Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
J Ethnopharmacol ; 312: 116454, 2023 Aug 10.
Article in English | MEDLINE | ID: mdl-37059246

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Polyrhachis vicina Roger (P. vicina), a traditional Chinese medicinal animal, has been used to treat rheumatoid arthritis, hepatitis, cancer, and other conditions. Due to its anti-inflammatory properties, our previous pharmacological investigations have demonstrated that it is effective against cancer, depression, and hyperuricemia. Nevertheless, the key active components and targets of P. vicina in cancers are still unexplored. AIM OF THE STUDY: The study aimed to evaluate the pharmacological treatment mechanism of the active fraction of P. vicina (AFPR) in treating colorectal cancer (CRC) and to further reveal its active ingredients and key targets. METHODS: To examine the inhibitory impact of AFPR on CRC growth, tumorigenesis assays, cck-8 assays, colony formation assays, and MMP detection were utilized. The primary components of AFPR were identified by GC-MS analysis. The network pharmacology, molecular docking, qRT-PCR, western blotting, CCK-8 assays, colony formation assay, Hoechst staining, Annexin V-FITC/PI double staining, and MMP detection were performed to pick out the active ingredients and potential key targets of AFPR. The function of Elaidic acid on necroptosis was investigated through siRNA interference and the utilization of inhibitors. Elaidic acid's effectiveness to suppress CRC growth in vivo was assessed using a tumorigenesis experiment. RESULTS: Studies confirmed that AFPR prevented CRC from growing and evoked cell death. Elaidic acid was the main bioactive ingredient in AFPR that targeted ERK. Elaidic acid greatly affected the ability of SW116 cells to form colonies, produce MMP, and undergo necroptosis. Additionally, Elaidic acid promoted necroptosis predominantly by activating ERK/RIPK1/RIPK3/MLKL. CONCLUSION: According to our findings, Elaidic acid is the main active component of AFPR, which induced necroptosis in CRC through the activation of ERK. It represents a promising alternative therapeutic option for CRC. This work provided experimental support for the therapeutic application of P. vicina Roger in the treatment of CRC.


Subject(s)
Colorectal Neoplasms , Necroptosis , Animals , Molecular Docking Simulation , Sincalide , Colorectal Neoplasms/drug therapy , Carcinogenesis
2.
Anal Chim Acta ; 1221: 340103, 2022 Aug 15.
Article in English | MEDLINE | ID: mdl-35934395

ABSTRACT

Controllable encapsulation of sulfur quantum dots (SQDs) into metal-organic frameworks (ZIF-8) by a surface-bound zinc ion-induced growth strategy, and SQDs@ZIF-8 was successfully prepared for alkaline phosphatase (ALP) detection. The new synthesis procedure involves first binding Zn2+ to the surface of SQDs to form SQDs/Zn, and then via zinc ion-induced in situ ZIF-8 growth to obtain SQDs@ZIF-8, which greatly improved the luminous efficiency of SQDs. The specific process of detecting ALP using pH-triggered fluorescence quenching of SQDs@ZIF-8: firstly ALP hydrolyzes 2-phosphate-l-ascorbic acid trisodium salt (AAP) to ascorbic acid (AA), and then the leakage of SQDs in the SQDs@ZIF-8 leads to a decrease in fluorescence intensity based on the destruction of ZIF-8 skeleton by H+ released by AA. A linear relationship was obtained between the fluorescence intensity and the ALP concentration in the range of 0.15-50 U/L, and the detection limit was 0.044 U/L. Moreover, it was found that free SQDs can be complexed with Fe2+ to produce wine red complexes, and the obtained UV absorbance and ALP concentration have a linear relationship in the range of 10-200 U/L. The detection range of ALP is significantly broadened based on the combination of the above two detection methods. Furthermore, SQDs@ZIF-8 exhibited excellent stability in water and was successfully applied to the fluorescence and colorimetric detection of ALP in human serum.


Subject(s)
Quantum Dots , Alkaline Phosphatase/chemistry , Ascorbic Acid , Colorimetry/methods , Coloring Agents , Humans , Limit of Detection , Quantum Dots/chemistry , Sulfur , Zinc
3.
Chem Asian J ; 17(13): e202200283, 2022 Jul 01.
Article in English | MEDLINE | ID: mdl-35460188

ABSTRACT

Metal-organic frameworks (MOFs) are a class of crystalline porous materials with simple synthesis conditions, large specific surface area, structural diversity, and a wide range of interesting properties. The integration of MOFs with other materials can provide new multifunctional composites that exhibit both component properties and new characteristics. In recent years, the integration of carbon dots (CDs) into MOFs to form composites has shown improved optical properties and fascinating new characteristics. This review focuses on the design and synthesis strategies of CDs@MOFs composites (including pore-confined synthesis, in situ encapsulation, post-synthesis modification and impregnation method) and their recent research progress in photocatalysis and detection of environmental pollutants. Both the achievements and problems are evaluated and proposed, and the opportunities and challenges of CDs@MOF composite are discussed.


Subject(s)
Environmental Pollutants , Metal-Organic Frameworks , Carbon , Metal-Organic Frameworks/chemistry , Porosity
SELECTION OF CITATIONS
SEARCH DETAIL
...