| Literature DB >> 30680812 |
Zhendong Lei1,2, Lin Ding1, Chenjie Yao1,3, Fengfeng Mo4, Chenchen Li1, Yanan Huang1, Xuelian Yin1, Min Li4, Jinliang Liu1, Yong Zhang1,2, Changquan Ling5, Yanli Wang1,3.
Abstract
Efficient tumor targeting has been a great challenge in the clinic for a very long time. The traditional targeting methods based on enhanced permeability and retention (EPR) effects show only an ≈5% targeting rate. To solve this problem, a new graphene-based tumor cell nuclear targeting fluorescent nanoprobe (GTTN), with a new tumor-targeting mechanism, is developed. GTTN is a graphene-like single-crystalline structure amphiphilic fluorescent probe with a periphery that is functionalized by sulfonic and hydroxyl groups. This probe has the characteristic of specific tumor cell targeting, as it can directly cross the cell membrane and specifically target to the tumor cell nucleus by the changed permeability of the tumor cell membranes in the tumor tissue. This new targeting mechanism is named the cell membrane permeability targeting (CMPT) mechanism, which is very different from the EPR effect. These probes can recognize tumor tissue at a very early stage and track the invasion and metastasis of tumor cells at the single cell level. The tumor-targeting rate is improved from less than 5% to more than 50%. This achievement in efficient and accurate tumor cell targeting will speed up the arrival of a new era of tumor diagnosis and treatment.Entities:
Keywords: cell membrane permeability; fluorescent nanoprobes; tumor cell nuclear targeting
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Year: 2019 PMID: 30680812 DOI: 10.1002/adma.201807456
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849