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Visualization of drug delivery processes using AIEgens
Youyong Yuan1, Bin Liu1,2
1Department of Chemical and Biomolecular Engineering , National University of Singapore , 4 Engineering Drive 4 , Singapore 117585 .
Abstract:
Drug delivery systems (DDSs) have been extensively studied as carriers to deliver small molecule chemo-drugs to tumors for cancer therapy. The therapeutic efficiency of chemo-drugs is crucially dependent on the effective drug concentrations in tumors and cancer cells. Novel DDSs that can simultaneously unveil drug distribution, drug release/activation behaviors and offer early evaluation of their therapeutic responses are highly desirable. Traditional fluorescent dye-labeled DDSs may suffer from notorious aggregation-caused quenching (ACQ) with limited sensitivity for bioimaging; in addition, the intrinsic fluorescence of these dyes requires careful selection of energy acceptor or quencher moieties for a light-up probe design, which complicates the development of self-reporting DDSs, especially the ones for reporting multiple processes. The recently emerged fluorogens with aggregation-induced emission characteristics (AIEgens) offer a straightforward solution to tackle this challenge. Thanks to the unique properties of AIEgens, new theranostic DDSs have been developed for simultaneous drug delivery and bioimaging with high signal to background ratio and multiple signal reporting capabilities. In this mini-review, we summarize the recent development of theranostic DDSs based on AIEgens for monitoring the drug distribution, drug activation and prediction of the therapeutic responses. Through illustration of their design principles and application examples, we hope to stimulate the interest in the design of more advanced theranostic DDSs for biomedical research.
Insights
Aggregation-induced emission (AIEgens) enable advanced theranostic drug delivery systems (DDSs) for cancer therapy. These systems allow simultaneous drug delivery, bioimaging, and prediction of therapeutic responses, overcoming limitations of traditional fluorescent probes.
Area of Science:
- Biomedical Engineering
- Materials Science
- Nanotechnology
Background:
- Traditional fluorescent dye-labeled drug delivery systems (DDSs) for cancer therapy face challenges like aggregation-caused quenching (ACQ) and limited sensitivity in bioimaging.
- Developing self-reporting DDSs that monitor drug distribution, release, and therapeutic response simultaneously is crucial for effective cancer treatment.
- Existing fluorescent probes often require complex designs for multi-process reporting, hindering the development of advanced theranostic tools.
Purpose of the Study:
- To review recent advancements in theranostic DDSs utilizing aggregation-induced emission characteristics (AIEgens).
- To highlight the design principles and applications of AIEgen-based DDSs for monitoring drug delivery and therapeutic outcomes.
- To encourage the development of sophisticated theranostic DDSs for enhanced cancer therapy and biomedical research.
Main Methods:
- Review of literature on theranostic DDSs incorporating AIEgens.
- Analysis of design strategies for AIEgen-based probes enabling simultaneous bioimaging and drug delivery.
- Examination of AIEgen properties for monitoring drug distribution, activation, and predicting therapeutic responses.
Main Results:
- AIEgens offer a solution to ACQ, enabling high signal-to-background ratio bioimaging for DDSs.
- AIEgen-based theranostic DDSs facilitate simultaneous monitoring of drug distribution and release kinetics.
- These novel DDSs show promise in predicting therapeutic responses, improving cancer treatment efficacy.
Conclusions:
- AIEgens are powerful tools for developing advanced theranostic DDSs with multiple reporting capabilities.
- AIEgen-based DDSs significantly enhance the sensitivity and functionality of cancer theranostics.
- Further research into AIEgen-based DDSs is expected to drive innovation in personalized cancer therapy.
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