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1.
ACS Appl Bio Mater ; 6(12): 5621-5629, 2023 Dec 18.
Article in English | MEDLINE | ID: mdl-37983123

ABSTRACT

Hydrogels with the features of softness, biocompatibility, and modifiability have emerged as excellent materials in the biomedical field. However, the poor mechanical properties of the hydrogels limit their further practical applications. Double-network and metal ion coordination, such as Cu2+ and Zn2+, have achieved a significant reinforcement of the mechanical strength of the hydrogels. Herein, we report a Zn2+-enhanced polyelectrolyte double-network hydrogel stent with a mechanical enhancement phenomenon in bile. The gelatin/poly(zinc acrylate) (PZA) stent was constructed by dip-coating and UV irradiation. Although the mechanical strength of the as-prepared stent was quite weak, it was discovered to be mechanically enhanced by the natural bile. After exploring the effect of different components on the stents according to the components of bile, we found that Ca2+ in bile made a contribution to the mechanical enhancement of the stent. It is envisioned that this bile-enhanced gelatin/PZA stent provides a train of thought for the potential application of hydrogels in the biliary environment.


Subject(s)
Gelatin , Zinc , Hydrogels/therapeutic use , Bile , Stents
4.
J Ethnopharmacol ; 141(1): 178-82, 2012 May 07.
Article in English | MEDLINE | ID: mdl-22366674

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Eupolyphaga sinensis Walker popularly known as "preferred drug to regulate blood flow" are traditionally used in folk medicine in the treatment of ecchymoma, posttraumatic wound, hepatic fibrosis and tumor. AIM OF THE STUDY: To characterize chemical compositions and to evaluate the antitumor and immunomodulatory of Eupolyphaga sinensis Walker ethanol extract (ESEE) in hepatocarcinoma H(22) bearing mice. MATERIALS AND METHODS: ESEE was obtained by ethanol reflux extraction and analyzed by gas chromatography-mass spectrometry (GC-MS) after methylation. ICR mice were treated with ESEE for 14 consecutive days at doses of 31mg/kg (low-dose), 62mg/kg (mid-dose) and 124mg/kg (high-dose) after H(22) tumor cells were implanted. At the end of the experiments, the tumor weight of each mouse was measured. Levels of serum TNF-α and IFN-γ was assayed by ELISA. Protein expressions of Bax, Bcl-2 and caspases-3 were detected by immunohistochemistry. RESULTS: Chemical analysis revealed the presence of 6 components that account for 97.55% of fatty acids, indicating the occurrence of saturated and polyunsaturated fatty acids. Oral administration of ESEE could inhibit tumor growth, promote Th1 type cytokine productions (TNF-α and IFN-γ) and induce apoptosis of hepatocarcinoma via increase of Bax/Bcl-2 ratio and activation of caspases-3. Oral administration of ESEE in a dosage of 6.2g/kg did not lead to toxic effects in mice. CONCLUSIONS: ESEE was effective in inhibiting tumor growth in vivo and could also serve as immunoadjuvant for tumor therapy.


Subject(s)
Adjuvants, Immunologic/pharmacology , Antineoplastic Agents, Phytogenic/pharmacology , Carcinoma, Hepatocellular/drug therapy , Cockroaches , Drugs, Chinese Herbal/pharmacology , Ethanol/chemistry , Liver Neoplasms/drug therapy , Plant Extracts/pharmacology , Solvents/chemistry , Adjuvants, Immunologic/chemistry , Adjuvants, Immunologic/isolation & purification , Animals , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/isolation & purification , Apoptosis/drug effects , Carcinoma, Hepatocellular/blood , Carcinoma, Hepatocellular/immunology , Carcinoma, Hepatocellular/pathology , Caspase 3/metabolism , Cell Line, Tumor , Chemical Fractionation , Cockroaches/chemistry , Dose-Response Relationship, Drug , Drugs, Chinese Herbal/chemistry , Drugs, Chinese Herbal/isolation & purification , Enzyme-Linked Immunosorbent Assay , Gas Chromatography-Mass Spectrometry , Immunohistochemistry , Interferon-gamma/blood , Liver Neoplasms/blood , Liver Neoplasms/immunology , Liver Neoplasms/pathology , Male , Mice , Mice, Inbred ICR , Phytotherapy , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Plants, Medicinal , Proto-Oncogene Proteins c-bcl-2/metabolism , Th1 Cells/drug effects , Th1 Cells/immunology , Time Factors , Tumor Burden/drug effects , Tumor Necrosis Factor-alpha/blood , bcl-2-Associated X Protein/metabolism
5.
J Ethnopharmacol ; 139(2): 668-71, 2012 Jan 31.
Article in English | MEDLINE | ID: mdl-22193174

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Mosla dianthera as an aromatic herb is used in folk medicine for the treatment of cough, colds, fever, bronchitis, nasal congestion and headache. AIM OF THE STUDY: To characterize chemical compositions and to evaluate the anti-influenza effects of essential oils of M. dianthera (MDEO) in influenza virus A (IVA) infected mice. MATERIALS AND METHODS: MDEO was obtained by hydrodistillation and analysed by gas chromatography-mass spectrometry (GC-MS). ICR mice were treated with MDEO for 5 consecutive days at doses of 90-360 mg/kg after post-infected. Levels of Serum IL-4 and IFN-γ were assayed by ELISA. Levels of MOD, SOD, TAOC and GSH-Px in lung tissue were determined by colorimetric method. RESULTS: GC-MS analysis revealed the presence of 29 components that account for 97.74% of phenolic sesquiterpenes and aromatic compounds. The major compounds were elemicin (16.51%), thymol (14.77%), ß-caryophyllene (14.49%), iso-elemicin (9.22%), asarone (6.09%) and α-caryophyllene (5.26%). It had significant effects on decreasing lung viral titers, inhibiting pneumonia, reducing levels of serum IFN-γ and IL-4, and enhancing antioxidant activity in the lung tissue of IVA infected mice. CONCLUSIONS: MPE could exhibit therapeutical effects in IVA infected mice as a suppressor of IVA replication and inflammatory mediators and a promoter of antioxidant potentials. Therefore, MDEO could provide a safe and effective therapeutic candidate for treatment of influenza and its subsequent viral pneumonia.


Subject(s)
Antiviral Agents/pharmacology , Influenza A Virus, H1N1 Subtype/drug effects , Lamiaceae , Lung/drug effects , Oils, Volatile/pharmacology , Orthomyxoviridae Infections/drug therapy , Plant Oils/pharmacology , Animals , Antiviral Agents/chemistry , Antiviral Agents/isolation & purification , Antiviral Agents/toxicity , Colorimetry , Disease Models, Animal , Enzyme-Linked Immunosorbent Assay , Gas Chromatography-Mass Spectrometry , Glutathione Peroxidase/metabolism , Inflammation Mediators/blood , Influenza A Virus, H1N1 Subtype/pathogenicity , Interferon-gamma/blood , Interleukin-4/blood , Lamiaceae/chemistry , Lung/metabolism , Lung/pathology , Lung/virology , Malondialdehyde/metabolism , Mice , Mice, Inbred ICR , Oils, Volatile/chemistry , Oils, Volatile/isolation & purification , Oils, Volatile/toxicity , Orthomyxoviridae Infections/blood , Orthomyxoviridae Infections/pathology , Orthomyxoviridae Infections/virology , Plant Components, Aerial , Plant Oils/chemistry , Plant Oils/isolation & purification , Plant Oils/toxicity , Plants, Medicinal , Ribavirin/pharmacology , Superoxide Dismutase/metabolism , Virus Replication/drug effects
6.
Article in Chinese | MEDLINE | ID: mdl-17361828

ABSTRACT

Immunohistochemical streptavidin biotin-peroxidase complex method was used to investigate the effect of gamma-interferon (IFN-gamma) on the hepatic granuloma formation and liver fibrosis in mice infected with Taenia saginata in Duyun area of Guizhou Province. The results reveal contrary relation between the level of IFN-gamma in the liver and the degree of liver fibrosis (p<0.01). The injection of IFN-gamma considerably decreased (p<0.01) the area and size of granuloma (p<0.01).


Subject(s)
Cysticercosis/drug therapy , Cysticercus/drug effects , Granuloma/drug therapy , Interferon-gamma/therapeutic use , Liver Diseases, Parasitic/drug therapy , Animals , Cysticercosis/parasitology , Cysticercus/growth & development , Female , Granuloma/parasitology , Immunohistochemistry , Interferon-gamma/administration & dosage , Interferon-gamma/pharmacokinetics , Liver/drug effects , Liver/metabolism , Liver/parasitology , Male , Mice , Taenia saginata/drug effects , Taenia saginata/growth & development
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