New methylene blue analogues with N-piperidinyl-carbinol units: Synthesis, optical properties and in vitro internalization in human ovarian cancer cells. (September 2022)
- Record Type:
- Journal Article
- Title:
- New methylene blue analogues with N-piperidinyl-carbinol units: Synthesis, optical properties and in vitro internalization in human ovarian cancer cells. (September 2022)
- Main Title:
- New methylene blue analogues with N-piperidinyl-carbinol units: Synthesis, optical properties and in vitro internalization in human ovarian cancer cells
- Authors:
- Stoean, Bianca
Gaina, Luiza
Cristea, Castelia
Silaghi-Dumitrescu, Radu
Branzanic, Adrian M.V.
Focsan, Monica
Fischer-Fodor, Eva
Tigu, Bogdan
Moldovan, Cristian
Cecan, Andra Diana
Achimas-Cadariu, Patriciu
Astilean, Simion
Silaghi-Dumitrescu, Luminita - Abstract:
- Abstract: In this work, two new phenothiazinium dyes containing N -piperidinyl-carbinol auxochrome units have been designed, synthesized and investigated in vitro for ovarian cancer cell fluorescence imaging and cytotoxicity. A solvent free mechanochemical procedure is described as a greener alternative to the previously reported synthetic methodology applied in the preparation of methylene blue analogues by the substitution of the phenothiazinium tetraiodide substrate with nucleophilic secondary amines in solution. The optical properties of the new dyes were evaluated by UV–vis absorption/emission spectroscopy which revealed maxima situated in the red region (λmax absorption = 668-664 nm and λmax emission = 715-698 nm) with large molar extinction coefficients (log ε = 4.5–5.1) and bathochromic shifts of 314–383 cm −1 occurring upon switching from less polar to more polar solvents. The theoretical DFT computational study performed in order to clarify the obtained data indicated that the vertical TD-DFT calculations (typically applied for simulating UV–vis spectra) were within ∼150 nm of the experimental data, but a better agreement with experiment was obtained by using the vibronic corrections which revealed a dominant vibronic component not only for the main absorption/emission maxima, but also for the displayed shoulders which are rather the effects of the vibronic coupling between S0 and S1 electronic states. The new dyes presented a hydrophilic character (logP nAbstract: In this work, two new phenothiazinium dyes containing N -piperidinyl-carbinol auxochrome units have been designed, synthesized and investigated in vitro for ovarian cancer cell fluorescence imaging and cytotoxicity. A solvent free mechanochemical procedure is described as a greener alternative to the previously reported synthetic methodology applied in the preparation of methylene blue analogues by the substitution of the phenothiazinium tetraiodide substrate with nucleophilic secondary amines in solution. The optical properties of the new dyes were evaluated by UV–vis absorption/emission spectroscopy which revealed maxima situated in the red region (λmax absorption = 668-664 nm and λmax emission = 715-698 nm) with large molar extinction coefficients (log ε = 4.5–5.1) and bathochromic shifts of 314–383 cm −1 occurring upon switching from less polar to more polar solvents. The theoretical DFT computational study performed in order to clarify the obtained data indicated that the vertical TD-DFT calculations (typically applied for simulating UV–vis spectra) were within ∼150 nm of the experimental data, but a better agreement with experiment was obtained by using the vibronic corrections which revealed a dominant vibronic component not only for the main absorption/emission maxima, but also for the displayed shoulders which are rather the effects of the vibronic coupling between S0 and S1 electronic states. The new dyes presented a hydrophilic character (logP n -octanol/water = −1.15 and −1.29 respectively) comparable to the parent methylene blue and no aggregation tendency was observed in aqueous solution at concentration range 75–150 μM used in this study. Cellular imaging experiments displayed the new dyes' ability to selectively stain the cytoplasm of tumoral OVCAR-3 and A2780 fixed cells. The evaluation of their biological activity encompassed cell grow inhibitory potential (dose-response activity and half maximal inhibitory concentration IC50 ), as well as their capacity to influence the tumoral OVCAR-3, A2780 and healthy BJ ovarian cells' metabolic activity. Dye 2 exhibited moderate cytotoxicity against human ovarian cancer cell lines, being the most active against the A2780 ovarian adenocarcinoma cells where its cellular uptake was noteworthy and displayed a deeper influence on the chemoresistant, highly malignant OVCAR-3 cells function by modulating FOLR1, ICAM-1 and VCAM-1 proteins with role in the growth and migration of cancer cells. Graphical abstract: Image 1 Highlights: New symmetrical Phenothiazinium dyes containing N-piperidinyl-carbinol auxochrome. Solvent free mechanochemical procedure for the synthesis of MB analogues. Optical properties enlightened by theoretical TD-DFT calculations with vibronic correction. In vitro cytoplasmatic accumulation and staining of ovarian tumor cell lines. Cytotoxicity and multitarget influence on ovarian tumor cell's functions. … (more)
- Is Part Of:
- Dyes and pigments. Volume 205(2022)
- Journal:
- Dyes and pigments
- Issue:
- Volume 205(2022)
- Issue Display:
- Volume 205, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 205
- Issue:
- 2022
- Issue Sort Value:
- 2022-0205-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-09
- Subjects:
- Methylene blue -- Phenothiazinium dyes -- Fluorescence emission -- Cellular imaging -- Cytotoxicity
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2022.110460 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22761.xml