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We have studied the effect of berberine on the recovery processes of liver xenobiotic-metabolizing function during its compensatory growth after 70% partial hepatectomy. It was found the hepatic ability to metabolize foreign substances are not restored up to day 8. Administration of berberine (10 mg/kg intraperitoneally) for 6 days led to normalization of both cytochrome P450-dependent and flavin-containing monooxygenases. It is suggested that in the biotransformation of berberine involved not only cytochrome P450, but also flavin-containing monooxygenases.
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http://dx.doi.org/10.18097/PBMC20156103381 | DOI Listing |
Drug Dev Res
September 2025
Department of Breast Disease Center, the First Affiliated Hospital of Nanchang University, the First Clinical Medical College of Nanchang University, Jiangxi Medical College, Nanchang, P.R. China.
Melanoma is a type of aggressive cancer distinguished by its high propensity for recurrence, the development of metastases, and an unfavorable outlook for recovery. Treatment modalities for melanoma encompass surgery, immunotherapy, and targeted therapies. In recent decades, berberine has garnered attention for its significant anticancer properties across various cancer types.
View Article and Find Full Text PDFRSC Adv
July 2025
Key Laboratory of Carbohydrate Science and Engineering, Chongqing Normal University Chongqing 401331 China.
The extraction methods of berberine hydrochloride include water, acidified water, lime milk, and ethanol extraction. The water extraction method is mainly a decoction method, whereas the alcohol extraction method mainly includes microwave, ultrasonic and cable reflux extraction. In the alcohol extraction method, the solvent has low restriction and can be used repeatedly, making the operation simple and increasing the extraction rate; however, the equipment investment for ultrasonic extraction and other methods is substantial.
View Article and Find Full Text PDFJ Chromatogr A
September 2025
Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of Ministry of Education, College of Pharmaceutical Sciences, College of Chemistry and Materials Science, Hebei University, Baoding 071002, China. Electronic address:
A urea-melamine-hexamethylenetetramine resin (UMHR) was synthesized using water as the reaction medium, with hexamethylenetetramine serving as an environmentally friendly crosslinking agent in place of traditional formaldehyde. The resin was optimized as an efficient solid-phase extraction (SPE) adsorbent through optimization of synthetic parameters. A precise detection method for berberine hydrochloride in Pudilan antiphlogistic oral liquid was established by optimizing extraction parameters.
View Article and Find Full Text PDFACS Appl Mater Interfaces
July 2025
State Key Laboratory of Food Nutrition and Safety, College of Food Science and Engineering, Tianjin University of Science and Technology, Tianjin 300457, PR China.
Bacterial wound infection tends to cause intense inflammation, while a lack of oxygen can lead to the destruction and contraction of blood vessels in the wound microenvironment. Here, a degradable hydrogel (denoted as PBCB hydrogel) was constructed with gelatin methacrylate (GelMA), tannic acid (TA), and polyphosphate (PolyP) by photopolymerization, and mesoporous polydopamine nanoparticles (MPDA) with berberine (BR), along with Cu and Bi nanoparticles grown in situ, were loaded into the hydrogel. PBCB hydrogel exhibits a high photothermal conversion efficiency (68.
View Article and Find Full Text PDFDrug Des Devel Ther
June 2025
Department of Pharmacy, Shengjing Hospital of China Medical University, Shenyang, Liaoning Province, People's Republic of China.
Propose: The co-treatment of ulcerative colitis with berberine hydrochloride (BBR), the Janus kinase(JAK) inhibitor Tofacitinib (TOFA), and Fligotinib (FIGA) is feasible and sophisticated in terms of mechanism. However, no studies have yet explored their interactions. This study aimed to establish a highly sensitive, specific, and reproducible HPLC-MS/MS method for investigating the pharmacokinetic interactions between BBR-TOFA and BBR-FIGA in rats.
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