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1.
The spectral properties and efficiency for photosensitizing the lysis of phosphatidylcholine liposomes have been measured for the components of hematoporphyrin derivative (Hpd) after alkaline hydrolysis and fractionation by polyacrylamidc gel chromatography. Two major and two minor Hpd fractions have been identified whose spectral properties correlate with the anoxic sensitizing efficiency and the oxygen enhancement ratio (OER). The fastest moving fraction, which is the putative biologically active component, comprised one-third of the starting material and had OER = 2.7. Liposome lysis by this fraction was inhibited in the presence of human serum albumin at concentration ratios comparable to those employed for photoradiation therapy. The present results show that Hpd can act as an oxic and anoxic photosensitizer of a model biomembrane and suggest that separation from serum proteins is required for in vivo photosensitization. 相似文献
2.
Hematoporphyrin as a photosensitizer of tumors 总被引:1,自引:0,他引:1
T J Dougherty 《Photochemistry and photobiology》1983,38(3):377-379
Abstract— The ability of hematoporphyrin (Hp) to act as a photosensitizer of cells in vitro or in vivo is a matter of dispute, while hematoporphyrin derivative (Hpd), a mixture of porphyrins including hematoporphyrin, has been consistently found to be an effective photosensitizer both in vitro and in vivo. Until recently the actual component of the Hpd mixture responsible for these effects had not been identified. We have found that those preparations of Hp which contain, as an impurity, a porphyrin similar to that found to be responsible for the tumor photosensitizing ability of Hpd, may be effective photosensitizers of tumors but are generally of low efficacy. This material accounts for the entire photosensitizing activity of both Hp and Hpd in the SMT-F mammary carcinoma in DBA/2 HeHa mice. 相似文献
3.
Elena Reddi Michael A. J. Rodgers John D. Spikes Giulio Jori 《Photochemistry and photobiology》1984,40(4):415-421
Abstract The 83 μM hematoporphyrin (HP)-sensitized photooxidation of 0.1 mM tryptophan in aqueous solution buffered at pH 7.4 or in binary mixtures of phosphate buffer and organic solvents of higher (formamide) or lower (N,N-dimethylformamide, methanol, ethanol, tetrahydrofuran) polarity proceeds by a pure singlet oxygen (1O2) mechanism as suggested by azide quenching experiments, the rate-enhancing action of deuterated solvents, and the lack of any significant reaction between triplet HP and tryptophan. Both the first-order rate constant of the photoprocess and the photooxidation quantum yield (φ= 0.011 in phosphate buffer at pH 7.4) increase when the medium polarity is increased (e.g. φ= 0.024 in 90% formamide); this results mainly from the greater quantum yield of 1O2 generation and the longer lifetime of 1O2. The intrinsic reactivity of 1O2 with tryptophan is independent of formamide concentration. A moderate decrease in the medium polarity (e.g. in the range 0-30% methanol) enhances the efficiency of tryptophan photooxidation (φ= 0.014 in 30% methanol) as a result of the enhanced quantum yields of triplet HP and 1O2 formation. In contrast, the overall photooxidation rate is depressed at high concentrations of low-polarity organic solvents (e.g. φ= 0.0039 in 90% methanol) due to a 5.5-fold drop of the rate constant for the 1O2-tryptophan reaction which counteracts the enhancement of the lifetime and quantum yield of triplet HP and 1O2. The solvent composition also affects the equilibria between monomeric and multimeric forms of HP. However, under our experimental conditions, the aggregation state of HP appears to exert only a minor influence on the efficiency of tryptophan photooxidation. 相似文献
4.
The effect of the acidity of the environment on the topography and photophysics of sensitizer molecules in homogeneous solutions, and when embedded in a lipid microenvironment, was studied. Four hematoporphyrin (HP) analogs were studied, which have chemical "spacers" of varying lengths between the chromophoric tetrapyrrole and the carboxylate moiety. These derivatives have essentially the same chemical attributes and reactivity as the parent compound, HP IX, which is used in clinical procedures of photodynamic therapy. The binding constants of these HP derivatives to membrane model systems increase with the length of carboxylate chain in the pH range 3.0-6.6. This effect of chain length is attributed to an increase in the hydrophobicity of the molecule on elongation of the alkyl chains. A strong pH dependence of the quenching efficiency of the porphyrins' fluorescence by iodide ions was observed in aqueous solution and is attributed to a unique electrostatic interaction between the fluorophore and the quencher. The quenching efficiency in liposomes, relative to the quenching in buffer, as a function of pH, shows that porphyrins in the neutral form penetrate deeper inside the lipid bilayer and are less exposed to external quenching than when negatively charged at the carboxylic moiety. This vertical displacement in the membrane is also evidenced in the effect of pH on the photosensitized oxidation efficiency of a membrane-bound chemical target. Increasing the pH causes a significant decrease in the sensitization efficiency in liposomes. This trend is attributed to the vertical localization, and protonation of the carboxylic groups on lowering the pH leads to sinking of the sensitizer into the lipid bilayer and to a consequent generation of singlet oxygen at a deeper point. This increases the dwell time of singlet oxygen within the bilayer, which results in greater photodamage to a membrane-residing singlet oxygen target. 相似文献
5.
Anna Kozinska Andrzej Zadlo Przemyslaw Labuz Agnieszka Broniec Pawel Pabisz Tadeusz Sarna 《Photochemistry and photobiology》2019,95(1):227-236
Photochemical properties of a new class of inorganic nanoparticles, namely a cationic C60 fullerene substituted with three quaternary pyrrolidinium groups (BB6) and a surface‐modified nanocrystalline TiO2 with bromopyrogallol red (Brp@TiO2) were examined for their effectiveness in photogenerating singlet oxygen and free radicals. In particular, their ability to photosensitize peroxidation of unsaturated lipids was analyzed in POPC:cholesterol liposomes and B16 mouse melanoma cells employing a range of spectroscopic and analytical methods. Because melanoma cells typically are pigmented, we examined the effect of melanin on the photosensitized peroxidation of lipids in liposomes and B16 melanoma cells, mediated by BB6 and Brp@TiO2 nanoparticles. The obtained results suggest that peroxidation of unsaturated lipids, photosensitized by BB6 occurs mainly, although not exclusively, via Type II mechanism involving singlet oxygen. On the other hand, if surface‐modified TiO2 is used as a photosensitizer, Type I mechanism of lipid peroxidation dominates, as indicated by the predominant formation of the free radical‐dependent cholesterol oxidation products. The protective effect of melanin was particularly evident when BB6 was used as a photosensitizer, suggesting that melanin could efficiently interfere with Type II processes. 相似文献
6.
Abstract— By a technique which combines rapid mixing of cells and hematoporphyrin (HP) with a short duration of illumination, the photodynamic inactivation of yeast cells was investigated, particularly, in seeking for the information of the location of HP at the time of action. The fluence-survival curves obtained under the conditions where the reaction mixture was kept in the dark for Is, 60s and even 35 min before illumination were indistinguishable from each other, indicating no interaction between cells and sensitizers took place in about 30 min in such a way that the photodynamic efficiency could be modified. It is unlikely that HP acted intracellularly, since the protective effect of N?3 was observed at concentrations as low as 0.5 mM. Furthermore, the rate constant kp related to the protective effect of NJ, was estimated to be 1 × 108M?1 s?1 under the assumption that 1O2 was the active intermediate and had a lifetime of 2 μs under the present conditions. This value of kp is rather close to that of kq, the quenching rate constant of N?3 for 1O2, of which the accepted value is 2 × 108M?1s?1 in the homogeneous aqueous system. This information, together with the absence of uptake of HP by cells and a well response of survival upon illumination to the D2O fraction of the reaction mixture, provide strong bases for the argument that direct interaction of HP with yeast cells is of minor importance in the photodynamic processes, and the photodynamic action is largely mediated by an intermediate (102) generated in bulk medium. 相似文献
7.
The lytic interactions of a series of alkyl glucosides (alkyl chain lengths ranging from C8 to C12) with liposomes formed by a mixture of lipids modeling the stratum corneum (SC) lipid composition were investigated. The
surfactant-to-lipid molar ratios (Re) and the normalized bilayer/aqueous phase partition coefficients (K) were determined by monitoring the changes in the static light-scattering (SLS) of the system during solubilization. The
fact that the free surfactant concentrations were always similar to their critical micelle concentrations indicates that the
liposome solubilization was mainly ruled by the formation of mixed micelles. At the two interaction levels studied (100 and
0% SLS) the nonyl glucoside showed the highest ability to saturate and to solubilize liposomes (lowest Re values), whereas
the dodecyl glucoside showed the highest degree of partitioning into liposomes or affinity with these structures (highest
K values). Comparison of the data for octyl glucoside with that reported for the interaction of this surfactant with phosphatidylcholine
(PC) liposomes shows that whereas the SC lipid liposomes were more resistant to the action of this surfactant (higher Re values),
its degree of partitioning into SC bilayers was both in the saturation and solubilization of liposomes similar to that exhibited
in PC vesicles (similar K values).
Received: 27 November 2000/Accepted: 19 February 2001 相似文献
8.
G De Guidi R Chillemi S Giuffrida G Condorelli M Cambria Famá 《Journal of photochemistry and photobiology. B, Biology》1991,10(3):221-237
The lysis of red blood cells photosensitized by diflunisal (DFN) was investigated. Photohemolysis is inhibited by butylated hydroxyanisole and reduced glutathione, but is unaffected by mannitol and enhanced by sodium azide; the presence of oxygen markedly reduces the lysis which is accelerated in anaerobic conditions. These results contrast with those expected for a photodynamic mechanism. High lytic activity is observed for pre-irradiated solutions, mainly under anaerobic conditions. Direct irradiation of DFN in buffer solution at pH 7.4 leads to the formation, under anaerobic conditions, of compound 2'-(2',4'-difluoro-3'-carboxy-[1',1'-biphenyl]-4'-oxy)-4'- fluoro-4-hydroxy-[1,1'-biphenyl]-3-carboxylic acid (PhP), whereas under aerobic conditions formation of PhP is accompanied by unidentified photo-oxidation products; only compound PhP displays strong lytic activity. The overall results for DFN-photosensitized hemolysis suggest a mechanism involving a concerted action of free radicals, superoxide anion, singlet oxygen and sensitizer photoproducts. 相似文献
9.
Philippe Richard Aleksander Blum Leonard I. Grossweiner 《Photochemistry and photobiology》1983,37(3):287-291
—The photosensitized inactivation of subtilisin BPN' by free hematoporphyrin (HP) followed exponential kinetics with positive mechanistic tests for the involvement of singlet oxygen (1 O2 ) as the principal intermediate. The photoinactivation quantum yield was 0.029 at 390 nm in oxygen-saturated, D2 O buffer at pH 7.0. The effects of HP binding were investigated for tryptophan oxidation in bovine serum albumin (BSA) and human serum albumin (HSA) at high protein:HP concentration ratios where the HP was > 97% complexed. The reaction kinetics were non-exponential and mimick a second-order process in the initial stages. The rate of HP photobleaching was 30-fold faster for complexed HP compared with free HP, which was shown to account for the observed kinetics. Mechanistic tests showed that 1 O2 was the dominant photooxidizing intermediate of tryptophan residues and that it was not involved in the accompanying photobleaching of HP. The quantum yield for tryptophan oxidation in BSA was 0.11 at 390 nm in oxygen-saturated, D2 O buffer at pH 8.0. The reactivity of HSA was approximately 2-fold lower than BSA for equivalent conditions. Estimates of the reaction cross sections led to 3 Å2 for the inactivation of subtilisin BPN' by 1 O2 and 20 Å2 for the oxidation of tryptophan in BSA. 相似文献
10.
Gianfranco Canti Ornella Marelli Laura Ricci Angelo Nicolin 《Photochemistry and photobiology》1981,34(5):589-594
Abstract— It has been known that haemoatoporphyrin derivative (Hpd) has a preferential distribution in tissues with high mitotic index. Furthermore, cytocidal activity of light activated Hpd within the cells has been exploited in the therapy of experimental and human cancer. It is reported here that maximum, long lasting, although reversible, inhibition of DNA synthesis was obtained in Hpd-treated lymphocytes. However, Hpd-treated lymphoid cells did not stimulate allogeneic lymphocytes in the primary mixed lymphocyte reaction (MLR) culture. Phytohaemagglutinin (PHA) stimulated murine lymphocytes treated with Hpd and exposed to laser light have shown higher susceptibility to lysis than resting, PHA unstimulated, lymphocytes. In vitro DBA/2 stimulated C57 lymphocytes, inoculated into X-irradiated BD2F1 mice, upon Hpd treatment followed by exposure to light, did not cause a lethal graft vs. host reaction (GVHR). Haematoporphyrin derivative was preferentially incorporated by large and metabolically active cells. inhibited the incorporation of [3H]-thymidine in the lymphocyte nucleus and could be exploited to selectively remove blast cells from resting lymphocytes. 相似文献
11.
Abstract— Studies were conducted to assess the interdependence of three discrete parameters known to influence hematoporphyrin derivative (Hpd)-induced photosensitization. The effects of fiuence, drug dose and oxygen environment were examined for their role in causing an inhibition of the activity of mitochondrial cytochrome c oxidase. Experiments were performed on R3230AC mammary tumor mitochondria in vitro and on mitochondria isolated from tumors of animals pre-treated with Hpd in vivo. Inhibition of cytochrome c oxidase activity was observed to be directly proportional to total energy density. Photosensitization was dependent on oxygen concentration, with total energy density dependent photosensitization being diminished in environments containing less than 5% oxygen. At 1% oxygen environments, photosensitization was significantly impaired and demonstrated no drug-dose relationship. These results suggest that tissue oxygen concentration may represent a critical factor for the therapeutic usefulness of Hpd photodynamic therapy in treatment of cancer. 相似文献
12.
Abstract Porphyrins used as sensitizers for the photodynamic therapy (PDT) of tumors are progressively destroyed (photobleached) during illumination. If the porphyrin bleaches too rapidly, tumor destruction will not be complete. However, with appropriate sensitizer dosages and bleaching rates, irreversible photodynamic injury to the normal tissues surrounding the tumor, which retain less sensitizer, may be significantly decreased. This paper surveys the quantum yields and kinetics of the photobleaching of four porphyrins: hematoporphyrin (HP), Photofrin II (PF II), tetra(4-sulfonatophenyOporphine (TSPP) and uroporphyrin I (URO). The initial quantum yields of photobleaching, as measured in pH 7.4 phosphate buffer in air, were: 4.7 × 10-5, 5.4 × 10-5, 9.8 × 10-5, and 2.8 × 10-5 for HP, PF II, TSPP and URO respectively; thus, the rates of photobleaching are rather slow. Low oxygen concentration (2 μM) significantly reduced the photobleaching yields. However, D2O increased the yields only slightly, and the singlet oxygen quencher, azide, had no effect, even at 0.1 M. Photosensitizing porphyrins in body fluids, cells and tissues may be closely associated with various photooxidizable molecules and electron acceptors and donors. Therefore, selected model compounds in these categories were examined for their effects on porphyrin photobleaching. A number inhibited and/or accelerated photobleaching, depending on the compound, the porphyrin and the reaction conditions. For example, 1.0 mM furfuryl alcohol increased the photobleaching yields of HP and URO more than 5-fold, with little effect on PF II or TSPP. In contrast, the electron acceptor, methyl viologen, increased the photobleaching yield of TSPP more than 10-fold, with little accelerating effect on the other porphyrins. These results suggest that the mechanism(s) of the photobleaching of porphyrin photosensitizers in cells and tissues during PDT may be complex. 相似文献
13.
Adeel Arsalan Iqbal Ahmad Syed Abid Ali Kiran Qadeer Shaukat Mahmud Fozia Humayun Anwar Ejaz Beg 《国际化学动力学杂志》2020,52(3):207-217
Cyanocobalamin (B12) is a photosensitive vitamin, and its photodegradation to hydroxocobalamin (B12b) in liposomes has been investigated. The values of apparent first-order rate constants (kobs) for the photodegradation of B12 in liposomes (nine preparations) are in the range of (0.52-2.24) × 10–3 min–1, compared to 3.21 × 10–3 min–1 for B12 in aqueous solution (pH 5.0). The entrapment efficiency of B12 in liposomes is 26.4-38.8%. The values of kobs show a linear relation with phosphatidylcholine (PC) content in liposomes, indicating the influence of PC in inhibiting the rate of photolysis of B12. The value of the bimolecular rate constant for photochemical interaction of B12 and PC is 0.32 M–1 min–1, indicating the stabilizing effect of PC on the photolysis of B12. The ratio of B12 stabilization in liposomal preparations is in the range 2-6 compared to that of the unentrapped vitamin The stabilization of B12 is mediated by a photoinduced charge-transfer B12-PC complex that leads to the reduction of B12 to B12r, which is then oxidized to B12b that has low susceptibility to photolysis. The extent of stabilization of B12 probably depends on the degree of interaction between the two compounds under the reaction conditions, indicated by the loss of B12 fluorescence. 相似文献
14.
The oxygen and ?-tryptophan (TRP) effect on the triplet state of hematoporphyrin IX (HP) has been investigated by means of the laser photolysis technique at room temperature, in various pH 7.4 buffered aqueous/formamide or methanol mixtures with different polarity. The quenching of the HP triplet state by oxysgen is not affected by the medium polarity (kq O2 = 1.5 × 109 M?1 s?1), whereas the quenching by TRP appears dependent on the composition. The mechanism of the HP-sensitized photooxidation of TRP is discussed. 相似文献
15.
Abstract— Egg lecithin liposomes were lysed by singlet oxygen (1O*2) generated by red light irradiation of oxygenated methylene blue (MB+) and by superoxide (O?2) generated by blue-green irradiation of oxygenated riboflavin (RF) in the presence of ethylenediaminetetraacetic acid (EDTA) or reduced nicotinamide adenine dinucleotide (NADH). The MB+/O2 sensitized process is more efficient in alkaline solutions, attributed to the stabilization of the triplet state di-cation. The small increase of the lysis efficiency from pH4 to pH9 for the RF/EDTA/O2 system suggests that HO?2 may be more damaging than O?2. Estimates based on large-target reaction kinetics indicate that 1O*2 is about 200 times more effective than superoxide for inducing liposome lysis. Similar experiments with saturated 1 -α-phosphatidylcholine dipalmitoyl liposomes showed no photosensitized lysis for either system. 相似文献
16.
EFFECT OF SINGLET OXYGEN QUENCHERS ON OXIDATIVE DAMAGE TO LIPOSOMES INITIATED BY PHOTOSENSITIZATION OR BY RADIOFREQUENCY DISCHARGE 总被引:5,自引:0,他引:5
S. M. Anderson N. I. Krinsky M. J. Stone D. C. Clagett 《Photochemistry and photobiology》1974,20(1):65-69
Abstract —Lipid model membrane systems, liposomes, may be oxidized by both toluidine blue Osensitized photo-oxidation and radiofrequency-discharge-generated singiet oxygen. Oxidation can be followed by the appearance of lipid peroxides, malondialdehyde formation, and ultimately by the lysis of the liposomes. Inhibition of oxidation is observed in both systems using either β-carotene or DABCO. These observations are consistent with the view that type II (singlet oxygen) reactions are involved in this photodynamic system. 相似文献
17.
Luciana Mercedes Pujol-Lereis Ana Massaldi Alejandro Rabossi Luis Alberto Quesada-Allué 《Photochemistry and photobiology》2010,86(3):639-644
Immature stages of Ceratitis capitata were tested as a model for hematoporphyrin IX (HP IX) phototoxicity. The lethal concentration 50 (LC50) of HP IX in the food was determined during postembryonic development until adult emergence as 0.173 mm (95% CI: 0.138–0.209). The corresponding HP IX LC50 during the dispersal period alone was 0.536 mm (95% CI: 0.450–0.633). HP IX toxicity was compared against Phloxine B (PhB) (0.5 mm ). HP IX elicited a mortality of 90.87%, which was mainly concentrated during prepupal and early pupal stages. PhB mortality was much lower (56.88%) and occurred mainly during the adult pharate stage. A direct correlation between light-dependent HP IX mortality, evidence of reactive oxygen species (ROS) and lipid peroxidation (conjugated dienes and thiobarbituric acid reactive substances) was established in C. capitata larvae. ROS were found to be very significant in both the brain and in the gut. 相似文献
18.
《Journal of polymer science. Part A, Polymer chemistry》2018,56(2):229-236
The benzaldehyde derivatives, such as 2,4‐dimethoxy benzaldehyde (PC1) and p‐anisaldehyde (PC2), were successfully used as photoredox catalysts (PCs) in combination with typical RAFT agent 4‐cyano‐4‐(phenylcarbonothioylthio)pentanoic acid (CTP) for the controlled photoinduced electron transfer RAFT polymerization (PET‐RAFT) of methyl methacrylate (MMA) and benzyl methacrylate (BnMA) at room temperature. The kinetics of the polymerizations showed first order with respect to monomer conversions. Besides, the average number molecular weights (Mn) of the produced polymers increased linearly with the monomer conversions and kept relatively narrow polydispersity (PDI = Mw/Mn). For example, the Mn of PMMA increased from about 3400 to 17,300 g mol−1 with the increasing in monomer conversion from 11% to 85%, and the PDI maintained around 1.36. The living features of polymerizations with the PC1 and PC2 as catalysts have also been further supported by chain extension and synthesis of PMMA‐b‐PBnMA diblock copolymer. As a result, the simplicity and efficiency of benzaldehyde derivatives catalyzed PET‐RAFT polymerization have been demonstrated under mild conditions. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 229–236 相似文献
19.
In order to design liposomes which release their contents in a glucose-sensitive manner, the surfaces of egg phosphatidylcholine
(egg PC) liposomes or dioleoylphosphatidylethanolamine (DOPE) liposomes were modified with the copolymer of N-isopropylacrylamide/methacrylic acid/octadecylacrylate and hydrophobically modified glucose oxidase (EC 1.1.3.4.). Whichever
the liposomes were prepared with egg PC or DOPE, an extensive release of calcein was observed at acidic conditions. And DOPE
liposomes were more pH sensitive than egg PC liposomes in terms of the release. In glucose-dependent calcein release experiment,
there was no release for 180 min when the suspension of liposome was free of glucose. When the glucose concentration was 50 mg/dl,
no appreciable amount of calcein was released for the first 50 min, but a significant release was observed for the last 130 min.
At glucose concentration of 200 mg/dl, calcein release became more extensive and the releases for 180 min from egg PC and
DOPE liposome were 84% and 98%, respectively. 相似文献
20.
Abstract— Hydroxyl radicals ('OH) are scavenged by 1,4-diazabicyclo[2.2.2]octane (DABCO) at a diffusion-controlled rate of 1.25 ± 0.1 × 109 M -1 s-1 . Unlike other efficient 'OH scavengers which exhibit protection of bacteria against irradiation both in oxic and hypoxic conditions, DABCO has been shown to protect Serratia marcescens and various strains of Escherichia coli only in oxic conditions.
DABCO appears to eliminate a component of the sensitization afforded by oxygen in all strains of E. coli tested. The level of this protection increases from ∼15% in the wild type AB 1157 to ∼100% in the recA uvrA mutant AB 2480. It is suggested that DABCO protects against lethal events that can occur on macromolecules other than DNA such as the cell membrane.
Results with added glycerol, as well as work in D2 O solution, indicate that DABCO is more likely to be acting by scavenging radicals rather than by quenching 1 O2 . If 1 O2 is a component of the sensitization afforded by oxygen, then it is unlikely to be formed in a hydrophilic environment in the cell. 相似文献
DABCO appears to eliminate a component of the sensitization afforded by oxygen in all strains of E. coli tested. The level of this protection increases from ∼15% in the wild type AB 1157 to ∼100% in the recA uvrA mutant AB 2480. It is suggested that DABCO protects against lethal events that can occur on macromolecules other than DNA such as the cell membrane.
Results with added glycerol, as well as work in D