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Sorption of three common nonsteroidal anti-inflammatory drugs (NSAIDs) to microplastics

The Science of The Total Environment 2020 178 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Armando Elizalde‐Velázquez, Seenivasan Subbiah, Todd A. Anderson, Micah J. Green, Xiaofei Zhao, Jaclyn E. Cañas‐Carrell

Summary

This study investigated the adsorption of three common nonsteroidal anti-inflammatory drugs (NSAIDs) onto microplastics, finding that polymer type, drug properties, and environmental conditions all influenced sorption capacity. The results suggest microplastics can act as vectors for pharmaceutical contaminants in aquatic environments.

Body Systems

High disposability, high durability, and indiscriminate use have led to the accumulation of plastics at uncontrolled rates in the environment. However, plastics are not the only source of water pollution in the environment. Nonsteroidal anti-inflammatory drugs (NSAIDs) are a group of pharmaceuticals widely and highly consumed in the market due to a low price and over-the-counter accessibility. NSAIDs are frequently detected in surface water environments at μg L concentrations. In the present study, the sorption behavior of three NSAIDs (ibuprofen, naproxen, diclofenac) was examined with four types of microplastics (polystyrene (PS), ultra-high molecular weight polyethylene (UHMWPE), average molecular weight medium density polyethylene (AMWPE), and polypropylene (PP)), under varying water conditions. Low sorption occurred between NSAIDs and microplastics under environmentally relevant conditions. The sorption process exhibited a pronounced pH dependency due to the effect of pH on the speciation of the compounds and the surface charge of the particles. Only under acidic conditions (pH: 2), NSAIDs were highly sorbed onto microplastics mainly ruled by hydrophobic interactions. Among NSAIDs tested, diclofenac exhibited the highest sorption coefficients to microplastics. Polyethylene particles exhibited the highest affinity for NSAIDs.

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