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Faculty of Pharmacy - Mahidol University

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300 <strong>Faculty</strong> <strong>of</strong> <strong>Pharmacy</strong><br />

vaccine against SARS is available. However, it was found that a<br />

mixture <strong>of</strong> two HIV-1 proteinase inhibitors, lopinavir and ritonavir,<br />

exhibited some signs <strong>of</strong> effectiveness against the SARS virus. To<br />

understand the fine details <strong>of</strong> the molecular interactions between these<br />

proteinase inhibitors and the SARS virus via complexation, molecular<br />

dynamics simulations were carried out for the SARS-CoV 3CL(pro)<br />

free enzyme (free SARS) and its complexes with lopinavir (SARS-<br />

LPV) and ritonavir (SARS-RTV). The results show that flap closing<br />

was clearly observed when the inhibitors bind to the active site <strong>of</strong><br />

SARS-CoV 3CL(pro). The binding affinities <strong>of</strong> LPV and RTV to<br />

SARS-CoV 3CL(pro) do not show any significant difference. In<br />

addition, six hydrogen bonds were detected in the SARS-LPV system,<br />

while seven hydrogen bonds were found in SARS-RTV complex.<br />

(Journal <strong>of</strong> Theoretical Biology Volume 254, Issue 4, 21 October<br />

2008, Pages 861-867) (This work was jointly supported by the<br />

Commission on Higher Education and the Thailand Research Fund<br />

(MRG4880041)<br />

FORENSIC DETECTION OF MARIJUANA TRACE<br />

(NO. 816)<br />

Thitika Kitpipit 1 , Nathinee Panvisavas 1,2 , Nuntavan<br />

Bunyapraphatsara 3<br />

1Forensic Science Graduate Programme, <strong>Faculty</strong> <strong>of</strong> Scinece,<br />

<strong>Mahidol</strong> Univerfsity, Bangkok 10400, Thailand; 2Department <strong>of</strong><br />

Plant Science, <strong>Faculty</strong> <strong>of</strong> Science, <strong>Mahidol</strong> <strong>University</strong>, Thailand;<br />

3Deparment <strong>of</strong> Pharmacognosy, <strong>Faculty</strong> <strong>of</strong> <strong>Pharmacy</strong>, <strong>Mahidol</strong><br />

<strong>University</strong>, Thailand.<br />

Key words : DNA, Forensic, Marijuana, TLC, Trace<br />

In this study, we compared the use <strong>of</strong> both chemical and<br />

biological tests for precise screening. Marijuana leaves had been<br />

treated in simulated conditions according to the way they are<br />

consumed; leaves materials were boiled in water for 5 min to 8 h.<br />

dried in hot-air oven, air-dried in shade and sunlight, and burned to<br />

black and white ashes. The THC band was detected in the TLC<br />

fingerprints <strong>of</strong> all samples, except the white ash extract. In contrast,<br />

the 197-bp mitochondrial trnL-F fragment was amplified in two<br />

samples, i.e., the DNA extracted from fresh marijuana leaves that<br />

were boiled for 5 min and some <strong>of</strong> the dried marijuana sample. The<br />

results suggested that TLC was a robust method for the detection <strong>of</strong><br />

THC in marijuana. However, DNA analysis seems to be limited when<br />

DNA from heat-treated materials were analyzed 2008 Elsevier<br />

Ireland Ltd. All rights reserved.<br />

(Forensic Science International : Genetics Supplement Series; 1(1)<br />

August 2008: 600-602.)<br />

THE SMOOTHNESS OF BLOOD PRESSURE<br />

CONTROL OF RAMIPRIL IN ESSENTIAL<br />

HYPERTENSIVE THAI PATIENTS EVALUATION<br />

BY 24-HOUR AMBULATORY BLOOD PRESSURE<br />

MONITORING. (NO. 817)<br />

Uchaipichat, V. 1,4 , Koanantakul, B 2 , Suthisisang, C 3<br />

1 Department <strong>of</strong> <strong>Pharmacy</strong> Practice, <strong>Faculty</strong> <strong>of</strong> Pharmaceutical<br />

Sciences, Khon Kaen <strong>University</strong>, Khon Kaen, Thailand; 2 Division<br />

<strong>of</strong> Medicine, Bhumibol Adulyadej Hospital, Bangkok, Thailand;<br />

3 Department <strong>of</strong> Pharmacology, <strong>Faculty</strong> <strong>of</strong> <strong>Pharmacy</strong>, <strong>Mahidol</strong><br />

<strong>University</strong>, Bangkok, Thailand; 4 Department <strong>of</strong> <strong>Pharmacy</strong><br />

Practice, <strong>Faculty</strong> <strong>of</strong> Pharmaceutical Sciences, Khon Kaen<br />

<strong>University</strong>, Khon Kaen 40002, Thailand.<br />

Key words : Angiotensin converting enzyme inhibitor; Blood<br />

pressure variability; Hypertension<br />

Objective: Evaluate the efficacy <strong>of</strong> ramipril 2.5 and 5 mg<br />

once daily on the degree and homogeneity <strong>of</strong> 24-hour blood pressure<br />

reduction in essential hypertensive Thai patients. Material and<br />

Method: Nineteen male subjects, aged 30 to 60 years, with newly<br />

diagnosed essential hypertension were evaluated using the 24-hour<br />

ambulatory blood pressure (24-h ABP) measurement. Results: Twelve<br />

subjects responded and/or normalized with ramipril once daily, where<br />

the <strong>of</strong>fice and 24-h ABP were decreased significantly from baseline<br />

(p < 0.01). The percentage and magnitude <strong>of</strong> 24-h SBP/DBP loads<br />

after treatment were significantly decreased from 92 9.7/91 15.9<br />

to 67 23.8/65 27.6 (p < 0.01) and from 23 10.6/16 5.3 mmHg<br />

to 17 10.3/10 4.8 mmHg (p < 0.05). Trough to peak ratio for<br />

SBP/DBP was 0.59/0.52 (overall estimated) and 0.68 0.23/0.52<br />

0.22 (individual estimated), while the smoothness index was 0.89/<br />

1.03. Conclusion: Ramipril 2.5 and 5 mg once daily exerted the<br />

smooth 24-hour blood pressure reduction in essential hypertensive<br />

Thai patients.<br />

(Journal <strong>of</strong> the Medical Association <strong>of</strong> Thailand Volume 91, Issue 9,<br />

September 2008, Pages 1468-1477.)<br />

EFFECT OF FENOFIBRATE THERAPY ON<br />

PARAOXONASE1 STATUS IN PATIENTS WITH<br />

LOW HDL-C LEVELS (NO. 818)<br />

Wimon Phuntuwate 1 , Chuthamanee Suthisisang 1 , Banhan<br />

Koanantakul .2 , Preecha Chaloeiphap 3 , Bharit Mackness 4 , Mike<br />

Mackness. 4<br />

1 Department <strong>of</strong> Pharmacology, <strong>Faculty</strong> <strong>of</strong> <strong>Pharmacy</strong>, <strong>Mahidol</strong><br />

<strong>University</strong>, Sri Ayudhaya Road, Bangkok, 10400, Thailand;<br />

2 Cardiac and Preventive Center, Bhumibol Adulyadej Hospital,<br />

Bangkok, 10200, Thailand; 3 Division <strong>of</strong> Preventive Medicine,<br />

Royal Thai Air Force, Bangkok, 10200, Thailand; 4 <strong>University</strong> <strong>of</strong><br />

Manchester, Department <strong>of</strong> Medicine, Manchester Royal<br />

Infirmary, Oxford Road, Manchester, M13 9WL, United<br />

Kingdom<br />

Key words : Fen<strong>of</strong>ibrate; HDL-C; Oxidized LDL; Paraoxonase1<br />

Objectives: We evaluated the effect <strong>of</strong> micro-coated<br />

fen<strong>of</strong>ibrate on lipid parameters, high sensitivity C-reactive protein<br />

and paraoxonase1 levels in dyslipidemic patients with low highdensity<br />

lipoproteins levels. In addition, the effects <strong>of</strong> the paraoxonase1<br />

polymorphisms on lipid and paraoxonase1 responses to fen<strong>of</strong>ibrate<br />

therapy were examined. Methods: A total <strong>of</strong> 61 dyslipidemic patients<br />

with low high-density lipoproteins levels were recruited into this study<br />

to receive micro-coated fen<strong>of</strong>ibrate (160 mg/day) for 12 weeks. Lipid<br />

parameters, C-reactive protein, paraoxonase1 concentration and<br />

activity were measured at baseline and after 6 and 12 weeks <strong>of</strong><br />

fen<strong>of</strong>ibrate treatment. Four polymorphisms in both the coding (L55M<br />

and Q192R) and regulatory regions (T-108C and G-909C) <strong>of</strong> human<br />

paraoxonase1 were also quantified. Results: Micro-coated fen<strong>of</strong>ibrate

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