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Related Concept Videos

Bioavailability Enhancement: Drug Solubility Enhancement01:16

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Body: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...
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Bioavailability Enhancement: Drug Permeability Enhancement01:27

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Body:After oral administration, poor permeability often limits the rate at which drugs are absorbed through the intestinal epithelium. Enhancing drug permeability is crucial for effective therapy, and several strategies have been developed to overcome this challenge.One effective strategy involves the use of lipid-based formulations. These formulations enhance dissolution and solubility, targeting physiological mechanisms to increase drug absorption. This includes stimulating bile salt...
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Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems01:22

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Body:Bioavailability is a critical pharmacological concept that measures the extent and rate at which an active drug ingredient or therapeutic moiety enters the systemic circulation, remaining unchanged. It's a pivotal factor in determining a drug's efficacy and safety.The Biopharmaceutics Classification System (BCS) plays an essential role in drug development by categorizing drugs into four classes based on their solubility and permeability. This classification aids in understanding drug...
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Bioavailability Enhancement: Drug Stability Enhancement and GI Retention01:05

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Body: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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Bioavailability Study Design: Absolute Versus Relative Bioavailability01:27

Bioavailability Study Design: Absolute Versus Relative Bioavailability

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Bioavailability refers to the proportion of an administered drug that reaches the systemic circulation in its active, unaltered form. It is a crucial pharmacokinetic parameter that determines the effectiveness of a drug in achieving its intended therapeutic outcomes. The route of administration significantly influences bioavailability, with intravenous administration achieving 100% bioavailability as the drug directly enters the bloodstream. In contrast, oral administration often results in...
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Self-Nanoemulsification of Healthy Oils to Enhance the Solubility of Lipophilic Drugs
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Enhanced Curcumin Bioavailability through Nonionic Surfactant/Caseinate Mixed Nanoemulsions.

Francesca Cuomo1, Luisa Perugini1, Emanuele Marconi1

  • 1Dept. of Agricultural, Environmental and Food Sciences (DiAAA), Univ. of Molise, Via De Sanctis, I-86100, Campobasso, Italy.

Journal of Food Science
|August 23, 2019
PubMed
Summary

Mixed emulsifier nanoemulsions significantly enhance curcumin delivery and bioavailability compared to sodium caseinate alone. This offers a promising strategy for oral delivery of lipophilic compounds like curcumin.

Keywords:
curcuminemulsifiersinterfacesnanoemulsionssodium caseinate

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Area of Science:

  • Food Science
  • Nanotechnology
  • Nutraceuticals

Background:

  • Curcumin, a lipophilic compound, has numerous health benefits but suffers from poor oral bioavailability.
  • Oil-in-water (O/W) nanoemulsions are explored as delivery systems for lipophilic compounds.
  • Sodium caseinate and mixed emulsifiers (caseinate/Tween 20) are investigated for stabilizing curcumin-loaded nanoemulsions.

Purpose of the Study:

  • To evaluate the efficacy of two types of O/W nanoemulsions in delivering curcumin.
  • To compare the curcumin solubilization and loading capacity of nanoemulsions stabilized by sodium caseinate versus a mixed emulsifier system.
  • To assess the impact of simulated gastrointestinal digestion on curcumin bioavailability from these nanoemulsions.

Main Methods:

  • Preparation of O/W nanoemulsions stabilized by sodium caseinate (Cas-O/W) and a mix of caseinate and Tween 20 (Mix-O/W).
  • Loading of curcumin into both nanoemulsion systems.
  • In vitro simulated gastrointestinal digestion process.
  • Evaluation of curcumin solubilization, loading capacity, and bioavailability.

Main Results:

  • Mix-O/W nanoemulsions showed higher curcumin solubilization (approx. 180 µg/mL) compared to Cas-O/W (approx. 55 µg/mL).
  • Curcumin loading capacity increased with higher incubation temperatures for both systems.
  • Mix-O/W nanoemulsions delivered more than double the amount of curcumin compared to Cas-O/W after simulated digestion.

Conclusions:

  • Mixed emulsifier systems (caseinate/Tween 20) are superior to sodium caseinate alone for oral delivery of curcumin.
  • These nanoemulsions offer a high intake of curcumin with low fat content, improving oral bioavailability.
  • Protein/surfactant-stabilized nanoemulsions are a viable solution for overcoming solubility limitations of lipophilic compounds in food and beverages.