제출 정보
이승준 (광주과학기술원)
이재영 (광주과학기술원)
초록
Acute kidney injury (AKI) often progresses to chronic kidney disease (CKD) due to complex pathophysiology involving reactive oxygen species (ROS) and renal fibrosis. We developed a multifunctional nanoplatform for kidney-specific targeting, ROS scavenging, and ROS-responsive anti-fibrotic drug release to prevent AKI-to-CKD transition. Hyaluronic acid (HA), targeting CD44 overexpressed in injured kidneys, was conjugated to reduced graphene oxide (rGO), an antioxidant and drug carrier, forming HA/rGO. Paricalcitol, an anti-fibrotic drug, was loaded onto HA/rGO and released under oxidative stress. HA/rGO showed strong antioxidant activity, protecting tubular cells from ROS-induced damage in vitro. In vivo, HA/rGO accumulated in ischemia/reperfusion (IR)-injured kidneys via HA-CD44 interaction, improved renal function, and reduced fibrosis in IR mouse models. This nanoplatform effectively mitigates AKI-to-CKD progression through targeted, ROS-responsive therapy.
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