There are 5 models of management for drug price currently in the world. Each model has combined with a private rule in order to stable drug price. In the situation of our country at the moment, we couldn’t apply one of among these methods. Some issues should be given priority as research of diseases model in practically and drug’s use, a tax system or fee for drug, promulgate of list of essential drugs needed in price’s management, an explanation of price should be given for a new drug and establishment of drug distribution system. In order to stable of drug’s price for a long term or in a certain duration, the key role is depended on the pharmacologist and the leaders of pharmacologic special management
Pharmacy ; Pharmaceutical Preparations ; Case Management ; drugs ; Commerce

Background: The postoperative residual spherical equivalent (SE) refractive error of the posterior chamber intraocular lens insertion is the cause result in significant distant vision loss. Objective: The study evaluated residual SE refractive error of the patients having ocular trauma undergoing a trans pars plana vitreo-lensectomy and posterior chamber intraocular lens insertion, for recorrection of the preoperative IOL power calculated formula are also investigated. Subjects: 43 consecutive patients who underwent a trans pars plana vitreo-lensectomy and posterior chamber intraocular lens insertion in the sulcus, in the Trauma Department of National Institute of Ophthalmology, from December 2005 to June 2007. Method: This was a prospective cross-sectional study. Results: Among 43 patients, there were 39 men and 4 women, age ranged from 10 to 45 years. In the most cases, the residual spherical equivalent deviation was planned to achieve final mild myopia (mean -1.75 D by manifest refraction; -1.9 D by autorefractor measurements). The surgery could provide a best corrected visual acuity at over 0.2 (81.4%). Conclusions: Intraocular lens implantation at the time of trans pars plana vitreo-lensectomy could provide a reasonable restoration of visual acuity and binocular function. However, recorrection of the IOL power calculation was necessary in these cases.
Postoperative spherical refractive error ; intraocular lens insertion

Introduction: Cataract and vitreous opacification caused by ocular injury results in significant visual loss. Objectives: to evaluate the initial outcome of patients with ocular blunt or penetrating trauma who underwent trans pars planar vitreo-lensectomy and posterior chamber intra ocular lens insertion. Comment on the indications and applications of surgical techniques. Subjects and method: In this prospective randomized study, a total of 30 patients (30 eyes) with blunt/penetrating ocular trauma were assessed using X-ray and ultrasound in the Trauma Department of National Institute of Ophthalmology, from December 2005 to August 2006. Results: 30 patients (28 men and 2 women) with an age range from 3 to 45 years. Penetrating injuries are more common than blunt ones. The cornea is the most common site of injury (73.3%). Conclusion: Intraocular lens were implanted at the time of trans pars planar vitreo-lensectomy can provide a reasonable restoration of visual acuity and binocular function.
Vitreo-lensectomy ; Intraocular lens

Background: In the period 2006-2010, a investigation on medical arthropod has been conducted\r\n', u'Objective: 1) To determine species composition and distribution of medical arthropod. 2) To find species transmitted disease \r\n', u'Subject and method: The cross sectional, descriptive and analytic investigation was conducted in 3 communes along the Ho Chi Minh road in Cao Bang province. \r\n', u'Results and conclusion: : A total of 3.437 of samples of medical arthropod belonging to 96 species have been collected including: three species of flea (Siphonaptera), two species of tick (Ixodoidea), four species of chigges (Trombiculidae), ten species of mites (Gamasoidea), twenty four species of flies (Muscoidea), and fifty-three species of mosquito (Culicidae). They belong to 39 genuses, 17 families, 3 orders: (Siphonaptera, Acarina and Diptera); two classes (Insecta and Arachnida). \r\n', u'Some species having epidemiological role such as Aedes albopictus, Culex tritaeniorhyncus, Cx. quinquefasciatus, Cx. vishnui ... were predominant at all study sites. Anopheles minimus, the main malaria vector, was mainly collected in cattle- sheds in Truong Ha and Bach Dang communes. \r\n', u'
Medical arthropod ; investigation

Background: Japanese Encephalitis (JE) is common in the plains and mountainous areas in Asia \u2013 Pacific. Japanese encephalitis vaccine shows effectiveness in protecting children from JE in some countries such as Japan and Korea. Objective: To evaluate the efficacy of Japanese Encephalitis (JE) vaccination in Thai Binh province during 2003-2007. Subject and Method: Prospective, retrospective and sero-epidemiological methods were carried out on 329 samples collected from viral encephalitis patients and tested by JE MAC-ELISA, the positive average was 41.6% (137/329). Result: It had dramatically dropped from 85.2% in 2003 to 8.5 % in 2007 related to the rate of JE vaccination for children from 1 to 5 years old increasing from 49 % in 2003 to 77 % in 2007. Most of JE confirmed cases were un-vaccinated. Conclusion: JE etiology cause viral encephalitis in children in Thai Binh province was reduced thanks to JE vaccination in EPI program for 1 to 5 year old children. But more than 96% (131/136) of viral encephalitis in 15 years old upward was unknown etiology, the need for further study of the etiology cause viral encephalitis in adults.
Japanese encephalitis ; virus encephalitis ; MAC-ELISA ; Vaccine

A new crinane-type alkaloid, 6-epihydroxypowelline (1), together with six known alkaloids, lycorine (2), 2-O-acetyllycorine (3), deacetylbowdensine (4), 1-epideacetylbowdensine (5), 8-demethyl-3-oxomaritidine (6), and (-)-marithamine (7) were isolated from the whole parts of the Crinum latifolium L. in Vietnam. The structure identification of all compounds was determined by 1D, 2D-NMR as well as HR-ESI-MS spectroscopic techniques. The absolute configuration of these compounds was established by the ECD data. In addition, in vitro inhibition of acetylcholinesterase (AChE) activities was assessed for all isolated alkaloids. All alkaloids had AChE inhibitory effects, with IC50 values ranging from 32.65 ± 2.72 to 212.76 ± 8.30 µM and compound 3 displayed the strongest inhibition of AChE, with IC50 values of 32.65 ± 2.72 µM (in comparison to the reference drug, galanthamine, which had an IC50 of 2.40 ± 0.45 µM).

A new crinane-type alkaloid, 6-epihydroxypowelline (1), together with six known alkaloids, lycorine (2), 2-O-acetyllycorine (3), deacetylbowdensine (4), 1-epideacetylbowdensine (5), 8-demethyl-3-oxomaritidine (6), and (-)-marithamine (7) were isolated from the whole parts of the Crinum latifolium L. in Vietnam. The structure identification of all compounds was determined by 1D, 2D-NMR as well as HR-ESI-MS spectroscopic techniques. The absolute configuration of these compounds was established by the ECD data. In addition, in vitro inhibition of acetylcholinesterase (AChE) activities was assessed for all isolated alkaloids. All alkaloids had AChE inhibitory effects, with IC50 values ranging from 32.65 ± 2.72 to 212.76 ± 8.30 µM and compound 3 displayed the strongest inhibition of AChE, with IC50 values of 32.65 ± 2.72 µM (in comparison to the reference drug, galanthamine, which had an IC50 of 2.40 ± 0.45 µM).

A new crinane-type alkaloid, 6-epihydroxypowelline (1), together with six known alkaloids, lycorine (2), 2-O-acetyllycorine (3), deacetylbowdensine (4), 1-epideacetylbowdensine (5), 8-demethyl-3-oxomaritidine (6), and (-)-marithamine (7) were isolated from the whole parts of the Crinum latifolium L. in Vietnam. The structure identification of all compounds was determined by 1D, 2D-NMR as well as HR-ESI-MS spectroscopic techniques. The absolute configuration of these compounds was established by the ECD data. In addition, in vitro inhibition of acetylcholinesterase (AChE) activities was assessed for all isolated alkaloids. All alkaloids had AChE inhibitory effects, with IC50 values ranging from 32.65 ± 2.72 to 212.76 ± 8.30 µM and compound 3 displayed the strongest inhibition of AChE, with IC50 values of 32.65 ± 2.72 µM (in comparison to the reference drug, galanthamine, which had an IC50 of 2.40 ± 0.45 µM).

A new crinane-type alkaloid, 6-epihydroxypowelline (1), together with six known alkaloids, lycorine (2), 2-O-acetyllycorine (3), deacetylbowdensine (4), 1-epideacetylbowdensine (5), 8-demethyl-3-oxomaritidine (6), and (-)-marithamine (7) were isolated from the whole parts of the Crinum latifolium L. in Vietnam. The structure identification of all compounds was determined by 1D, 2D-NMR as well as HR-ESI-MS spectroscopic techniques. The absolute configuration of these compounds was established by the ECD data. In addition, in vitro inhibition of acetylcholinesterase (AChE) activities was assessed for all isolated alkaloids. All alkaloids had AChE inhibitory effects, with IC50 values ranging from 32.65 ± 2.72 to 212.76 ± 8.30 µM and compound 3 displayed the strongest inhibition of AChE, with IC50 values of 32.65 ± 2.72 µM (in comparison to the reference drug, galanthamine, which had an IC50 of 2.40 ± 0.45 µM).

A new crinane-type alkaloid, 6-epihydroxypowelline (1), together with six known alkaloids, lycorine (2), 2-O-acetyllycorine (3), deacetylbowdensine (4), 1-epideacetylbowdensine (5), 8-demethyl-3-oxomaritidine (6), and (-)-marithamine (7) were isolated from the whole parts of the Crinum latifolium L. in Vietnam. The structure identification of all compounds was determined by 1D, 2D-NMR as well as HR-ESI-MS spectroscopic techniques. The absolute configuration of these compounds was established by the ECD data. In addition, in vitro inhibition of acetylcholinesterase (AChE) activities was assessed for all isolated alkaloids. All alkaloids had AChE inhibitory effects, with IC50 values ranging from 32.65 ± 2.72 to 212.76 ± 8.30 µM and compound 3 displayed the strongest inhibition of AChE, with IC50 values of 32.65 ± 2.72 µM (in comparison to the reference drug, galanthamine, which had an IC50 of 2.40 ± 0.45 µM).