Pharmaceuticals in the environment /
Medicines play an important role in the treatment and prevention of disease in humans and animals, but residues from these medicines can be released into the environment through a number of routes during their manufacture, use and disposal. It is only recently that the potential environmental impact...
Clasificación: | Libro Electrónico |
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Otros Autores: | , |
Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
[Cambridge] :
Royal Society of Chemistry,
[2015]
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Colección: | Issues in environmental science and technology.
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Temas: | |
Acceso en línea: | Texto completo |
Tabla de Contenidos:
- The Pharmaceutical Industry and the Future of Drug Development
- Distribution of Pharmaceutical Residues in the Environment
- Pharmaceuticals in the Marine Environment
- Sources of Residues in the Environment and their Control
- Persistence of Pharmaceutical Residues both in Sewage Treatment Works and the Receiving Environment
- Ecotoxicology, Environmental Risk Assessment and Potential Impact on Human Health
- Impacts of Pharmaceuticals on Terrestrial Wildlife
- Veterinary Pharmaceuticals.
- Machine generated contents note: The Pharmaceutical Industry and the Future of Drug Development / David Taylor
- 1. Introduction
- 1.1. Historical Background
- 1.2. What is a Pharmaceutical?
- 1.3. Environmental Impact
- 2. The Pharmaceutical Industries
- 3. Research, Discovery and Development
- 3.1. Pre-clinical Trials
- 3.2. Clinical Trials
- 3.3. Environmental Issues
- 4.Commercial Realities
- 4.1. Problems with Patents
- 4.2. Maintaining a Viable Business
- 4.3. Access to Medicines
- 5. The Pharmaceutical Industry in the Future
- 5.1.Commercial Pressures
- 5.2. Environmental Challenges
- 6. Conclusions
- References
- Distribution of Pharmaceutical Residues in the Environment / Vince D'Aco
- 1. Introduction
- 2. Occurrence of Pharmaceuticals
- 3. Reviews of Pharmaceutical Products
- 4. Measured Concentrations
- 5. Modelling to Complement and Extend the Utility of Field Programs
- 5.1. Measure or Model?
- 5.2. Estimates of API Consumption for Use in Modelling Analysis.
- Note continued: 5.3. Modelling for Design of Field Surveys
- 5.4. Elucidating Fate and Transport Mechanisms
- 5.5. Critical Evaluation of Measured Concentrations
- 5.6. Modelling to Support Human Health and Environmental Risk Assessments
- 5.7. Models to Evaluate Potential Impacts of Natural and Synthetic Estrogens
- 5.8. Using Models to Evaluate Mitigation Strategies
- 6. Conclusion
- References
- Pharmaceuticals in the Marine Environment / Thomas H. Hutchinson
- 1. Introduction
- 2. Key Sources of Pharmaceuticals Entering the Marine Environment
- 2.1. Human Pharmaceuticals and Illicit Drugs
- 2.2. Veterinary Medicines
- 2.3. Environmental Fate of PhACs in Marine Environments
- 2.4. Concentrations of PhACs Measured in the Marine Environment
- 2.5. Impacts on Marine Organisms
- 2.6. Human Health Concerns
- 3. Conclusions
- References
- Sources of Pharmaceutical Residues in the Environment and their Control / Daniel J. Caldwell
- 1. Introduction and Overview.
- Note continued: 2. Pathways of Exposure
- 3. Patient Consumption and Excretion
- 3.1. Human Excretion
- 3.2. APIs Excreted into the Sewage System Undergo Wastewater Treatment
- 4. Emissions from Pharmaceutical Manufacturing
- 5. Unused Medicines and their Disposal
- 5.1. Disposal in Municipal Solid Waste
- 6. Wastewater Treatment
- 7. Hospitals
- 8. Minor Pathways
- 8.1. Exposure through the Consumption of Foods
- 8.2. Exposure through Water Consumption
- 9. Conclusions
- References
- Pharmaceutical Residues in Sewage Treatment Works and their Fate in the Receiving Environment / Paola Verlicchi
- 1. Introduction
- 2. Pharmaceuticals in Municipal Wastewaters
- 2.1. Occurrence in Municipal Sewage
- 2.2. The Fate and Behaviour of Pharmaceuticals in Sewage Works
- 2.3. Removal of Pharmaceuticals during Conventional Wastewater Treatment
- 2.4. Occurrence in Sewage Sludge
- 3. Need for Advanced Treatment and Sustainability Implications.
- Note continued: 4. Pharmaceuticals in Receiving Waters
- 4.1. Occurrence
- 4.2. Fate and Behaviour
- 5. Significance of Levels of Pharmaceuticals in Waters
- 6. Discussion
- 6.1. Recommendations to Reduce Pharmaceutical Inputs
- 7. Summary
- References
- Ecotoxicology, Environmental Risk Assessment and Potential Impact on Human Health / Reinhard Lange
- 1. Introduction
- 2. Some Relevant Pharmacology
- 2.1. Pharmacokinetics
- 2.2. Pharmacodynamics
- 3. General Approaches and Data Availability
- 3.1. Dealing with Data Distributions
- 3.2. What is a `Safe' Concentration?
- 3.3. Data Feast and Famine
- 4. Potential Risks to Humans
- 4.1. Predicted Environmental Concentrations versus Acceptable Daily Intakes
- 4.2. Measured Environmental Concentrations versus Acceptable Daily Intakes
- 4.3. Genotoxicity
- 4.4. Hormonal Disruption
- 4.5. Susceptible Sub-populations
- 4.6. Conclusions on Human Risks
- 5. Potential Risks to Aquatic Life.
- Note continued: 5.1. Limitations of Available Ecotoxicity Data
- 5.2. Predicted Environmental Concentrations versus Predicted No Effect Concentrations
- 5.3. Measured Environmental Concentrations versus Predicted No Effect Concentrations
- 5.4. Estrogenic APIs
- 5.5. Antidepressants
- 5.6. Plasma Concentration Model
- 5.7. Conclusions on Risks to Aquatic Life
- 6. Antibiotics, Clinical Resistance and Potential Risks to Beneficial Microbes
- References
- Impacts of Pharmaceuticals on Terrestrial Wildlife / Chad A. Kinney
- 1. Introduction
- 1.1.A Global Context
- 1.2. Scale and Pathways
- 1.3. Recognised Impacts on Non-target Wildlife
- 1.4. Aim of this Chapter
- 2. Pathways, Exposure and Effects in Terrestrial Wildlife
- 2.1. Pathways, Exposure and Effects Associated with Freshwater Contamination
- 2.2. Pathways, Exposure and Effects within the Terrestrial Landscape
- 3. Known Impacts in Terrestrial Wildlife.
- Note continued: 3.1. Case Study: Non-steroidal Anti-inflammatory Drugs and Avian Scavengers
- 4. Analytical and Monitoring Approaches and Challenges
- 4.1. Analytical Tools
- 4.2. Monitoring Approaches
- Transformation Products
- 4.3. Wildlife Exposure: Novel Biomarkers and Endpoints
- 4.4. Field Monitoring and Sample Matrices
- 5. Legislative Perspectives
- 5.1. Case 1: Scavenging Wildlife and Pentobarbital in the US
- 5.2. Case 2: Veterinary NSAIDs in the EU, South Africa and on the Indian Subcontinent
- 6. Future Priorities
- 6.1. Better Quantify Potential Risks for Terrestrial Wildlife
- 6.2. Improve Risk Assessment for Terrestrial Environments
- 6.3. Better Understand the Risks Posed by Pharmaceutical Transformation Products
- 6.4. Develop New Ways of Monitoring Across a Wider Range of Taxa
- 7. In Conclusion
- References
- Veterinary Pharmaceuticals / Silke Hickmann
- 1. Introduction.
- Note continued: 2. Legal and Regulatory Demands Concerning Environmental Impact of VMPs in the EU
- 3. The Impact of VMPs on the Environment
- 3.1. Emission of VMP Residues Related to Production
- 3.2. Emission of VMPs Residues Related to Use
- 3.3. Emission of VMPs Residues Related to Disposal
- 4. Specific Toxic Effects of VMPs
- 4.1. Antiparasitics in the Aquatic Environment
- 4.2. Antimicrobials in Aquatic and Terrestrial Environments
- 4.3. Antiparasitics for Pasture Animals
- 4.4. Risks to Vultures and other Necrophagous Bird Populations in the European Union in Connection with the Use of Veterinary Medicines Containing Diclofenac
- 5. Monitoring and Ecopharmacovigilance
- References.