Stanislaw Schastak
Leipzig University
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Featured researches published by Stanislaw Schastak.
PLOS ONE | 2010
Stanislaw Schastak; Svitlana Ziganshyna; Burkhard Gitter; Peter Wiedemann; Thomas Claudepierre
The worldwide rise in the rates of antibiotic resistance of bacteria underlines the need for alternative antibacterial agents. A promising approach to kill antibiotic-resistant bacteria uses light in combination with a photosensitizer to induce a phototoxic reaction. Concentrations of 1, 10 and 100µM of tetrahydroporphyrin-tetratosylat (THPTS) and different incubation times (30, 90 and 180min) were used to measure photodynamic efficiency against two Gram-positive strains of S.aureus (MSSA and MRSA), and two Gram-negative strains of E.coli and P.aeruginosa. We found that phototoxicity of the drug is independent of the antibiotic resistance pattern when incubated in PBS for the investigated strains. Also, an incubation with 100µM THPTS followed by illumination, yielded a 6lg (≥99.999%) decrease in the viable numbers of all bacteria strains tested, indicating that the THPTS drug has a high degree of photodynamic inactivation. We then modulated incubation time, photosensitizer concentration and monitored the effect of serum on the THPTS activity. In doing so, we established the conditions to obtain the strongest bactericidal effect. Our results suggest that this new and highly pure synthetic compound should improve the efficiency of photodynamic therapy against multiresistant bacteria and has a significant potential for clinical applications in the treatment of nosocomial infections.
Journal of Photochemistry and Photobiology B-biology | 2003
Michael Oertel; Stanislaw Schastak; Andrea Tannapfel; Ralf Hermann; Ulrich Sack; Joachim Mössner; Frieder Berr
Photodynamic therapy of bile duct cancer using hematoporphyrin derivative (HPD) and laser light of 630 nm wavelength is confined to a tumouricidal tissue penetration of 4 mm, which might be doubled with laser light between 700 and 800 nm. Therefore, we investigated the photosensitising properties of a novel bacteriochlorine, tetrakis-pyridyl-tetrahydroporphyrin tosylat (THP) with high absorption at 763 nm. Two biliary cancer cell lines (BDC, GBC) were incubated with HPD or THP to assess cellular uptake kinetics, dark cytotoxicity, and photodynamic cytotoxicity (laser light exposure 1-20 J/cm2). Tumours grown from BDC cells in subcutaneous tissue of severe combined immunodeficient mice were treated with laser light of 30 J/cm2 after injection of THP. The concentrations that killed 50% of cells in the dark were 680 microg/ml of HPD, but > 6400 microg/ml of THP in BDC cells, and 220 microg/ml of HPD, but 6400 microg/ml of THP in GBC cells. Both cell lines exhibited uptake and retention of THP and photodynamic cytotoxicity (up to 86% cells killed). THP induced tumour-selective phototoxicity in the cholangiocarcinoma model. The novel bacteriochlorine THP exhibits photosensitiser properties in biliary tract cancer cells in vitro and in vivo and could achieve deep tumouricidal tissue penetration due to photoactivation at 763 nm.
Journal of Physical Chemistry B | 2014
Yasser M. Riyad; Sergej Naumov; Stanislaw Schastak; Jan Griebel; Axel Kahnt; Tilmann Häupl; Jochen Neuhaus; Bernd Abel; Ralf Hermann
Reactive oxygen species (ROS) formed by light activated photosensitizers (PSs) are the hallmark of photodynamic therapy (PDT). It is generally accepted that commonly used PSs generate singlet oxygen ((1)O2) as the cell-toxic species via type II photosensitization. We explored here the consequences of chemical modification and the influence of the net charge of a cationic tetrahydroporphyrin derivative (THPTS) relative to the basic molecular structure on the red-shift of absorption, solubility, mechanistic features, and photochemical as well as cell-toxic activity. In order to shed light into the interplay between chemical modification driven intra- and intermolecular photochemistry, intermolecular interaction, and function, a number of different spectroscopic techniques were employed and our experimental studies were accompanied by quantum chemical calculations. Here we show that for THPTS neither (1)O2 nor other toxic ROS (superoxide and hydroxyl radicals) are produced directly in significant quantities in aqueous solution (although the formation of singlet oxygen is energetically feasible and as such observed in acetonitrile). Nevertheless, the chemically modified tetrapyrrole photosensitizer displays efficient cell toxicity after photoexcitation. The distribution and action of THPTS in rat bladder caricinoma AY27 cells measured with fluorescence lifetime imaging microscopy shows accumulation of the THPTS in lysosomes and efficient cell death after irradiation. We found evidence that THPTS in water works mainly via the type I mechanism involving the reduction rather than oxidation of the excited triplet state THPTS(T1) via efficient electron donors in the biosystem environment and subsequent electron transfer to produce ROS indirectly. These intriguing structure-activity relationships may indeed open new strategies and avenues in developing PSs and PDT in general.
Optical Fibers and Sensors for Medical Applications II | 2002
Georg Hillrichs; Hartmut Dietz; Martin Ruetting; Stanislaw Schastak; Peter Wiedemann; Yuji Matsuura; Mitsunobu Miyagi; Karl-Friedrich Klein
Many potential microsurgical applications of UV laser radiation need a flexible beam guiding system. Especially for the argon fluorine excimer laser ((lambda) equals 193 nm) and for the 5th harmonic of the Nd:YAG laser ((lambda) equals 213 nm) the use of optical fused silica fibers is difficult. In this work we designed and tested a laboratory prototype of a scalpel for surgical treatments of the retina based on UV laser ablation. To achieve the necessary flexibility and to provide laser fluences above the ablation threshold of retina we developed a new type of beam guiding device. A hollow core waveguide is used in combination with a short length of a special fused silica optical fiber to guide the laser beam. To increase the laser fluence at the distal scalpel tip and to achieve a very small cut width a fused silica fiber (core diameter 600 micrometers ) has been tapered down to a diameter of about 150 micrometers .
Photodiagnosis and Photodynamic Therapy | 2017
Mandy Berndt-Paetz; Annett Weimann; Nadine Sieger; Stanislaw Schastak; Yasser M. Riyad; Jan Griebel; Vinodh Kumar Adithyaa Arthanareeswaran; Jens-Uwe Stolzenburg; Jochen Neuhaus
BACKGROUND Efficacy of PDT in muscle-invasive bladder cancer is hampered by low tissue penetration of most photosensitizers by short excitation wavelength. THPTS is excitable at near-infrared (760nm) allowing tissue penetration up to 15mm. We examined the cellular effects of THPTS-PDT in human bladder cancer cells. MATERIAL AND METHODS We used four human transitional carcinoma cell lines, epithelial bladder progenitors (HBLAK) and bladder smooth muscle cells (HBSMC). We used flow cytometry to examine pharmacokinetics of THPTS, confocal laser scanning microscopy to analyze subcellular localization and production of reactive oxidative species (ROS), examined cytotoxicity and cell death pathways (qRT-PCR). RESULTS Total uptake varied between cell lines and was significantly high in HBLAK and HBSMC. Lysosomal localization was mainly seen in cancer cells and HBLAK, while THPTS was distributed throughout the cytoplasm in HBSMC. Significant ROS production was detected 30min after THPTS-PDT. Growth arrest occurred within 4h and resulted in apoptotic and necrotic cytotoxicity after 24h. Cytotoxicity was dose-dependent and specifically high in cancer cells and HBLAK and significantly low in HBSMC. CONCLUSION THPTS-PDT induces cellular mechanisms leading to cellular growth arrest, apoptosis and necrosis in human bladder cancer cells. These effects are only partly dependent on the total amount of THPTS uptake and rather dependent on its subcellular compartmentalization. HBSMC are hardly affected by THPTS-PDT confirming tumor specificity and safety. THPTS is a promising new photosensitizer with the unique advantage of deep tissue penetration allowing the treatment of solid tumors and warranting further animal studies.
Laser-Medizin: eine interdisziplinäre Zeitschrift ; Praxis, Klinik, Forschung | 1998
Stanislaw Schastak; N. Kondratjuk; D. Molotkov; A. Schagov; Peter Wiedemann
Summary Laser radiation has found wide application in medicine because of the ability to control is effect by manipulation of energy distribution, regulation of power and precise selection of wavelength. The argon fluoride excimer laser with high energy output at 193 nm is known for its ability to ablate biologic tissue and has been widely accepted for refractive surgery. In addition to the common excimer the use of fifth harmonic of Nd:YAG at 213 nm has become popular. The solid state fifth harmonic laser system is compact, low in cost, easier to maintain as excimer laser and utilizes not toxic gases. In this article, we present our numerical calculations of the pulse energy at 193 nm of a solid state sum frequency generator (SFG) and discussed the basic principles of building high efficiency laser systems generating tunable radiation in the range from 190 to 199 nm.
Journal of Photochemistry and Photobiology B-biology | 2005
Stanislaw Schastak; Benedikt Jean; Romy Handzel; Genady Kostenich; Ralf Hermann; Ulrich Sack; Arie Orenstein; Yu-Sheng Wang; Peter Wiedemann
Lasers in Surgery and Medicine | 2006
Benjamin Funke; Astrid Jüngel; Stanislaw Schastak; Katharina Wiedemeyer; Frank Emmrich; Ulrich Sack
Archive | 1999
Stanislaw Schastak; Alexander Shulga; Frieder Berr; Peter Wiedemann
Lasers in Surgery and Medicine | 2007
Stanislaw Schastak; Yousef Yafai; Tsutomu Yasukawa; Yu-Sheng Wang; Georg Hillrichs; Peter Wiedemann