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1.
China Pharmacy ; (12): 3060-3063, 2023.
Article in Chinese | WPRIM | ID: wpr-1003547

ABSTRACT

OBJECTIVE To investigate the role of clinical pharmacists in the treatment of a patient with Epstein-Barr (EB) virus encephalitis. METHODS Clinical pharmacist participated in drug diagnosis and therapy for a patient with EB virus encephalitis. According to the physiological characteristics of the disease and the pharmacokinetic-pharmacodynamic characteristics of antibiotics, clinical pharmacists suggested that the dose should be adjusted as ceftriaxone 2 g, q12 h+meropenem 2 g, q8 h. Based on the uncontrolled infection of the patient, pharmacists suggested that ceftriaxone should be stopped and vancomycin 1 million U and q12 h should be used as alternative therapy. According to the results of etiology, pharmacists suggested that acyclovir should be discontinued and replaced with ganciclovir 5 mg/kg, q12 h. The electrolyte disturbance of the patient may be adverse drug reactions caused by Mannitol injection, it was recommended to stop the drug. RESULTS The clinician followed the advice of the clinical pharmacists. After treatment, the patient improved and was discharged. CONCLUSIONS Clinical pharmacists can carry out pharmaceutical care for patients with EB virus encephalitis, assist physicians in optimizing the treatment plan of patients, and ensure the effectiveness and safety of drug treatment.

2.
China Pharmacy ; (12): 173-178, 2020.
Article in Chinese | WPRIM | ID: wpr-817357

ABSTRACT

OBJECTIVE:To establis h HPLC fingerprint of Chinese gall leaven ,simultaneous determination of 5 components and optimization of distillers ’grains. METHODS :HPLC method was adopted. The determination was carried out on Waters Symmetry Shield TM RP18 column with mobile phase consisted of acetonitrile- 0.1% trifluoroacetic acid aqueous (gradient elution )at the flow rate of 0.8 mL/min. The column temperature was 30 ℃,and detection wavelength was set at 280 nm. The sample size was 5 µL. Using gallic acid as reference ,HPLC fingerprints of 14 batches of sample were drawn. The similarity evaluation was performed by using Similarity Evaluation System of Chromatogram Fingerprint of TCM (2012 edition)to determine common peaks;SPSS 20.0 software was used for cluster analysis. RESULTS :There were 11 common peaks in 14 batches of samples ,and the similarity range of 14 batches of samples was 0.424-0.998,A1-A5 was less than 0.850;5 components were identified in B 1-B9 sample,i.e. gallic acid ,(-)-epigallocatechin,methyl gallate ,2,4,6-tri-O-galloyl-α-D-glucose and 2,4,6-tri-O-galloyl- β-D-glucose. The results of cluster analysis showed that 14 batches of samples could be grouped into 3 categories,i.e. A1-A5 into one category,B1 and B 6 into one category ,B2-B5 and B 7-B9 into one category. The linear ranges of above 5 components were 29.96-599.2 μg/mL(r=0.999 6),0.832-416 μg/mL(r=0.999 6),0.102-51 μg/mL(r=0.999 8),0.286 4-143.2 μg/mL(r=0.999 8), 0.286 4- 143.2 μg/mL(r=0.999 8),respectively. The limits of quantitation were 0.060,0.104,0.017,0.029,0.057 μg/mL;the limits of detection were 0.018,0.031,0.005,0.009,0.017 μg/mL,respectively. RSDs of precision ,stability,reproducibility and durability tests were all lower than 3%. The recoveries were 97.16%-101.88%(RSD=1.60%,n=6),96.98%-99.24%(RSD= 0.85%,n=6),97.7%-101.64%(RSD=1.54%,n=6),97.77%-103.08%(RSD=1.82%,n=6),98.16%-101.88%(RSD=1.24%, n=6),respectively. CONCLUSIONS:The established HPLC fingerprint and cluster analysis can be used to evaluate the quality of Chinese gall leaven. The established method is simple to Δ 基金项目:国家重点研发计划项目(No.2018YFC1707200);公 operate and can be used to determine the contents of 5 益性行业科研专项项目(No.201507004-03);河南中医药大学研究生 components simultaneously ;rice husk distillers ’grains were 科研创新基金项目(No.YJS2018B14) *硕士研究生 。研究方向 :中药饮片及新药研究 。E-mail: not suitable for fermented Chinese gall leaven . 401327039@qq.com

3.
China Pharmacy ; (12): 1601-1607, 2020.
Article in Chinese | WPRIM | ID: wpr-822626

ABSTRACT

OBJECTIVE:To establish the fingerprint of raw produc ts and different processed products of Pinellia pedatisecta , to determine the contents of 5 kinds of nucleosides ,and to compare the differences of components between the raw products and processed products. METHODS :P. pedatisecta raw products ,processed products by Processing Standard of Chinese Medicine in Henan Province (called“Standard processed product ”for short )and processed products by new integrated processing technology in the production area (called“new integrated processed product ”for short )were collected as investigation objects (12 batches of each). The determination was performed on SymmetryShield RP 18 column with mobile phase consisted of acetonitrile (A)-0.1% acetic acid aqueous water solution (B)(gradient elution )at the flow rate of 0.8 mL/min,with the column temperature of 30 ℃, the detection wavelength of 270 nm,and the injection volume of 15 µL. HPLC fingerprints of 3 kinds of P. pedatisecta samples were established by using Similarity Evaluation System of TCM Chromatographic Fingerprints (2004 A version ) ,and the similarity of fingerprints was evaluated. The chromatographic peaks were identified by comparing with the reference chromatogram. Five nucleosides (adenine,hypoxanthine,uridine,xanthine,inosine)were quantitatively analyzed. SPSS 21.0 software was used for cluster analysis of 36 batches of samples. RESULTS :The results of fingerprint and content determination met the relevant requirements. The similarity of 3 kinds of sample with their control fingerprint were all greater than 0.990. There were 22 common peaks in the raw products of P. pedatisecta ,and 16 common peaks were identified in the 2 kinds of processed products (the same 6 peaks disappeared from 2 kinds of processed products ). Fivecomponents were identified in 3 kinds of samples ,such as adenine(peak 3),hypoxanthine(peak 7),uridine(peak 8), 1064056472@qq.com xanthine(peak 9)and inosine (peak 11). Results of content determination showed that total contents of 5 kinds of nucleosides in 2 kinds of proc essed products were all· decreased;the contents of them in descending order w as raw product >new i ntegrated processed products >Standard processed products. Results of cluster analysis showed that 36 batches of samples could be clustered into 2 categories,i.e. raw product was clustered into one category and 2 kinds of processed products into other one . CONCLUSIONS :Established method is stable , feasible and suitable for the quality evaluation of raw products and different processed products of P. pedatisecta . Fingerprints have changed significantly and the total content of 5 kinds of nucleosides in P. pedatisecta are all decreased after processing ,but that of new integrated processed products is slightly higher than that of Standard processed products .

4.
Chinese Journal of Dermatology ; (12): 302-305, 2018.
Article in Chinese | WPRIM | ID: wpr-710379

ABSTRACT

Objective To investigate therapeutic effects and complications of three kinds of minimally invasive therapies for varicosis of the lower extremities.Methods Totally,79 patients with 94 affected limbs were enrolled into this study.According to their clinical manifestations,3 kinds of minimally invasive therapies alone or in combination were selected,including endovenous laser treatment (EVLT) with saphenofemoral ligation and stripping of the great saphenous vein,microphlebectomy,foam sclerotherapy,EVLT with saphenofemoral ligation and stripping of the great saphenous vein + microphle-bectomy,and EVLT with saphenofemoral ligation and stripping of the great saphenous vein + foam sclerotherapy.Physical examination and color Doppler ultrasonography were performed to evaluate the regression and recurrence of varicosis,as well as complications.Meanwhile,dermatology life quality index (DLQI) was used to evaluate the improvement of life quality of the patients after the treatment.Results All the patients were followed up for 1-6 months (average,4.2 months),and no recurrence was observed.One month after the treatment,all the patients were re-evaluated.Of the 94 affected limbs,46 (48.9%) were cured,43 (45.7%) were improved,and 5 (5.3%) were unimproved.Three months after the treatment,69 patients with 82 limbs completed the re-examination.Of the 82 limbs,71 (86.6%)were cured,9 (11.0%) were improved,and 2 (2.4%) were unimproved.Six months after the treatment,61 patients with 70 limbs completed the follow-up.Of the 70 limbs,62 (88.6%) were cured,7 (10.0%) were improved,1 (1.4%) was unimproved.Repeated-measures analysis of variance revealed that the total DLQI scores before the treatment (9.12 ± 2.87),one month after the treatment (6.97 ± 2.39),3 months after the treatment (5.12 ± 1.96) and 6 months after the treatment (3.69 ± 1.45) significantly differed (F =328.84,P < 0.01),and there were significantly differences between any two time points of re-evaluations (all P < 0.01).In the 79 patients,postoperative complications included subcutaneous ecchymosis (7 patients,8.9%),numb sensation in the foot and boot area of the legs (6 patients,7.6%),and cord-like subcutaneous induration =(3 patients,3.8%).Conclusions The three kinds of minimally invasive therapies alone or in combination are all effective for the treatment of varicosis of the lower extremities with rapid recovery.The life quality of patients was obviously improved after the treatment,and the complications were acceptable.

5.
Chinese Journal of Dermatology ; (12): 885-888, 2018.
Article in Chinese | WPRIM | ID: wpr-734721

ABSTRACT

Objective To evaluate the therapeutic effect of endovenous laser ablation (ELA) combined with foam sclerotherapy (FS) and mucopolysaccharide polysulfate (MP)cream on stasis dermatitis.Methods From December 2015 to May 2017,52 patients with 60 lesional limbs were enrolled from Department of Dermatology of Sichuan Provincial People's Hospital.The 60 lesional limbs were randomly and equally divided into 3 groups by a random number table and remainder grouping:combination group,MP group and control group.All the 3 groups were firstly treated with ELA in the main great saphenous vein.Then,the combination group was treated with FS followed by topical MP cream for 4 weeks.After the laser therapy,the MP group was treated with topical MP cream for 4 weeks,and the control group was treated with topical mometasone furoate cream alone for 4 weeks.The eczema area and severity index (EASI) and visual analogue scale (VAS) for itching scores in the above 3 group were recorded before treatment and 4 weeks after treatment.Statistical analysis was done by paired t-test for comparisons before and after treatment,one-way analysis of variance (ANOVA) for intergroup comparison,and least significant difference (LSD)-t test for multiple comparisons.Results No significant difference was observed before treatment among the combination group,MP group and control group in the EASI (9.64 ± 4.58,9.94 ± 4.18,9.50 ± 4.41 respectively,F =0.052,P > 0.05) or VAS scores (7.25 ± 1.29,7.50 ± 1.19,7.45 ± 1.32 respectively,F =0.218,P > 0.05).After 4-week treatment,the combination group,MP group and control group all showed significantly decreased EASI (3.54 ± 1.57,5.86 ± 2.39,7.04 ± 2.75 respectively) and VAS scores (2.35 ± 0.67,3.85 ± 0.67,4.65 ± 1.23 respectively) compared with those before treatment (t =4.30-18.80,all P < 0.05).After 4-week treatment,the EASI score was significantly lower in the combination group than in the MP group and control group (both P < 0.05),while there was no significant difference between the MP group and control group (P > 0.05).Additionally,the VAS score was significantly lower in the combination group than in the MP group and control group (both P < 0.05),as well as in the MP group than in the control group (P < 0.05).Conclusions ELA combined with FS and topical MP cream shows better short-term efficacy for the treatment of stasis dermatitis compared with ELA combined with topical MP cream or mometasone furoate cream.The combination with topical MP cream is superior to that with topical mometasone furoate cream in improving itching.The long-term efficacy needs to be observed further.

6.
Chinese Journal of Immunology ; (12): 1000-1004, 2017.
Article in Chinese | WPRIM | ID: wpr-616462

ABSTRACT

Objective:To investigated the activity inhibition and inhibitory type of polyphenol oxidase (PPO) induced by galangin and the interaction mechanism of galangin with polyphenol oxidase was preliminarily indicated,and prove the related mechanism of galangin on proliferation of on human melanoma A375 cells.Methods: The activity inhibition and inhibitory type of PPO induced by galangin were investigated by spectrophotometric method,and interation mechanism of galangin with PPO was preliminarily indicated by fluorescence quenching and molecular docking,and chelating copper ions with the inhibitory mechanism of galangin on polyphenol oxidase was measured.Results: Galangin was a competitive inhibitor,the IC50 and Ki on PPO were obtained to be (47.86±3.33) and (24.83±1.45)μmol/L,respectively.Fluorescence spectrum indicated the fluorescence of PPO was quenched effectively by galangin and the binding constant Ka was obtained to be (4.67±0.43)×104 L/mol.Chelating copper ions and molecular simulation further showed that galangin was combined with active center of copper ions,and formed hydrogen bonds with catalytic site His259.Luteolin could induce the apoptosis of A375 cells significantly,and the tyrosinase activity and melanin synthesis were decreased.Conclusion: Galangin as a competitive polyphenol oxidase inhibitor and reduced the activity of polyphenol oxidase.which provides the theoretical basis for the clinical anti skin cancer.

7.
Chongqing Medicine ; (36): 1048-1051, 2017.
Article in Chinese | WPRIM | ID: wpr-515058

ABSTRACT

Objective To research the effect of pure interbody fusion and interbody cage fusion under minimally invasive transforaminal lumbar interbody fusion treat to single segment of lumbar disc herniation,analysis clinical value the two methods.Methods A total of 61 cases single segment lumbar disc herniation were treated with MIS-TLIF surgery,were divided into pure interbody fusion group (group A) and interbody fusion Cage group (group B) according to different fusion methods.Operative time,blood loss and postoperative drainage were recorded in two groups,the clinical efficacy were tested by using of visual analogue score (VAS),Japanese Orthopedic Association scores (JOA),Oswestry disability index (ODI) score and Macnab standard,the interbody fusion ability were evaluated by power lumbar X-ray film and CT 3D reconstruction.Results The gender,age,disease duration and disease segments in two gracps were not found statistically significant difference (P>0.05).Also,two groups of patients,blood loss,postoperative drainage has no significant difference (P>0.05).After the operation,the VAS score,ODI score,JOA score and Macnab criteria,the last follow-up of intervertebral fusion rate in in tuo groups were not found statistically significant difference (P>0.05).While the operative time,postoperative disc height changes were found significant difference between two groups (P< 0.05).Conclusion MIS-TLIF simple fusion for lumbar disc herniation will be available with equal clinical efficacy fusion rate compared with cage fusion.

8.
Chinese Journal of Immunology ; (12): 66-71, 2017.
Article in Chinese | WPRIM | ID: wpr-508446

ABSTRACT

Objective:To investigate the effect and the related mechanism of c-Myc on the proliferation,invasion and migration ability of malignant melanoma B16-F10 cells. Methods:We detected the expression of PIK3R3 in malignant melanoma and normal tis-sues. Efficiency of gene silencing of c-Myc and PIK3R3 was determined by qPCR and Western blot. We detected the proliferate ability of B16-F10 cells after silencing c-Myc and PIK3R3 using EdU assay. We detected the migration and invasion ability of B16-F10 cells after silencing c-Myc and PIK3R3 using wound healing assays and Transwell matrigel invasion assays. The expression of miR-199a after silencing c-Myc and PIK3R3 using qPCR. The expression of c-Myc and PIK3R3 was detected by qPCR after transfecting miR-199a mimics or miR-199a inhibitor. Dual-luciferase reporter assay system was used to detect miR-199a regulating c-Myc and PIK3R3. Results:Compared normal skin tissue,expression of PIK3R3 was significantly increased in malignant melanoma tissue;after silencing c-Myc and PIK3R3 gene,the proliferation,invasion and metastasis of melanoma cell line B16-F10 were significantly reduced;expression of miR-199a upregulated after silencing c-Myc and PIK3R3 genes, expression of c-Myc and PIK3R3 decreased after transfecting miR-199a mimics, expression of c-Myc and PIK3R3 upregulated after transfecting miR-199a inhibitor, dual luciferase reporter system test results revealed miR-199a can directly regulate c-Myc and PIK3R3 transcription activity. Conclusion: miR199a regulated the expression of c-Myc,then promote proliferation,migration and invasion in malignant melanoma cells.

9.
Journal of Central South University(Medical Sciences) ; (12): 1129-1135, 2017.
Article in Chinese | WPRIM | ID: wpr-669196

ABSTRACT

Objective:To investigate the effect of mH2A and Butein on mitogen-activation protein kinase (MAPK) signaling pathway through targeting glucose regulated protein of 78 (GRP78) in regulating the biological behavior of melanoma.Methods:Immunohistochemistry was used to detect the expressions of mH2A and GRP78 in melanoma and adjacent normal tissues.The relationship between mH2A and GRP78,and the dinicopathological data was analyzed.The relationship between GRP78 and mH2A protein was detected by immunoprecipitation assay.The protein expressions of mH2A and GRP78 was detected by Western blot.The invasion ability of melanoma after sliencing mH2A was detected by Transwell invasion assay.The migration ability of melanoma after sliencing mH2A was detected by wound healing assays.The protein expressions of MEK and ERK1 after sliencing mH2A was detected by Westem blot.Results:The expressions of mH2A and GRP78 in melanoma tissues was significantly lower than that in adjacent normal tissues (P<0.05).Butein enhanced the expression of mH2A (P<0.05).The mH2A regulated the GRP78 protein (P<0.05).Silencing mH2A promoted the invasion and migration of melanoma A375 cells.The MEK and ERK1 protein expressions were up-regulated after silencing Butein.Conclusion:Butein promotes the role of mH2A in regulating GRP78 and modulating the biological behavior of melanoma cells through MAPK signaling pathway.

10.
Journal of Practical Stomatology ; (6): 649-652, 2014.
Article in Chinese | WPRIM | ID: wpr-458959

ABSTRACT

Objective:To investigate the effects of scutellarin on Bcl-2 and Bax expression in human tongue squamous carcinoma Tca-8113 cell.Methods:Tca8113 cells were treated with 80,120 and 160μg/ml scutellarin for 48 h respectively.Immunocytochem-istry method and RT-PCR were applied to observe the expression of Bcl-2 and Bax protein and mRNA in the cells.Results:With the increase of scutellarin concentration,Bcl-2 protein and mRNA decreased(P<0.05),Bax protein and mRNA increased(P<0.05). Conclusion:Scutellarin may downregulate Bcl-2 expression and upregulate Bax expression in Tca-8113 cells.

11.
Acta Pharmaceutica Sinica ; (12): 406-10, 2014.
Article in Chinese | WPRIM | ID: wpr-448775

ABSTRACT

In this paper, microcrystalline cellulose WJ101 was used as a model material to investigate the effect of various process parameters on granule yield and friability after dry granulation with a single factor and the effect of comprehensive inspection process parameters on the effect of granule yield and friability, then the correlation between process parameters and granule quality was established. The regress equation was established between process parameters and granule yield and friability by multiple regression analysis, the affecting the order of the size of the order of the process parameters on granule yield and friability was: rollers speed > rollers pressure > speed of horizontal feed. Granule yield was positively correlated with pressure and speed of horizontal feed and negatively correlated rollers speed, while friability was on the contrary. By comparison, fitted value and real value, fitted and real value are basically the same of no significant differences (P > 0.05) and with high precision and reliability.

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