PLGA公司
材料科学
荧光
光致发光
猝灭(荧光)
胶质瘤
量子点
钙钛矿(结构)
纳米晶
量子产额
生物物理学
纳米技术
色散(光学)
纳米颗粒
荧光寿命成像显微镜
化学
光电子学
癌症研究
生物
结晶学
光学
物理
作者
Dongdong Wu,Jimei Chi,Meng Zhang,Lijun Cheng,Xuning Wang,Junzhen Fan,Zengqi Huang,Huadong Wang,Hongfei Xie,Qi Pan,Zeying Zhang,Bingda Chen,Meng Su,Bainan Xu,Yanlin Song
标识
DOI:10.1002/adom.202101835
摘要
Abstract Real‐time in vitro detection of glioma cells facilitates precise tumor removal. However, the fluorescent labeling of tumor cells in clinical practice is limited by many factors, including the time consumed, low recognition efficiency, and fluorescence quenching. Here, a general strategy for building perovskite quantum dot (PQD)‐based biological probes utilizing the attraction between positive and negative electric charges is reported. Poly (lactic‐co‐glycolic acid) (PLGA) is chosen for encapsulating PQDs to completely prevent their aggregation, decomposition, or release in water or oxygen. The carboxyl group of PLGA has anchoring coordination with the PQDs, which reduces the surface defects. Moreover, it causes PQD‐based nanocrystals (P‐PNCs) to be surrounded by a positively charged layer in water. Given the specific recognition of chlorotoxin for the channels, rapid imaging of glioma cells is successfully performed in 15 min using P‐PNCs modified with chlorotoxin via charge attraction. The photoluminescence quantum yield of P‐PNC probes reached 87% and remained at 93% after 30 days of dispersion in water, while maintaining a much longer fluorescence lifetime of 15 µs. Therefore, this promising biological probe will be a general nanoplatform for identifying distinct cellular compartments using different biomarker imaging methods.
科研通智能强力驱动
Strongly Powered by AbleSci AI