journal article·2017-08-30

Environment Activatable Nanoprodrug: Two-Step Surveillance in the Anticancer Drug Release

Sandipan Biswas, Joyjyoti Das, Shrabani Barman, Bhaskara Rao Pinninti, Tapas K. Maiti, N. D. Pradeep Singh

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Abstract

Remedial cancer therapy deals with a large number of theranostic applications. However, systems, so far known, are only capable of single surveillance for both diagnostic and therapeutic modes of action. A nanosystem, which can be localized to the cancer and deliver the chemotherapeutic agent on demand, will provide effective therapeutic activity. Herein, we designed a single component nanoprodrug ANPD-X (Activatable Nano Pro-Drug-X) which indentified the tumor sites by fluorescent color change (signal 1, blue to green fluorescence) using H 2 O 2 -mediated oxidation of boronate fluorophore. In the next step, precise spatiotemporal irradiation of light only on identified tumor sites resulted in the release of anticancer drug chlorambucil. The real time information on drug release was achieved by a second fluorescence color change (signal 2, green to blue fluorescence). Thus, nanoprodrug ANPD-X provided overall two-step surveillance in the anticancer drug delivery. Activation of the ANPD-X after addition of H 2 O 2 and drug release upon photoirradiation was investigated in vitro by monitoring its fluorescence in the HeLa cell line.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Luminescence and Fluorescent Materials · Advanced biosensing and bioanalysis techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry and ‡Department of Biotechnology, Indian Institute of Technology, Kharagpur 721302, West Bengal, India

Funding

University Grants Commission · Science and Engineering Research Board

References (26)

Show source-provided references
1. 10.1021/bm400257410.1021/bm4002574 ↗
2. 10.1038/ncomms790710.1038/ncomms7907 ↗
3. 10.1002/adma.20120445510.1002/adma.201204455 ↗
4. 10.1002/adhm.20120042310.1002/adhm.201200423 ↗
5. 10.1021/am400572b10.1021/am400572b ↗
6. 10.1021/acs.macromol.5b0170910.1021/acs.macromol.5b01709 ↗
7. 10.1021/acsami.6b0160210.1021/acsami.6b01602 ↗
8. 10.1039/C5CC04087F10.1039/C5CC04087F ↗
9. Szatrowski T. P. · Cancer Res. · 1991 · 51 · 794
10. 10.1021/jm401349g10.1021/jm401349g ↗
11. 10.1186/1477-7819-11-910.1186/1477-7819-11-9 ↗
12. 10.1016/j.canlet.2008.12.01110.1016/j.canlet.2008.12.011 ↗
13. 10.1016/j.ccr.2006.08.01510.1016/j.ccr.2006.08.015 ↗
14. 10.1038/nrd280310.1038/nrd2803 ↗
15. 10.1021/ja207382410.1021/ja2073824 ↗
16. 10.1021/ja507768410.1021/ja5077684 ↗
17. 10.1021/ja510421q10.1021/ja510421q ↗
18. 10.1021/ja302482k10.1021/ja302482k ↗
19. 10.1016/j.snb.2017.01.00810.1016/j.snb.2017.01.008 ↗
20. 10.1039/C4TB01583E10.1039/C4TB01583E ↗
21. 10.1039/c3cc46078a10.1039/c3cc46078a ↗
22. 10.1039/C5TB02045J10.1039/C5TB02045J ↗
23. 10.1002/anie.20150890110.1002/anie.201508901 ↗
24. 10.1021/acs.bioconjchem.6b0043710.1021/acs.bioconjchem.6b00437 ↗
25. 10.1021/bc050050z10.1021/bc050050z ↗
26. 10.1021/ol400084510.1021/ol4000845 ↗