“…[277,278] Endogenous biomarkers, including small molecules, enzymes, cell receptors, and cytokines, are involved in the pathological process of CVD and can be exploited as stimuli to trigger in situ assembly/ disassembly of nanomaterials or as targets to guide the enrichment of nanomaterials in the lesion area. [279][280][281] These endogenous biomarker-responsive nanomaterials not only nicely circumvent the issues with CVD theranostics, such as off-target effects, short blood circulation, low bioavailability, poor solubility, and nonspecific distribution but also improve the targetability of drug delivery, accuracy of detection, imaging diagnostic capability and therapeutic outcome. In this review, we systematically and comprehensively summarized recent studies of various nanomaterials responsive to endogenous biomarkers (e.g., pH, ROS, lipids, enzymes, macrophage receptors, VSMC receptors, platelet receptors, inflammation and OPN) and their application in CVD theranostics, including diagnosis (e.g., FL Integration of diagnosis and treatment Real-time monitoring of treatment effect Difficulty in nanocarrier synthesis; preclinical [273,276] imaging, PA imaging, MR imaging, US imaging, multimodal imaging and POCT) and treatment (e.g., gene therapy, drug therapy, US-based therapy, optical therapy, synergistic therapy and integration of diagnosis and treatment).…”