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Related Concept Videos

Factors Influencing Drug Absorption: Pharmaceutical Parameters01:28

Factors Influencing Drug Absorption: Pharmaceutical Parameters

Solid dosage forms such as tablets and capsules undergo rigorous manufacturing processes to ensure stability and effectiveness. Their dissolution and absorption properties are influenced significantly by the choice of excipients (inactive ingredients that serve various roles in the formulation), and the methodology applied during production. The manufacturing parameters, such as compression force and granulation techniques, significantly affect dissolution rates. Elevated compression forces...
Bioavailability Enhancement: Drug Solubility Enhancement01:16

Bioavailability Enhancement: Drug Solubility Enhancement

Bioavailability is a critical factor in determining a drug's effectiveness. It refers to the proportion of a drug that enters the circulation when introduced into the body and is, as a result, able to have an active effect. Enhancing bioavailability is essential for drugs with poor solubility, as it can significantly impact their therapeutic efficacy. Various methods are employed to increase the solubility of drugs, thereby enhancing their bioavailability.Micronization and nanonization are...
Factors Affecting Dissolution: Particle Size and Effective Surface Area01:23

Factors Affecting Dissolution: Particle Size and Effective Surface Area

Dissolution kinetics, an essential aspect of oral drug delivery, is significantly influenced by the drug's particle size. According to the Noyes-Whitney dissolution model, the dissolution rate correlates directly with the drug's surface area. The larger the surface area, the higher the drug's solubility in water, leading to a faster drug dissolution rate. Reducing particle size increases the effective surface area, enhancing the dissolution process. Micronization and nanosizing are employed to...
Bioavailability Enhancement: Drug Stability Enhancement and GI Retention01:05

Bioavailability Enhancement: Drug Stability Enhancement and GI Retention

Improving a drug's stability in the gastrointestinal (GI) tract is paramount for enhancing its bioavailability and therapeutic effectiveness. Various strategies are employed to protect the drug from the harsh gastric milieu and to ensure its release and absorption at the desired site within the GI tract.Polymer coatings are one such method used to shield drugs from the stomach's acidic environment. By preventing premature drug release, these coatings improve the bioavailability of unstable...
Supercritical Fluid Chromatography01:18

Supercritical Fluid Chromatography

Supercritical fluid chromatography (SFC) provides a beneficial substitute for gas chromatography (GC) and liquid chromatography (LC) for certain samples because it merges the top attributes of both techniques. SFC allows the separation and analysis of compounds that GC or LC does not easily manage. These compounds are traditionally nonvolatile or thermally unstable, making GC unsuitable and lacking functional groups required for HPLC analysis.
SFC utilizes a supercritical fluid mobile phase,...
In Vitro Drug Dissolution: Alternative Methods01:17

In Vitro Drug Dissolution: Alternative Methods

Alternative drug dissolution methods include the rotating bottle, intrinsic dissolution test, peristalsis, and the Franz diffusion cell method. The rotating bottle method involves meticulously rotating tightly capped controlled-release beads in a temperature-controlled bath. Periodic decanting of samples allows for residue assay, followed by refilling with fresh medium and testing at various pH levels to emulate the gastrointestinal tract conditions.In contrast, the intrinsic dissolution test...

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Related Experiment Video

Updated: Jul 7, 2026

Transport Properties of Ibuprofen Encapsulated in Cyclodextrin Nanosponge Hydrogels: A Proton HR-MAS NMR Spectroscopy Study
10:10

Transport Properties of Ibuprofen Encapsulated in Cyclodextrin Nanosponge Hydrogels: A Proton HR-MAS NMR Spectroscopy Study

Published on: August 15, 2016

Drug loading into beta-cyclodextrin granules using a supercritical fluid process for improved drug dissolution.

Khaled Hussein1, Michael Türk, Martin A Wahl

  • 1Pharmazeutische Technologie, Eberhard-Karls-Universität Tübingen, Auf der Morgenstelle 8, D-72076 Tübingen, Germany.

European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|February 20, 2008
PubMed
Summary

Supercritical fluid technology effectively loaded ibuprofen into beta-cyclodextrin granules, significantly enhancing drug dissolution. This controlled particle deposition method offers a solvent-free approach for improving drug solubility.

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Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials
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Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials

Published on: May 15, 2015

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Last Updated: Jul 7, 2026

Transport Properties of Ibuprofen Encapsulated in Cyclodextrin Nanosponge Hydrogels: A Proton HR-MAS NMR Spectroscopy Study
10:10

Transport Properties of Ibuprofen Encapsulated in Cyclodextrin Nanosponge Hydrogels: A Proton HR-MAS NMR Spectroscopy Study

Published on: August 15, 2016

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials
09:05

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials

Published on: May 15, 2015

Area of Science:

  • Pharmaceutical Technology
  • Materials Science
  • Chemical Engineering

Background:

  • Poor water-solubility of drugs limits their bioavailability and therapeutic efficacy.
  • Supercritical fluid (SCF) technology offers a green and efficient method for drug formulation.
  • Beta-cyclodextrin (betaCD) is a suitable carrier for enhancing the solubility of poorly water-soluble drugs.

Purpose of the Study:

  • To evaluate the efficacy of controlled particle deposition (CPD), an SCF technique, for loading ibuprofen into betaCD granules.
  • To compare the CPD technique with a conventional solution immersion (SI) method for drug loading.
  • To assess the impact of drug loading on the physical properties and dissolution of ibuprofen.

Main Methods:

  • Ibuprofen was loaded into betaCD granules using two methods: CPD (SCF process) and SI (conventional method).
  • Drug loading efficiency was quantified by weight percentage.
  • Physical characterization included BET surface area analysis and X-ray diffraction.
  • Drug dissolution rates were measured and compared to unprocessed ibuprofen.

Main Results:

  • CPD resulted in significantly higher ibuprofen loading (17.42 wt.%) compared to SI (3.8 wt.%).
  • BET surface area reduction confirmed drug loading in the CPD product, unlike the SI product.
  • X-ray patterns indicated crystalline ibuprofen in loaded granules.
  • Both methods improved drug dissolution compared to unprocessed ibuprofen, with CPD showing greater potential.

Conclusions:

  • Controlled particle deposition using supercritical fluids is a highly effective technique for loading poorly water-soluble drugs into solid carriers like betaCD.
  • This SCF-based method significantly enhances drug loading capacity and improves drug dissolution properties.
  • CPD offers a promising, solvent-free alternative to conventional methods for pharmaceutical formulation.