Quimicamente, o ecstasy é a 3,4-metilenodioximetanfetamina (MDMA), um composto sintético com propriedades estimulante central e alucinogênicas. Algumas substâncias análogas à MDMA, já identificadas em comprimidos de ecstasy, são principalmente: 3,4-metilenodioxietilanfetamina (MDEA), 3,4-metilenodioxianfetamina (MDA), metanfetamina e anfetamina. Os adulterantes mais comuns, normalmente encontrados são: cafeína e efedrinas. O objetivo deste trabalho foi a validação de um método analítico para quantificar a MDMA em comprimidos e cápsulas de ecstasy, através da cromatografia em fase gasosa com detector de nitrogênio/fósforo (GC/NPD). Substâncias análogas à MDMA e adulterantes também foram identificados. Amostras de comprimidos e cápsulas de 25 diferentes lotes, apreendidos como ecstasy em São Paulo (SP), foram analisadas pelo método proposto. Desse total de amostras, 21 continham somente MDMA (84%) e apenas 1 delas apresentou MDMA associada com cafeína (4%). A concentração total de MDMA nessas amostras variou entre 30,9 e 92,7mg, resultando em uma média aritmética de 63mg. / Chemically, \"ecstasy\" is 3,4-methylenedioxymethamphetamine (MDMA), a synthetic compound with stimulant and hallucinogenic properties. Some MDMA analog substances such as 3,4-methylenedioxyethylamphetamine (MDEA), 3,4-methylenedioxyamphetamine (MDA), methamphetamine and amphetamine have already been identified in \"ecstasy\" tablets. Caffeine and ephedrines are the most common adulterants also found. The aim of this paper is to describe the validation of an analytical method to quantify MDMA in \"ecstasy\" tablets and capsules. Gas chromatography with nitrogen/phosphorus detector was used in the method. Analog substances to MDMA and adulterant compounds were also identified. Samples from 25 lots of tablets seized in the city of São Paulo were analyzed. From that total, 21 showed only MDMA (84%) and just 1 of them presented MDMA plus caffeine (4%). MDMA total concentration in these samples had a variation between 30.9 and 92.7mg, resulting in an arithmetic average of 63mg.

Quimicamente, o ecstasy é a 3,4-metilenodioximetanfetamina (MDMA), um composto sintético com propriedades estimulante central e alucinogênicas. Algumas substâncias análogas à MDMA, já identificadas em comprimidos de ecstasy, são principalmente: 3,4-metilenodioxietilanfetamina (MDEA), 3,4-metilenodioxianfetamina (MDA), metanfetamina e anfetamina. Os adulterantes mais comuns, normalmente encontrados são: cafeína e efedrinas. O objetivo deste trabalho foi a validação de um método analítico para quantificar a MDMA em comprimidos e cápsulas de ecstasy, através da cromatografia em fase gasosa com detector de nitrogênio/fósforo (GC/NPD). Substâncias análogas à MDMA e adulterantes também foram identificados. Amostras de comprimidos e cápsulas de 25 diferentes lotes, apreendidos como ecstasy em São Paulo (SP), foram analisadas pelo método proposto. Desse total de amostras, 21 continham somente MDMA (84%) e apenas 1 delas apresentou MDMA associada com cafeína (4%). A concentração total de MDMA nessas amostras variou entre 30,9 e 92,7mg, resultando em uma média aritmética de 63mg. / Chemically, \"ecstasy\" is 3,4-methylenedioxymethamphetamine (MDMA), a synthetic compound with stimulant and hallucinogenic properties. Some MDMA analog substances such as 3,4-methylenedioxyethylamphetamine (MDEA), 3,4-methylenedioxyamphetamine (MDA), methamphetamine and amphetamine have already been identified in \"ecstasy\" tablets. Caffeine and ephedrines are the most common adulterants also found. The aim of this paper is to describe the validation of an analytical method to quantify MDMA in \"ecstasy\" tablets and capsules. Gas chromatography with nitrogen/phosphorus detector was used in the method. Analog substances to MDMA and adulterant compounds were also identified. Samples from 25 lots of tablets seized in the city of São Paulo were analyzed. From that total, 21 showed only MDMA (84%) and just 1 of them presented MDMA plus caffeine (4%). MDMA total concentration in these samples had a variation between 30.9 and 92.7mg, resulting in an arithmetic average of 63mg.

The illegal drug ecstasy, chemically known as 3,4-methylenedioxymethamphetamine (MDMA), sometimes contains additional chemicals which can pose health risks to users. This thesis examines strategies that recreational ecstasy users in Victoria, British Columbia utilize to determine the purity of their ecstasy. It also examines why they use these strategies and if they are concerned about impure ecstasy affecting their health because this information can help explain the use of these strategies. I performed a quantitative analysis of data collected by the Centre for Addictions Research of BC’s survey, the Canadian Recreational Drug Use Survey, to determine the strategies participants utilized to minimize potential harms caused by ecstasy use. This analysis revealed that 73.9% of survey participants discussed purity of ecstasy with friends, 33.3% checked drug information websites, 17.4% used an ecstasy testing kit, 2.9% asked harm reduction services for advice, and 0% owned a testing kit. In addition, the data revealed that the participants were more likely to take ecstasy from a friend than a stranger. Next, I developed an interview guide based on these findings and I interviewed 10 female recreational ecstasy users. I chose to interview women only because recreational drug use by women is underrepresented in the drug literature. The most common strategy the women utilized to determine ecstasy purity was to discuss ecstasy with friends. They preferred this strategy because it was a convenient, practical strategy. Also, they perceived their friends to be a trusted source of ecstasy and ecstasy information. Half the women analyzed how they felt after ingesting ecstasy to determine its purity because they believed different chemicals caused different effects. Others assessed the physical characteristics of their ecstasy to try to determine purity because they believed these characteristics could reveal its chemical contents. One participant used an ecstasy testing kit, but the rest cited multiple barriers to their use. Some women also had negative attitudes towards testing kits and felt no social pressure to use them. I asked the participants about their use of ecstasy testing laboratories, but none used this service because they did not know it existed. Overall, none of the women seemed concerned about ecstasy impurity harms. This could be due to four factors. First, their ecstasy use patterns made them feel safe from harms related to ecstasy use. Second, recreational ecstasy use was “normal” amongst young adults in Victoria who attend parties, raves, or clubs. Third, they primarily obtained ecstasy and ecstasy information from trusted friends. Fourth, they had never suffered significant harm caused by ecstasy impurity, even though all of the women believed they had ingested impure ecstasy. / Graduate

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The amphetamine derivative, 3,4-methylenedioxymethamphetamine (MDMA), is a popular drug often taken by young adults at dance clubs or rave parties. Laser light shows, fast-paced electronic music, and hot crowded dance floors are characteristic of these events, and Ecstasy users report that the acute effects of the drug are potentiated by these stimulatory conditions. However, it remains largely unknown how environmental stimuli impact the neurochemical and physiological effects of MDMA. The aim of the first study presented in this dissertation was to investigate how auditory stimuli (music, white noise, and no additional sound) influence MDMA conditioned place preference (CPP), self-administration, and nucleus accumbens (NAcc) dopamine (DA) and serotonin (5-HT) responses. Findings revealed a significant CPP for animals exposed to white noise during MDMA conditioning trials. After self-administration of MDMA (1.5 mg/kg), NAcc DA and 5-HT were highest in rats exposed to music during the test session. The second study aimed to investigate the effects of ambient temperature (23°or 32°C) on long-term MDMA self-administration and neurochemical responses. Results indicated no difference in self-administration or locomotor activity rates for the high versus room temperature groups across sessions. However, MDMA (3.0 mg/kg) administered in high ambient temperature resulted in significantly greater NAcc serotonin release compared to when taken at room temperature, but no differences in dopamine response was determined between the two conditions. Overall, these results indicate that auditory and thermal stimuli can effect MDMA-induced behavioral and neurochemical responses. The last aim tested a novel apparatus and method for use in animal models of drug reinforcement. By combining traditional CPP and self-administration procedures, this approach provided more informative data and circumvented some inherent drawbacks of each method alone. In addition to confirming the ability to produce drug conditioned place preferences after short- and long-term experiments, the long-term version of the procedure revealed a significant positive relationship between lever response rate and CPP magnitude. Therefore, this experimental design can be used to identify subgroups of rats that may vary in sensitivity to drug motivational effects. Further study of these populations may be useful in the development of behavioral and pharmacological therapies for drug addiction. / text