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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    World journal of urology 5 (1987), S. 259-261 
    ISSN: 1433-8726
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Until recently, the indications for extracorporeal shock wave lithotripsy (ESWL) have been limited to renal calculi and ureteral calculi above the pelvic brim. However, the distal ureter can be made available for shock wave treatment as well, by modifying the position of the patient on the support of the Dornier lithotripter HM-3. Using this “sitting position” technique, 133 patients with stones or stone fragments in the lower ureter were treated from January through November 1986. Treatment was successful in 125 patients (94%), 14 of whom required 2 sessions. In 8 patients, treatment failed and stone removal was accomplished using ureteroscopy or open surgery. No complications or adverse side effects were encountered in the entire series. We consider ESWL the treatment of choice in the management of distal ureteral calculi and Steinstrassen.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 19 (1991), S. 353-356 
    ISSN: 1434-0879
    Keywords: Bladder cancer ; Electron microscopy ; Photodynamic therapy ; Photosan ; Phototoxicity ; Tumor selectivity ; Video fluorescence microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The uptake of photosan and the intracellular sites of photoradiation-induced damage were investigated in vitro in bladder carcinoma cells and in normal bladder cells. Cells were examined by phase contrast, fluorescence and electron microscopy. The concentration of photosan, measured in μg/106 cells, showed a good correlation to the incubation time. At all incubation times, control cells showed a lower uptake when compared with tumor cells. Following photodynamic therapy (PDT), phase-contrast microscopy revealed marked changes in tumor cells, whereas only minor effects could be detected at the cell membrane of the control cells. Following PDT, most of the investigated cells showed onanges of the mitochondria and cytoplasma. These changes consisted of dissolution of the cristae, predominantly in the central part of the mitochondria. Twenty-four hours after PDT the shape of the mitochondria had changed markedly and the cristae were found to be completely destroyed. Moreover, the cystoplasma showed numerous vacuoles, and the number of mitochondria was decreased compared to non-treated cells.
    Type of Medium: Electronic Resource
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  • 13
    ISSN: 1434-0879
    Keywords: Photodynamic therapy ; Porphycene ; pH-sensitive liposomes ; Transmission electron microscopy ; Scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In vitro experiments were performed on human bladder carcinoma cells to evaluate the efficiency of the recently synthesized photosensitizer 9-acetoxy-tetra-n-propylporphycene (ATPPn) for photodynamic therapy. To improve cytoplasmic delivery of this hydrophobic compound, we prepared pH-sensitive liposomes composed of phosphatidylethanolamine (PE) and cholesteryl hemisuccinate (CHEMS) in comparison with pH-insensitive liposomes consisting of phosphatidylcholine (PC) and CHEMS. Dynamic light scattering measurements were used to monitor the acid-induced liposome destabilization. After incubation with liposome-bound ATPPn, bladder carcinoma cells were irradiated by a dye laser with increasing light fluence rates from 1 to 48 J/cm2. The photodynamic effects were then assessed from cell survival curves. No dark or phospholipid toxicity was measured for 2 μg ATPPn/1.5 ml medium. Qualitative cellular uptake of ATPPn was determined by fluorescence microscopy, while photodamage was elucidated by transmission and scanning electron microscopy. Absorption spectra performed up to 42 days revealed changes in shape for the pH-sensitive liposomes after storage at room temperature. ATPPn was proved to be an encouraging photosensitizer, capable of reducing cell survival to 0.1% after short-term incubation of 60 min with a drug dose of 2 μg ATPPn/1.5 ml medium. Although pH-sensitive PE/CHEMS liposomes showed significantly (P〈0.05) more photokilling effects at 24 J/cm2 and 48 J/cm2, no further advantages over non-pH-sensitive PC/CHEMS liposomes were found.
    Type of Medium: Electronic Resource
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  • 14
    ISSN: 1434-0879
    Keywords: Phototoxicity ; Aluminum-chlorophtalocyanine ; Electron microscopy ; DAB staining
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In vitro experiments were performed on human bladder carcinoma cells to evaluate the uptake of aluminum-chlorophthalocyanine (AlSPc) and the subcellular target of phototoxicity. In order to quantify the correlation of intracellular uptake and incubation time and to identify the primary subcellular target of phototoxicity, fluorescence and absorption measurements have been carried out as well as electron microscopic studies. Absorption and fluorescence measurements showed the largest value after 24 h of incubation time. Fluorescence microscopic studies suggested the sensitizer to be located in a brighter patch within cytoplasm. Electron microscopic studies using DAB (3,3′ diaminobenzidine) staining showed that the mitochondria are the primary target of phototoxic activity of AlSPc and that the majority of vacuoles of treated cells were originally mitochondria.
    Type of Medium: Electronic Resource
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  • 15
    ISSN: 1434-0879
    Keywords: Bladder carcinoma ; Tetramethyl hematoporphyrin ; Liposomes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The main problems presented by superficial bladder carcinoma, its high recurrence rate and multifocal appearance, require treatment of the bladder as a whole. Photodynamic therapy (PDT) is one such experimental treatment for superficial bladder carcinoma, involving the administration of a photosensitizer that accumulates in the tumor tissue, and subsequent irradiation of the tumor with light. Since the photosensitizers used in PDT suffer from several drawbacks, new photosensitizers are being sought. Drug delivery systems are also being investigated for the administration of hydrophobic photosensitizers and enhancement of photodynamic efficiency and tumor selectivity. In this study we examined a new photosensitizer, tetramethyl hematoporphyrin (TMHP), in two human bladder cancer cell lines. In the first pair of the experiments, TMHP was bound to unilamellar liposomes. Cellular uptake, dark toxicity and photodynamic efficiency were then studied. Fluorescence microscopy showed TMHP localization in the cytoplasm in a perinuclear region, sparing the nucleus. Dark toxicity occurred after incubation of cells with TMHP above a concentration of 20 μg/ml. Irradiation was carried out using an argon-pumped dye laser emitting a wavelength of 630 nm at a fluence of 3.6 and 7.2 J/cm2. Before irradiation, cells were incubated with TMHP at concentrations of 2.5 and 5 μg/ml for 1 h. Cell survival rates after incubation with 5 μg/ml TMHP and irradiation at 7.2 J/cm2 were 15.7% of control cells for Rec and 4.5% for Waf cells. Uptake studies showed a higher intracellular TMHP concentration in Waf than in Rec cells. This correlates with the higher PDT efficiency seen in Waf cells. Our results show that TMHP can be encapsulated into unilamellar liposomes without losing its photodynamic efficiency. TMHP is taken up by human bladder carcinoma cells after an incubation time of only 1 h. This short incubation time seems to be appropriate for an intravesical instillation of the photosensitizer for PDT in bladder cancer patients. Intravesical instillation might demonstrate higher phototoxic efficiency with reduced side effects. TMHP acts as a potent photosensitizer and shows drug- and light-dose-dependent cell destruction. Thus, TMHP has the potential for use in PDT in bladder cancer.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 24 (1996), S. 285-289 
    ISSN: 1434-0879
    Keywords: Bladder cancer ; Photodynamic therapy ; Aminolevulinic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A new concept in photosensitizing tumor cells is photosensitizer synthesis in situ. Aminolevulinic acid (ALA) is a precursor of protoporphyrin IX (PP IX), a potent photosensitizer. The goal of our study was to examine dark toxicity, phototoxic potential, metabolism of ALA and morphological alterations in Waf bladder cancer cells. Dark toxicity of Waf cells was observed after incubation with ALA, beginning at a concentration of 15 mM. Photodynamic treatment with ALA at concentrations of 1,5 and 10 mM showed a drug- and light-dose-dependent cell survival rate in comparison to a control group. Two incubation times of 3.5 and 5.5 h were compared for cell survival. After a longer incubation time of 5.5 h, cell survival was decreased in all experiments; this is consistent with our extraction data where higher fluorescence was found after 5.5 than after 3.5 h. The results show that ALA-induced photosensitization has a high potential for photodynamic therapy (PDT) of superficial bladder carcinoma.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 22 (1994), S. 21-23 
    ISSN: 1434-0879
    Keywords: Bladder cancer ; Photodynamic therapy ; Intravenous injection ; Intravesical instillation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Photodynamic therapy (PDT) consists in administration of a photosensitizer and subsequent irradiation of the tumor with visible light. Routinely the photosensitizer is given intravenously (i.v.). The goal of our study was to examine whether intravesical (i.b.) instillation of the photosensitizer for PDT of bladder cancer might be feasible. Therefore, the uptake of chlor-aluminum-sulfonated phthalocyanine (CASPc) in bladder, bladder tumor, skin, and muscle in a rat bladder cancer model after i.v. injection and i.b instillation was compared. The efficacy of PDT after either method of administration was also evaluated. The CASPc concentration in bladder tumor after i.v. injection was approximately 1.5-fold that after i.b. instillation. The ratio of CASPc concentration between bladder tumor and normal bladder was approximately 2:1 after administration by either route. There was no systemic absorption of CASPc after i.b. instillation; hence no systemic side effects are expected. PDT showed similar effects on bladder tumor after either method of administration, but less side effects on normal bladder wall after i.b instillation. Our results demonstrate that i.b. instillation of CASP for PDT of superficial bladder cancer seems to have advantages over i.v. injection.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    World journal of urology 1 (1983), S. 94-98 
    ISSN: 1433-8726
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Repeated instillation of adriamycin, mitomycin C and cisplatinum into the bladder of female Wistar rats induced epithelial proliferation and tumors. The induction rate depends on the total dose of the cytotoxic agent administered. No lesions were found in the control group. The biological behavior of the induced lesions is followed up in long-term experiments.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Springer
    World journal of urology 1 (1983), S. 113-113 
    ISSN: 1433-8726
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    World journal of urology 1 (1983), S. 186-191 
    ISSN: 1433-8726
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The aim of therapeutic management in cystinuria is simply to keep the urinary cystine concentration less than supersaturation and thus to prevent cystine precipitation and subsequent stone formation. However, the results in clinical experience with cystinuria treatment continue to be poor. The most promising form of therapy at present is changing cystine to a chemically more soluble form. Until now, treatment has relied primarily on d-penicillamine. However, the drug has serious side effects that limit its application. MPG is a newly developed drug, promising higher effectiveness and lack of toxic side effects. From 1970 to 1983, 38 female and 61 male cystinuric stone formers with a mean age of 36 years have been treated with MPG. Of these 99 patients, 42 form the basis of a report on long-term follow-up, i.e., MPG treatment for a period greater than 3 years. The dose of MPG required was adjusted to the urinary cystine level, which should be less than 100 mg/d if calculi are to be prevented. The results were as follows: 1) There was no recurrent stone formation except at the immediate onset of the MPG therapy when 14 of the 42 patients continued to pass small calculi. However, in these patients this must be attributed to their failure to follow the MPG regimen appropriately in the early days of the therapy. 2) The routinely performed tests were normal through the years, and there were no major side effects necessitating withdrawal of the drug. 3) Unfortunately, continued use of MPG during this 10-year period resulted in a slight loss of effectiveness in 27 of the 42 patients. In these patients the dosage had to be increased stepwise from 600 to 2,000 mg/d. 4) After a dosage increase to finally 2,500 mg/d after a treatment period of 9 years, the cystine excretion in only one patient showed no further response and thus this patient is the only treatment failure. Because of its high effectiveness and lack of toxicity MPG currently should be the treatment of choice in cystinuric stone-forming patients.
    Type of Medium: Electronic Resource
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