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Application of targeted liposomes-based salvianolic acid A for the treatment of ischemic stroke

Mingyan Yang, Yu Liu, Ya-Wen Yu, Bai-Fang Gong, Jian Ruan, Huaying Fan

2024Neurotherapeutics12 citationsDOIOpen Access PDF

Abstract

Novel therapeutics for the treatment of ischemic stroke remains to be the unmet clinical needs. Previous studies have indicated that salvianolic acid A (SAA) is a promising candidate for the treatment of the brain diseases. However, SAA has poor absolute bioavailability and does not efficiently cross the intact blood-brain barrier (BBB), which limit its efficacy. To this end we developed a brain-targeted liposomes for transporting SAA via the BBB by incorporating the liposomes to a transport receptor, insulin-like growth factor-1 receptor (IGF1R). The liposomes were prepared by ammonium sulfate gradients loading method. The prepared SAA-loaded liposomes (Lipo/SAA) were modified with IGF1R monoclonal antibody to generate IGF1R antibody-conjugated Lipo/SAA (IGF1R-targeted Lipo/SAA). The penetration of IGF1R-targeted Lipo/SAA into the brain was confirmed by labeling with Texas Red, and their efficacy were evaluate using middle cerebral artery occlusion (MCAO) model. The results showed that IGF1R-targeted Lipo/SAA are capable of transporting SAA across the BBB into the brain, accumulation in brain tissue, and sustained releasing SAA for several hours. Administration o IGF1R-targeted Lipo/SAA notably reduced infarct size and neuronal damage, improved neurological function and inhibited cerebral inflammation, which had much higher efficiency than no-targeted SAA.

Topics & Concepts

LiposomeMedicineInsulin-like growth factor 1 receptorPharmacologyNeuroprotectionBioavailabilityBlood–brain barrierMonoclonal antibodyChemistryInternal medicineReceptorImmunologyAntibodyBiochemistryGrowth factorCentral nervous systemNanoparticle-Based Drug DeliveryNeuroinflammation and Neurodegeneration MechanismsTraditional Chinese Medicine Analysis