Intrarenal pH-Responsive Self-Assembly of Luminescent Gold Nanoparticles for Diagnosis of Early Kidney Injury.
Zhipeng ZhaoKui HeBen LiuWenyan NieXiaoxi LuoJinbin LiuPublished in: Angewandte Chemie (International ed. in English) (2024)
Metabolic acidosis-induced kidney injury (MAKI) is asymptomatic and lack of clinical biomarkers in early stage, but rapidly progresses to severe renal fibrosis and ultimately results in end-stage kidney failure. Therefore, developing rapid and noninvasive strategies direct responsive to renal tubular acidic microenvironment rather than delayed biomarkers are essential for timely renoprotective interventions. Herein, we develop pH-responsive luminescent gold nanoparticles (p-AuNPs) in the second near-infrared emission co-coated with 2,3-dimethylaleic anhydride conjugated β-mercaptoethylamine and cationic 2-diethylaminoethanethiol hydrochloride, which showed sensitive pH-induced charge reversal and intrarenal self-assembly for highly sensitive and long-time (~24 h) imaging of different stages of MAKI. By integrating advantages of pH-induced intrarenal self-assembly and enhanced interactions between pH-triggered positively charged p-AuNPs and renal tubular cells, the early- and late-stage MAKI could be differentiated rapidly within 10 min post-injection (p.i.) with contrast index (CI) of 3.5 and 4.3, respectively. The corresponding maximum CI could reach 5.1 and 9.2 at 12 h p.i., respectively. Furthermore, p-AuNPs were demonstrated to effectively real-time monitor progressive recovery of kidney injury in MAKI mice after therapy, and also exhibit outstanding capabilities for drug screening. This pH-responsive strategy showed great promise for feedback on kidney dysfunction progression, opening new possibilities for early-stage diagnosis of pH-related diseases.
Keyphrases
- living cells
- gold nanoparticles
- high glucose
- early stage
- diabetic rats
- drug induced
- endothelial cells
- quantum dots
- multiple sclerosis
- emergency department
- oxidative stress
- magnetic resonance
- radiation therapy
- early onset
- sensitive detection
- cell death
- photodynamic therapy
- reduced graphene oxide
- magnetic resonance imaging
- adipose tissue
- cell proliferation
- bone marrow
- computed tomography
- locally advanced
- drug delivery
- signaling pathway
- endoplasmic reticulum stress
- rectal cancer