口服當(dāng)歸補(bǔ)血湯后阿魏酸在大鼠體內(nèi)的組織分布

1、口服當(dāng)歸補(bǔ)血湯后阿魏酸在大鼠體內(nèi)的組織分布        【摘要】     目的研究大鼠灌胃給予當(dāng)歸補(bǔ)血湯后阿魏酸在體內(nèi)的組織分布特性。方法采用高效液相色譜法；色譜柱為Kromasil C18（4.6 mm×150 mm,5 m）；流動(dòng)相為0.2%甲醇乙腈-0.2%磷酸0.2%三乙胺水溶液（18：82）；檢測(cè)波長(zhǎng)322 nm；柱溫40；流速0.8 ml/min。結(jié)果各組織中的阿魏酸在10400 ng范圍內(nèi)與峰面積呈良好的線性關(guān)系；回收率平均為87.97%&

2、#177;1.95%；日內(nèi)和日間的RSD分別1.92% 3.87% 和3.21%6.39% 之間。阿魏酸在各組織器官中濃度差異較大。結(jié)論大鼠灌胃給予當(dāng)歸補(bǔ)血湯后阿魏酸主要在肝臟和腎臟分布，阿魏酸不能通過(guò)血腦屏障。     【關(guān)鍵詞】  當(dāng)歸補(bǔ)血湯； 阿魏酸； 反相-高效液相色譜； 組織分布； 大鼠    Tissue Distribution of Ferulic Acid after Oral Administration of Tangkuei Blood-Supplementing Decoctio

3、n to RatsWANG Yonglu, WANG Liyao,  CHENG Guoguang, ZHANG Dongxu, WEI Ping(1. Nanjing University of Technology, Nanjing, 210009, China;. China Pharmacological University, Nanjing, 210009, China)Abstract:ObjectiveTo investigate the tissue distribution of ferulic acid in rats after oral administra

4、tion of Tangkuei blood-supplementing decoction.MethodsHPLC was used；Column: Kromasil C18（150mm×4.6mm ，5m）; mobile phase: 0.2%methanol acetonitrile-0.2% phosphoric acid 0.2%triethylamine solution（18：82）; detection wavelength was at 322nm; temperature was at 40; flow velocity was 0.8ml/min.Result

5、sThe linear ranges of ferulic acid in the heart, liver, spleen, lung and kidney were 10400ng. The recovery of  ferulic acid was 87.97%±1.95% on average . The intra-day and inter-day RSD were 1.92%3.87% and 3.21%6.39%, respectively. The concentrations of ferulic acid were very different in

6、organs. ConclusionThe major distribution organs of ferulic acid in rats are liver and kidney. Ferulic acid can not pass though the blood-barrier.Key words:Tangkuei blood-Supplementing decoction ;   Ferulic acid;   Tissue distribution；  Rats    Tangkuei Blood-S

7、upplementing Decoction has been widely used for tonifying blood and treating anemia, female irregular menstruation and amenorrhoea in the traditional Chinese medicine for hundreds of years. Previous studies have demonstrated that Tangkuei Blood-Supplementing Decoction can inhibit lipid peroxidation,

8、 maintain activities of SOD and GSH, enhance cell ability against oxidation, improve immune function, and lessen ischemia/reperfusion injury in the heart and the brain1. Ferulic acid, one of the important components of Tangkuei Blood-Supplementing Decoction2, diminished the production of H2O2 in hep

9、atocytes and protected membrane lipid after ischemia/reperfusion. It also plays a role of dilating blood vessel3, inhibiting platelet aggregation, inhibiting inflammatory reaction, anti-oxydation and cleaning free radical, acting on eliminating and inhibiting. In the present study, the tissue distri

10、bution of ferulic acid in rats was investigated by high-performance liquid chromatography after oral administration of Tangkuei blood-supplementing decoction.1  Material and methods1.1  Apparatus and reagentsThe DIONEX HPLC system consisted of a P680 quaternary pump and a UVD170U variable

11、wavelength detector. The data were collected and processed with a CHROMELEON (Version 6.60) chromatographic workstation. HT-230A thermostated column compartment was bought from Heng-ao Co. (Tianjin, China).   Ferulic acid (FA) was provided by National Institute for the Control of Pharmaceu

12、tical and Biological Products (batch number: 0773-9910; for use of determination).The ultrapure water and HPLC-grade solvents, including methanol and acetonitrile were bought from Wan-qing Co. (Nanjing, China). All other chemicals were of analytical grade. Astragali radix and angelicae radix were bo

13、ught from Nanjing Pharmaceutical Co. (Nanjing, China).1.2  AnimalsSprague-Dawley rats aged 6-8 weeks (provided by the Department of Laboratory Animals of Dongnan University, Nanjing China) weighing 160-250 g were used in the experiments.1.3  Chromatographic conditionColumn: Kromasil C18（15

14、0 mm×4.6 mm，5 m）; mobile phase: 0.2% methanol acetonitrile-0.2% phosphoric acid 0.2% triethylamine solution（18：82）; detection wavelength was at 322 nm; temperature:40; flow velocity:0.8 ml/min; the injected volume:20 l.1.4  Extraction process of the decoctionAccording to the recipe, angeli

15、cae radix 25 g and astragali radix 175 g were weighed, and decocted together. The extraction processes were repeated twice. The added water was 2 400 milliliter and the decocted time was 2 hours. Then the resulting solution was collected and concentrated. Finally 1g primary herbs were contained in 1

16、ml.1.5  Sample collectionAfter a day of fast, the rats were given orally the decoction of Tangkuei blood-supplementing at the dose of 1.5 ml/100 g. Twenty minutes after the administration, the rats were decollated quickly and the heart, liver, spleen, lung, kidney and brain were dissected out a

17、nd put into normal saline solution to remove the blood. The water was removed with filter paper, and then the tissue samples were weighed for wet weight and homogenized in saline solution, respectively. The supernatant was collected and centrifuged , which was stored at -20.1.6  Sample preparat

18、ionThe procedures for analyzing the frozen tissue samples consisted of the following steps. The frozen tissue samples were thawed at 25 and were mixed with 500 l HCl(0.1mol/L) and 6ml ethyl acetate. The resulting mixture was vortexed for an additional 1 min. The samples were centrifuged for 20 min a

19、t 3 000 r/min.The supernatant liquor about 5 ml was transfered to a suitable tube and evaporated to dryness under a stream of nitrogen gas at 40. After 5 l methanolic acid was added, the residue was dissolved in 0.5ml of mobile phase. After filtration by millipore filter of 0.22m, 20 l of solution w

20、as injected into the chromatographic system, and the chromatograms were recorded.1.7  Method validation experiment1.8  Quantitation The concentrations of ferulic acid in tissue sample were quantified from the calibration curve according to the peak areas.2  Results2.1  Performanc

21、e of the HPLC systemRepresentative chromatograms are shown in Figure 1. The retention time of ferulic acid was about 9.3±0.7 min; No interference was observed. Ferulic acid can not be detected in cerebrum.2.2  Linearity and LODThe peak area (A) and concentration of ferulic acid (C) were su

22、bjected to regression analysis to calculate the calibration equation and correlation coefficient. The calibration equations of ferulic acid in each organ were shown in Table 1.The results showed an excellent correlation between the peak area and the concentration of ferulic acid. The limit of detect

23、ion of the assay was calculated to be 9.8ng/ml by the ratio of signal to noise 3:1.2.3  Recoveries and precisionThe results are given in Table 2. The recoveries were over 86%. The average recoveries(87.97%±1.95%) were high enough to reach the normal analytical criterion. The intra-day RSD

24、ranged from 1.92% to 3.87%. The inter day RSD ranged from 3.21% to 6.39%.2.4  The concentrations of ferulic acid in each organThe concentrations of ferulic acid (ng/g) in such major organs as heart, liver, spleen, lung and kidney are shown in Figure 2.3  Discussion    Feruli

25、c acid absorbed quickly in rats4 and rabbits5. The Tmax ranged from ten to twenty minutes. The sample collection time was decided to be twenty minutes, in which the concentrations of organ sample were the highest according to the preliminary experiment. Figure 2 illustrated the distribution of ferul

26、ic acid in different rat organs. The concentrations of ferulic acid were very different in organs:Cliver>Ckidney>Clung>Cheart>Cspleen>Ccerebrum at 15min after administration of Tangkuei blood-supplementing decoction. Ferulic acid could not be detected in rat brain, one possible reason

27、 was that ferulic acid could not pass though the blood-barrier and thus could not act on the central nervous system. The concentration of ferulic acid in heart was lower too, just as one-tenth of which in liver. This study clarifies that the major distribution organs of ferulic acid in rats are live

28、r and kidney, where the blood flow rate is faster than other organs. Although Tangkuei Blood-Supplementing Decoction is efficient in lessening ischemia/reperfusion injury in heart and brain, the experiment result illustrated that the major site of ferulic acid may not the heart and brain.Table1  Linear equations and correlation coefficients of ferulic acid in each organ（略）Table2  Recovery and precision of the HPLC method to determine Ferulic Acid in rat tissues（略）    【參考文獻(xiàn)】  1Deng Zhi-feng, Li Min