2022
DOI: 10.1002/anie.202217291
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Back Cover: An Enzymatically Gated Catalytic Hairpin Assembly Delivered by Lipid Nanoparticles for the Tumor‐Specific Activation of Signal Amplification in miRNA Imaging (Angew. Chem. Int. Ed. 51/2022)

Abstract: Tumor‐specific miRNA imaging is achieved through the integration of enzyme‐triggered catalytic hairpin assembly with lipid‐nanoparticle‐based delivery. The approach enables controlled activation of signal amplification in cancer cells with improved imaging contrast, as reported by Lele Li, Mengyuan Li, and co‐workers in their Research Article (e202214230).

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Cited by 47 publications
(17 citation statements)
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“…[28]; 18 from ref. [29]; This study provides P7 to P11 with excellent toughness and ductility. c Recycle of the polymers completed through two cycles: Cycle 1 via hydrolysis, esterification, and polymerization; Cycle 2 via methanolysis and polycondensation.…”
Section: Resultsmentioning
confidence: 91%
“…[28]; 18 from ref. [29]; This study provides P7 to P11 with excellent toughness and ductility. c Recycle of the polymers completed through two cycles: Cycle 1 via hydrolysis, esterification, and polymerization; Cycle 2 via methanolysis and polycondensation.…”
Section: Resultsmentioning
confidence: 91%
“…In addition to CaB, they also constructed an enzyme-regulated amplification strategy using the AP site-specific cleavage of APE1 as a molecular switch coupled with CHA signal amplification (Figure 1C-ii). 43 In this work, tumor-cell-specific miRNA amplified imaging in vivo with enhanced spatial accuracy was achieved. Wang's group 44 also used a similar strategy to achieve precise and amplified imaging of miR-21 in mice.…”
Section: Molecular Switchesmentioning
confidence: 98%
“…As a classical enzyme-free nucleic acid circuit amplication method, catalytic hairpin assembly (CHA) [19][20][21] achieves cyclic amplication of the target through toehold-mediated strand displacement [22][23][24] with simplicity and versatility, [25][26][27][28][29] which is one of the best candidates to achieve sensitive detection and versatility of APE1. Nevertheless, traditional CHA reactions relied on random collisions of reactants in a homogeneous solution with low collision efficiency and long reaction time, resulting in a low reaction rate and nonspecic background leakage, which limit further exploration and application of CHA.…”
Section: Introductionmentioning
confidence: 99%