Rapid response human testing of smokeless tobacco products
Rapid response human testing of smokeless tobacco products
批准号:
8534749
负责人:
PAMELA I CLARK
金额:
$73.87万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-01 至 2015-08-31
关键词:
AcuteAdoptionAdultAromatic Polycyclic HydrocarbonsBiological MarkersBreath TestsCamelsCigaretteCross-Over StudiesDevelopmentDimensionsEducational workshopElectroencephalographyEmployee StrikesEvaluation ResearchEvent-Related PotentialsExhalationHumanIndividualLaboratoriesLeadLengthManufacturer NameMarketingMass FragmentographyMeasurementMeasuresMethodsMonitorNamesNeurocognitiveNicotineNitrosaminesOral TobaccoPhysiologicalPositioning AttributePrevalenceProceduresRecommendationResearchRiskRosaSalivaSalivarySamplingSeriesSmokeSmokelessSmokeless TobaccoSmokingSystemTechniquesTestingTimeTobaccoTobacco SurveillanceTobacco useToxic effectWithdrawalWorkaddictioncigarette smokingcravingfallsin vivoiq&aposmiknon-smokingprogramsresponsesmoking cessationsnuffsnustime usetobacco advertisingtoxicantuptakevectorvolatile organic compound
中文摘要
描述(由申请人提供):虽然成人吸烟率持续下降,但无烟烟草(ST)的使用正在增加。自2005年以来,几乎所有主要的卷烟生产商都进入了st市场,其中一些使用其流行的卷烟品牌(如万宝路鼻烟、骆驼鼻烟、好彩鼻烟)生产产品。这些新产品的大量涌现,使现有的非吸烟烟草(如湿鼻烟、咀嚼烟草、伊克米克、颗粒烟草)种类更加丰富。在如此快速变化的环境中表征这些ST产品需要比传统的长期交叉试验更快速的手段。这是一项应用急性检测措施的建议,以更好地了解人类使用不同ST产品的后果。我们将进行一系列急性交叉试验,系统地测试目前市场上的ST产品,以及在工作过程中引入的任何ST产品,以确定其滥用责任和潜在毒性。为此,我们提出以下具体目标:描述和对比滥用责任潜力和采用一系列ST产品的可能性。与药用尼古丁(已知低滥用潜力的对照)相比,ST的滥用责任评估(ALA)将包括喜欢和缓解渴望/戒断和神经认知功能(脑电图频谱分析和事件相关电位);使用对一次性使用烟草制品敏感的boost生物标志物,包括唾液烟草特异性亚硝胺(TSNAs)和多环芳烃(PAHs)以及呼出的挥发性有机化合物(VOCs),表征和对比ST产品的潜在毒性,所有这些都是在一次性使用每种产品之前和之后测量的;通过测量一系列ST产品中挥发性有机化合物的含量,以及产品中tsna和PAHs的含量,并评估pH值、水分、总尼古丁和游离尼古丁的含量,来表征和对比ST产品的潜在毒性和滥用潜力。
英文摘要
DESCRIPTION (provided by applicant): While rates of adult cigarette smoking continue to decline, smokeless tobacco (ST) use is increasing. Since 2005, virtually every major producer of cigarettes has entered the market for ST. Some are producing products using their popular cigarette brand names (e.g., Marlboro Snus, Camel Snus, Lucky Strike Snus). The proliferation of these new products is adding to the already wide array of available non-smoked tobacco (e.g., moist snuff, chewing tobacco, iqmik, pellets). Characterizing these ST products in such a rapidly changing landscape requires more rapid means than traditional long term cross-over trials. This is a proposal to apply acute testing measures to better understand the consequences of human use of varying ST products. We will perform a series of acute cross-over trials, systematically testing ST products currently on the market, and any introduced in the course of the work to determine their abuse liability and potential toxicity. To that end, we propose the following specific aims: To characterize and contrast the abuse liability potential and likelihood of adoption of a range of ST products. Abuse liability assessment (ALA) of ST will include liking and relief of craving/withdrawal and neurocognitive function (EEG spectral analysis and event- related potentials) in comparison to medicinal nicotine (control with known low abuse potential); to characterize and contrast the potential toxicity of ST products using boost biomarkers that are sensitive to one-time use of a tobacco product, including salivary tobacco-specific nitrosamines (TSNAs) and polycyclic aromatic hydrocarbons (PAHs) and exhaled breath volatile organic compounds (VOCs), all measured before and after single-use of each product; and, to characterize and contrast the potential toxicity and abuse potential of ST products by measuring levels of VOCs emitted from a range of ST products, as well as product levels of TSNAs and PAHs, and assessing pH, moisture, total nicotine, and free nicotine levels.
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海外基金