Autor: Agata Szczepanik

Zapytanie ofertowe nr 02/FENG.01.01-IP.01-A05T/23z dnia 04 września 2024 r.

Zapytanie ofertowe nr 02/FENG.01.01-IP.01-A05T/23z dnia 04 września 2024 r. Zapytanie ofertowe nr 02/FENG.01.01-IP.01-A05T/23 z dnia 04 września 2024 r. Przedmiotem zamówienia jest: „Zakup układów FPGA 2” w ramach rekomendowanego do dofinansowania projektu nr 02/FENG.01.01-IP.01-A05T/23 o tytule: „Opracowanie mobilnego urządzenia do lokalnych badań nowotworów skóry, poziomu utlenowania oraz biodozymetrii poekspozycyjnej” współfinansowanego ze środków Unii Europejskiej w ramach Programu Fundusze Europejskie dla Nowoczesnej Gospodarki Priorytet 1. Wsparcie dla przedsiębiorców Nabór FENG.01.01-IP.01-002/23 – Ścieżka SMART. Zapytanie ofertowe nr 02/FENG.01.01-IP.01-A05T/23 z dnia 04 września 2024 r. Załącznik nr 1. – szczegółowe warunki zamówienia Załącznik nr 2 – formularz ofertowy – wzór Załącznik nr 3 – oświadczenie dotyczące przesłanek wykluczenia Attachment no.3 Załącznik nr 4 – oświadczenie dotyczące przesłanek wykluczenia Attachment no.4 Załącznik nr 5 – wzór umowy sprzedaży Rozstrzygnięcie zapytania ofertowego

Zapytanie ofertowe nr 02/FENG.01.01-IP.01-A05T/23z dnia 04 września 2024 r. Dowiedz się więcej »

Zapytanie ofertowe nr 01/FENG.01.01-IP.01-A05T/23z dnia 09 luty 2024 r.

Zapytanie ofertowe nr 01/FENG.01.01-IP.01-A05T/23 z dnia 09 luty 2024 r. Przedmiotem zamówienia jest: „Zakup układów FPGA” w ramach ewaluowanego projektu nr 01/FENG.01.01-IP.01-A05T/23 o tytule: „Opracowanie mobilnego urządzenia do lokalnych badań nowotworów skóry, poziomu utlenowania oraz biodozymetrii poekspozycyjnej” współfinansowanego ze środków Unii Europejskiej w ramach Programu Fundusze Europejskie dla Nowoczesnej Gospodarki Priorytet 1. Wsparcie dla przedsiębiorców Nabór FENG.01.01-IP.01- 002/23 – Ścieżka SMART. Zapytanie ofertowe nr 01/FENG.01.01-IP.01-A05T/23 z dnia 09 luty 2024 r. Request for Proposal no. 01/FENG.01.01-IP.01-A05T/23of 9 February 2024 Załącznik nr 1. – szczegółowe warunki zamówienia Załącznik nr 2 – formularz ofertowy – wzór Załącznik nr 3 – oświadczenie dotyczące przesłanek wykluczenia Attachment no.3 Załącznik nr 4 – oświadczenie dotyczące przesłanek wykluczenia Attachment no.4 Protokół odbioru cząstkowego do zapytania ofertowego Protokół z rozstrzygnięcia zapytania ofertowego

Zapytanie ofertowe nr 01/FENG.01.01-IP.01-A05T/23z dnia 09 luty 2024 r. Dowiedz się więcej »

Konkurs nr 01/FENG.01.01-IP.01-A05T/23 na pozycję Starszy Konstruktor z dnia 26 czerwca 2024 r

W związku z przyznaniem dofinansowania projektu nr FENG.01.01-IP.01-A05T/23 o tytule: „Opracowanie mobilnego urządzenia do lokalnych badań nowotworów skóry, poziomu utlenowania oraz biodozymetrii poekspozycyjnej” współfinansowanego ze środków Unii Europejskiej w ramach Programu Fundusze Europejskie dla Nowoczesnej Gospodarki Priorytet 1. Wsparcie dla przedsiębiorców Nabór FENG.01.01-IP.01-002/23 – Ścieżka SMART

Konkurs nr 01/FENG.01.01-IP.01-A05T/23 na pozycję Starszy Konstruktor z dnia 26 czerwca 2024 r Dowiedz się więcej »

Zapytanie ofertowe nr 29/POIR.01.02.00-00-0077/18 z dnia 21 kwietnia 2023 r.

Zapytanie ofertowe nr 29/POIR.01.02.00-00-0077/18 z dnia 21 kwietnia 2023 r. Przedmiotem zamówienia jest: „Przeprowadzeniu kompletu badań na zgodność z dyrektywą kompatybilności elektromagnetycznej (dyrektywa 2014/30/UE)” w ramach projektu nr POIR.01.02.00-00-0077/18 o tytule: „Innowacyjny tomograf impulsowy do przestrzennego obrazowania zmian neurodegeneracyjnych z wykorzystaniem techniki rezonansu elektronowego” współfinansowanego ze środków Unii Europejskiej w ramach Programu Operacyjnego Inteligentny Rozwój, działanie 1.2., sektorowe programy B+R InnoNeuroPharm. Zapytanie ofertowe nr 29/POIR.01.02.00-00-0077/18 z dnia 21 kwietnia 2023 r. Załącznik nr 1.pdf Załącznik nr 2.pdf Załącznik nr 3.pdf Załącznik nr 4.pdf

Zapytanie ofertowe nr 29/POIR.01.02.00-00-0077/18 z dnia 21 kwietnia 2023 r. Dowiedz się więcej »

redox status

It is possible to obtain 3D map of redox status in a fast and non-invasive way?

It is possible to obtain 3D map of redox status in a fast and non-invasive way? Antioxidant defence system and stabilized level of reactive oxygen species (ROS) protect organisms against various diseases such as stroke or inflammation. In order to create an effective therapy for such diseases, the in vivo redox status map may be useful. The fact is that EPR imaging, with a suitable external imaging probe, is a great tool for monitoring the balance or imbalance between oxidation and reduction reactions and assessing the redox state of the brain. That issue was considered by Hirotada Fujii and his research group in the paper “Mapping of Redox Status in a Brain-Disease Mouse Model by Three-Dimensional EPR Imaging”. Control mice and transient middle cerebral artery occlusion (MCAO) mice were used as the subjects in this experiment. The in vivo redox state in the brains of control and MCAO mice was measured by improved EPR imager that enabled rapid data acquisition, engineered by Fuji and colleagues. Reduction of the acquisition time has allowed to obtain high-quality 3D images in a very short time. A nitroxide, 3-hydroxymethyl-2,2,5,5-tetramethylpyrrolidine-1-oxy (HMP), was used as a redox-sensitive spin probe. HMP has passed freely through the brain-blood barrier, which was also confirmed by MRI examination.  The redox status of MCAO mice was visualized as 3D maps, where each voxel represents   half-live of HMP in the difference part of brain. The half-life mapping of HMP has shown a significant heterogeneity of the redox state in brain of MCAO mice. It was also revealed that there is an increase of HMP in the brain of ischemia-reperfusion-treated mice, and consequently, the reduction rate of nitroxide is slower in MCAO mice. This study confirmed that with the use of an EPR scanner and given an appropriate time of data acquisition, is it possible to provide a 3D map of the in vivo redox state in the mouse brain . Therefore, the role of EPR imaging systems in the research on redox status is significant. References: Fujii H, Sato-Akaba H, Kawanishi K, Hirata H.; Mapping of redox status in a brain-disease mouse model by three-dimensional EPR imaging; Magn Reson Med. 2011 Jan;65(1):295-303; DOI: 10.1002/mrm.22598.

It is possible to obtain 3D map of redox status in a fast and non-invasive way? Dowiedz się więcej »

invivo po2

It is possible to conduct in-vivo pO2 measurements in mouse?

It is possible to conduct in-vivo pO2 measurements in conscious mouse? It is a well-known fact that the oxygenation level is a significant determinant when it comes to identifying and monitoring neoplastic changes. Another fact is that anesthetics affect the physiology of the oxygen inside the animal’s body, which could cause inaccuracies during in vivo experiments. The question is whether it is possible to monitor conscious animal, avoiding the anesthesia’s impact and, simultaneously, collect high-quality data. To answer this question, we begin by taking a closer look at the study conducted by Matsumoto et al. “Dynamic Monitoring of Localized Tumor Oxygenation Changes Using RF Pulsed Electron Paramagnetic Resonance in Conscious Mice”. The authors used an electron paramagnetic resonance (EPR) spectroscopy at frequency of 750 MHz to assess the pO2 level in tumor bearing mice. Crystals of lithium phthalocyanine (LiPc) was implanted into squamous cell carcinoma (SCC) tumor and femoral muscle on opposing legs of mice. It has been examined whether there is a correlation between oxygenation and factors such as anesthesia, body temperature and carbogen inhalation. As a consequence of the conducted experiment, this correlation has been confirmed by Matsumoto and colleagues. In conclusion, EPR spectroscopy, due to a rapid acquisition of spectral data, enables the pO2 measurements in conscious mice and minimizing the influence of anesthetics. This ability makes the EPR with LiPc a powerful tool in oncology researches, especially. in studies on tissues oxygenation. References: Matsumoto S. et al.; Dynamic monitoring of localized tumor oxygenation changes using RF pulsed electron paramagnetic resonance in conscious mice; Magn Reson Med. 2008 Mar;59(3):619-25; DOI: 10.1002/mrm.21500.

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cancerous tissues

Biological differences between cancerous tissues and healthy ones.

Biological differences between cancerous tissues and healthy ones. Nowadays, a fight against cancer seems to be one of the most important issue for scientists. Research groups all around the world are working on new cancer therapies which target tumour cells. One of the approaches to this problem consists in learning the physiological differences between normal and neoplastic tissue. The differences could appeared among physiological parameters such as redox state, oxygenation and pH value. The fact is that Electron Paramagnetic Resonance is a non-invasive and rapid method that enables detection of insignificant changes of above-mentioned characteristics and thus it is a great tool for preclinical cancer research and has a great potential to become a method used in clinical trials. A hypothesis that the redox state and pO2 value differ in normal and neoplastic tissue, have been presented in a paper “Noninvasive Imaging of Tumor Redox Status and Its Modification by Tissue Glutathione Levels” by Kuppusamy et al. The main goal of the research was:  i) develop a non-invasive technique that enables measurement and imaging of the tissue’s redox state ii)  acquire images of redox state from normal and malignant tissue iii) analyse the role of glutathione (GSH) in changes of the redox status. In examinations conducted by the research group, in vivo EPR spectroscopy and imaging (EPRI) with a nitroxide spin probe were used. Buthionine sulfoximine (BSO), as a GSH synthesis inhibitor, was applied to decrease the level of GSH in a tissue. The subject was tumour-bearing mice with implanted radiation-induced fibrosarcoma (RIF-1) tumour growing in the right leg. The normal tissue from the left leg was used as a control. The results of experiments have confirmed the hypothesis posed by the research group. It has been shown that physiological parameters such as redox status, in the normal tissue and in the neoplastic tissue significantly differ from each other. Obtained data showed that it was a higher concentration of GSH in malignant tissue. It was also noted that BSO treatment causes differences in reduction of GSH level. Tumour tissue showed higher reduction rate in comparison to healthy tissue. Physiological differences between malignant tissue and normal tissue are a significant factor involved in improving cancer treatments, and what is important, EPR technique is a very promising and helpful tool in such researches.  References: Kuppusamy P. et al.; Noninvasive imaging of tumor redox status and its modification by tissue glutathione levels; Cancer Res. 2002 Jan 1;62(1):307-12.

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cancer

Differences Between Normal Tissue and Tumour Tissue

EPR is making its way to clinical studies There are  subtle physiological differences between normal tissue and tumour tissue. These differences mainly concern characteristics such as redox status and pO2 levels. Thus, imaging methods that enable detection of these biological variations may be valuable in developing treatment strategies. Electron Paramagnetic Resonance Imaging is capable of non-invasive measurements of redox state and pO2 level, involving proper nitroxide probes. The study of the distribution and lifetime of nitroxides in normal and tumour tissue was the aim of Kuppusamy’s research paper “In vivo Electron Paramagnetic Resonance Imaging of Tumour Heterogeneity and Oxygenation in a Murine Model”. As has been pointed out, nitroxides occur in biological systems in two forms: as a free radical and/or as a diamagnetic hydroxylamine which is a product of one-electron reduction of the nitroxide free radical. The reduction rate of nitroxides is increasing during  hypoxia conditions. A specificity of these compounds may indicate some of the physiological differences in tissues, which exist under various oxygenation levels. In order to detect tissue heterogeneity, three nitroxides were used: TPL (4-OH, 2,2,6,6-tetramethylpiperidine-1-oxyl ), 3-CP (3-carbamoyl-proxyl) and PDT (4-oxo-L,2,6,6-tetramethylpiperadine-1-oxyl). TPL has been specified as an in vitro radioprotector, the 3-CP, due to greater biostability in tissues, was used in in vivo EPRI experiments and PDT was used as a probe for pO2 levels assessment.  Mice bearing tumour in size approximately 10 – 15 mm in diameter were examined. Electron Paramagnetic Resonance Imaging was used to perform measurements of reduction rates, distribution and levels of nitroxides in normal and tumour tissues. The obtained results have shown that the peak level of nitroxides was significantly lower in the tumour tissue. Moreover, the reduction rate of nitroxides was much higher in tumours, compared to normal tissues. 3D imaging has confirmed a significant heterogeneity in the distribution of spin probes and redox state in tumour tissue, whereas normal tissues has remained homogenous. With the use of PDT, a significant difference in pO2 level between normal tissue and tumour tissue have been shown. An average level of oxygenation in tumours was three times lower, then in normal tissue. A state of hypoxia in tumours is linked to lower nitroxides content and its greater reduction rate. The study conducted by Kuppusamy’s group has confirmed, that EPRI is a technique that enables performing both the spatial bio-distribution and functional imaging as a result of spectral properties of nitroxides. EPRI may be a breakthrough approach to plan  treatment of neoplastic diseases. References:  Kuppusamy P et al.;In vivo electron paramagnetic resonance imaging of tumor heterogeneity and oxygenation in a murine model; Cancer Res. 1998 Apr 1;58(7):1562-8. 

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neurodegenerative diseases

A new therapeutic approach for neurodegenerative diseases.

A new therapeutic approach for neurodegenerative diseases. Nowadays, neurodegenerative diseases are a very serious problem. Scientists are trying to discover all the mechanisms for the formation of diseases such as Alzheimer’s, as well as finding a way to diagnose them faster and treat them more effectively. An interesting fact is that a research group led by professor Emoto has conducted a series of animal studies, the result of which was the discovery of a potential therapeutic approach for neurodegenerative diseases. The details of those experiments were shown in the article “Non-invasive imaging of the levels and effects of glutathione on the redox status of mouse brain using electron paramagnetic resonance imaging”. The authors’ purpose was to determine the influence of gluthathione (GSH) on the redox state in the mouse brain. In order to measure the GSH level in animal models, electron paramagnetic resonance (EPR) imaging and a redox-sensitive nitroxide imaging probe, 3-methoxycarbonyl-2,2,5,5-tetramrthylpiperidine-1-oxyl (MCP), were used. As emphasized, the antioxidants defence system, endogenous antioxidants compounds and enzymatic systems are able to protect the brain from oxidative damage. On the one hand, GSH and ascorbic acid (AsA) are the main endogenous antioxidants. More importantly, their level of concentration could change in the case of a disease. It should be mentioned that AsA, in contrast to GSH, directly influences the reduction of nitroxides. On the other hand, nitroxide probes, once introduced into the animal’s body, are easily reduced under the oxidative stress condition. The reduction rate of nitroxides may be considered as a ratio of in vivo redox state. Therefore, the capabilities of EPR imaging and the MCP probe have been used in this examination. On the basis of the map of MCP reduction rate, a visualization of the redox state in an animal model under oxidative stress has been made. Due to the reduction of GSH levels in the animal’s body, the redox map of mice brain (control and GSK-depleted) has shown a significant change in the redox state. The linear relationship between the reduction rate of nitroxide probe and the GSH concentration in both control and GSH-depleted mice, has been observed. Therefore, this correlation could be used as a potential method for estimating the GSK levels in vivo from the redox map. Of course, this type of measurement could be conducted with the use of EPR and a nitroxide probe. It is important to emphasize that GSH levels decrease in the case of diseases related to oxidative stress, such as Alzheimer’s disease. The increase of GSK levels has a potential approach for creating therapies against neurodegenerative disorders. The contribution of GSK to neurodegenerative diseases needs detailed studies, and fortunately EPR imaging could be helpful in such research. References Emoto MC, Matsuoka Y, Yamada KI, Sato-Akaba H, Fujii HG; Non-invasive imaging of the levels and effects of glutathione on the redox status of mouse brain using electron paramagnetic resonance imaging; Biochem Biophys Res Commun. 2017 Apr 15;485(4):802-806; DOI: 10.1016/j.bbrc.2017.02.134.

A new therapeutic approach for neurodegenerative diseases. Dowiedz się więcej »

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