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首页> 外文期刊>Journal of Analytical Toxicology >Anodyne by Design; Measuring the Prevalence of Esoteric Designer Opioids in Pain Management Patients
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Anodyne by Design; Measuring the Prevalence of Esoteric Designer Opioids in Pain Management Patients

机译:anodyne按设计; 测量疼痛管理患者中的深度设计者阿片类药物的患病率

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摘要

The recent increase in illicit opioids sold on the black market, cut into heroin and masqueraded as prescription pills prompts a significant public health concern. Most designer opioids possess unknown potencies and unknown pharmacokinetics and their unregulated, variable dosages lead to rashes of overdoses. Additionally, many of the designer opioids, especially the fentanyl analogs are significantly more potent than heroin. High-profile cases involving overdoses of U-47700 and carfentanil have been reported in the media; however, the true prevalence of these and other designer opioids is unknown. Independent LC-MS-MS screen and confirmation methods have been developed and validated to identify and quantify fentanyl, and 18 designer opioids and their metabolites; methods were then exercised on urine specimens from contract pain management clients. Assuming patients in a pain management program may have a higher probability to seek out self-medication, samples from pain management patients were investigated for designer opioids. Similarly, pain management patients identified as using heroin may be more likely to experiment with or be accidentally exposed to designer opioids, specimens screening positive for the heroin metabolite 6-acetylmorphine were specifically chosen for designer opioid screening. Within this small group of pain management and heroin-positive samples, nine designer opioids were detected at a total prevalence of 25%. When screening random pain management samples not positive for heroin, a considerably lower percentage of samples ( 1%) were identified as positive for designer opioids. Furanyl fentanyl, fluorobutyryl fentanyl and acetylfentanyl were the most prevalent designer opioids detected in both test groups.
机译:最近在黑色市场上出售的非法表阿片类药物的增加,切成海洛因并伪装成处方药,促使具有重要的公共卫生问题。大多数设计师阿片类药物具有未知的效力和未知的药代动力学以及其未调节的可变剂量导致过量的皮疹。另外,许多设计师阿片类药物,尤其是芬太尼类似物比海洛因的有效性显着更高。媒体报道了涉及U-47700和Carfentanil过量的高调案例;然而,这些和其他设计师阿片类药物的真正患病率未知。已经开发并验证了独立的LC-MS-MS筛网和确认方法以鉴定和量化芬太尼,18名设计者阿片类药物及其代谢物;然后对来自合同疼痛管理客户的尿标本进行方法。假设患者在止痛药管理计划中可能具有较高的概率来寻求自我用药,研究了来自疼痛管理患者的样品进行设计师阿片类药物。类似地,鉴定为使用海洛因的疼痛管理患者可能更有可能对设计者阿片类药物进行实验或意外地暴露于设计者阿片类药物中,筛选阳性的海洛因代谢物6-乙酰甘氨酸的阳性被特别选择用于设计者阿片类药物筛选。在这一小群疼痛管理和海洛因阳性样本中,九个设计者阿片类药物的总患病率为25%。当筛选出对海洛因不阳性的随机疼痛管理样品时,将百分比的样品(1%)较低的百分比被鉴定为设计者阿片类药物阳性。呋喃基,氟丁基芬太尼和乙酰芬太尼是在两个测试组中检测到的最普遍的设计者阿片类药物。

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