Publications by authors named "Yao Si-De"

In this paper, the photochemical and photobiological characters of the active radicals of berberine (BBR) was investigated for finding an efficient and safe photosensitizer with highly active transient products using in Photodynamic therapy (PDT) study. The active species of BBR was generated and identified by using pulse radiolysis method. In neutral aqueous solution, BBR react with hydrated electron and hydroxyl radical, forming the radical anion and neutral radical of BBR, and the related reaction rates were determined as 3.

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In the present paper, the interaction between model protein lysozyme (Lys) and antitumorigenic berberine (BBR) was investigated by spectroscopic methods, for finding an efficient and safe photosensitizer with highly active transient products using in photodynamic therapy study. The fluorescence data shows that the binding of BBR could change the environment of the tryptophan (Trp) residues of Lys, and form a new complex. Static quenching is the main fluorescence quenching mechanism between Lys and BBR, and there is one binding site in Lys for BBR and the type of binding force between them was determined to be hydrophobic interaction.

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Using 266 nm laser flash photolysis it has been demonstrated that Berberine (BBR) in aqueous solution is ionized via a mono-photonic process giving a hydrated electron, anion radical that formed by hydrated electron react with steady state of BBR, and neutral radical that formed from rapid deprotonation of the radical cation of BBR. The quantum yield of photoionization is determined to be 0.03 at room temperature with KI solution used as a reference.

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Titanium dioxide (TiO(2)) has been considered as non-toxic mineral particles widely used in the fields like cosmetics, food and drug. When the scale come to nanometer, TiO(2) nanoparticles (nano-TiO(2)) exhibits multiple specific characteristics coupled with unknown risks on health. The purpose of this study was to systematically research the influence of nano-TiO(2) on erythrocyte.

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Laser flash photolysis study was carried out for the first time in the binary mixture of room-temperature ionic liquid (RTIL) and traditional organic solvent. Photochemical properties of the ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate [bmim][PF6] and its binary mixed solutions with MeCN were investigated by laser photolysis technique at an excitation wavelength of 355 nm, using anthraquinone (AQ) as a probe molecule. It was indicated that [bmim] [PF6] itself participates in the reaction with 3AQ*.

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Background & Objective: Choosing suitable gene carrier is very important in gene therapy. Recently, polyethylenimine (PEI), a new polycation compound, is particularly attractive due to its high transduction efficiency and low toxicity. This study was to synthesize a series of PEI nanogels of different particle diameters by photochemistry, investigate the relation between the transfection efficiency and particle diameter, and screen ideal gene carrier.

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Polyethyleneimine nanogels (named as M-PEIs) with different sizes were prepared by photo-Fenton reaction in aqueous solution from which samples of 38, 75, 87, 121, 132 and 167nm were selected for in vitro transfection. The homogeneous structure and the same component made it possible to study the size effect of M-PEIs nanogels on gene transfection efficiency when loading the same quantity of plasmid DNA (pLEGFP-C1) into A549, Bel7402, BGC-823 and Hela cells. M-PEIs and its DNA complexes were characterized by photo correlation spectroscopy and atomic force microscopy.

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Article Synopsis
  • The study investigates the photo-ionization and excited state properties of benzoic acid and its methyl derivatives using a 248 nm laser flash photolysis technique.
  • It determines key factors such as quantum yields of hydrated electrons, excited triplet lifetimes, and self-quenching rate constants, revealing minimal impact from the position of methyl groups on the triplet state.
  • Additionally, the research explores resonant excitation of the triplet state through a two-step laser flash method and makes conjectures about the upper excited states and radicals involved in the processes.
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Quinoline's degradation was studied by pulse radiolysis. It was found that hydrated electron, hydrogen radical, hydroxyl radical and SO4*- can react with quinoline. The absorption spectra of the transient species of quinoline were obtained, and related constants were determined, but it was found that the species of Br2*- and N3*- can't react with quinoline.

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Article Synopsis
  • - The study investigated how hydroxyl radicals (*OH) and hydrated electrons (*e(aq)-) react with azo dye AO7 in water using specialized techniques in nano-second pulse radiolysis.
  • - Researchers tracked the formation of transient absorption spectra to calculate second-order reaction rate constants based on how these absorptions developed over time.
  • - By analyzing changes in the UV-Vis absorption of AO7 after exposure to gamma radiation, the researchers clarified the mechanisms behind the reactions taking place.
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The catalysis effect of water-soluble calix[4]arene C[4] (calix[4]arene-5,11,17,23-tetrasulfonate) on hydrolysis of ATP in aqueous solution was studied by HPLC. Using laser photolysis and pulse radiolysis, the supramolecular interaction between water-soluble calix[4]arene and ATP was investigated.

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