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Microplastics are synthetic polymer particles measuring less than 5 millimeters in diameter, originating from the degradation of plastic waste or intentional manufacture for industrial and consumer products [1]. They are not biological targets, such as receptors or enzymes, but rather exogenous environmental contaminants that have been increasingly identified within human biological systems, including the bloodstream, lungs, and placenta [2]. Upon entry into the body via ingestion or inhalation, microplastics can trigger localized and systemic inflammatory responses and promote oxidative stress [4]. Recent clinical evidence has linked the presence of microplastics, such as polyethylene and polyvinyl chloride, within arterial plaques to an increased risk of myocardial infarction, stroke, and all-cause mortality [3]. Additionally, these particles can serve as carriers for toxic additives like phthalates and bisphenol A, which interfere with endocrine signaling [4]. Because they are not therapeutic targets, there are no drugs designed to interact with them; instead, medical interest focuses on their role as pathogenic drivers of chronic disease. The accumulation of these non-biodegradable materials in tissues poses a significant challenge for long-term human health and environmental safety. Research is currently focused on quantifying the threshold of toxicity and the specific mechanisms by which different polymer types interact with cellular membranes.
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