Jove
Visualize
Contact Us
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 Concept Videos

Bioavailability Enhancement: Drug Stability Enhancement and GI Retention01:05

Bioavailability Enhancement: Drug Stability Enhancement and GI Retention

69
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...
69
Bioavailability Enhancement: Drug Solubility Enhancement01:16

Bioavailability Enhancement: Drug Solubility Enhancement

75
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...
75
Bioavailability Enhancement: Drug Permeability Enhancement01:27

Bioavailability Enhancement: Drug Permeability Enhancement

76
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...
76
Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems01:22

Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems

58
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...
58
Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry01:20

Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry

338
Orally administered drugs primarily enter the systemic circulation via passive diffusion through the intestinal membranes. The drug's absorption is influenced by drug stability in the gastrointestinal GI tract, membrane permeability, the surface area available for absorption, luminal drug concentration, and residence time in the lumen. Drug permeability can be enhanced by adjusting the lipophilicity, polarity, or molecular size of the drug, promoting its passive transport across intestinal...
338
Methods for Studying Drug Absorption: In vitro01:16

Methods for Studying Drug Absorption: In vitro

446
In vitro experiments are crucial for understanding the transport and absorption of drugs through biological materials. These studies employ varied methods such as the diffusion cell method, the everted sac technique, and the everted ring technique.
The diffusion cell method uses a two-compartment cell, including a donor compartment with the drug solution, which simulates the environment where the drug is applied, and a receptor compartment with a buffer solution, which simulates the environment...
446

You might also read

Related Articles

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

Sort by
Same author

Evaluation of allergenicity of the alternative food protein sources microalga Spirulina and rapeseed cake - A study in Brown Norway rats.

Food research international (Ottawa, Ont.)·2025
Same author

Novel Fibre-Rich Breads Yield Improved Glucose Release Curves and Are Well Accepted by Children in Primary School Breakfast Clubs.

Nutrients·2025
Same author

Effects of Ferulic Acid on Cognitive Function: A Systematic Review.

Molecular nutrition & food research·2024
Same author

Effect of beta glucan coating on controlled release, bioaccessibility, and absorption of β-carotene from loaded liposomes.

Food & function·2024
Same author

Small intestine vs. colon ecology and physiology: Why it matters in probiotic administration.

Cell reports. Medicine·2023
Same author

The role of food structure in gastric-emptying rate, absorption and metabolism.

The Proceedings of the Nutrition Society·2023

Related Experiment Video

Updated: Nov 12, 2025

In vitro Digestion of Emulsions in a Single Droplet via Multi Subphase Exchange of Simulated Gastrointestinal Fluids
10:20

In vitro Digestion of Emulsions in a Single Droplet via Multi Subphase Exchange of Simulated Gastrointestinal Fluids

Published on: November 18, 2022

2.9K

Improving carvacrol bioaccessibility using core-shell carrier-systems under simulated gastrointestinal digestion.

Taskeen Niaz1, Muhammad Imran2, Alan Mackie3

  • 1Department of Biosciences, COMSATS University Islamabad (CUI), Park Road, Islamabad, Pakistan; Food Colloids and Bioprocessing Group, School of Food Science and Nutrition, University of Leeds, Leeds LS2 9JT, UK.

Food Chemistry
|March 18, 2021
PubMed
Summary

Chitosan-albumin nano-carriers effectively stabilize carvacrol, enhancing its delivery. These core-shell structures improve the bioaccessibility of carvacrol for functional food applications.

Keywords:
CarvacrolConfocal laser scanning microscopyCore-shell nano-systemsIn vitro bioaccessibilitySustained delivery

More Related Videos

Development, Characterization, and Evaluation of CAGE-based Ionic Liquid Systems for Transdermal Delivery
09:58

Development, Characterization, and Evaluation of CAGE-based Ionic Liquid Systems for Transdermal Delivery

Published on: September 26, 2025

135
Extraction of Plant-based Capsules for Microencapsulation Applications
10:54

Extraction of Plant-based Capsules for Microencapsulation Applications

Published on: November 9, 2016

12.3K

Related Experiment Videos

Last Updated: Nov 12, 2025

In vitro Digestion of Emulsions in a Single Droplet via Multi Subphase Exchange of Simulated Gastrointestinal Fluids
10:20

In vitro Digestion of Emulsions in a Single Droplet via Multi Subphase Exchange of Simulated Gastrointestinal Fluids

Published on: November 18, 2022

2.9K
Development, Characterization, and Evaluation of CAGE-based Ionic Liquid Systems for Transdermal Delivery
09:58

Development, Characterization, and Evaluation of CAGE-based Ionic Liquid Systems for Transdermal Delivery

Published on: September 26, 2025

135
Extraction of Plant-based Capsules for Microencapsulation Applications
10:54

Extraction of Plant-based Capsules for Microencapsulation Applications

Published on: November 9, 2016

12.3K

Area of Science:

  • Food Science
  • Nanotechnology
  • Biomaterials

Background:

  • Carvacrol is a hydrophobic bioactive compound with potential health benefits.
  • Encapsulation is crucial for improving the stability and delivery of hydrophobic compounds.
  • Chitosan-albumin core-shell nanocarriers offer a promising platform for encapsulation.

Purpose of the Study:

  • To evaluate the stability and bioaccessibility of carvacrol encapsulated in chitosan-albumin core-shell nanocarriers.
  • To characterize the physicochemical properties of these nanocarriers.
  • To assess their performance under simulated digestion conditions.

Main Methods:

  • Fabrication of chitosan-albumin core-shell nanocarriers (NCs).
  • Characterization of NCs size and zeta potential.
  • Assessment of NCs stability and carvacrol bioaccessibility during simulated gastrointestinal digestion.

Main Results:

  • Chitosan-albumin NCs exhibited particle sizes ranging from 52.4 to 203 nm and zeta potentials from +21 to -18 mV.
  • Core-shell NCs demonstrated enhanced stability and reduced aggregation compared to chitosan-only NCs under simulated digestion.
  • Carvacrol bioaccessibility was significantly improved when encapsulated within the core-shell NCs.

Conclusions:

  • Chitosan-albumin core-shell nanocarriers provide an effective system for encapsulating and protecting carvacrol.
  • These nanocarriers enhance the stability and bioaccessibility of carvacrol.
  • The findings suggest potential applications of these nanocarriers in functional foods for improved delivery of bioactive compounds.