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Related Concept Videos

Bioavailability Enhancement: Drug Permeability Enhancement01:27

Bioavailability Enhancement: Drug Permeability Enhancement

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 secretion,...
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...
Factors Influencing Drug Absorption: Presystemic Elimination01:24

Factors Influencing Drug Absorption: Presystemic Elimination

The pharmacokinetic journey of oral drugs begins with a crucial first pass through the hepatic portal system, called the first-pass effect. This first pass significantly impacts bioavailability — the proportion of a drug that enters systemic circulation and is available for therapeutic action. The primary route sees the drug absorbed by intestinal membranes and then shunted to the liver via the hepatic portal vein. Here, pre-systemic elimination occurs as drugs face metabolism or biliary...
Modified-Release Drug Delivery Systems: Bioavailability01:30

Modified-Release Drug Delivery Systems: Bioavailability

Modified-release (MR) dosage forms are designed to extend drug release over time, thereby maintaining stable plasma concentrations and reducing dosing frequency. However, their bioavailability is typically below 100% due to incomplete drug release and presystemic metabolism, and limitations in drug permeability across the gastrointestinal epithelium, all of which can restrict the fraction of the drug reaching systemic circulation. Consequently, studying the in vivo bioavailability of MR...
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...
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...

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Related Experiment Video

Updated: Jun 7, 2026

Isolation of Intrapulmonary Artery and Smooth Muscle Cells to Investigate Vascular Responses
07:56

Isolation of Intrapulmonary Artery and Smooth Muscle Cells to Investigate Vascular Responses

Published on: June 8, 2022

Modification of propranolol's bioavailability by Eurycoma longifolia water-based extract.

S A B Salman1, S Amrah, M S A Wahab

  • 1Department of Pharmacology, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Penang, Malaysia.

Journal of Clinical Pharmacy and Therapeutics
|November 9, 2010
PubMed
Summary

Eurycoma longifolia significantly reduces propranolol bioavailability and absorption in healthy males. Caution is advised when combining this herb with propranolol due to potential drug interactions.

Related Experiment Videos

Last Updated: Jun 7, 2026

Isolation of Intrapulmonary Artery and Smooth Muscle Cells to Investigate Vascular Responses
07:56

Isolation of Intrapulmonary Artery and Smooth Muscle Cells to Investigate Vascular Responses

Published on: June 8, 2022

Area of Science:

  • Pharmacology
  • Pharmacokinetics
  • Herbal Medicine Interactions

Background:

  • Eurycoma longifolia (E. longifolia) is a herb used for aphrodisiac properties, often by Asian males, including those with hypertension on propranolol.
  • Propranolol, a beta-blocker, can cause sexual dysfunction as a side effect.
  • No prior studies have investigated the pharmacokinetic interaction between E. longifolia and propranolol.

Purpose of the Study:

  • To investigate the pharmacokinetic effects of Eurycoma longifolia on propranolol in healthy male volunteers.
  • To compare propranolol's pharmacokinetics when administered with E. longifolia versus a placebo.

Main Methods:

  • A placebo-controlled, randomized, single-blinded, crossover study involving 14 healthy, non-smoking young males.
  • Participants received a single oral dose of 80 mg propranolol with either a placebo or 200 mg of a water-based E. longifolia extract.
  • Plasma concentrations of propranolol were measured over 10 hours using high-performance liquid chromatography (HPLC).

Main Results:

  • Co-administration with E. longifolia decreased propranolol's bioavailability (AUC0-∞) by 29%.
  • Maximum plasma concentration (Cmax) of propranolol was reduced by 42%, and the time to reach Cmax (Tmax) was significantly prolonged by 86%.
  • The terminal elimination half-life of propranolol was not significantly affected.

Conclusions:

  • Eurycoma longifolia significantly reduces propranolol bioavailability, primarily by decreasing its absorption.
  • The interaction does not appear to be mediated by increased propranolol metabolism.
  • While pharmacodynamics were unaffected in healthy volunteers, caution is recommended when co-administering E. longifolia and propranolol.