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Technically, LBNP-PC@M addresses the core limitations of current PE therapies by utilizing cell membrane hybridization to preserve key biological properties of trophoblast cells: this design not only mitigates maternal immune clearance but also significantly enhances placental accumulationproperties that could be extended to other placental disorders (e.g., fetal growth restriction, placental abruption) requiring targeted drug delivery

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This makes the brain more susceptible to both Parkinsons disease and damage following stroke or other insult[11]