Related Experiment Video
Updated: Aug 5, 2026

08:00
Screening for Endocrine Activity in Water Using Commercially-available In Vitro Transactivation Bioassays
Published on: December 4, 2016
Incorporating a Screening-Level Risk Quotient (RQ_screen) for Assessing Human Health Risk of Pharmaceutical Residues
Gabriel Souza-Silva1, Igor F C Santos2, Inês B Gomes3
1Faculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte 31270-901, Brazil.
Summary
Pharmaceutical residues in Portugal
Area of Science:
- Environmental Science
- Public Health
- Pharmacology
Background:
- Pharmaceutical residues are emerging contaminants in aquatic environments.
- Their presence poses potential risks to human health and ecosystems.
- Understanding their distribution and risk is crucial for public health management.
Purpose of the Study:
- To systematically review and evaluate pharmaceutical residues in Portuguese water bodies.
- To assess potential human health risks using risk quotient (RQ) and screening-level risk quotient (RQ_screen) methods.
- To prioritize contaminants for monitoring and risk management.
Main Methods:
- Systematic literature review of published data on pharmaceutical residues in bottled, tap, and surface water in Portugal.
- Application of risk quotient (RQ) and screening-level risk quotient (RQ_screen) approaches.
- Age-specific risk assessment considering body weight and water intake.
Main Results:
- Bottled and tap water showed low risk, while surface water presented the highest concern.
- Hormones, ramipril, betamethasone, citalopram, and amoxicillin were key risk contributors.
- RQ_screen identified carbamazepine, diclofenac, and others for ongoing monitoring.
- Infants and children exhibited higher risk values due to physiological factors.
Conclusions:
- Pharmaceutical residues are an emerging public and environmental health concern in Portugal.
- Surface water poses a higher risk than tap or bottled water.
- Age-specific risk evaluation and targeted monitoring are essential for effective management within a One Health framework.
Related Concept Videos
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions
PK–PD modeling has significantly influenced FDA regulatory decisions, particularly drug approval, dosage optimization, and labeling. These models integrate pharmacokinetics (PK) and pharmacodynamics (PD) to predict drug behavior and effects, aiding in optimizing dosing regimens and enhancing the probability of clinical trial success.One notable example is Nesiritide (Natrecor®), a recombinant human brain natriuretic peptide for treating acute decompensated congestive heart failure (CHF).
Toxicity Testing in Animals
Toxicity tests in animals are grounded on two main assumptions: first, the effects observed in laboratory animals can be extrapolated to humans, especially when adjusted for body surface area; second, high-dose exposure in animals is essential to identify potential human hazards from lower doses. This is based on the quantal dose-response concept, which faces the challenge of extrapolating results from relatively few test animals to much larger human populations. For example, a 0.01% incidence...
