journal article·2014-05-28

1-Acetylpyrene–Salicylic Acid: Photoresponsive Fluorescent Organic Nanoparticles for the Regulated Release of a Natural Antimicrobial Compound, Salicylic Acid

Shrabani Barman, Sourav K. Mukhopadhyay, Krishna Kalyani Behara, Satyahari Dey, N. D. Pradeep Singh

Publisher page

Abstract

Photoresponsive 1-acetylpyrene-salicylic acid (AcPy-SA) nanoparticles (NPs) were developed for the regulated release of a natural antimicrobial compound, salicylic acid. The strong fluorescent properties of AcPy-SA NPs have been extensively used for potential in vitro cell imaging. The phototrigger capability of our newly prepared AcPy-SA NPs was utilized for the efficient release of an antimicrobial compound, salicylic acid. The photoregulated drug release of AcPy-SA NPs has been shown by the subsequent switching off and on of a visible-light source. In vitro biological studies reveal that AcPy-SA NPs of ∼68 nm size deliver the antimicrobial drug salicylic acid into the bacteria cells (Pseudomonas aeruginosa) and efficiently kill the cells upon exposure to visible light (≥410 nm). Such photoresponsive fluorescent organic NPs will be highly beneficial for targeted and regulated antimicrobial drug release because of their biocompatible nature, efficient cellular uptake, and light-induced drug release ability.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Antimicrobial Peptides and Activities · Polydiacetylene-based materials and applications

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

References (39)

Show source-provided references
1. Gristina A. G. · Int. J. Artif. Organs · 1993 · 16 · 75510.1177/039139889301601103 ↗
2. Lungren M. P. · Bacteriophage · 2013 · 3 · e2682510.4161/bact.26825 ↗
3. Litzler P. Y. · J. Thorac. Cardiovasc. Surg. · 2007 · 134 · 102510.1016/j.jtcvs.2007.06.013 ↗
4. Trautner B. W. · Am. J. Infect. Control · 2004 · 32 · 11710.1016/j.ajic.2003.08.005 ↗
5. Segev G. · J. Vet. Int. Med. · 2013 · 27 · 3910.1111/j.1939-1676.2012.01027.x ↗
6. Frank D. N. · PLoS One · 2009 · 4 · e781110.1371/journal.pone.0007811 ↗
7. Fux C. A. · Clin. Microbiol. Infect. · 2006 · 12 · 33110.1111/j.1469-0691.2006.01361.x ↗
8. Imamura Y. · Antimicrob. Agents Chemother. · 2008 · 52 · 17110.1128/AAC.00387-07 ↗
9. Wu Y. T. · Invest. Ophthalmol. Visual Sci. · 2010 · 51 · 632910.1167/iovs.10-5796 ↗
10. Wiley L. · Invest. Ophthalmol. Visual Sci. · 2012 · 53 · 389610.1167/iovs.11-8762 ↗
11. Abidi S. H. · BMC Ophthalmol. · 2013 · 13 · 5710.1186/1471-2415-13-57 ↗
12. Passerini L. · Crit. Care Med. · 1992 · 20 · 66510.1097/00003246-199205000-00020 ↗
13. Strachan C. J. · J. Hosp. Infect. · 1995 · 30 · 5410.1016/0195-6701(95)90006-3 ↗
14. Whitchurch C. B. · Science · 2002 · 295 · 148710.1126/science.295.5559.1487 ↗
15. Knezevic N. Z. · Chem. Commun. · 2011 · 47 · 281710.1039/c0cc04424e ↗
16. Norman R.S. · Nano Lett. · 2008 · 8 · 30210.1021/nl0727056 ↗
17. Parelshtein I. · J. Mater. Chem. B · 2013 · 1 · 196810.1039/c3tb00555k ↗
18. Wang L. · Bioconjugate Chem. · 2007 · 18 · 29710.1021/bc060255n ↗
19. Ghosh S. · RSC Adv. · 2012 · 2 · 93010.1039/C1RA00815C ↗
20. Agasti S. S. · J. Am. Chem. Soc. · 2009 · 131 · 572810.1021/ja900591t ↗
21. Angelos S. · J. Am. Chem. Soc. · 2009 · 131 · 1134410.1021/ja9042752 ↗
22. Zhu Y. · Angew. Chem., Int. Ed. · 2007 · 46 · 224110.1002/anie.200604850 ↗
23. Lin Q. · J. Am. Chem. Soc. · 2010 · 132 · 1064510.1021/ja103415t ↗
24. Lv C. · Langmuir · 2012 · 28 · 938710.1021/la301534h ↗
25. Viger M. L. · Adv. Mater. · 2013 · 25 · 373310.1002/adma.201300902 ↗
26. Yan B. · J. Am. Chem. Soc. · 2012 · 134 · 1655810.1021/ja308876j ↗
27. Knezevic N. Z. · Chem.—Eur. J. · 2011 · 17 · 333810.1002/chem.201002960 ↗
28. Karthik S. · ACS Appl. Mater. Interfaces · 2013 · 5 · 523210.1021/am401059k ↗
29. Karthik S. · Chem. Commun. · 2013 · 49 · 1047110.1039/c3cc46078a ↗
30. Liu G. · Biomacromolecules · 2012 · 13 · 157310.1021/bm300304t ↗
31. Liu Y. C. · Langmuir · 2009 · 25 · 571310.1021/la803588d ↗
32. Mizukami S. · J. Am. Chem. Soc. · 2010 · 132 · 952410.1021/ja102167m ↗
33. Jana A. · J. Am. Chem. Soc. · 2012 · 134 · 765610.1021/ja302482k ↗
34. Halim V. A. · Mol. Plant–Microbe Interact. · 2007 · 20 · 134610.1094/MPMI-20-11-1346 ↗
35. Polonio R. E. · Antimicrob. Agents Chemother. · 2001 · 45 · 326210.1128/AAC.45.11.3262-3266.2001 ↗
36. Kupferwasser L. I. · J. Clin. Invest. · 2003 · 112 · 22210.1172/JCI200316876 ↗
37. Wiegand I. · Nat. Protoc. · 2008 · 3 · 16310.1038/nprot.2007.521 ↗
38. Bauer A. W. · Am. J. Clin. Pathol. · 1966 · 45 · 49310.1093/ajcp/45.4_ts.493 ↗
39. Brayner R. · Nano Lett. · 2006 · 6 · 86610.1021/nl052326h ↗