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Related Concept Videos

Methods for Studying Drug Absorption: In vitro01:16

Methods for Studying Drug Absorption: In vitro

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...
Bioavailability: Influencing Factors01:22

Bioavailability: Influencing Factors

Bioavailability refers to the extent and rate at which a drug reaches systemic circulation in its active form. Extent refers to the amount of the drug that makes it into circulation, while rate is the speed at which it enters circulation. It is influenced by several factors critical for optimizing drug formulations, dosing regimens, and therapeutic outcomes.Physicochemical properties of drugs and formulationsThe solubility, stability, and dissolution rate of a drug significantly impact its...
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...
Bioavailability: Overview01:17

Bioavailability: Overview

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...
Bioavailability: Overview01:13

Bioavailability: Overview

Bioavailability refers to the proportion of an unaltered drug that, after administration, enters the systemic circulation and can be distributed to the desired action site. Factors such as gastrointestinal (GI) absorption and liver biotransformation influence the bioavailability of a drug when it is administered orally. When a drug is administered intravenously, it enters the systemic circulation directly; by definition, its bioavailability is assumed to be 100%. The bioavailability of an...
Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems01:22

Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems

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 absorption...

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The Caco-2 Cell Bioassay for Measurement of Food Iron Bioavailability
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From Rice Grain to Rice Bran: Processing Effects on Nutrient Retention, In Vitro Bioaccessibility and Caco-2 Cellular

Valery Conejo-Lopez1, Stefanny Campos-Boza1,2, Paola Fuentes-Schweizer3

  • 1Centro para Investigaciones en Granos y Semillas, Universidad de Costa Rica, San Pedro, San José, 11501-2060, Costa Rica.

Plant Foods for Human Nutrition (Dordrecht, Netherlands)
|May 15, 2026
PubMed
Summary

Rice milling significantly reduces vitamin E and minerals. Rice bran retains these nutrients, but bioaccessibility varies for compounds like ferulic acid, γ-oryzanol, and γ-tocotrienol.

Keywords:
Oryza sativaCaco-2 cellFerulic acidMineralsVitamin Eγ-oryzanol

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High-throughput, Microscale Protocol for the Analysis of Processing Parameters and Nutritional Qualities in Maize (Zea mays L.)

Published on: June 16, 2018

Area of Science:

  • Agricultural Science
  • Food Science
  • Nutritional Science

Background:

  • White rice, a global staple, undergoes milling that removes nutrient-rich outer layers.
  • Milling causes substantial loss of vitamin E, minerals, and bioactive compounds like γ-oryzanol and polyphenols.

Purpose of the Study:

  • To assess the impact of rice milling on nutrient retention in different rice subspecies.
  • To evaluate the in vitro bioaccessibility and Caco-2 cellular absorption of key bioactive compounds in rice bran.

Main Methods:

  • Analyzed vitamin E and mineral content in milled white rice and rice bran from 11 Costa Rican rice samples.
  • Utilized in vitro digestion followed by Caco-2 cell assays to measure bioaccessibility and absorption of γ-tocotrienol, γ-oryzanol, and ferulic acid.

Main Results:

  • White rice had 66% less vitamin E and 75% fewer minerals compared to rice bran.
  • Nutrient loss variation was linked to intrinsic sample characteristics, not milling degree.
  • Ferulic acid showed high bioaccessibility (186-1159%) and absorption (0-20%).
  • γ-Oryzanol had moderate bioaccessibility (59-162%) and low absorption (0.1-0.7%).
  • γ-Tocotrienol was bioaccessible (32-241%) but not absorbed by Caco-2 cells.

Conclusions:

  • Rice bran is a rich source of bioavailable antioxidants.
  • Processing methods should be optimized to preserve the nutritional value of rice bran.
  • Understanding the bioaccessibility and absorption of specific compounds is crucial for nutritional applications.