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    药物研究
  • 药物研究
    ZHANG Qinghong;DING Guohua;ZHANG Jiane;BAI Shoujun
    2008, 27(6): 615-618.
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    (1. ABSTRACTObjectiveTo study inhibitory effect of NS398 ,a selective cyclooxygenase2 inhibitor, on the expression of connective tissue growth factor (CTGF) in culture rat mesangial cell. MethodsRat glomerular mesangial cells were incubated with NS398 20 μmol•L-1 for 0,12,24,48,72 h. Reverse transcriptionpolymerase chain reaction and immunocytochemitry were used to evaluate the expression of connective tissue growth factor mRNA and protein,repectively. ResultsThe level of CTGFmRNA and protein were both significantly increased after exposing to high glucose (30 mmol•L-1) for 6 h, peaking at 12 h and declining after 18 h. Expression of CTGF mRNA and protein was also significantly decreased after NS398 stimulation for 30 min.ConclusionA selective cyclooxygenase2 inhibitor NS398 can downregulate the expression of CTGF in cultured mesangial cell with hyperglycemia.
  • 药物研究
    ZHANG Lifang;HU Xiao;GAN Xiaojian;XU Wenwei; ZHANG Hong
    2008, 27(6): 618-620.
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    ABSTRACTObjectiveTo study the pharmacokinetics and relative bioavailability of rapid oral disintegrating tablets of ambroxol hydrochloride in Chinese healthy volunteers. MethodsEighteen healthy volunteers were divided into 2 groups( n=9) randomizedly. Rapid oral disintegrating or common ambroxol hydrochloride tablets were given to volunteers respectively in an open crossover pattern. The concentration of ambroxol hydrochloride in plasma was determined by HPLC at different time points after a single oral dose of 90 mg. The pharmacokinetic parameters and relative bioavailability were evaluated to analyse the bioequivalence of 2 differents drug forms. ResultsMain pharmacokinetic parameters in the test preparation and the reference preparation were as follow: tmax were(1.3±0.6) and (1.5 ± 0.9) h;Cmax were(195.20 ±57.24) and (177.80 ±50.33) ng•mL-1;t1/2 were (6.69 ±1.75) and (6.91±1.57) h;AUC024 were (1 186.54±321.35) and (1 215.64±368.93) ng•h-1•mL-1; AUC0∞ were (1 375.05±388.37) and (1 371.22±419.52) ng•h-1•mL-1,respectively. The relative bioavailability of the test preparation was (102.1±29.8)%. ConclusionThe results showed that two preparation forms were bioequivalent.
  • 药物研究
    YAN Xia;SHENG Guorong
    2008, 27(6): 621-622.
    ABSTRACTObjectiveTo study the safety of compound cream of adenosine cyclophosphate by evaluating the skin irritation in guinea pigs . MethodsCompound cream of adenosine cyclophosphate was spreaded on the normal or damaged derma of animal back once or repetitiously and observe the situation of irritation. Results The average reaction value of compound cream of adenosine cyclophosphate in normal skin was lower than 0.50, and from 0.50 to 3.00 in damaged skin after 1 and 24 h, but lower than 0.50 after 48 h. ConclusionCompound cream of adenosine cyclophosphate had no irritation to normal skin and a modest stimulation to the damaged skin, but with a less than 48 h duration.
  • 药物研究
    CHEN Yunzhou;DU Guang;ZONG Kai
    2008, 27(6): 623-624.
    ABSTRACTObjectiveTo study the acute toxicities and antitumor activity of STEMX in vivo. MethodsThe acute toxicity of STEMX was assayed as followed : thirty mice were averagely divided into three groups. After 24 hours fasting, STEMX was given to the mice. The numbers and time of death mice, and primary toxic symptom were observed. The antitumor activity of STEMX was research as followed: forty mice were randomly divided to four groups (each group with 10 mice): low dose group (concentrated STEMX 10 mL•kg1), high dose group (concentrated STEMX 20 mL•kg1), 5Fu control group(20 mg•kg1) and blank control group and transplanted with the sarcocarcinoma 180 according to a standard method.The STEMX solution was given to mice for 10 days by i.g route. ResultsNo dead mouse was observed in three STEMX groups in acute toxicity assay. The LD50 of concentrated STEMX was over than 50 mL•kg1.For the antitumor activity of STEMX, the tumor weight in high dose group and 5Fu control group is obviously different from that in control group. The inhibitory rate has no marked difference between high dose group and 5Fu control group, but is higher than that in low dose group. Conclusion In the normal dose, STEMX is a safe agent with lowly toxicity and shows an obvious antitumor activity to sarcocarcinoma 180.
  • 药物研究
    WANG Xiaoxue;ZHOU Zewei;SHEN Xiu;TANG Weisheng;HAN Ying;WANG Jie
    2008, 27(6): 625-628.
    (1. ABSTRACTObjectiveTo study the antitumor effect of JH07 in vitro and in vivo and identify a highefficient and lowtoxic compound recipe. MethodsHalfinhibitory concentration (IC50) was assessed in human esophageal cell EC9706, human leukemia cell K562 resistant line and sensitive line, human fibroblastic cell L929 and human glioma cell TJ905 by MTT method. Meantime , mice model(n=40,10 mice in each group) transplanted liver cancer H22 were treated by JH07 and DDP and tumor inhibitoryrate, thymus gland and spleen indexes, and liver weight were measured. ResultsIC50 of JH07 in K562 resistant line, K562 sensitive line and TJ905 were 9.55,15.40,15.02 μg•mL1, respectively. Tumor inhibitory rates of low,midest and high dose group in H22 mice were 48.7%,36.5% and 46.7% ,and significantly higher than that of control group (P<0.01).However, JH07 groups showed small differences in spleen index, thymus index and liver weight compared with control group (P>0.05). Nevertheless, compared with cisplatinum group, the differences were marked (P<0.01).ConclusionJH07 had obvious antitumor activities in vitro and in vivo, further study on JH07 might be required
  • 妇产科用药专栏
  • 妇产科用药专栏
    CHEN Lu;ZHU Jianqing;QIAN Lijuan;GU Linghui;ZHEN Zhiguo;MA Shenglin;XIA Ting
    2008, 27(6): 637-639.
    (1. ABSTRACTObjectiveTo study the suppression effect of shenyi capsule (ginsenoside Rg3) combined with cisplatin on highmetastasis human ovarian cancer cell line HO8910PM. MethodsThe cell line was divided into 6 groups randomly: negative control group(A); low concentration Rg3(10 μg•mL1 )group(B); middle concentration Rg3(20 μg•mL1 ) group(C); high concentration Rg3 (40 μg•mL1 )group (D); cisplatin(10 μg•mL1 ) positive control group (E); combination of cisplatin+Rg3 group(F):10 μg•mL-1 cisplatin +20 μg•mL1 Rg3. CCK8 method and microscopic observation were used to investigate the suppression effects. ResultsRg3 has a significant cytotoxic effect to human ovarian cancer cell, especially under the high concentration (P<0.05). Combination of Rg3 and cisplatin has the similar antitumor effect to D group,but shows a stronger injury in the morphology and structure of cell. ConclusionRg3 has the antitumor effect with human ovarian cancer cell line HO8910PM and combination of Rg3 and cisplatin may be a more appropriate strategy.
  • 妇产科用药专栏
    ZHAO Ding;LIU Weina;WANG Wei;LI Yang;JIAO Junjie;REN Leiming
    2008, 27(6): 640-642.
    ABSTRACTObjectiveTo investigate the effects of extractives from Herba Leonuri on contractile activity of the uterine smooth muscle isolated from normal, estrogentreated and postpartum mice. MethodsMedlab/4s Vital Signal Recorder was used to measure the effects of extractives (0.54.0 mg•mL1) on contractile amplitude and frequency of the isolated uterus from mice. ResultsHerba Leonuri extractives increased the contractile frequency and contractile activity of the smooth muscle cells from normal nonpregnancy and treated with estrogen lightly, but strongly accelerated that of muscle cells isolated from postpartum uterus. In the isolated uterus from normal, estrogentreated and postpartum mice, Herba Leonuri extract significantly inhibited the increased contractile frequency and amplitude, and relieved the spasm induced by oxytocin. ConclusionHerba Leonuri significantly increased the contractile frequency and contractile activity of the uterus isolated from postpartum mouse, inhibited the spasm of the uterine smooth muscle induced by oxytocin, which is contributed to its antidysmenorrhea effect.
  • 妇产科用药专栏
    XIE Shouzhen;SONG Chengwen;CHEN Zhilan;WANG Jing;YAN Xiaofang;JIANG Hongwei
    2008, 27(6): 644-646.
    (1. ABSTRACTObjectiveTo investigate the inhibitory effects of medroxyprogesteron acetate (MPA) combined with chemotherapy on pathologic angiogenesis in postoperation patients with ovarian epithelial cancer , and evaluate the prognosis of patients .Methods53 patients including phaseⅠ/Ⅱ 30 cases (56.6%) and Ⅲ/Ⅳ 23 cases(43.4%) were admitted to the experimental group. PAC or PC chemotherapy regime was taken from 1998, and PT chemotherapy regime was taken from 2001. Six cycles were conducted. The internal iliac artery chemoembolization was performed and then pelvic angiography was scanned by DSA durring the seventh chemotherapy. One year after embolization, the internal iliac artery chemoembolization and DSA were conducted once more. The MAP 250 mg•d-1 was orally administered 6-30 months. CA125 was monitored before each cycle of chemotherapy. ②37 patients including phaseⅠ/Ⅱ 20 cases (54.1%) and Ⅲ/Ⅳ 17 cases(45.9%) were admitted to the control group.The patients received the same treatment as the experimental group except MPA. The three and five years survival rate was followedup.Results①One year later after chemotherapy and chemoembolization, the decline of CA125 in the experimental group of phaseⅠ/Ⅱ and Ⅲ/Ⅳ were more significant than those in the control group, respectively ( P<0.05, P<0.05 ; P<0.05, P<0.01) . ②The tortuous branches of internal iliac arterial and flaming pathlogical vessels in the experimental group were obviously mild than those in the control group ( P<0.05 ). The change of pelvic pathlogical vessels was positively relevant to the value of CA125 (r=0.95, P<0.001 ).③ The three and five years survival rates of Ⅰ/Ⅱ in experimental group were higher than those in control group ,88.33% , 41.23%, vs 79.59% , 34.31% respectively (P<0.05) . The same results was observed in Ⅲ/Ⅳ patients (17.52% , 1.34% in experimental group vs 12.49% ,0.00% in control group,P<0.05) .ConclusionThe MPA was able to inhibit the angiogenesis of ovarian cancer. The combination of MPA and chemotherapy was well tolerance and improved the survival of patients. Pelvic pathologic vessels might be an one factor to evaluate the effects and prognosis.
  • 妇产科用药专栏
    ZHANG Hanwang;RAO Qun;AI Jihui;YUE Jing;LAI Qiaohong;LIU Yuqin;LI li
    2008, 27(6): 647-650.
    ABSTRACTObjectiveTo evaluate the clinical effect of letrozole(LE) with HMG or clomiphene citrate(CC) with HMG in treatment of polycystic ovarian syndrome(PCOS) .MethodsOne hundred and twentysix patients with PCOS were divided into 2 groups treated with letrozole ( 70 cycles) or CC (82 cycles). Letrozole 5 mg was given daily d 37 of menses and CC 100 mg was given daily d59 of menses. Patients were monitorized with transvaginal ultrasonography and combined with HMG if needed. When the dominant follicle diameter reached 18 mm, HCG (5 000 U ,IM) was given to trigger ovulation. Levels of serum E2,LH,T,P were detected on the day of HCG administration and E2,P on more than 7 days after follicular rupture. The primary endpoints were the number of follicles, endometrial thickness, pregnancy rate and miscarriage rate. ResultsNo significant difference was found between LE group and CC group for endometrial thickness measured on the day of HCG,the duration to reach a dominant follicle and the total dose of HMG. The number of follicles ≥14 mm were significantly less in the LE group, but no significant differences in the ≥18 mm follicles. Levels of serum E2 ,P/E2 were more lower in LE group, but similar for LH,T,P. The rates of pregnancy, twin gestation, ectopic pregnancy and OHSS were almost consistent in 2 groups. Moreover, withdrawal rate as inefficacy was significantly lower in the LE group.ConclusionLE might be an alternative method in PCOS to induce ovulation, especially for patients no responsing to CC ,or with OHSS or thin endometrium.
  • 药物与临床
  • 药物与临床
    ZHANG Zhiqiang;MI Shukun;PAN Lijuan;HAO Shan;ZHAO Shirong;LIU Qiang
    2008, 27(6): 655-658.
    (1. ABSTRACTObjectiveTo observe the therapeutic effect and safety of shangkesan for acute closed injury of parenchyma. Methods100 cases were randomly divided into two groups. Fifty patients in group one were externally applied with shangkesan and another group (50 patients) with 701 paste. After 7day treatment, the reduction of pain, tendness, swelling, ecchymosis and dysfunction was assessed. Meanwhile, three routine examinations, liver and kidney function tests were conducted to each group. ResultsCompared to that in the controls, the symptom scores of pain, tendness, swelling, ecchymosis and dysfunction in shangkesan group were reduced markedly(P<0.05) and the treatment effect was improved(P<0.05) with a total effective rate of 100.0%(17 cases were healed, none was ineffective) .Abnormal reports of three routine examination, liver and kidney function tests were observed.The treatment effects for dampens and sprains were also much better(P<0.05). ConclusionShangkesan has more significant effect,through promoting blood circulation and removing blood stasis,lessening swelling and pain, and more safety than 701 paste.
  • 药物与临床
    WU Shimin;ZHANG Xianwei;WEN Weihao
    2008, 27(6): 658-660.
    (1. ABSTRACTObjectiveTo compare analgesic efficacy and safety of flurbiprofen axeyil combined with a small dose of fentanyl with fentanyl alone in postoperative intravenous analgesia for total hysterectomy patients. Methods120 patients undergoing total hysterectomy in general anesthesia were randomly divided into four groups with thirty cases each. The dose assignment followed as: fentanyl 1 mg in group A, fentanyl 0.5 mg in group B, flurbiprofen axeyil 50 mg plus fentanyl 0.5 mg in group C, flurbiprofen axeyil 100 mg combined with fentanyl 0.375 mg in group D. The drugs in each group were diluted to 100 mL and infused by pumps. The visual analog scale(VAS),times of PCIA and incidence of side effects were recorded during the period of postoperative 24 hours. ResultsThe VAS of group B at 2 h after operation was significantly higher than that of group A,C and D(P<0.05),which became similar 2 h later(P>0.05). The times required for supplemental bolus in group B was also more than that of A,C and D(P<0.05). The incidences of nausea ,vomiting, itching and somnolence in group B,C and D were significantly less than those in group A(P<0.05).No respiratory depression or abnormal bleeding occurred in four groups. Conclusion Intravenous analgesia of flurbiprofen axeyil combined with a small dose of fentanyl had a better effect and safety than fentanyl alone and was able to reduce fentanyl requirement in total hysterectomy patients.
  • 药物与临床
    HU Mingpin;LI Xingwang;LIAN Qingquan;CHEN Lingyang;MAO Fangmin
    2008, 27(6): 661-663.
    (1. ABSTRACTObjectiveTo investigate the effects of different antalgic methods on postoperative pain after internal fixation of thoracolumbar vertebrae fractures. MethodsNinety patients undergoing thoracolumbar spinal surgery were randomly divided into three groups of thirty patients each according to the methods of postoperative pain management: group PCIA received patientcontrolled intravenous analgesia with morphine 0.5 mg•mL-1(n=30); group PCEA1 received patientcontrolled epidural analgesia with 0.125% bupivacaine+morphine 0.04 mg•mL-1(n=30), epidural space was opened during surgery; group PCEA2 received patientcontrolled epidural analgesia with 0.125% bupivacaine+morphine 0.04 mg•mL-1(n=30),epidural space was not opened during surgery. PCA was maintained for 48 h in all three groups. VAS scores were used to assess analgesia at rest and movement. Cumulative morphine requirement and side effects(nausea, Vomiting and pruritus)were recorded after 4,8,12,24,36,48h of postoperative analgesia. ResultsDuring the 36 hours after operation, the VAS scores in group PCEA2 at rest and motion were significantly lower than those in group PCIA and PCEA1 (P<0.05). During the 24 hours after operation, the degree of sedation was higher in group PCIA than that in other two groups(P<0.05), The total morphine requirement was significantly larger in group PCIA than that in other two groups(P<0.01). The prevalences of postopertive nausea, vomiting and pruritus were markedly higher in group PCIA than those in other two groups(P<0.05).ConclusionPCEA2 is more effective than PCIA with lower opioid consumption, fewer side effects, and a higher satisfaction for patients with thoracolumbar vertebrae fractures .
  • 药物与临床
    WANG Long;LI Danfeng;XU Jingjing;ZHOU Qingshan
    2008, 27(6): 664-667.
    ABSTRACTObjectiveTo examine the effects of sufentanil and remifentanil administered by targetcontrolled infusion (TCI) on postoperative analgesia and recovery of craniotomy patients. Methods Foutyeight adult patients scheduled for craniotomy were enrolled into our prospective,randomized study.Both Sufentanil by TCI(S group) and remifentanil by TCI(R group) were administered during operation.In the R group, at 30 min before surgery completion, morphine 0.15 mg•kg1 was addministered i.v.In the S group ,an plasma concentration of 0.25 ng•mL1 was targeted at extubation.In 2 groups,postoperative pain was controlled by titration of i.v. morphine and then patientscontrolled analgesia with morphine. Results The extubation time was similar in the two groups.VAS was significantly higher during the first 2 h after tracheal extubation in R group than that in S group. The time to first analgesic request in ICU was significantly longer in the S group than that in R group(P<0.01). The cumulative morphine dose for titration was significantly increased in R group(P<0.01).The cumulative morphine doses on 4,12 and 24 h after extubation and PCiA were significantly greater in R group (P<0.05). ConclusionSufentanil by TCI was more effective than the combination of remifentanil by TCI with moephine bolus for postoperative pain after craniotomy and did not compromise recovery.
  • 药物与临床
    YUAN Hong fei;WU Hailing;YE Lijun
    2008, 27(6): 667-669.
    ABSTRACTObjectiveTo evaluate the clinical efficacy of gatifloxacin sequential therapy for the elderly patients with communityacquired pneumonia(CPA). MethodsTwohundred and fortysix patients were divided into two groups : treatment group with 120 cases assigned by gatifloxacin for intravenous injection once daily 400 mg for 3~5 d ays and then with oral gatifloxacin 400 mg once daily, and control group with 126 cases treated by gatifloxacin for intravenous injection once daily 400 mg.The overall period of treatment was 7 10 days . The patients from two groups were not given any other antibiotics. ResultsThe total effective rate of the treatment group was higher , compared with control group (98.33% vs 94.44%, P>0.05), but no obvious differences of bacteria clearance rate was observed in the two groups( P>0.05).ConclusionGatifloxacin sequential therapy offered a safety, utility,strategy for elderly patients of CPA .
  • 药物与临床
    FANG Jianming;XIA Honghui;LIU Junhui;YU Xiaoyong;TANG Jun
    2008, 27(6): 669-671.
    ABSTRACTObjectiveTo assess the effect of tamsuiosin (alpha 1 receptors blocker) in treatment of ureterolithiasis localized in the lower ureters. MethodsFrom July 2004 to December 2006,278 patients with ureterolithiasis in the lower ureters were randomly divided into two groups: group A (n=138) was subjected to our regular treatment(0.5 g PSKL tid)and group B (n=140) was regular treatment combined with tamsulosin 0.4 mg qd. ResultsIn group A, 52.17% of the patients expelled the calculi and was lower than 84.29% in group B.The mean time discharged calculis in group A was more longer and incidence of renal colics more frequent, compared with group B [(10±7) days vs (7±3) days, 2.0 times vs 1.0 times,respectively)]. ConclusionThe treatment by tamsulos might accelerate calculi discharge from the lower ureters and be safety.
  • 药物制剂
  • 药物制剂
    XUE Lian;LI Linyan;XU Yiqing
    2008, 27(6): 687-688.
    ABSTRACTObjectiveTo study preparation technics of huangqijing effervescent tablets. MethodsThe optimum extraction technics of radix astragal was selected by orthogonal test and tiptop molding technics was screened out through single factor test such as disintegration time and taste. ResultsThe best preparation process was that 8 times of percolation liquid was gathered, percolation speed was 5.00-6.25 mL per minute, percolation yield was inspissated, and then dried using dextrin. At last,aluminum citrate and sodium bicarbonate as effervescent materials and CMSNa and pregelatinized starch as disintegrating agent were applied. ConclusionOur preparation procedure was optimum and simple.
  • 药物制剂
    HUANG Jie;XU Wenqing;LANG Yujiao;WANG Xuejiao
    2008, 27(6): 689-692.
    (1. ABSTRACTObjectiveTo obtain the best scheme to remove protein from the polysaccharide of parmelia tinctorium. MethodsFive methods, such as sevag, enzyme, sevag plus enzyme, trichloroaceticacidnbutanol, enzyme plus trichloroaceticacidnbutanol, were used to remove protein from the polysaccharide of parmelia tinctorium. ResultsThe scheme of enzyme combined with trichloroaceticacidnbutanol was that using 1% protease,the polysaccharide solution was hydrolysis for 3 hours in 50 ℃ water of pH 7.0,and then added trichloroaceticacidnbutanol once as much as polysaccharide solution,stirred for 20 minutes,and stayed in static state for an hour.The removal of protein reached the maximum and the loss of polysaccharide was lowest.ConclusionThe scheme of enzyme combined with trichloroaceticacidnbutanol was best than others.
  • 药品质量控制
  • 药品质量控制
    ZHAO Li;YAN Keli;BAI Yu
    2008, 27(6): 698-700.
    ABSTRACTObjectiveTo establish an HPLC method to determine cinobufagin and resibufogenin in meihuadianshe dan. MethodsHPLC system applied ODS column, 4.6 mm×250 mm ,5 μm with a mobile phase of acetonitrilewater(43.5:56.5)and 20 μL sample. The flow rate was 1.0 mL•min-1. The detection wavelength was 296 nm. ResultsThe calibration curves of cinobufagin and resibufogenin showed a linear relation in the range of 5.31-63.75 μg•mL-1,6.00-72.00 μg•mL-1 (r=0.999 8,0.999 7). The average recovery rate (n=6) and RSD were 98.74% and 1.91% for cinobufagin,and 99.74% and 0.92% for resibufogenin,respectively. Conclusion The HPLC was a rapid, accurate and reliable method.
  • 药品质量控制
    JIANG Junyong;YANG Jingjing
    2008, 27(6): 701-703.
    (1. ABSTRACTObjectiveTo establish an RPHPLC method for the simultaneous determination of contents of triamcinolone acetonide acetate and miconazole nitrate in triamcinolone acetonide acetate and miconazole nitrate and neomycin sulfate cream.MethodsRPHPLC was conducted using a Diamonsil C18 column (200 mm×4.6 mm,5 μm),with a mobile phase of 0.5% ammonium acetate solutionacetonitrilemethanol (15:42.5:42.5) and flow rate of 1.0 mL•min1. Samples was detected at 272 nm, with dibutyl phthalate as internal standard. ResultsThe linear range was 64.08-149.52 μg•mL-1(r=0.999 9)and the average recovery rate was 99.6%,RSD=0.43%(n=6) for triamcinolone acetonide acetate. The linear range was 600.6-1 401.4 μg•mL-1(r=0.999 9),the average recovery rate was 100.0%,RSD=0.49%(n=6) for miconazole nitrate. ConclusionThe method was accurate,simple and effective. It might effectively be applied to control the quality of agent.
  • 药品质量控制
    HONG Yi;XIAO Xuecheng;XUE Daquan;ZHOU Benhong
    2008, 27(6): 704-707.
    (1. ABSTRACTObjectiveTo establish a method for determination of the contents of ibuprofen, pseudoephedrine hydrochloride and chlorphenamine maleate capsule. MethodsHPLC was undertaken using Zorbax C18(4.6 mm×250 mm,5 μm)with a flow rate 1 mL•min1 and detected at 259 nm and 265 nm. Mobile phase was consisted of methanol(6 mmol•L-1), sodium lauryl sulfate(0.025 mol•L-1), potassium dihydrogen phosphate and triethylamine(75:20:20:0.25,pH=3.25). ResultsThe linearity between concentration and absorption was found in the range of 100.6-704.2 μg•mL-1 for ibuprofen , 50.0-600.0 μg•mL-1 for pseudoephedrine hydrochloride and 5.02-50.20 μg•mL-1 for chlorphenamine maleate. The average recycle rate of ibuprofen,pseudoephedrine hydrochloride and chlorphenamine maleate was 99.7%, 99.1% and 99.1%, and RSD was 0.71%,0.73% and 0.71% (n=5), respectively.ConclusionHPLC was a reliable,accurate and suitable method for the determination of the ibuprofen, pseudoephedrine hydrochloride and chlorphenamine maleate in the capsuley.
  • 药品质量控制
    WU Guang;XIE Baiyan;ZHANG Yonghui;RUAN Hanli;PI Huifang;WU Jizhou
    2008, 27(6): 707-710.
    ABSTRACTObjectiveTo determine the optimum plant age, size and manure scheme of Fritillaria hupehensis, and supply the fundamental data for GAP. MethodsAcid dye colorimetry was used to determine total alkaloids in Fritillaria hupehensis at 415 nm. The fingerprints are performed by HPLCELSD, with gradient elution. ResultsThe contents of total alkaloids in the group of oneyear old and big size are higher (0.526%) than that in other groups and peimine is higher (0.065%)in the group of oneyear old and big size. Hupehenine in the oneyear group of small size is the highest, 0.069%. The contents of total alkaloids, hupehenine and peimine (respectively 0.551%, 0.060% and 0.042%) in the group without fertilizer are higher than those in other groups. ConclusionUnder the other same conditions, the quality of oneyear and big size Fritillaria hupehensis and without fertilizer is better than that of other Fritillaria hupehensis .