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Related Concept Videos

Biopharmaceutical Factors Influencing Drug Product Design: Overview01:22

Biopharmaceutical Factors Influencing Drug Product Design: Overview

Rational drug product design integrates knowledge of the drug’s physicochemical properties, formulation components, manufacturing techniques, and intended route of administration. Each factor influences the drug’s performance, including how it is released, absorbed, and eliminated in the body.The physicochemical properties of a drug—such as solubility, stability, and particle size—affect its compatibility with excipients and the choice of dosage form. Excipients, though pharmacologically...
Site-Targeted Drug Delivery Systems: Polymeric Carriers01:24

Site-Targeted Drug Delivery Systems: Polymeric Carriers

Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
Clinically Relevant Drug Product Specifications: Methods of Establishment01:29

Clinically Relevant Drug Product Specifications: Methods of Establishment

Product specifications define the acceptable quality of a pharmaceutical product by ensuring identity, purity, potency, and strength. These specifications serve as benchmarks during development, manufacturing, and post-approval quality control. Clinically relevant specifications are particularly important because they directly relate to a drug's safety and efficacy in clinical use.Dissolution studies are critical biopharmaceutic tools that link in vitro behavior to in vivo performance. They...
Biopharmaceutics and Pharmacokinetics: Overview01:28

Biopharmaceutics and Pharmacokinetics: Overview

Understanding drugs, drug products, and their performance in pharmaceutical science is pivotal. Drugs, whether simple molecules or complex compounds, are designed to interact with the body's biological systems to diagnose, treat, or prevent diseases. Drug products include various delivery systems such as tablets, capsules, injections, and inhalers. The performance of these drug products is gauged by their ability to deliver the active ingredient to the desired site of action at the appropriate...
Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

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Changes in polymorphic forms can significantly influence the bioavailability of poorly soluble drugs. Although the FDA defines pharmaceutical equivalence based on having the same active ingredient, dosage form, and route of administration, it does not automatically disqualify products with different polymorphic forms. This means two products with different polymorphs can still be deemed pharmaceutically equivalent. However, polymorphic differences can affect properties like wettability,...
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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...

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Updated: Jun 7, 2026

Transport Properties of Ibuprofen Encapsulated in Cyclodextrin Nanosponge Hydrogels: A Proton HR-MAS NMR Spectroscopy Study
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Published on: August 15, 2016

Pharmaceutical applications of cyclodextrins: basic science and product development.

Thorsteinn Loftsson1, Marcus E Brewster

  • 1Faculty of Pharmaceutical Sciences, University of Iceland, Reykjavik, Iceland. thorstlo@hi.is

The Journal of Pharmacy and Pharmacology
|November 3, 2010
PubMed
Summary

Cyclodextrins are effective excipients for improving the solubility and dissolution of poorly soluble drugs. Their application in drug formulation is crucial for developing new parenteral and oral dosage forms, enhancing bioavailability.

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Published on: January 22, 2015

Area of Science:

  • Pharmaceutical Science
  • Drug Delivery
  • Formulation Development

Background:

  • A significant percentage of marketed drugs (40%) and a higher proportion of drugs in development (90%) exhibit poor solubility.
  • Poor aqueous solubility presents a major challenge in developing effective oral and parenteral drug formulations.
  • Cyclodextrins offer a promising approach to overcome solubility limitations in drug development.

Purpose of the Study:

  • To review the fundamental science of cyclodextrins.
  • To present data on the development of drug formulations utilizing cyclodextrins.
  • To highlight cyclodextrins as a key tool for enhancing drug solubility and bioavailability.

Main Methods:

  • Review of scientific literature on cyclodextrin properties and applications.
  • Analysis of data from studies on cyclodextrin-drug complexation.
  • Evaluation of factors influencing the biopharmaceutical characteristics of cyclodextrin formulations.

Main Results:

  • Cyclodextrins are established as valuable solubilizing excipients with successful marketed products.
  • New product introductions confirm the significant added value of cyclodextrin-based formulations.
  • Understanding cyclodextrin properties and interactions is key to predicting formulation success.

Conclusions:

  • Cyclodextrins are essential in the formulator's toolkit for improving apparent solubility and dissolution rates.
  • These excipients are vital for developing dosage forms for poorly water-soluble drug candidates.
  • Continued research and application of cyclodextrins indicate their ongoing importance in pharmaceutical R&D and marketing.