锰
体内
材料科学
基质金属蛋白酶
配体(生物化学)
生物物理学
化学
生物化学
受体
生物
生物技术
冶金
作者
Hongyu Zhang,Panpan Chen,Wenxiong Shi,Aihua Qu,Maozhong Sun,Hua Kuang
标识
DOI:10.1002/adma.202415656
摘要
Abstract In this study, polypeptide TGGGPLGVARGKGGC‐induced chiral manganese dioxide supraparticles (MnO 2 SPs) are prepared for sensitive quantification of matrix metalloproteinase‐9 (MMP‐9) in vitro and in vivo. The results show that L ‐type manganese dioxide supraparticles ( L ‐MnO 2 SPs) exhibited twice the affinity for the cancer cell membrane receptor CD47 (cluster of differentiation, integrin‐associated protein) than D ‐type manganese dioxide supraparticles ( D ‐MnO 2 SPs) to accumulate at the tumor site after surface modification of the internalizing arginine‐glycine‐aspartic acid (iRGD) ligand, specifically reacting with the MMP‐9, disassembling into ultrasmall nanoparticles (NPs), and efficiently underwent renal clearance. Furthermore, L ‐MnO 2 facilitates the quantification of MMP‐9 in mouse tumor xenografts, as demonstrated by circular dichroism (CD) and magnetic resonance imaging (MRI) within 2 h. A strong linear relationship is observed between MMP‐9 concentration and both CD and MRI intensity, ranging from 0.01 to 10 ng mL −1 . The corresponding limits of detection (LOD) are 0.0054 ng mL −1 for CD and 0.0062 ng mL −1 for MRI, respectively. hese SPs provide a new approach for exploring chiral advanced biosensors for early diagnosis of cancer.
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