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1.
ChemistryOpen ; 10(6): 645-652, 2021 06.
Artículo en Inglés | MEDLINE | ID: mdl-34126002

RESUMEN

3-Chloroquinoline-2,4-diones react with cyanide ions in dimethyl formamide to give 3-cyanoquinoline-2,4-diones in small yields due to the strong hindrance of the substituent at the C-3 atom. Good yields can be achieved if the substituent at this position is the methyl group. In the methanol solution, the reaction proceeds by an addition mechanism to form 2-oxo-1a,2,3,7b-tetrahydrooxireno[2,3-c]quinoline-7b-carbonitriles, from which 4-hydroxy-3-methoxy-2-oxo-1,2,3,4-tetrahydroquinoline-4-carbonitriles are subsequently formed by opening of the epoxide ring with methanol. Some minor products of these reactions have also been isolated. The 1 H, 13 C and 15 N NMR spectra of the prepared compounds were measured, and all resonances were assigned using appropriate two-dimensional spectra.

2.
In Vivo ; 35(2): 731-741, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33622866

RESUMEN

BACKGROUND/AIM: Anastomotic leakage is a feared complication in colorectal surgery. Postoperative peritoneal adhesions can also cause life-threatening conditions. Nanofibrous materials showed their pro-healing properties in various studies. The aim of the study was to evaluate the impact of double-layered nanofibrous materials on anastomotic healing and peritoneal adhesions formation. MATERIALS AND METHODS: Two versions of double-layered materials from polycaprolactone and polyvinyl alcohol were applied on defective anastomosis on the small intestine of healthy pigs. The control group remained with uncovered defect. Tissue specimens were subjected to histological analysis and adhesion scoring after 3 weeks of observation. RESULTS: The wound healing was inferior in the experimental groups, however, no anastomotic leakage was observed and the applied material always kept covering the defect. The extent of adhesions was larger in the experimental groups. CONCLUSION: Nanofibrous materials may prevent anastomotic leakage but delay healing.


Asunto(s)
Fuga Anastomótica , Nanofibras , Anastomosis Quirúrgica/efectos adversos , Fuga Anastomótica/etiología , Fuga Anastomótica/patología , Fuga Anastomótica/prevención & control , Animales , Colon/patología , Porcinos , Adherencias Tisulares/prevención & control , Cicatrización de Heridas
3.
Anticancer Res ; 40(12): 6817-6833, 2020 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-33288574

RESUMEN

BACKGROUND: In patients with colorectal liver metastases, the possibility for radical liver resection can be limited by oxaliplatin-induced sinusoidal obstruction syndrome (SOS). This study investigates the potential of mesenchymal stem cells (MSC) to improve the outcome of liver resections in pigs with SOS. MATERIALS AND METHODS: SOS was induced in all animals (n=20) on day 0. Animals in the experimental group (n=8) received allogeneic MSC on day 7. Liver resection was performed in all animals on day 14 and the animals were observed until day 28. Ultrasound volumetry, biochemical analysis and histological examination of liver parenchyma was performed during the follow-up period. RESULTS: Six animals from the control group died prematurely, while all animals survived in the experimental group. According to histology, biochemical analysis and ultrasound volumetry, there were no significant differences between the groups documenting the effect of MSC. CONCLUSION: Single dose allogeneic MSC administration improved survival of animals with SOS undergoing partial liver resection. Further experiments with different timing of liver resection and MSC administration should be performed to investigate the effect of MSC in more detail.


Asunto(s)
Hepatectomía , Enfermedad Veno-Oclusiva Hepática/patología , Enfermedad Veno-Oclusiva Hepática/terapia , Trasplante de Células Madre Mesenquimatosas , Células Madre Mesenquimatosas , Animales , Biomarcadores , Neoplasias Colorrectales/patología , Terapia Combinada , Modelos Animales de Enfermedad , Femenino , Hepatectomía/métodos , Enfermedad Veno-Oclusiva Hepática/etiología , Inmunohistoquímica , Inmunofenotipificación , Neoplasias Hepáticas/complicaciones , Neoplasias Hepáticas/secundario , Masculino , Células Madre Mesenquimatosas/citología , Porcinos , Resultado del Tratamiento
4.
Anticancer Res ; 39(12): 6603-6620, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31810926

RESUMEN

BACKGROUND: In clinical medicine, little is known about the use of allografts for portal vein (PV) reconstruction after pancreaticoduodenectomy (PD). Portal and caval systems are physiologically different, therefore the properties of allografts from caval and portal systems were studied here in a pig model. MATERIALS AND METHODS: PD with PV reconstruction with allogeneic venous graft from PV or inferior vena cava (IVC) was performed in 26 pigs. Biochemical analysis and ultrasonography measurements were performed during a 4-week monitoring period. Computer simulations were used to evaluate haemodynamics in reconstructed PV and explanted allografts were histologically examined. RESULTS: The native PV and IVC grafts varied in histological structure but were able to adapt morphologically after transplantation. Computer simulation suggested PV grafts to be more susceptible to thrombosis development. Thrombosis of reconstructed PV occurred in four out of five cases in PV group. CONCLUSION: This study supports the use of allografts from caval system for PV reconstruction in clinical medicine when needed.


Asunto(s)
Simulación por Computador , Pancreaticoduodenectomía , Vena Porta/cirugía , Vena Cava Inferior/trasplante , Aloinjertos , Anastomosis Quirúrgica/métodos , Animales , Cadáver , Femenino , Hemodinámica , Masculino , Tamaño de los Órganos , Tratamientos Conservadores del Órgano , Vena Porta/anatomía & histología , Vena Porta/diagnóstico por imagen , Vena Porta/fisiología , Complicaciones Posoperatorias/etiología , Píloro , Procedimientos de Cirugía Plástica/métodos , Flujo Sanguíneo Regional , Porcinos , Recolección de Tejidos y Órganos , Ultrasonografía , Vena Cava Inferior/anatomía & histología , Vena Cava Inferior/diagnóstico por imagen , Vena Cava Inferior/fisiología , Trombosis de la Vena/etiología
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