11 research outputs found

    New way to create high-speed LCDs based on the use of modified nanomaterials

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    Modified β€œdetonation nanodiamond” (MDND), graphene oxide (MGO) and nanoclay (MNC) were doped to nematic (NLCs) and ferroelectric liquid crystals (FLCs). The effect of modified nanomaterials on the physical and electro-optical properties of liquid crystals was investigated

    ΠžΠŸΠ’Π˜Π§Π•Π‘ΠšΠ˜Π• Π‘Π’ΠžΠ™Π‘Π’Π’Π ΠšΠžΠœΠŸΠ›Π•ΠšΠ‘ΠžΠ’ Π£Π›Π¬Π’Π ΠΠ”Π˜Π‘ΠŸΠ•Π Π‘ΠΠ«Π₯ ΠΠ›ΠœΠΠ—ΠžΠ’ Π”Π•Π’ΠžΠΠΠ¦Π˜ΠžΠΠΠžΠ“Πž Π‘Π˜ΠΠ’Π•Π—Π Π‘ Π˜ΠΠ”ΠžΠ’Π Π˜ΠšΠΠ Π‘ΠžΠ¦Π˜ΠΠΠ˜ΠΠžΠ’Π«Πœ ΠšΠ ΠΠ‘Π˜Π’Π•Π›Π•Πœ

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    A method to create complexes of detonation nanodiamonds with molecules of an indotricarbocyanine dye was developed. The process of complex formation was shown to depend on the nanodiamond annealing conditions. Nanodiamonds that were vacuum annealed at 750oC display the most effective interaction with the dye molecules. Formation of the complexes was studied with the aid of optical spectroscopy in the visible and infrared regions.Π Π°Π·Ρ€Π°Π±ΠΎΡ‚Π°Π½ ΠΌΠ΅Ρ‚ΠΎΠ΄ получСния комплСксов ΡƒΠ»ΡŒΡ‚Ρ€Π°Π΄ΠΈΡΠΏΠ΅Ρ€ΡΠ½Ρ‹Ρ… Π°Π»ΠΌΠ°Π·ΠΎΠ² Π΄Π΅Ρ‚ΠΎΠ½Π°Ρ†ΠΈΠΎΠ½Π½ΠΎΠ³ΠΎ синтСза с ΠΌΠΎΠ»Π΅ΠΊΡƒΠ»Π°ΠΌΠΈ ΠΈΠ½Π΄ΠΎΡ‚Ρ€ΠΈΠΊΠ°Ρ€Π±ΠΎΡ†ΠΈΠ°Π½ΠΈΠ½ΠΎΠ²ΠΎΠ³ΠΎ краситСля. Показано, Ρ‡Ρ‚ΠΎ Π½Π° процСсс комплСксообразования Π²Π»ΠΈΡΡŽΡ‚ условия тСрмичСской ΠΎΠ±Ρ€Π°Π±ΠΎΡ‚ΠΊΠΈ Π½Π°Π½ΠΎΠ°Π»ΠΌΠ°Π·ΠΎΠ². НаиболСС эффСктивноС взаимодСйствиС с краситСлСм проявляСтся для ΡƒΠ»ΡŒΡ‚Ρ€Π°Π΄ΠΈΡΠΏΠ΅Ρ€ΡΠ½Ρ‹Ρ… Π°Π»ΠΌΠ°Π·ΠΎΠ², ΠΎΡ‚ΠΎΠΆΠΆΠ΅Π½Π½Ρ‹Ρ… Π² Π²Π°ΠΊΡƒΡƒΠΌΠ΅ ΠΏΡ€ΠΈ 750ΠΎΠ‘. ΠŸΡ€ΠΎΡ†Π΅ΡΡ образования комплСксов ΠΈΠ·ΡƒΡ‡Π΅Π½ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠΌ оптичСской спСктроскопии Π² Π²ΠΈΠ΄ΠΈΠΌΠΎΠΉ ΠΈ инфракрасной областях

    ΠšΠ°Ρ‚Π°Π»ΠΈΡ‚ΠΈΡ‡Π΅ΡΠΊΠΈΠ΅ систСмы для Ρ€Π΅Π°ΠΊΡ†ΠΈΠΉ кросс-сочСтания Π½Π° основС ΠΌΠΎΠ΄ΠΈΡ„ΠΈΡ†ΠΈΡ€ΠΎΠ²Π°Π½Π½Ρ‹Ρ… ΡƒΠ»ΡŒΡ‚Ρ€Π°Π΄ΠΈΡΠΏΠ΅Ρ€ΡΠ½Ρ‹Ρ… Π°Π»ΠΌΠ°Π·ΠΎΠ²

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    Methods for preparation of nanocomposites of modified detonation nanodiamonds (DND) with metallic palladium have been developed and their catalytic activity in the Suzuki-Miyaura cross-coupling reaction in various reaction media has been studied. Methods for the regeneration of palladium-containing nanocomposites from the reaction mixture have been developed. The high catalytic activity of nanocomposites is confirmed by kinetic analysis based on the results of chromatographic analysis of the reaction mixture and is comparable to the literature data about similar catalytic systems. Regenerated nanocomposites showed the retention of catalytic activity for 3 consecutive cross-coupling cycles on model systems.Π Π°Π·Ρ€Π°Π±ΠΎΡ‚Π°Π½Ρ‹ ΠΌΠ΅Ρ‚ΠΎΠ΄Ρ‹ получСния Π½Π°Π½ΠΎΠΊΠΎΠΌΠΏΠΎΠ·ΠΈΡ‚ΠΎΠ² ΠΌΠΎΠ΄ΠΈΡ„ΠΈΡ†ΠΈΡ€ΠΎΠ²Π°Π½Π½ΠΎΠ³ΠΎ ΡƒΠ»ΡŒΡ‚Ρ€Π°Π΄ΠΈΡΠΏΠ΅Ρ€ΡΠ½ΠΎΠ³ΠΎ Π°Π»ΠΌΠ°Π·Π° Π΄Π΅Ρ‚ΠΎΠ½Π°Ρ†ΠΈΠΎΠ½Π½ΠΎΠ³ΠΎ синтСза с мСталличСским ΠΏΠ°Π»Π»Π°Π΄ΠΈΠ΅ΠΌ ΠΈ ΠΈΠ·ΡƒΡ‡Π΅Π½Π° ΠΈΡ… каталитичСская Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ Π² Ρ€Π΅Π°ΠΊΡ†ΠΈΠΈ кросс-сочСтания Π‘ΡƒΠ·ΡƒΠΊΠΈ-ΠœΠΈΡΡƒΡ€Ρ‹ Π² Ρ€Π°Π·Π»ΠΈΡ‡Π½Ρ‹Ρ… Ρ€Π΅Π°ΠΊΡ†ΠΈΠΎΠ½Π½Ρ‹Ρ… срСдах. Π˜ΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½Ρ‹ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΈΠΊΠΈ Ρ€Π΅Π³Π΅Π½Π΅Ρ€Π°Ρ†ΠΈΠΈ палладийсодСрТащих Π½Π°Π½ΠΎΠΊΠΎΠΌΠΏΠΎΠ·ΠΈΡ‚ΠΎΠ² ΠΈΠ· Ρ€Π΅Π°ΠΊΡ†ΠΈΠΎΠ½Π½ΠΎΠΉ смСси. ΠšΠ°Ρ‚Π°Π»ΠΈΡ‚ΠΈΡ‡Π΅ΡΠΊΠ°Ρ Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΡΡ‚ΡŒ Π½Π°Π½ΠΎΠΊΠΎΠΌΠΏΠΎΠ·ΠΈΡ‚ΠΎΠ² ΠΏΠΎΠ΄Ρ‚Π²Π΅Ρ€ΠΆΠ΄Π΅Π½Π° исслСдованиСм ΠΊΠΈΠ½Π΅Ρ‚ΠΈΠΊΠΈ Ρ€Π΅Π°ΠΊΡ†ΠΈΠΈ кросс-сочСтания хроматографичСским Π°Π½Π°Π»ΠΈΠ·ΠΎΠΌ Ρ€Π΅Π°ΠΊΡ†ΠΈΠΎΠ½Π½ΠΎΠΉ смСси ΠΈ сопоставима с ΡƒΠΆΠ΅ ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΠ΅ΠΌΡ‹ΠΌΠΈ ΠΏΠΎΠ΄ΠΎΠ±Π½Ρ‹ΠΌΠΈ ΠΊΠ°Ρ‚Π°Π»ΠΈΠ·Π°Ρ‚ΠΎΡ€Π°ΠΌΠΈ. Π Π΅Π³Π΅Π½Π΅Ρ€ΠΈΡ€ΠΎΠ²Π°Π½Π½Ρ‹Π΅ Π½Π°Π½ΠΎΠΊΠΎΠΌΠΏΠΎΠ·ΠΈΡ‚Ρ‹ ΠΏΠΎΠΊΠ°Π·Π°Π»ΠΈ сохранСниС каталитичСской активности для 3 ΠΏΠΎΡΠ»Π΅Π΄ΠΎΠ²Π°Ρ‚Π΅Π»ΡŒΠ½Ρ‹Ρ… Ρ†ΠΈΠΊΠ»ΠΎΠ² кросс-сочСтания Π½Π° ΠΌΠΎΠ΄Π΅Π»ΡŒΠ½Ρ‹Ρ… систСмах

    Π‘ΠΏΠ΅ΠΊΡ‚Ρ€Π°Π»ΡŒΠ½Ρ‹Π΅ свойства ΠΈΠ½Π΄ΠΎΡ‚Ρ€ΠΈΠΊΠ°Ρ€Π±ΠΎΡ†ΠΈΠ°Π½ΠΈΠ½ΠΎΠ²ΠΎΠ³ΠΎ краситСля Π² тканях ΡΠΊΡΠΏΠ΅Ρ€ΠΈΠΌΠ΅Π½Ρ‚Π°Π»ΡŒΠ½Ρ‹Ρ… ΠΆΠΈΠ²ΠΎΡ‚Π½Ρ‹Ρ…

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    The paper presents the results of studies of the spectral properties of a photosensitizer based on indotricarbocyanine dye when accumulating in tissues of experimental animals. Using laser fluorescence spectroscopy, the in vivo and ex vivo fluorescence spectra of tissue-localized indotricarbocyanine dye were obtained for different time counts after intravenous administration. The profile of the pharmacokinetics of its accumulation and withdrawal was determined from the change in the intensity of fluorescence in the tumor and healthy muscle tissues of the photosensitizer. A monotonic deformation of its fluorescence spectrum was revealed in the tissues of tumor nodes and muscles of the thigh when registered through the skin over time after intravenous administration. The achievement of the maximum accumulation of the photosensitizer in the tumor correlates with the stabilization of the shape of its in vivo fluorescence spectrum. Thus, the maximum shift can be used as a diagnostic indicator of the maximum accumulation of indotricarbocyanine photosensitizer in the tumor tissues. The results were confirmed for two groups of animals: the first one – black mice of the C57Bl/6 line with an inoculated tumor of Clone M3 melanoma, the second – white mice of the ICR line with an inoculated tumor of Ehrlich ascites carcinoma. The analysis of the shape of the fluorescence spectrum of the photosensitizer during registration through the skin for animals with different colors has been carried out.Π’ Ρ€Π°Π±ΠΎΡ‚Π΅ ΠΏΡ€ΠΈΠ²Π΅Π΄Π΅Π½Ρ‹ Ρ€Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Ρ‹ исслСдований ΡΠΏΠ΅ΠΊΡ‚Ρ€Π°Π»ΡŒΠ½Ρ‹Ρ… свойств фотосСнсибилизатора Π½Π° основС ΠΈΠ½Π΄ΠΎΡ‚Ρ€ΠΈΠΊΠ°Ρ€Π±ΠΎΡ†ΠΈΠ°Π½ΠΈΠ½ΠΎΠ²ΠΎΠ³ΠΎ краситСля ΠΏΡ€ΠΈ Π½Π°ΠΊΠΎΠΏΠ»Π΅Π½ΠΈΠΈ Π² тканях ΡΠΊΡΠΏΠ΅Ρ€ΠΈΠΌΠ΅Π½Ρ‚Π°Π»ΡŒΠ½Ρ‹Ρ… ΠΆΠΈΠ²ΠΎΡ‚Π½Ρ‹Ρ…. Π‘ ΠΏΠΎΠΌΠΎΡ‰ΡŒΡŽ Π»Π°Π·Π΅Ρ€Π½ΠΎΠΉ флуорСсцСнтной спСктроскопии ΠΏΠΎΠ»ΡƒΡ‡Π΅Π½Ρ‹ спСктры флуорСсцСнции in vivo ΠΈ ex vivo Π»ΠΎΠΊΠ°Π»ΠΈΠ·ΠΎΠ²Π°Π½Π½ΠΎΠ³ΠΎ Π² тканях ΠΈΠ½Π΄ΠΎΡ‚Ρ€ΠΈΠΊΠ°Ρ€Π±ΠΎΡ†ΠΈΠ°Π½ΠΈΠ½ΠΎΠ²ΠΎΠ³ΠΎ краситСля для Ρ€Π°Π·Π½Ρ‹Ρ… Π²Ρ€Π΅ΠΌΠ΅Π½Π½Ρ‹Ρ… отсчСтов послС Π²Π½ΡƒΡ‚Ρ€ΠΈΠ²Π΅Π½Π½ΠΎΠ³ΠΎ ввСдСния. По измСнСнию интСнсивности флуорСсцСнции Π² ΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΠΎΠΉ ΠΈ Π·Π΄ΠΎΡ€ΠΎΠ²ΠΎΠΉ ΠΌΡ‹ΡˆΠ΅Ρ‡Π½ΠΎΠΉ тканях фотосСнсибилизатора ΠΎΠΏΡ€Π΅Π΄Π΅Π»Π΅Π½ ΠΏΡ€ΠΎΡ„ΠΈΠ»ΡŒ Ρ„Π°Ρ€ΠΌΠ°ΠΊΠΎΠΊΠΈΠ½Π΅Ρ‚ΠΈΠΊΠΈ Π΅Π³ΠΎ накоплСния ΠΈ Π²Ρ‹Π²ΠΎΠ΄Π°. ВыявлСна монотонная дСформация Π΅Π³ΠΎ спСктра флуорСсцСнции Π² тканях ΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²Ρ‹Ρ… ΡƒΠ·Π»ΠΎΠ² ΠΈ ΠΌΡ‹ΡˆΡ† Π±Π΅Π΄Ρ€Π° ΠΏΡ€ΠΈ рСгистрации Ρ‡Π΅Ρ€Π΅Π· ΠΊΠΎΠΆΡƒ с Ρ‚Π΅Ρ‡Π΅Π½ΠΈΠ΅ΠΌ Π²Ρ€Π΅ΠΌΠ΅Π½ΠΈ послС Π²Π½ΡƒΡ‚Ρ€ΠΈΠ²Π΅Π½Π½ΠΎΠ³ΠΎ ввСдСния. ДостиТСниС максимального накоплСния фотосСнсибилизатора Π² ΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΠΎΠΌ ΡƒΠ·Π»Π΅ ΠΊΠΎΡ€Ρ€Π΅Π»ΠΈΡ€ΡƒΠ΅Ρ‚ со стабилизациСй Ρ„ΠΎΡ€ΠΌΡ‹ Π΅Π³ΠΎ спСктра флуорСсцСнции in vivo. ΠŸΡ€ΠΈ этом смСщСниС максимума ΠΌΠΎΠΆΠ΅Ρ‚ ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΠΎΠ²Π°Ρ‚ΡŒΡΡ Π² качСствС диагностичСского ΠΈΠ½Π΄ΠΈΠΊΠ°Ρ‚ΠΎΡ€Π° максимального накоплСния ΠΈΠ½Π΄ΠΎΡ‚Ρ€ΠΈΠΊΠ°Ρ€Π±ΠΎΡ†ΠΈΠ°Π½ΠΈΠ½ΠΎΠ²ΠΎΠ³ΠΎ фотосСнсибилизатора Π² тканях ΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²Ρ‹Ρ… ΡƒΠ·Π»ΠΎΠ². Π Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Ρ‹ ΠΏΠΎΠ΄Ρ‚Π²Π΅Ρ€ΠΆΠ΄Π΅Π½Ρ‹ для Π΄Π²ΡƒΡ… Π³Ρ€ΡƒΠΏΠΏ ΠΆΠΈΠ²ΠΎΡ‚Π½Ρ‹Ρ…: пСрвая – Ρ‡Π΅Ρ€Π½Ρ‹Π΅ ΠΌΡ‹ΡˆΠΈ Π»ΠΈΠ½ΠΈΠΈ C57Bl/6 с ΠΏΠ΅Ρ€Π΅Π²ΠΈΡ‚ΠΎΠΉ ΠΎΠΏΡƒΡ…ΠΎΠ»ΡŒΡŽ ΠΌΠ΅Π»Π°Π½ΠΎΠΌΡ‹ Clone M3, вторая – Π±Π΅Π»Ρ‹Π΅ ΠΌΡ‹ΡˆΠΈ Π»ΠΈΠ½ΠΈΠΈ ICR с ΠΏΠ΅Ρ€Π΅Π²ΠΈΡ‚ΠΎΠΉ ΠΎΠΏΡƒΡ…ΠΎΠ»ΡŒΡŽ асцитной ΠΊΠ°Ρ€Ρ†ΠΈΠ½ΠΎΠΌΡ‹ Π­Ρ€Π»ΠΈΡ…Π°. ΠŸΡ€ΠΎΠ²Π΅Π΄Π΅Π½ Π°Π½Π°Π»ΠΈΠ· Ρ„ΠΎΡ€ΠΌΡ‹ спСктра флуорСсцСнции фотосСнсибилизатора ΠΏΡ€ΠΈ рСгистрации Ρ‡Π΅Ρ€Π΅Π· ΠΊΠΎΠΆΡƒ для ΠΆΠΈΠ²ΠΎΡ‚Π½Ρ‹Ρ… с Ρ€Π°Π·Π½ΠΎΠΉ окраской

    Optical properties of the complexes of detonation nanodiamonds with an indotricarbocyanine dye

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    A method to create complexes of detonation nanodiamonds with molecules of an indotricarbocyanine dye was developed. The process of complex formation was shown to depend on the nanodiamond annealing conditions. Nanodiamonds that were vacuum annealed at 750oC display the most effective interaction with the dye molecules. Formation of the complexes was studied with the aid of optical spectroscopy in the visible and infrared regions

    Optical properties of the complexes of detonation nanodiamonds with an indotricarbocyanine dye

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    Π Π°Π·Ρ€Π°Π±ΠΎΡ‚Π°Π½ ΠΌΠ΅Ρ‚ΠΎΠ΄ получСния комплСксов ΡƒΠ»ΡŒΡ‚Ρ€Π°Π΄ΠΈΡΠΏΠ΅Ρ€ΡΠ½Ρ‹Ρ… Π°Π»ΠΌΠ°Π·ΠΎΠ² Π΄Π΅Ρ‚ΠΎΠ½Π°Ρ†ΠΈΠΎΠ½Π½ΠΎΠ³ΠΎ синтСза с ΠΌΠΎΠ»Π΅ΠΊΡƒΠ»Π°ΠΌΠΈ ΠΈΠ½Π΄ΠΎΡ‚Ρ€ΠΈΠΊΠ°Ρ€Π±ΠΎΡ†ΠΈΠ°Π½ΠΈΠ½ΠΎΠ²ΠΎΠ³ΠΎ краситСля. Показано, Ρ‡Ρ‚ΠΎ Π½Π° процСсс комплСксообразования Π²Π»ΠΈΡΡŽΡ‚ условия тСрмичСской ΠΎΠ±Ρ€Π°Π±ΠΎΡ‚ΠΊΠΈ Π½Π°Π½ΠΎΠ°Π»ΠΌΠ°Π·ΠΎΠ². НаиболСС эффСктивноС взаимодСйствиС с краситСлСм проявляСтся для ΡƒΠ»ΡŒΡ‚Ρ€Π°Π΄ΠΈΡΠΏΠ΅Ρ€ΡΠ½Ρ‹Ρ… Π°Π»ΠΌΠ°Π·ΠΎΠ², ΠΎΡ‚ΠΎΠΆΠΆΠ΅Π½Π½Ρ‹Ρ… Π² Π²Π°ΠΊΡƒΡƒΠΌΠ΅ ΠΏΡ€ΠΈ 750 ΠΎΠ‘. ΠŸΡ€ΠΎΡ†Π΅ΡΡ образования комплСксов ΠΈΠ·ΡƒΡ‡Π΅Π½ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠΌ оптичСской спСктроскопии Π² Π²ΠΈΠ΄ΠΈΠΌΠΎΠΉ ΠΈ инфракрасной областях. A method to create complexes of detonation nanodiamonds with molecules of an indotricarbocyanine dye was developed. The process of complex formation was shown to depend on the nanodiamond annealing conditions. Nanodiamonds that were vacuum annealed at 750 oC display the most effective interaction with the dye molecules. Formation of the complexes was studied with the aid of optical spectroscopy in the visible and infrared regions

    Indotricarbocyanine dyes relevant for photodynamic therapy and their radicals: Substituent effects studied by optical and electrochemical methods

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    Photodynamic therapy is an effective and minimally invasive treatment method for cancer. A deeper under- standing of the photocytotoxicity mechanism of cyanine dyes is necessary for the development of more efficient photosensitizers. We combine electrochemistry, optical and ESR spectroscopy, and quantum chemical calcula- tions to study indotricarbocyanine dyes relevant for photodynamic therapy. The incorporation of 4-meso-chloride and a 3,5-o-phenylene bridge into the polymethine chain results in a hypsochromic shift of the absorption spectrum by ca. 30 nm and in a downward shift of the frontier orbitals energy levels by 0.1–0.3 eV. In addition, such substitution imparts stability to the electrogenerated radical dications of the dyes. The presence of 4-meso- chloride and a 3,5-trimethylene bridge in the polymethine chain causes the absorption spectrum to shift bath- ochromically by almost 40 nm and the HOMO–LUMO energy gap to decrease by ca. 0.1 eV. The radical dication of the dye with such substitution is particularly stable and exhibits improved electron delocalization. The radical dication of the dye with an unsubstituted polymethine chain is unstable due to its propensity to form dimers. The substituents at the nitrogen atoms are shown to have almost no influence on the optical and electrochemical properties of the indotricarbocyanine dyes. The radical dications of the dyes with an o-phenylene bridge can oxidize bromide ions, unlike the radical dications of the dyes with an unsubstituted polymethine chain or with a trimethylene bridge. The reported data can be used to develop new indotricarbocyanine dyes with desired characteristics

    Novel indotricarbocyanine dyes covalently bonded to polyethylene glycol for theranostics

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    The synthesis methods for the indotricarbocyanine dyes covalently bonded to polyethylene glycols with varying degrees of polymerization have been developed. New indotricarbocyanine was synthesized in one step using the Mukayama reagent in polyethylene glycol with cesium fluoride as a basic catalyst. In vivo investigation of the phototherapeutic dye activity has shown selective recognition of malignant tissues, where accumulation of the dye was 4–5 times higher than in normal tissues. The necrotic area after local photoirradiation at the effective energy fluence 180 J/cm2, l = 780 nm was observed to a depth of 2.5 cm making the synthesized dyes very promising for further pharmaceutic researc

    Novel indotricarbocyanine dyes covalently bonded to polyethylene glycol for theranostics

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    The synthesis methods for the indotricarbocyanine dyes covalently bonded to polyethylene glycols with varying degrees of polymerization have been developed. New indotricarbocyanine was synthesized in one step using the Mukayama reagent in polyethylene glycol with cesium fluoride as a basic catalyst. In vivo investigation of the phototherapeutic dye activity has shown selective recognition of malignant tissues, where accumulation of the dye was 4–5 times higher than in normal tissues. The necrotic area after local photoirradiation at the effective energy fluence 180 J/cm2, l = 780 nm was observed to a depth of 2.5 cm making the synthesized dyes very promising for further pharmaceutic researc

    Spectral and luminescent properties and morphology of self-assembled nanostructures of an indotricarbocyanine dye

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    Spectral and luminescent properties of an indotricarbocyanine dye are studied in solutions and after deposition on quartz or silicon substrates. It is found that the dye molecules self-assemble in aqueous EtOH solutions to form H*-aggregates. The absorption band of the H*-aggregates shows a hypsochromic shift of 192 nm (5291 cm–1) relative to the absorption maximum of dye monomers (706 nm) and has a full width at half maximum of 21 nm (797 cm–1). The morphology of the H*-aggregates of the indotricarbocyanine dye is studied for the fi rst time. It is found that the aggregates are rod-like species ~10 nm high, 100 nm wide, and several micrometers long. H-aggregates with a fl uorescence maximum at 560 nm and Stokes shift of 325 cm–1 in addition to non-fl uorescent H*-aggregates form in aqueous EtOH solutions and are nanoparticles with a height of 1–3 nm and lateral dimensions of ~100 nm
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