methylcellulose has been researched along with Necrosis* in 8 studies
8 other study(ies) available for methylcellulose and Necrosis
Article | Year |
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Injectable methylcellulose hydrogel containing silver oxide nanoparticles for burn wound healing.
A thermo-sensitive methylcellulose (MC) hydrogel containing silver oxide nanoparticles (NPs) was prepared via one-pot synthesis in which a silver acetate precursor salt (CH Topics: Acetates; Animals; Anti-Bacterial Agents; Burns; Drug Liberation; Hydrogels; Inflammation; Male; Methylcellulose; Nanoparticles; Necrosis; Oxides; Porosity; Rats, Sprague-Dawley; Silver Compounds; Wound Healing | 2018 |
Evaluation of methylcellulose and dimethyl sulfoxide as the cryoprotectants in a serum-free freezing media for cryopreservation of adipose-derived adult stem cells.
Developing effective techniques for the cryopreservation of human adipose-derived adult stem cells (ASCs) could increase the usefulness of these cells in tissue engineering and regenerative medicine. To this end, we investigated the post-freeze/thaw viability and apoptotic behavior of Passage 1 (P1) adult stem cells (ASCs) in 11 different media: (i) the traditional media containing Dulbecco's modified Eagle's medium (DMEM) with 80% fetal calf serum (FCS) and 10% dimethyl sulfoxide (DMSO), (ii) DMEM with 80% human serum (HS) and 10% DMSO, (iii) DMEM with 1% methyl cellulose (MC) and 10% of either HS or FCS or DMSO, and (iv) DMEM with 0%, 2%, 4%, 6%, 8%, or 10% DMSO. Approximately 1 mL (10(6) cells/mL) of P1 ASCs were frozen overnight in a -80 degrees C freezer and stored in liquid nitrogen for 2 weeks before being rapidly thawed in a 37 degrees C water bath (1-2 min of agitation), resuspended in culture media, and seeded in separate wells of a 6-well plate for a 24-h incubation period at 37 degrees C. After 24 h, the thawed samples were analyzed by bright-field microscopy and flow cytometry. The results suggest that the absence of DMSO (and the presence of MC) significantly increases the fraction of apoptotic and/or necrotic ASCs. However, the percentage of viable cells obtained with 2% DMSO and DMEM was comparable with that obtained in freezing media with 10% DMSO and 80% serum (HS or FCS), that is, approximately 84% +/- 5% and approximately 84% +/- 8%, respectively. Adipogenic and osteogenic differentiation behavior of the frozen thawed cells was also assessed using histochemical staining. Our results suggest that post-thaw ASC viability, adipogenic and osteogenic differentiability can be maintained even when they are frozen in the absence of serum but with a minimal concentration of 2% DMSO in DMEM. Topics: Adipocytes, White; Adult Stem Cells; Apoptosis; Cell Differentiation; Cell Separation; Cell Survival; Cells, Cultured; Cryopreservation; Cryoprotective Agents; Culture Media, Serum-Free; Dimethyl Sulfoxide; Humans; Methylcellulose; Necrosis; Osteocytes | 2010 |
Induced acute ocular hypertension: mode of retinal cell degeneration.
The effects of experimental hypertension on retinal cells were studied. Evaluation was made of IOP levels and degree of cell damage by cytochemical and DNA analysis, and degeneration modes: necrosis and apoptosis. Topics: Acute Disease; Animals; Apoptosis; DNA; Follow-Up Studies; Intraocular Pressure; Male; Methylcellulose; Necrosis; Ocular Hypertension; Rats; Retina; Retinal Degeneration | 1998 |
The protective effect of polyriboinosinic acid-polyribocytidylic acid against the occurrence of galactosamine-induced liver cell injury in rat.
A marked increase of serum transaminase activities, histological changes of livers similar to those seen in viral hepatitis in man, and inhibition of hepatic protein synthesis were observed in rats following a single injection of D-galactosamine-HCl. These galactosamine-induced phenomena were prevented by the pretreatment of polyriboinosinic acid-polyribocytidylic acid 24 h before the galactosamine administration. Topics: Alanine Transaminase; Animals; Aspartate Aminotransferases; Carboxymethylcellulose Sodium; Chemical and Drug Induced Liver Injury; Galactosamine; Liver; Liver Diseases; Male; Methylcellulose; Necrosis; Peptides; Poly I-C; Polylysine; Rats; Rats, Inbred Strains | 1983 |
Thermography and microangiography in the investigation of local toxic effects of contrast media and anaesthetics.
Topics: Anesthetics, Local; Angiography; Animals; Capillary Permeability; Contrast Media; Dextrans; Diatrizoate; Ear, External; Lidocaine; Mepivacaine; Methods; Methylcellulose; Microcirculation; Microradiography; Necrosis; Rabbits; Regional Blood Flow; Sodium Chloride; Thermography; Time Factors; Transillumination | 1972 |
The influence of the autonomic nervous system on phagocytosis. VII. Changes caused by chronic administration of cobefrin.
Topics: Animals; Antibodies; Body Weight; Carbon Isotopes; Complement System Proteins; Guinea Pigs; Leukocytes; Methylcellulose; Necrosis; Norepinephrine; Opsonin Proteins; Phagocytosis; Salmonella typhimurium; Shigella; Sodium Chloride; Staphylococcus; Sympathetic Nervous System | 1969 |
[Further observations on the storage of carboxymethyl-cellulose in the medulla of the adrenal gland].
Topics: Adrenal Medulla; Animals; Cricetinae; Cytoplasm; Endoplasmic Reticulum; Female; Golgi Apparatus; Histocytochemistry; Male; Methods; Methylcellulose; Microscopy; Microscopy, Electron; Mitochondria; Necrosis; Ribosomes | 1969 |
Production and prevention of two distinctive kinds of destruction of adrenal cortex.
Topics: Adrenal Glands; Adrenalectomy; Animals; Benz(a)Anthracenes; Corticosterone; Heparin; Heparin Antagonists; In Vitro Techniques; Liver; Methylcellulose; Methylcholanthrene; Necrosis; Oxidoreductases; Polyvinyls; Povidone; Quaternary Ammonium Compounds; Rats; Sulfonic Acids | 1965 |