Jove
Visualize
Contact Us

Related Concept Videos

Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism01:21

Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism

389
Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
389
Solubility03:00

Solubility

18.2K
Solution, Solubility, and Solubility Equilibrium
A solution is a homogeneous mixture composed of a solvent, the major component, and a solute, the minor component. The physical state of a solution—solid, liquid, or gas—is typically the same as that of the solvent. Solute concentrations are often described with qualitative terms such as dilute (of relatively low concentration) and concentrated (of relatively high concentration).
In a solution, the solute particles (molecules,...
18.2K
Entropy and Solvation02:05

Entropy and Solvation

7.2K
The process of surrounding a solute with solvent is called solvation. It involves evenly distributing the solute within the solvent. The rule of thumb for determining a solvent for a given compound is that like dissolves like. A good solvent has molecular characteristics similar to those of the compound to be dissolved. For example, polar solutions dissolve polar solutes, and apolar solvents dissolve apolar solutes. A polar solvent is a solvent that has a high dielectric constant (ϵ...
7.2K
Solubility Equilibria03:07

Solubility Equilibria

53.2K
Solubility equilibria are established when the dissolution and precipitation of a solute species occur at equal rates. These equilibria underlie many natural and technological processes, ranging from tooth decay to water purification. An understanding of the factors affecting compound solubility is, therefore, essential to the effective management of these processes. This section applies previously introduced equilibrium concepts and tools to systems involving dissolution and precipitation.
The...
53.2K
Solubility Equilibria: Ionic Product of Water01:16

Solubility Equilibria: Ionic Product of Water

1.1K
Pure water is a weak electrolyte; only a small amount ionizes into hydrogen and hydroxide ions. At any given temperature, the concentration of undissociated water is almost constant, so the ionic product of water is the product of the hydrogen and hydroxide ion concentrations, denoted as Kw. The square root of Kw gives the individual ion concentrations.
The ionic product of water varies with temperature, and its value is 1.0 x 10−14 at standard experimental conditions. Per Le...
1.1K
Analyte Adsorption and Distribution01:09

Analyte Adsorption and Distribution

850
In certain chromatographic separations, solutes transfer between the mobile phase and the stationary phase via sorption, which typically refers to the process of adsorption. For many chromatographic systems, the sorption process often depends on the polarity of the compounds—an expression of the overall dipole moment within the molecule. During the separation process, there is competition between the solute and solvent for adsorption to the stationary phase. Highly polar compounds and...
850

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Combining PC-SAFT and ML to Access Unknown API Solubilities.

Molecular pharmaceutics·2026
Same author

The More the Better?─Vitamin E TPGS as a Release Enhancer for Ritonavir/PVPVA Amorphous Solid Dispersions.

Molecular pharmaceutics·2025
Same author

The Hidden Crux of Correctly Determining Octanol-Water Partition Coefficients.

Molecular pharmaceutics·2025
Same author

Water-Assisted Drying of PVPVA-Based Amorphous Solid Dispersions.

Molecular pharmaceutics·2025
Same author

Water Activity as an Indicator for Antibody Storage Stability in Lyophilized Formulations.

Molecular pharmaceutics·2025
Same author

Simultaneous Water Sorption and Crystallization in ASDs 2: Modeling Long-Term Stabilities.

Molecular pharmaceutics·2024
Same journal

RETRACTED: Meligy et al. Therapeutic Potential of Mesenchymal Stem Cells Versus Omega n - 3 Polyunsaturated Fatty Acids on Gentamicin-Induced Cardiac Degeneration. <i>Pharmaceutics</i> 2022, <i>14</i>, 1322.

Pharmaceutics·2026
Same journal

Correction: Mohite et al. Bioactive Compound-Fortified Nanomedicine in the Modulation of Reactive Oxygen Species and Enhancement of the Wound Healing Process: A Review. <i>Pharmaceutics</i> 2025, <i>17</i>, 855.

Pharmaceutics·2026
Same journal

Metal Nanoparticle-Reinforced Hydrogels Applied in the Inhibition of Clinical Pathogens: Structural Features, Mechanisms, and Biomedical Prospects.

Pharmaceutics·2026
Same journal

Development and Evaluation of a Physiologically Based Pharmacokinetic Model for Cipepofol Across Diverse Clinical Populations.

Pharmaceutics·2026
Same journal

Artificial Intelligence in Nanopharmaceutical Development: From Predictive Design to Clinical Translation.

Pharmaceutics·2026
Same journal

Textilinin-1, a Snake Venom-Derived Kunitz-Type Protease Inhibitor, Accelerates Wound Healing Through Anti-Inflammatory, Antibacterial, and Pro-Regenerative Activities.

Pharmaceutics·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Video

Updated: Sep 6, 2025

Author Spotlight: Advancing Agricultural Land Ecosystem Research with a Hydraulic Property Analyzer to Assess Soil Health
07:21

Author Spotlight: Advancing Agricultural Land Ecosystem Research with a Hydraulic Property Analyzer to Assess Soil Health

Published on: August 9, 2024

1.1K

Predicting the Water Sorption in ASDs.

Dominik Borrmann1, Andreas Danzer1, Gabriele Sadowski1

  • 1Laboratory of Thermodynamics, Department of Chemical and Biochemical Engineering, TU Dortmund University, Emil-Figge-Str. 70, 44227 Dortmund, Germany.

Pharmaceutics
|June 24, 2022
PubMed
Summary
This summary is machine-generated.

This study presents a new method to predict water sorption in amorphous solid dispersions (ASDs), crucial for pharmaceutical stability. The approach accurately forecasts water absorption extent and rate using polymer and drug properties alone.

Keywords:
ASDsNET-GPPC-SAFTwater-sorption isothermswater-sorption kinetics

More Related Videos

Deposition of Porous Sorbents on Fabric Supports
05:58

Deposition of Porous Sorbents on Fabric Supports

Published on: June 12, 2018

6.6K
In Situ Soil Moisture Sensors in Undisturbed Soils
08:20

In Situ Soil Moisture Sensors in Undisturbed Soils

Published on: November 18, 2022

6.5K

Related Experiment Videos

Last Updated: Sep 6, 2025

Author Spotlight: Advancing Agricultural Land Ecosystem Research with a Hydraulic Property Analyzer to Assess Soil Health
07:21

Author Spotlight: Advancing Agricultural Land Ecosystem Research with a Hydraulic Property Analyzer to Assess Soil Health

Published on: August 9, 2024

1.1K
Deposition of Porous Sorbents on Fabric Supports
05:58

Deposition of Porous Sorbents on Fabric Supports

Published on: June 12, 2018

6.6K
In Situ Soil Moisture Sensors in Undisturbed Soils
08:20

In Situ Soil Moisture Sensors in Undisturbed Soils

Published on: November 18, 2022

6.5K

Area of Science:

  • Pharmaceutical Science
  • Materials Science
  • Physical Chemistry

Background:

  • Water sorption compromises the stability of amorphous solid dispersions (ASDs).
  • Preventing water uptake during storage is critical for maintaining ASD integrity.
  • Predictive models for water sorption in ASDs are needed to guide formulation and storage.

Purpose of the Study:

  • To develop and validate a methodology for predicting water sorption isotherms and kinetics in ASDs.
  • To assess the accuracy of predictions based solely on neat polymer and active pharmaceutical ingredient (API) properties.
  • To provide insights into water-sorption behavior relevant to pharmaceutical formulation.

Main Methods:

  • Combining the Perturbed-Chain Statistical Association Theory (PC-SAFT) with the Non-Equilibrium Thermodynamics of Glassy Polymers (NET-GP) approach for isotherm prediction.
  • Utilizing Maxwell-Stefan diffusion coefficients for predicting water sorption kinetics.
  • Experimental validation using ASD films of polyvinylpyrrolidone-based polymers and indomethacin at various drug loads and relative humidity (RH) levels.

Main Results:

  • Accurate prediction of water sorption isotherms and kinetics in ASDs was achieved.
  • The model successfully predicted water sorption for drug loads of 0.2 and 0.5 across a humidity range of 0 to 0.9 RH at 25 °C.
  • Predictions relied exclusively on the sorption properties of the neat polymer and API.

Conclusions:

  • The proposed methodology offers a reliable way to predict water sorption in ASDs.
  • This predictive capability is valuable for optimizing ASD formulation and storage conditions.
  • Understanding and controlling water sorption is key to enhancing the long-term stability of amorphous pharmaceutical systems.