Miljöpåverkan
Travoprost
Miljörisk:
Risk för miljöpåverkan av travoprost kan inte uteslutas då det inte finns tillräckliga ekotoxikologiska data.
Nedbrytning:
Travoprost är potentiellt persistent.
Bioackumulering:
Travoprost har hög potential att bioackumuleras.
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Detaljerad miljöinformation
Environmental Risk Classification
Predicted Environmental Concentration (PEC)
PEC is calculated according to the following formula:
PEC (μg/L) = (A*109*(100-R))/(365*P*V*D*100) = 1.37*10-6 * A * (100 - R) = 1.37*10-6 * 0.0301 * 100 = 0.000004 μg/L = 0.04 ng/L
Where:
A = 0.0301 kg travoprost (total sold amount API in Sweden year 2022, data from IQVIA).
R = 0 % removal rate (due to loss by adsorption to sludge particles, by volatilization, hydrolysis or biodegradation) = 0, if no data is available.
P = number of inhabitants in Sweden = 10 *106
V (L/day) = volume of wastewater per capita and day = 200 (ECHA default) (ECHA 2008)
D = factor for dilution of waste water by surface water flow = 10 (ECHA default) (ECHA 2008)
Predicted No Effect Concentration (PNEC)
Ecotoxicological studies
Algae: no data available
Crustacean (Daphnia magna): no data available
Fish: no data available
Other ecotoxicity data: No data available
PNEC derivation:
No PNEC can be calculated since there is no environmental toxicity data available
Environmental risk classification (PEC/PNEC ratio)
Calculation of a risk ratio is not possible, due to the lack of environmental toxicity data. Therefore, the following phrase is used "Risk of environmental impact of travoprost cannot be excluded, since there is not sufficient ecotoxicity data available. According to the European Medicines Agency guideline on environmental risk assessment of medicinal products (EMA/CHMP/SWP/4447/00), use of travoprost is unlikely to represent a risk for the environment, because the predicted environmental concentration (PEC) at the time of registration is below the action limit 0.01 μg/L."
Degradation
Biotic degradation
Ready degradability:
3-4%, not readily biodegradable (OECD301B) (Study No. 511319)
Justification of chosen degradation phrase:
As travoprost does not fulfil the criteria for ready biodegradability, the following phrase is used: Travoprost is potentially persistent.
Bioaccumulation
Partitioning coefficient:
logKow = 4.647 (OECD123) (TDOC-0018065)
Justification of chosen bioaccumulation phrase:
As the logKow exceeds the trigger level for a bioaccumlative substance (logKow > 4.0), the following statement is used for travoprost: Travoprost has high potential for bioaccumulation.
Excretion (metabolism)
Travoprost is hydrolyzed by esterases in the cornea to the biologically active form (travoprost free acid). Systemically, travoprost free acid is metabolized to inactive metabolites. Travoprost free acid is rapidly eliminated from plasma; plasma levels are below the limit of quantitation within one hour following ocular instillation. Less than 2% of the topical ocular dose is excreted in urine within 4 hours as travoprost free acid. (AHSF Drug Information, 2017)
PBT/vPvB assessment
Based on screening information, travoprost can be considered a potential PBT substance as the criteria for persistence are fulfilled, the octanol-water partition coefficient exceeds the trigger level for a bioaccumulative substance and travoprost is labeled as a category 2 reprotoxic substance.
References
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ECHA 2008, European Chemicals Agency. 2008 Guidance on information requirements and chemical safety assessment. http://guidance.echa.europa.eu/docs/guidance_document/information_requirements_en.htm
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EMA 2006, European Medicines Agency. European Medicines Agency guideline on environmental risk assessment of medicinal products (EMA/CHMP/SWP/4447/00). https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-environmental-risk-assessment-medicinal-products-human-use-first-version_en.pdf
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Study No. 511319. Determination of 'Ready' Biodegradability: Carbon Dioxide (CO2) Evolution Test (Modified Sturm Test) of TRAVOPROST. Final report: 31 October 2016.
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TDOC-0018065. Determination of Partitioning Coefficient (1-Octanol/Water) for Travoprost Using Slow-Stirring Method at 25°C According to OECD/OCDE 123. Final report: 26 June 2014.
AHSF Drug Information, 2017. Medicines Complete. Pharmaceutical Press.