摘要
Objective UPLC-MS/MS bio-analysis method was developed for the simultaneous determination ofberberine,naringin,hesperidin,and neohesperidin in plasma of rats.Methods UPLC Acquity BEH C18 (50 rmm × 2.1 mm,1.7 μm) column was used,mobile phases were containing 0.05％ formic acid and 2 mmol/L ammonium formate in water (A)-containing 0.05％ formic acid in acetonitrile (B) as the mobile phase gradient elution;SD rats were randomly divided into oral administration berberine group,Citrus aurantium extract group,and berberine and C.aurantium extract compatibility group.Results UPLC-MS/MS method could be applied to determination of berberine,naringin,hesperidin,and neohesperidin,method validation meets the requirements of biological sample analysis.When rats were administered with berberine and C.aurantium extract compatibility,the plasma concentration of berberine was much more than single dose of berberine group and the bioavailability of berberine was increased.Meanwhile,naringin and neohesperidin can be detected in rat's plasma.Conclusion The bioavailability of flavonoids is significantly improved as well compared to the single dose of C.aurantium extract.This suggests that berberine and C.aurantium extract compatibility has significant drug-drug interaction.
摘要
<p><b>OBJECTIVE</b>To develop a method for determining the content of mercury contained in Yuhong ointment.</p><p><b>METHOD</b>The wet catalytic digestion method was adopted for the pretreatment, and the mercury content in Yuhong ointment was determined by hydride generation-atomic absorption spectrometry (HG-AAS).</p><p><b>RESULT</b>The mercury showed a good linear relation in the range from 2 to 20 microg x L(-1), with the average recovery of 104.27% and RSD of 3.37%. The RSD for real sample repeated measurement was determined to be 8.4%. The mercury content in Yuhong ointment was detected in range from 0.7 to 1.5 mg x g(-1).</p><p><b>CONCLUSION</b>The proposed method is accurate, highly reproducible and it can be used to control mercury content of Yuhong ointment.</p>
Subject(s)
Catalysis , Drugs, Chinese Herbal , Chemistry , Mercury , Ointments , Reference Standards , Reproducibility of Results , Spectrophotometry, Atomic , Methods摘要
AIM: To study the chromatographic fingerprint for Schizonepeta tenuisfolia Briq. by gas chromatography (GC). METHODS: The GC equipped with FID detector and a Varian CP-Sil 24 CB capillary column was used. The temperature program of column oven was as follows: 50℃, held for 3 min; increased at a rate of 2 ℃/min to 110℃, then at 6℃/min to 250℃, held for 5 min. RESULTS: The analytic method for fingerprint of Schizonepeta tenuisfolia Briq. was developed and validated. The fingerprint for Schizonepeta tenuisfolia Briq. was established. CONCLUSION: The method is simple, precise and reliable. The fingerprint is helpful to the quality control of Schizonepeta tenuisfolia Briq. in Chaijing Injection.