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Photoacoustic imaging-guided, synchronously targeted thrombolysis and neuroprotection of acute ischemic stroke.


ABSTRACT: Acute ischemic stroke (AIS) is a major cause of disability and mortality worldwide, typically resulting from a thrombus that blocks cerebral blood flow. Current treatments focus on thrombolysis and neuroprotection, with recombinant tissue plasminogen activator (rt-PA) and edaravone (Eda) as key drugs. However, their therapeutic efficacy is constrained by poor targeting, leading to suboptimal drug delivery to the brain. Herein, we develop a biomimetic delivery system (PLEA, platelet membrane-liposome hybrid delivery system encapsulating Eda and rt-PA) by hybridizing platelet membranes with liposomes, leveraging natural thrombus-targeting ability of the platelet membrane to enhance drug delivery efficiency. PLEA effectively targeted thrombus sites, synchronously enhancing thrombolysis and providing neuroprotection in a mouse model of AIS. Photoacoustic (PA) imaging was used to monitor clot formation and assess changes in intracranial blood flow and oxygen levels. These findings indicate that PA imaging-guided PLEA treatment represents a promising approach for precise stroke treatment.

SUBMITTER: Han M 

PROVIDER: S-EPMC12907673 | biostudies-literature | 2026 Feb

REPOSITORIES: biostudies-literature

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Photoacoustic imaging-guided, synchronously targeted thrombolysis and neuroprotection of acute ischemic stroke.

Han Mengtao M   Zhong Haoming H   Zhang Yuling Y   Zhang Min M   Ren Yaguang Y   Xu Zhiqiang Z   Ling Lu L   Xue Zhiwei Z   He Yiming Y   Liu Chengbo C   Tan Yizhou Y   Zhang Lingyan L   Chen Jingqin J   Wang Donghai D  

iScience 20260122 2


Acute ischemic stroke (AIS) is a major cause of disability and mortality worldwide, typically resulting from a thrombus that blocks cerebral blood flow. Current treatments focus on thrombolysis and neuroprotection, with recombinant tissue plasminogen activator (rt-PA) and edaravone (Eda) as key drugs. However, their therapeutic efficacy is constrained by poor targeting, leading to suboptimal drug delivery to the brain. Herein, we develop a biomimetic delivery system (PLEA, platelet membrane-lipo  ...[more]

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