Abstract
Substance use, for the most part, encompasses plant products and diverted pharmaceuticals. Other substances called designer drugs, novel psychoactive substances (bath salts/flakka, spice/K2/Bombay Blue, pinky, N-bomb), possess similar chemical structures or pharmacological profiles to known or familiar substance use. According to the Monitoring the Future Survey of 2019, 3.3% of high school seniors used synthetic cannabinoids in the past year, 2.2% of them used methylenedioxymethamphetamine (MDMA) (ecstasy/molly) and 4.6% of them used hallucinogens. The chemical properties of designer drugs are uncertain, posing a challenge to detect or identify them accurately. The risk of cardiac arrest, coma, cognitive impairment, and death is not uncommon among users. In this chapter, we will discuss several typical designer drug classes: synthetic cannabinoids, synthetic stimulants, synthetic hallucinogens, and synthetic opioids. We will cover their mechanism of action, metabolism, mode of detection, potential treatment, and management as well as their adverse reactions and life-threatening consequences, which are critical keys to mitigating potential dire health consequences associated with these substances.
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References
Algren DA, Monteilh CP, Punja M, Schier JG, Belson M, Hepler BR, et al. Fentanyl-associated fatalities among illicit drug users in Wayne County, Michigan (July 2005–May 2006). J Med Toxicol. 2013;9(1):106–15.
Banister SD, Stuart J, Kevin RC, Edington A, Longworth M, Wilkinson SM, et al. Effects of bioisosteric fluorine in synthetic cannabinoid designer drugs JWH-018, AM-2201, UR-144, XLR-11, PB-22, 5F-PB-22, APICA, and STS-135. ACS Chem Neurosci. 2015;6(8):1445–58.
Baumann MH, Ayestas MA Jr, Partilla JS, Sink JR, Shulgin AT, Daley PF, et al. The designer methcathinone analogs, mephedrone and methylone, are substrates for monoamine transporters in brain tissue. Neuropsychopharmacology. 2012;37(5):1192.
Baumann MH, Partilla JS, Lehner KR. Psychoactive “bath salts”: not so soothing. Eur J Pharmacol. 2013;698(1–3):1–5.
Baumann MH, Partilla JS, Lehner KR, Thorndike EB, Hoffman AF, Holy M, et al. Powerful cocaine-like actions of 3, 4-methylenedioxypyrovalerone (MDPV), a principal constituent of psychoactive ‘bath salts’ products. Neuropsychopharmacology. 2013;38(4):552.
Bowdle TA. Adverse effects of opioid agonists and agonist-antagonists in anaesthesia. Drug Saf. 1998;19(3):173–89.
Boyer EW. Management of opioid analgesic overdose. N Engl J Med. 2012;367(2):146–55.
Brewer TL, Collins M. A review of clinical manifestations in adolescent and young adults after use of synthetic cannabinoids. J Spec Pediatr Nurs. 2014;19(2):119–26.
Carhart-Harris RL, King LA, Nutt DJ. A web-based survey on mephedrone. Drug Alcohol Depend. 2011;118(1):19–22.
Chahl LA. Opioids-mechanisms of action. Aust Prescr. 1996;19(3):63–5.
Chimalakonda KC, Bratton SM, Le VH, Yiew KH, Dineva A, Moran CL, et al. Conjugation of synthetic cannabinoids JWH-018 and JWH-073, metabolites by human UDP-glucuronosyltransferases. Drug Metab Dispos. 2011;39(10):1967–76.
Collins M. Some new psychoactive substances: precursor chemicals and synthesis-driven end-products. Drug Test Anal. 2011;3(7–8):404–16.
Cooper ZD. Adverse effects of synthetic cannabinoids: management of acute toxicity and withdrawal. Curr Psychiatry Rep. 2016;18(5):52.
Crowther SM, Reynolds LA, Tansey EM. The medicalization of cannabis. London, UK: Wellcome Trust Centre for the History of Medicine; 2010. p. 4–5.
Dargan PI, Albert S, Wood DM. Mephedrone use and associated adverse effects in school and college/university students before the UK legislation change. QJM Int J Med. 2010;103(11):875–9.
Dean BV, Stellpflug SJ, Burnett AM, Engebretsen KM. 2C or not 2C: phenethylamine designer drug review. J Med Toxicol. 2013;9(2):172–8.
Dolengevich-Segal H, Rodríguez-Salgado B, Gómez-Arnau J, Sánchez-Mateos D. Severe psychosis, drug dependence, and hepatitis C related to slamming mephedrone. Case Rep Psychiatry. 2016;2016:8379562.
Drug Enforcement Administration - Department of Justice. 2015. FY 2015 Performance Budget Congressional Submission. Retrieeved from https://www.justice.gov/sites/default/files/jmd/legacy/2013/10/13/dea-justification.pdf.
Drug Enforcement Administration, Department of Justice. Schedules of controlled substances: temporary placement of three synthetic cathinones in Schedule I. Final Order. Federal register. 2011;76(204):65371.
Fantegrossi WE, Murnane KS, Reissig CJ. The behavioral pharmacology of hallucinogens. Biochem Pharmacol. 2008;75(1):17–33.
Fantegrossi WE, Moran JH, Radominska-Pandya A, Prather PL. Distinct pharmacology and metabolism of K2 synthetic cannabinoids compared to Δ9-THC: mechanism underlying greater toxicity? Life Sci. 2014;97(1):45–54.
Froberg BA, Levine M, Beuhler MC, Judge BS, Moore PW, Engebretsen KM, et al. Acute methylenedioxypyrovalerone toxicity. J Med Toxicol. 2015;11(2):185–94.
Garcia-Romeu A, Kersgaard B, Addy PH. Clinical applications of hallucinogens: a review. Exp Clin Psychopharmacol. 2016;24(4):229–68.
Gibbons, S., & Arunotayanun, W. (2013). Natural product (fungal and herbal) novel psychoactive substances. In Novel psychoactive substances. Academic Press. pp. 345–62.
Gourlay GK, Kowalski SR, Plummer JL, Cousins MJ, Armstrong PJ. Fentanyl blood concentration-analgesic response relationship in the treatment of postoperative pain. Anesth Analg. 1988;67(4):329–37.
Harrison Cook. 2018. FDA approves opioid 10 times stronger than fentanyl.Retrieved from https://www.beckershospitalreview.com/opioids/fda-approves-opioid-stronger-than-fentanyl.html.
Hill SL, Thomas SH. Clinical toxicology of newer recreational drugs. Clin Toxicol. 2011;49(8):705–19.
Hill SL, Doris T, Gurung S, Katebe S, Lomas A, Dunn M, et al. Severe clinical toxicity associated with analytically confirmed recreational use of 25I–NBOMe: case series. Clin Toxicol. 2013;51(6):487–92.
Holm NB, Nielsen LM, Linnet K. CYP3A4 mediates oxidative metabolism of the synthetic cannabinoid AKB-48. AAPS J. 2015;17(5):1237–45.
Holpuchin A. 2018. 'It's not just New Haven': mass K2 overdose symptom of national crisis. The Guardian. Retrieved from https://www.theguardian.com/society/2018/aug/17/k2-spice-synthetic-marijuana-new-haven-green-overdose.
Hu X, Primack BA, Barnett TE, Cook RL. College students and use of K2: an emerging drug of abuse in young persons. Subst Abuse Treat Prevent Policy. 2011;6(1):16.
Iversen L, White M, Treble R. Designer psychostimulants: pharmacology and differences. Neuropharmacology. 2014;87:59–65.
Izaguirre A, Parascandola R, Rayman G. 2016. Thirty-three people treated in Brooklyn from possible K2 synthetic marijuana overdoses; scene compared to 'The Walking Dead'. New York daily news. Retrieved from https://www.nydailynews.com/new-york/brooklyn/multiple-people-hospitalized-k-2-overdoses-article-1.2708254.
Johnson LA, Johnson RL, Portier RB. Current “legal highs”. J Emerg Med. 2013;44(6):1108–15.
Johnston LD, O'Malley PM, Bachman JG, Schulenberg JE, Miech RA. Monitoring the Future National Survey Results on Drug Use, 1975-2013. Volume 2, college students & adults ages 19–55. Institute for Social Research. 2014.
Khan S, Shaheen F, Sarwar H, Molina J, Mushtaq S. “Bath salts”–induced psychosis in a young woman. The primary care companion for CNS disorders. 2013;15(1).
Kelly, J. P. (2011). Cathinone derivatives: a review of their chemistry, pharmacology and toxicology. Drug testing and analysis, 3(7-8), 439-453.\.
Kerrigan S, Savage M, Cavazos C, Bella P. Thermal degradation of synthetic cathinones: implications for forensic toxicology. J Anal Toxicol. 2016;40(1):1–11.
Kukanich B, Clark TP. The history and pharmacology of fentanyl: relevance to a novel, long-acting transdermal fentanyl solution newly approved for use in dogs. J Vet Pharmacol Ther. 2012;35:3–19.
Maxwell JC. Psychoactive substances—some new, some old: a scan of the situation in the US. Drug Alcohol Depend. 2014;134:71–7.
Mechoulam R, Feigenbaum JJ, Lander N, Segal M, Järbe TUC, Hiltunen AJ, Consroe P. Enantiomeric cannabinoids: stereospecificity of psychotropic activity. Experientia. 1988;44(9):762–4.
Mechoulam R, Lander N, Zahalka J. Synthesis of the individual, pharmacologically distinct, enantiomers of a tetrahydrocannabinol derivative. Tetrahedron Asymmetry. 1990;1(5):315–8.
Meyer RP, Gehlhaus M, Knoth R, Volk B. Expression and function of cytochrome p450 in brain drug metabolism. Curr Drug Metab. 2007;8(4):297–306.
Mills B, Yepes A, Nugent K. Synthetic cannabinoids. Am J Med Sci. 2015;350(1):59–62.
Nelson L, Schwaner R. Transdermal fentanyl: pharmacology and toxicology. J Med Toxicol. 2009;5(4):230.
Nichols DE, Frescas SP, Chemel BR, Rehder KS, Zhong D, Lewin AH. High specific activity tritium-labeled N-(2-methoxybenzyl)-2, 5-dimethoxy-4-iodophenethylamine (INBMeO): a high-affinity 5-HT2A receptor-selective agonist radioligand. Bioorg Med Chem. 2008;16(11):6116–23.
Palamar JJ, Salomone A, Vincenti M, Cleland CM. Detection of “bath salts” and other novel psychoactive substances in hair samples of ecstasy/MDMA/ “Molly” users. Drug Alcohol Depend. 2016;161:200–5.
Papaseit E, Pérez-Mañá C, Mateus JA, Pujadas M, Fonseca F, Torrens M, et al. Human pharmacology of mephedrone in comparison with MDMA. Neuropsychopharmacology. 2016;41(11):2704.
Peiper NC, Clarke SD, Vincent LB, Ciccarone D, Kral AH, Zibbell JE. Fentanyl test strips as an opioid overdose prevention strategy: findings from a syringe services program in the southeastern United States. Int J Drug Policy. 2019;63:122–8.
Pertwee RG. Cannabinoid pharmacology: the first 66 years. Br J Pharmacol. 2006;147(S1):S163–71.
Rafaeli JS. 2017. The story of Mephedrone, the party drug that boomed and went bust. Vice magazine. Retrieved from https://www.vice.com/en_us/article/9aa53a/the-story-of-mephedrone-the-party-drug-that-boomed-and-went-bust.
Reschly-Krasowski JM, Krasowski MD. A difficult challenge for the clinical laboratory: accessing and interpreting manufacturer cross-reactivity data for immunoassays used in urine drug testing. Acad Pathol. 2018;5:2374289518811797. https://doi.org/10.1177/2374289518811797.
Shulgin AT, Shulgin A. PIHKAL: a chemical love story. Berkeley: Transform Press; 1995. p. 733–9.
Simmons J, Cookman L, Kang C, Skinner C. Three cases of “spice” exposure. Clin Toxicol. 2011;49(5):431–3.
Sivagnanam K, Chaudari D, Lopez P, Sutherland ME, Ramu VK. “Bath salts” induced severe reversible cardiomyopathy. Am J Case Rep. 2013;14:288.
Spiller HA, Ryan ML, Weston RG, Jansen J. Clinical experience with and analytical confirmation of “bath salts” and “legal highs” (synthetic cathinones) in the United States. Clin Toxicol. 2011;49(6):499–505.
Stanley TH. The history and development of the fentanyl series. J Pain Symptom Manag. 1992;7(3):S3–7.
Su MK, Seely KA, Moran JH, Hoffman RS. Metabolism of classical cannabinoids and the synthetic cannabinoid JWH-018. Clin Pharmacol Ther. 2015;97(6):562–4.
Substance Abuse and Mental Health Services Administration, Center for Behavioral Health Statistics and Quality. 2011. The DAWN report: highlights of the 2011 Drug Abuse Warning Network (DAWN) Findings on Drug-Related Emergency Department Visits. Retrieved from https://www.samhsa.gov/data/sites/default/files/DAWN2k11ED/DAWN2k11ED/DAWN2k11ED.pdf.
Taba P, Lees AJ, Sikk K. The neuropsychiatric complications of stimulant abuse, vol. 120. Burlington: Academic Press; 2015.
Thornton SL, Gerona RR, Tomaszewski CA. Psychosis from a bath salt product containing flephedrone and MDPV with serum, urine, and product quantification. J Med Toxicol. 2012;8(3):310–3.
UN Office on Drugs and Crime. 2013. "The challenge of new psychoactive substances: a report from the Global SMART Programme" (Vienna, Austria: UNODC Laboratory and Scientific Section, March 2013), pp. 10–11. Retrieved from http://www.unodc.org/documents...
United Nations Office on Drugs, & Crime. 2011. 2011 World Drug Report.Retrieved from https://www.unodc.org/documents/scientific/Synthetic_Cannabinoids.pdfpdf.
United Nations Office on Drugs, & Crime. 2016. 2016 world drug report. United Naetions Publications. Retrieved from http://www.unodc.org/doc/wdr2016/WORLD_DRUG_REPORT_2016_web.pdf.
Vardakou I, Pistos C, Spiliopoulou C. Drugs for youth via internet and the example of mephedrone. Toxicol Lett. 2011;201(3):191–5.
Watanabe K, Itokawa Y, Yamaori S, Funahashi T, Kimura T, Kaji T, et al. Conversion of cannabidiol to Δ 9-tetrahydrocannabinol and related cannabinoids in artificial gastric juice, and their pharmacological effects in mice. Forensic Toxicol. 2007;25(1):16–21.
Weaver MF, Schnoll SH. Addictions: a comprehensive guidebook. In: Stimulants: amphetamines and cocaine. New York: Oxford University Press USA; 1999. p. 105–20.
Weaver MF, Hopper JA, Gunderson EW. Designer drugs 2015: assessment and management. Addict Sci Clin Pract. 2015;10(1):8.
Weaver M, Schnoll S. Hallucinogens and club drugs. In: The American Psychiatric Publishing textbook of substance abuse treatment. 4th ed. Washington, D.C.: American Psychiatric Publishing Inc; 2008. p. 191–200.
Winstock A, Mitcheson L, Ramsey J, Davies S, Puchnarewicz M, Marsden J. Mephedrone: use, subjective effects and health risks. Addiction. 2011;106(11):1991–6.
Zaami S, Giorgetti R, Pichini S, Pantano F, Marinelli E, Busardo FP. Synthetic cathinones related fatalities: an update. Eur Rev Med Pharmacol Sci. 2018;22(1):268–74.
Zawilska JB, Wojcieszak J. Designer cathinones—an emerging class of novel recreational drugs. Forensic Sci Int. 2013;231(1–3):42–53.
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Revadigar, N., Yu, C.T., Silverstone-Simard, I. (2022). Designer Drugs. In: Akerele, E. (eds) Substance and Non-Substance Related Addictions. Springer, Cham. https://doi.org/10.1007/978-3-030-84834-7_16
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