Self-assembled vesicle and rod-like aggregates of functionalized perylene diimide: reaction-based near-IR intracellular fluorescent probe for selective detection of palladium. Issue 21 (5th May 2016)
- Record Type:
- Journal Article
- Title:
- Self-assembled vesicle and rod-like aggregates of functionalized perylene diimide: reaction-based near-IR intracellular fluorescent probe for selective detection of palladium. Issue 21 (5th May 2016)
- Main Title:
- Self-assembled vesicle and rod-like aggregates of functionalized perylene diimide: reaction-based near-IR intracellular fluorescent probe for selective detection of palladium
- Authors:
- Singh, Prabhpreet
Mittal, Lalit Singh
Vanita, Vanita
Kumar, Kapil
Walia, Amandeep
Bhargava, Gaurav
Kumar, Subodh - Abstract:
- Abstract : Aggregates ofPS-PDI after Pd 0 based depropargylation show de-aggregation and near-IR, ratiometric absorbance changes in water and live HeLa cells. Abstract : Herein, we report design, synthesis, and self-assembly of perylene diimide (PDI) based near-IR intracellular probe (PS-PDI ).PS-PDI molecules undergo aggregation to form self-assembled nanospheres and nanorods morphology in THF : H2 O (1 : 1) and DMSO : H2 O (1 : 9), respectively. The nanospheres have an open hole on surface reminiscent of vesicle structure (with a diameter of internal void in the range of 20–25 nm) whereas lengths of the nanorods extended up to few μm range. The Pd 0 based depropargylation leads to de-aggregation of thesePS-PDI aggregates into smaller spherical aggregates as evidenced by DLS, SEM, and TEM studies. Interestingly, these aggregates ofPS-PDI in solution show highly sensitive behavior in the presence of Pd 0 showing absorbance changes in NIR region ( λ max = 710 nm) and quenching of emission at λ em 630 nm (DMSO : H2 O, 1 : 9) with a limit of detection = 6.6 × 10 −9 M or at λ em 564 nm (THF : H2 O, 1 : 1) with limit of detection = 2.1 × 10 −8 M. Time and concentration dependent kinetics profiles ofPS-PDI aggregates revealed an impressive rate constant value of 0.4 s −1 and 0.21 s −1 (DMSO : H2 O, 1 : 9), respectively in fluorescence and UV-Vis spectroscopy using 2 × 10 −5 M concentration of Pd 0 .PS-PDI undergoes rapid internalization into HeLa cells with low cytotoxicity andAbstract : Aggregates ofPS-PDI after Pd 0 based depropargylation show de-aggregation and near-IR, ratiometric absorbance changes in water and live HeLa cells. Abstract : Herein, we report design, synthesis, and self-assembly of perylene diimide (PDI) based near-IR intracellular probe (PS-PDI ).PS-PDI molecules undergo aggregation to form self-assembled nanospheres and nanorods morphology in THF : H2 O (1 : 1) and DMSO : H2 O (1 : 9), respectively. The nanospheres have an open hole on surface reminiscent of vesicle structure (with a diameter of internal void in the range of 20–25 nm) whereas lengths of the nanorods extended up to few μm range. The Pd 0 based depropargylation leads to de-aggregation of thesePS-PDI aggregates into smaller spherical aggregates as evidenced by DLS, SEM, and TEM studies. Interestingly, these aggregates ofPS-PDI in solution show highly sensitive behavior in the presence of Pd 0 showing absorbance changes in NIR region ( λ max = 710 nm) and quenching of emission at λ em 630 nm (DMSO : H2 O, 1 : 9) with a limit of detection = 6.6 × 10 −9 M or at λ em 564 nm (THF : H2 O, 1 : 1) with limit of detection = 2.1 × 10 −8 M. Time and concentration dependent kinetics profiles ofPS-PDI aggregates revealed an impressive rate constant value of 0.4 s −1 and 0.21 s −1 (DMSO : H2 O, 1 : 9), respectively in fluorescence and UV-Vis spectroscopy using 2 × 10 −5 M concentration of Pd 0 .PS-PDI undergoes rapid internalization into HeLa cells with low cytotoxicity and was successfully used as an intracellular imaging reagent for Pd 0 in live HeLa cells. For practical applications, we exploited these nano-aggregates ofPS-PDI for estimation of Pd 2+ in the presence of a NaBH4 –PPh3 mixture, Pd 0 in drug and environmental samples, and Pd 2+ in urine samples with excellent selectivity and sensitivity. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 4:Issue 21(2016)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 4:Issue 21(2016)
- Issue Display:
- Volume 4, Issue 21 (2016)
- Year:
- 2016
- Volume:
- 4
- Issue:
- 21
- Issue Sort Value:
- 2016-0004-0021-0000
- Page Start:
- 3750
- Page End:
- 3759
- Publication Date:
- 2016-05-05
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Biomedical materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tb# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6tb00512h ↗
- Languages:
- English
- ISSNs:
- 2050-750X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205200
British Library DSC - BLDSS-3PM
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