Please use this identifier to cite or link to this item:
https://doi.org/10.1002/adfm.201502728
DC Field | Value | |
---|---|---|
dc.title | Light-Up Probe for Targeted and Activatable Photodynamic Therapy with Real-Time In Situ Reporting of Sensitizer Activation and Therapeutic Responses | |
dc.contributor.author | YUAN YOUYONG | |
dc.contributor.author | Zhang Chongjing | |
dc.contributor.author | Kwok, Ryan TK | |
dc.contributor.author | XU SHIDANG | |
dc.contributor.author | ZHANG RUOYU | |
dc.contributor.author | WU JI'EN | |
dc.contributor.author | Tang, Ben Zhong | |
dc.contributor.author | LIU BIN | |
dc.date.accessioned | 2020-06-11T02:22:38Z | |
dc.date.available | 2020-06-11T02:22:38Z | |
dc.date.issued | 2015-11-11 | |
dc.identifier.citation | YUAN YOUYONG, Zhang Chongjing, Kwok, Ryan TK, XU SHIDANG, ZHANG RUOYU, WU JI'EN, Tang, Ben Zhong, LIU BIN (2015-11-11). Light-Up Probe for Targeted and Activatable Photodynamic Therapy with Real-Time In Situ Reporting of Sensitizer Activation and Therapeutic Responses. Advanced Functional Materials 25 (42) : 6586-6595. ScholarBank@NUS Repository. https://doi.org/10.1002/adfm.201502728 | |
dc.identifier.issn | 1616-301X | |
dc.identifier.issn | 1616-3028 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/169648 | |
dc.description.abstract | Integrated systems that offer traceable cancer therapy are highly desirable for personalized medicine. Herein, a probe is reported that is composed of a red-emissive photosensitizer (PS) with aggregation-induced emission characteristics and a built-in apoptosis sensor with activatable green emission for targeted cancer cell ablation and real-time monitoring of PS activation and therapeutic response. The probe is nonemissive in aqueous media and can be selectively uptaken by αvβ3 integrin overexpressed cancer cells. Cleavage of the probe by intracellular glutathione leads to release of the apoptosis sensor and red fluorescence turn-on to report the PS activation. Upon light irradiation, the PS can generate reactive oxygen species to induce cell apoptosis and activate caspase-3/-7, which will cleave the apoptosis sensor to yield intense green fluorescence. Both the red and green emission can be obtained through a single wavelength excitation, which makes the probe very convenient for therapeutic protocol development. A novel light-up probe is developed for targeted and activatable photodynamic therapy with real-time in situ reporting of sensitizer activation and therapeutic responses. | |
dc.language.iso | en | |
dc.publisher | Wiley-VCH Verlag | |
dc.source | Elements | |
dc.subject | Science & Technology | |
dc.subject | Physical Sciences | |
dc.subject | Technology | |
dc.subject | Chemistry, Multidisciplinary | |
dc.subject | Chemistry, Physical | |
dc.subject | Nanoscience & Nanotechnology | |
dc.subject | Materials Science, Multidisciplinary | |
dc.subject | Physics, Applied | |
dc.subject | Physics, Condensed Matter | |
dc.subject | Chemistry | |
dc.subject | Science & Technology - Other Topics | |
dc.subject | Materials Science | |
dc.subject | Physics | |
dc.subject | AGGREGATION-INDUCED-EMISSION | |
dc.subject | NEAR-INFRARED LIGHT | |
dc.subject | REACTIVE OXYGEN | |
dc.subject | CANCER-THERAPY | |
dc.subject | MAGNETIC-RESONANCE | |
dc.subject | INDUCED APOPTOSIS | |
dc.subject | SINGLET OXYGEN | |
dc.subject | DRUG-DELIVERY | |
dc.subject | FAR-RED | |
dc.subject | NANOPARTICLES | |
dc.type | Article | |
dc.date.updated | 2020-06-10T08:19:14Z | |
dc.contributor.department | CHEMICAL & BIOMOLECULAR ENGINEERING | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1002/adfm.201502728 | |
dc.description.sourcetitle | Advanced Functional Materials | |
dc.description.volume | 25 | |
dc.description.issue | 42 | |
dc.description.page | 6586-6595 | |
dc.published.state | Published | |
Appears in Collections: | Staff Publications Elements |
Show simple item record
Files in This Item:
File | Description | Size | Format | Access Settings | Version | |
---|---|---|---|---|---|---|
adfm201502728.docx | Accepted version | 35.04 MB | Microsoft Word XML | OPEN | Post-print | View/Download |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.