AQUASOMIC

Our main objective is to develop and apply high-throughput analytical strategies to assess environmental and human exposure to emerging contaminants

The main tools that we will develop in the framework of Aquasomics are:

  • Validated target and reliable nontarget methods of analysis of emerging contaminants in surface waters and biofluids
  • Millifluidic devices to run innovative sample treatments and bioassays

These tools, among many others, will be applied in a large variety of cases to:

a. Assess the effects of identified CECs in waters and strategies for mitigation.

b. Estimate the bioaccessible and bioavailable fractions of CECs

c. Support millifluidic devices to run innovative in-vitro bioassays

d. Study the relationships between certain diseases with the exposure to CECs

e. Assess the exposure to CECs through urine analysis and wastewater-based epidemiology

Research methodology

The main strategy to study the external and the internal doses is the (bio)monitoring of target chemicals in biofluids and tissues and in the environment. The combined application of target and nontarget analysis (NTA) in human biofluids, organisms' tissues and in water samples will allow us to tackle those biomonitoring requirements. In addition to this, it is necessary to understand the way the contaminants can reach to the vascular system. In this sense, bioaccesibility and bioavailability concepts must become reliable and measurable.  

Project Work Packages (WP) 

There are 4 work packages in AQUASOMIC, which are all interconnected. WP1 will be monitoring and in contact with all of these work packages.

WP1. Coordination and Project management, Formation and Outreach Activities

Task 1.1. Project and Data Management Plan

Task 1.2. Project Coordination

Task 1.3. Formative activities

Task 1.4. Outreach activities

WP2. Development and validation of high-throughput analytical methods

Task 2.1. Development of target and nontarget methods

Task 2.2. Development of more efficient pipelines to annotate and identify compounds

Task 2.3. Development of 3D printed flow-injection platforms for miniaturized bioassays

Task 2.4. Novel sorptive composite materials based on 3D printing and periodic porous solids for on-line sample preparation

WP3. Environmental health assessment

Task 3.1. Occurrence, fate, and risk of emerging pollutants in aquatic ecosystems

Task 3.2. Development of 3D dispersal models of microfibers and microplastics (MP) in coastal waters

Task 3.3. Integrative optimization of a drinking water treatment pilot plant (DWTP)

Task 3.4. Millifluidic platforms for on-line oral bioaccessibility testing of additives from MPs and food-borne MPs

Task 3.5. In-vitro bioavailability tests of organic species associated to microplastics using lipid nanovesicles

Task 3.6 In-vivo bioavailability tests and advanced biochemical assays for microplastic additives using murine models

Task 3.7. Miniaturized 3D printed fluidic platforms for in-vitro cytotoxicity and ecotoxicity testing

WP4. Human health monitoring

Task 4.1. Toxicity of emerging contaminants onto human leukocyte populations using a 3D printed blood vessel

Task 4.2. Case study A: PFAS and xenobiotics in children plasma samples

Task 4.3. Case studies B and C: exposure to xenobiotics via urine analysis

Task 4.4. Case study D: Exposure effects on congenital anomalies of the kidney and urinary tract

Task 4.5. Case study E: Determination of xenobiotics in breast milk

Task 4.6 Human exposure assessment through Wastewater-based epidemiology (WBE)

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