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1.
Zhongguo Yi Liao Qi Xie Za Zhi ; (6): 267-269, 2020.
Artigo em Chinês | WPRIM | ID: wpr-942741

RESUMO

OBJECTIVE@#In order to find whether there is the correlation between the non-oil particle filtration efficiency(PFE) and the bacterial filtration efficiency(BFE) of medical surgical masks.@*METHODS@#Non-oil particle filtration efficiency and bacterial filtration efficiency were compared and analyzed through the test data of medical surgical masks from 2012 to 2018.@*RESULTS@#When the non-oil particle filtration efficiency of medical surgical mask is over 80%, the bacterial filtration efficiency can reach 95%.@*CONCLUSIONS@#In order to reach the requirement of 95% bacterial filtration efficiency, surgical medical mask must improve the limit of non-oil particle filtration efficiency. The results of data analysis can provide reference for emergency inspection and filter material rapid inspection, and also provide reference for the revision of YY 0469 standard.


Assuntos
Filtração , Máscaras , Tamanho da Partícula
2.
China Pharmacist ; (12): 171-173, 2018.
Artigo em Chinês | WPRIM | ID: wpr-705482

RESUMO

Objective:To establish a method for determining styrene monomer migration amount in ofloxacin and sodium chloride injection from three layer coextrusion infusion bags by GC-MS.Methods:The styrene monomer content in ofloxacin and sodium chlo-ride injection was detected by GC-MS in order to study the migration amount of styrene from the packaging bag ( three layer coextrusion infusion) of ofloxacin and sodium chloride injection .A DB-624123-1334 capilary column (30 m ×0.32 mm, 1.8 μm) was used, and the detection was carried out with programmed temperature and headspace sampling by the electron bombardment source (EI) in a selective ion monitoring (SIM) mode.Results:The linear concentration range of styrene was 46.96-543.60 ng· ml-1(r=0.9999), and the average recovery was 101.2%(RSD=3.1%, n=9).Conclusion:The method is simple, accurate and reproducible.It can be used for the compatibility testing between medicine and its package .

3.
Zhonghua xinxueguanbing zazhi ; (12): 782-784, 2015.
Artigo em Chinês | WPRIM | ID: wpr-317691

RESUMO

<p><b>OBJECTIVE</b>To compare the efficacy and safety of 3 rivaroxaban regimen in patients with venous thromboembolism (VTE).</p><p><b>METHODS</b>This is a retrospective study. Thirty three inpatients with VTE received rivaroxaban were divided into 3 groups, in which 16 patients were treated with 15 mg rivaroxaban twice daily for 21 days then followed by 20 mg once per day till 3 months (group 1), 9 patients were treated with 20 mg rivaroxaban once daily for 3 months (group 2), 8 patients were treated with 10 mg rivaroxaban once daily for 3 months. The reduction rate of D-Dimer on the third therapy day, the duration of D-Dimer normalization and hospital stay as well as symptom remission, the imaging assessment results after three months treatment, rate of recurrent VTE, bleeding, liver and kidney function were compared among the 3 groups.</p><p><b>RESULTS</b>The reduction rates of D-Dimer on the third therapy day were significantly higher ((46.12 ± 15.42) % vs. (26.59 ± 8.11) % and (25.55 ± 14.00) %, P = 0.02, P = 0.01), and the duration of D-Dimer normalization was significantly shorter ((17.9 ± 7.7) days vs. (24.1 ± 5.1) days and (26.3 ± 6.2) d, P = 0.03, P < 0.01) in group 1 than in group 2 and 3. There was one recurrent deep-vein thrombosis in group 3, one non-major bleeding in group 1 and group 3. Major bleeding or liver and kidney dysfunction were not observed in these patients.</p><p><b>CONCLUSIONS</b>Venous thromboembolism can be safely and effectively treated by rivaroxaban, and does of 15 mg twice daily for 21 days followed by 20 mg once daily for 3 months are superior to the other 2 tested therapy regimen in this patient cohort.</p>


Assuntos
Humanos , Produtos de Degradação da Fibrina e do Fibrinogênio , Hemorragia , Tempo de Internação , Estudos Retrospectivos , Rivaroxabana , Tromboembolia Venosa , Trombose Venosa
4.
China Pharmacist ; (12): 876-877, 2015.
Artigo em Chinês | WPRIM | ID: wpr-669785

RESUMO

Objective:To establish a method for the determination of antioxygen 1178 in 5-layer co-extrusion bags used for infu-sion. Methods:A Uitimat XB-C8 (250 mm × 4. 6 mm,5μm) column was used,the mobile phase was methanol-water with gradient elu-tion, the flow rate was 1. 0 ml·min-1 ,the detection wavelength was 223 nm,the column temperature was 35℃ and the injection vol-ume was 20 μl. Results:The concentration of antioxygen 1178 had the linear relationship within the range of 1. 64-205. 10 μg·ml-1 (r=0. 999 9),and the average recovery was 92. 05% (RSD=1. 94%, n=9). Conclusion:The method is accurate,stable and spe-cific,and can be used to determine antioxygen 1178 in 5-layer co-extrusion bags used for infusion.

5.
China Pharmacist ; (12): 1693-1694, 2015.
Artigo em Chinês | WPRIM | ID: wpr-670071

RESUMO

Objective:To establish a method for the determination of Si migration in penehyclidine hydrochloride injection packed with low borosilicate glass ampoule. Methods: Si migration was determined by graphite furnace-atomic absorption spectrometry. Re-sults:The linear concentration range was 0-85 ng·ml-1(r=0. 995 6). The average recovery was 95. 85% and RSD was 4. 60% (n=9). Conclusion:The method is sensitive, rapid and accurate with good repeatability, which can be used to determine Si migration in penehyclidine hydrochloride injection packed with low borosilicate glass ampoule.

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