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1.
China Pharmacy ; (12): 464-467, 2020.
Artigo em Chinês | WPRIM | ID: wpr-817293

RESUMO

OBJECTIVE:To study the anti-tumor effect of artemether (ARM)self-microemulsifying drug delivery system (SMEDDS) on human glioma subcutaneously transplanted model mice. METHODS :Human glioma cell line SHG 44 was inoculated and passed on to establish subcutaneous transplanted tumor model of nude mice. At the 5th,10th,15th,20th and 25th day after inoculation ,the tumor tissue volume was measured and the growth curve was drawn to confirm the initial stage of rapid tumor proliferation. Thirty nude mice was collected to establish subeutaneously transplanted tumor nude model ,and then divided into control group (normal saline ),ARM suspension group [ 60 mg/(kg·d)],ARM-SMEDDS low-dose ,medium-dose and high-dose groups [ 10,20,30 mg/(kg·d)] at the initial stage of rapid tumor proliferation. They were given normal saline and relevant solution intragastrically once a day ,for consecutive 30 d. The weight change and general sibuation of mice were recorded. The change of tumor volume was determined and relative tumor proliferation rate was calculated. RESULTS :The subcutaneously transplanted tumor tissue entered the initial stage of rapid tumor proliferation from the 10th day after transplantation. The general situation was normal ,and there was no obvious abnormal reaction in mice of each group during treatment. Since 10th day of administration,tumor tissue volume of mice in ARM-SMEDDS groups were shortened significantly than control group (P<0.05). At 15th day of administration ,tumor volume of mice in ARM-SMEDDS groups were shortened significantly than ARM suspension group(P<0.05). After last administration ,relative tumor proliferation rates of mice in ARM-SMEDDS groups were decreased significantly,compared with ARM suspension group (P<0.05). CONCLUSIONS :ARM-SMEDDS show significant inhibitory effect on the proliferation of human glioma ,and are better than suspension with higher dosage.

2.
Chinese Journal of Medical Education Research ; (12): 871-875, 2019.
Artigo em Chinês | WPRIM | ID: wpr-790249

RESUMO

Virtual reality technology is an emerging product of science and technology and has great potential in medical education. It can break through the limits of traditional teaching, establish a modern teaching model, improve teachers' teaching ability and quality, and thus promote the development of medical education. This study discussed the necessity and application practice of virtual reality technology in the medical education of China and explores its development in medical education with reference to the construction cases of the virtual experiment platform in Chongqing Medical University, so as to provide new ideas for improving the overall quality of medical education.

3.
Chinese Journal of Medical Education Research ; (12): 871-875, 2019.
Artigo em Chinês | WPRIM | ID: wpr-797446

RESUMO

Virtual reality technology is an emerging product of science and technology and has great potential in medical education. It can break through the limits of traditional teaching, establish a modern teaching model, improve teachers' teaching ability and quality, and thus promote the development of medical education. This study discussed the necessity and application practice of virtual reality technology in the medical education of China and explores its development in medical education with reference to the construction cases of the virtual experiment platform in Chongqing Medical University, so as to provide new ideas for improving the overall quality of medical education.

4.
China Pharmacy ; (12): 4738-4740, 2017.
Artigo em Chinês | WPRIM | ID: wpr-668323

RESUMO

OBJECTIVE:To provide reference for improving the teaching quality of pharmaceutical analysis course. METH-ODS:WeChat public platform was registered firstly,and supplement teaching was provided before class,during class and after class. RESULTS:WeChat public platform named Pharmaceutical Analysis of Chongqing Medical and Pharmaceutical College was registered and included 2 first-level-modules of"excellent resource"and"learning interaction",and 6 second-level-modules of"classic courseware""pre-course lesson plan""classic video""classroom exercises""question answering""classic case". Before class, students could preview through the platform;during class,the teachers could review teaching according to the platform;after class,the teachers could test students'learning results and answer questions for students,and students could consolidate classroom knowledge. Post-course effect evaluation showed that there was statistical significance in pass rate of student's grade between teach-ing reform class and control class (P<0.05). And the students of teaching reform class had good satisfactory degree (87.07%). CONCLUSIONS:WeChat mobile learning model supplements pharmaceutical analysis course,improves students'enthusiasm for learning and students,academic records. Students are satisfied with it. It can provide reference for improving the teaching quality of the course.

5.
China Pharmacy ; (12): 2207-2209, 2016.
Artigo em Chinês | WPRIM | ID: wpr-504491

RESUMO

OBJECTIVE:To study relative bioavailability of dauricine self-microemulsifying drug delivery system (SMEDDS) in rats. METHODS:12 rats were randomly divided into dauricine SMEDDS group (20 mg/kg) and dauricine solution group (50 mg/kg),6 rats in each group. They were given relevant medicine intragastrically. Then,0.3 ml plasma was collected from orbital venous plexus before medication and 0.167,0.333,0.5,0.75,1,2,4,8,12,24,36 h after medication. The plasma concentration of da- uricine was determined by HPLC-MS/MS,and DAS 3.0 was used to calculate pharmacokinetic parameters and evaluate the relative bioavailability of dauricine with dauricine SMEDDS. RESULTS:The linear range of dauricine in plasma were 2.12-424 ng/ml (r=0.999 9);RSDs of intra-day and inter-day were all lower than 10%. Pharmacokinetic parameters of dauricine solution and dau-ricine SMEDDS were that cmax were(126.3±37.4)ng/ml and(179.6±51.5)ng/ml;t1/2 were(11.48±4.58)and(21.79±6.59)h;AUC0-t were (1 963.5±638.3)ng·h/ml and(2 535.8±739.5)ng·h/ml;AUC0-∞ were(2 256.3±703.5)ng·h/ml and(2 854.6± 768.7)ng·h/ml,respectively. The relative bioavailability of dauricine SMEDDS were 323% and 316% by calculating with AUC0-t and AUC0-∞,respectively. CONCLUSIONS:Intragastric administration of dauricine SMEDDS can improve relative bioavailability of dauricine significantly.

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