extrusion (HME) and enhances proper understanding of the underlying critical process parameters....

    Kevin Kayser, Marius Monschke, Karl G. Wagner in AAPS PharmSciTech
    Article Open access 25 June 2022
  4. Influence of Particle Size and Drug Load on Amorphous Solid Dispersions Containing pH-Dependent Soluble Polymers and the Weak Base Ketoconazole

    Among the great number of poorly soluble drugs in pharmaceutical development, most of them are weak bases. Typically, they readily dissolve in an...

    Marius Monschke, Kevin Kayser, Karl G. Wagner in AAPS PharmSciTech
    Article Open access 12 January 2021
  5. Precipitation Technologies for Nanoparticle Production

    Precipitation technologies have been widely studied for nanoparticle production because they provide more control over particle size, shape, and...
    Tuangrat Praphawatvet, Robert O. Williams in Formulating Poorly Water Soluble Drugs
    Chapter 2022
  6. Third Generation Solid Dispersion-Based Formulation of Novel Anti-Tubercular Agent Exhibited Improvement in Solubility, Dissolution and Biological Activity

    The long treatment period and development of drug resistance in tuberculosis (TB) necessitates the discovery of new anti-tubercular agents. The drug...

    Gourav Paudwal, Rigzin Dolkar, ... Prem N. Gupta in The AAPS Journal
    Article 22 April 2024
  7. Multivariate Analysis of Solubility Parameters for Drug-Polymer Miscibility Assessment in Preparing Raloxifene Hydrochloride Amorphous Solid Dispersions

    The success of obtaining solid dispersions for solubility improvement invariably depends on the miscibility of the drug and polymeric carriers. This...

    Guilherme G. Moreira, Stephânia F. Taveira, ... Ricardo N. Marreto in AAPS PharmSciTech
    Article 06 June 2024
  8. Machine Learning in Additive Manufacturing of Pharmaceuticals

    The application of machine learning and deep learning in additive manufacturing, also called 3D printing, is expected in industrial fields to be an...
    Tatsuaki Tagami, Koki Ogawa, Tetsuya Ozeki in Additive Manufacturing in Pharmaceuticals
    Chapter 2023
  9. Advancements of hot-melt extrusion technology to address unmet patient needs and pharmaceutical quality aspects

    Background

    Hot-melt extrusion (HME) significantly affects pharmaceutical manufacturing by enhancing drug solubility and bioavailability. Advancements...

    Chulhun Park, Vanamane S. Renuka, ... Jun-Bom Park in Journal of Pharmaceutical Investigation
    Article 22 June 2024
  10. Flux-Based Formulation Development—A Proof of Concept Study

    The work aimed to develop the Absorption Driven Drug Formulation (ADDF) concept, which is a new approach in formulation development to ensure that...

    Szabina Kádár, Petra Tőzsér, ... Bálint Sinkó in The AAPS Journal
    Article Open access 05 January 2022
  11. Identification of a Multi-Component Formulation for Intestinal Delivery of a GLP-1/Glucagon Co-agonist Peptide

    Purpose

    Oral delivery of therapeutic peptides has been challenging due to multiple physiological factors and physicochemical properties of peptides....

    Huyen Tran, Phenil J. Patel, ... Amita Datta –Mannan in Pharmaceutical Research
    Article 01 September 2022
  12. Preparation and Characterization of Ibrutinib Amorphous Solid Dispersions: a Discussion of Interaction Force

    The aim of this study was to improve the solubility and dissolution of Ibrutinib (IBR), a biopharmaceutical classification system (BCS) class II...

    **angjun Shi, Baibai Fan, ... Yu Deng in Journal of Pharmaceutical Innovation
    Article 30 September 2021
  13. Application of Liquisolid Pellets Technology for Improving Dissolution of Posaconazole: A DoE Based Process Optimization

    Purpose

    Posaconazole (PSZ) is BCS class-II drug that displays variable bioavailability upon oral administration due to extremely low and pH-dependent...

    Sunny Shah, Parth Devani, ... Dhavalkumar Mori in Journal of Pharmaceutical Innovation
    Article 24 April 2024
  14. Continuous Manufacturing and Molecular Modeling of Pharmaceutical Amorphous Solid Dispersions

    Amorphous solid dispersions enhance solubility and oral bioavailability of poorly water-soluble drugs. The escalating number of drugs with poor...

    Amritha G Nambiar, Maan Singh, ... Dinesh Kumar in AAPS PharmSciTech
    Article 02 September 2022
  15. Therapeutic Polymer Conjugates and Their Characterization

    Drugs, proteins, and nanoparticles delivered into the body are exposed to numerous mechanisms for premature elimination and deterioration within the...
    Victor M. Quiroz, Joshua Devier, Joshua C. Doloff in Biomaterials and Biopolymers
    Chapter 2023
  16. The Development of a Novel Pharmaceutical Formulation of D-Tagatose for Spray-Drying

    Purpose

    D-tagatose is an alternative sweetener with superior properties for reducing overall sugar absorption, which is especially important in the...

    Heather R. Campbell, Fahd M. Alsharif, ... Robert A. Lodder in Journal of Pharmaceutical Innovation
    Article 16 October 2020
  17. Application of Insoluble Excipients in Solid Dispersion of Chinese Medicines

    In recent years, as the great success of arteannuin in the area of antimalarial treatment and commercial benefit, traditional Chinese medicine (TCM)...
    Hangyi Wu, Huixia Lv, Zhenhai Zhang in Novel Drug Delivery Systems for Chinese Medicines
    Chapter 2021
  18. Combination of co-crystal and nanocrystal techniques to improve the solubility and dissolution rate of poorly soluble drugs

    Purpose

    Solubility and dissolution rate are essential for the oral absorption and bioavailability of poorly soluble drugs. The aim of this study was...

    Zun Huang, Sven Staufenbiel, Roland Bodmeier in Pharmaceutical Research
    Article Open access 12 May 2022
  19. Osmolality of Excipients for Parenteral Formulation Measured by Freezing Point Depression and Vapor Pressure – A Comparative Analysis

    Purpose

    To investigate the difference in methods to determine the osmolality in solutions of stabilizers used for long-acting injectable suspensions.

    ...
    Mariana Hugo Silva, Sarah P. Hudson, ... René Holm in Pharmaceutical Research
    Article 22 April 2022
  20. Impact of Surfactants on the Performance of Clopidogrel-Copovidone Amorphous Solid Dispersions: Increased Drug Loading and Stabilization of Nanodroplets

    Purpose

    Surfactants are increasingly being added to amorphous solid dispersion (ASDs) formulations to enhance processability and release performance....

    Clara E. Correa Soto, Yi Gao, ... Lynne S. Taylor in Pharmaceutical Research
    Article 10 January 2022
Did you find what you were looking for? Share feedback.