OBJECTIVE:To facilitate the construction of Chinese pharmaceutical profession associations. METHODS: We analyzed the current situation and problems existing in Chinese pharmaceutical profession association as well as the developmental experience of foreign pharmaceutical associations then put forward suggestions for the development of pharmaceutical profession associations in China. RESULTS & CONCLUSIONS: The sound development of pharmaceutical profession associations calls for the cooperated efforts of government, profession association and pharmaceutical enterprises, meanwhile its function as bridge and tie between pharmaceutical enterprises and government should be brought into full play.

Arthralgia ; etiology ; Arthroplasty, Replacement, Knee ; adverse effects ; Humans ; Knee Joint ; surgery ; Pain, Postoperative ; etiology

Humans ; Pulpitis ; diagnosis

Excitatory Amino Acids ; secretion ; Humans ; Neurotransmitter Agents ; secretion ; Pain, Postoperative ; etiology ; metabolism ; prevention & control

Chronic Disease ; Cone-Beam Computed Tomography ; Humans ; Periapical Abscess ; pathology ; Periapical Granuloma ; pathology ; Periapical Periodontitis ; diagnostic imaging ; pathology ; Problem Solving ; Prognosis ; Radicular Cyst ; diagnostic imaging ; pathology

By using the method of eross-sectional anatomy, we examined human eerebral asymmetries in 31 Chinese adult brain.The left cortical language areas is larger than the right. The distribution of the hemispheric asymmetries is compatible with that reported by CT scan.The asymmetry of the posterior language areas mainly reflect the asymmetry of the occipital length and the asymmetries of the wide occipital lobe and the wide occipital horn might be in relation to the handedness. Though both the anterior and the posterior language area are mostly larger on the left hemisphere,there is no relationship between them

Objective:To study the enrichment and purification method of astragaloside Ⅳ from Radix astragali with macroporous resin,so as to lay a foundation for the large scale production of astragaloside Ⅳ.Methods: A HPLC-MSD method was established to determine the content of astragaloside Ⅳin Radix astragali.The adsorption ability and capability of different macroporous resins were investigated.The optimal alcohol concentration and capability of alcohol for elution were also confirmed through the determination of astragaloside Ⅳ in the eluted solution.Results: HPLC-MSD achieved satisfactory results in determination of astragaloside Ⅳ.D101 was proven to be the most potent macroporous resin;its adsorption capability of astragaloside Ⅳ was 0.42 mg/g when the elution solution was 5 folds of 70% alcohol.Conclusion: D101 macroporous resin can be used to effectively enrich and purify astragaloside Ⅳ,laying a foundation for analyzing the constituents of total astragalosides.

Objective To study the role of the specific short hairpin RNA(NS-shRNA) of nucleostemin in inhibiting the expression of nucleostemin(NS) gene and evaluate the effect of NS-shRNA on differentiation antigen and biological properties of HL-60 cells,so as to explore the relationship between the biological functions of NS and acute leukemia,the potential perspective of NS gene therapy with RNA interference(RNAi).Methods HL60 cells were directly transfected NS-shRNA by using special transfection reagent.After 48 h,the inhibition rate of NS-shRNA to NS gene was detected by RTPCR,the proliferation ability of HL-60 cells was detected by MTT,the differentiation antigens were assayed by flow cytometry(FCM),the morphologic peculiarities such as cell shape,growth condition were observed,and the volume and granularity of HL-60 cells were analyzed by blood cell analyzer.Results The expression of NS gene were significantly inhibited by both two NS-shRNA,the inhibition rate were 37.82% and 71.88%,respectively.The significant inhibition effect of NS-shRNA to the proliferation of HL-60 cells existed in a time-dependent and concentration-dependent manner,and the best time was 48 h,the best concentration was 10 nmol/L.The change of differentiation antigen included increase of CD11b,CD33,CD14,CD64,HLA-DR and decrease of CD38,indicating continuous maturation of HL-60 cells to granulocytes and redifferentiation trend to monocytes.The aggregation of cells declined and the cell fragments increased.Myeloperoxidase(MPO) and ?-naphthol acetate esterase(?-NAE) activity increased after NS-shRNA-2 transfection.Furthermore,some HL-60 cells changed from round to fusiform shape even to pseudopod.The cells of small volume and karyorrhexis increased. Conclusion Through blocking the expression of NS gene,NS-shRNA can inhibit the cell proliferation and induce the differentiation of HL-60 cells,weaken malignant degree of HL-60 cells and trigger cell apoptosis.NS-shRNA is of clinical potential in gene therapy for acute leukemia.

Aim In order to further explore the feasibility of gene therapy with RNA interference(RNAi) for acute leukemia,we synthesized short hairpin RNA(shRNA)for nucleostemin(NS)in vitro.Methods The designed DNA template consists of the sequence complementary to target mRNA,which was screened out consensus motif of three variants of NS gene,using 5′-UCUCUUGAA-3′ as loop sequence,The sequence of 5′-GGATCCTAATACGACTCACTATA-3′ acts as T7 promoter.Two shRNA were produced by T7 RNA polymerase and named as shRNA-NS-1 and shRNA-NS-2,respectively.The purified shRNA was quantified by gel electrophoresis.The interference effect of shRNA-NS transfected into HL-60 cell was examined by resultant cell morphology and inhibition rate of NS-mRNA expression.Results The concentrations of two shRNA-NS without degradation and diffusion were 5.24 ?mol?L~(-1)and 3.35 ?mol?L~(-1),respectively.There were significant decline in density and aggregation of cells and significant differences in size between cells after interfering HL-60 cell for 48 h.Furthermore,some of HL-60 cells treated by shRNA-NS-2 were changed from round to fusiform shape even with pseudopod.Compared with control group,the inhibition rates of shRNA-NS-1 and shRNA-NS-2 to NS-mRNA expression were 37.82% and 71.88%,respectively.Conclusion The two shRNA for NS gene were successfully constructed,which suppress NS gene expression significantly.shRNA-NS-2 also can chang HL-60 cell′s morphology and might be a useful tool to explore NS gene function and possible therapy for acute leukemia.

OBJECTIVE:To provide references for Chinese drug distribution reform.METHODS:The drug distribution model in USA was briefly introduced and compared with that in China.The difficulties and orientations in Chinese drug distribution reform were put forward.RESULTS &CONCLUSIONS:Drug distribution reform should be carried out cautiously.Our government should deal well with the relationships between different interested parties and set up a reimbursement mechanism in medical institutions in order to facilitate the reform.