Poppers
A selection of over-the-counter poppers on display | |
| Clinical data | |
|---|---|
| Other names | popper, poppe, pops |
| Routes of administration | Inhalation |
| Drug class | Vasodilator |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Bioavailability | When inhaled,
|
| Metabolism | Liver |
| Metabolites |
|
| Onset of action | 15 seconds |
| Elimination half-life | Suspected to be minutes to less than an hour |
| Duration of action | 30 seconds to 5 minutes |
| Excretion | Primarily urine |
| Chemical and physical data | |
| Formula | Depends on primary active ingredient |
| Molar mass | Depends on primary active ingredient |
| Boiling point | Depends on primary active ingredient |
Poppers are recreational drugs belonging to the alkyl nitrite family of chemical compounds. When fumes from these substances are inhaled, they act as potent vasodilators, producing mild euphoria, warmth, and dizziness. Most effects have a rapid onset and are short-acting.[2] Its recreational use is believed to be potentially dangerous for people with heart problems, anaemia, or glaucoma. Reported adverse effects include fainting, retinal toxicity, and vision loss.[3][4]
As poppers include a broad range of chemical types, their legality differs across different jurisdictions. They are often packaged under the guise of room deodorizer, leather polish, nail polish remover, or videotape head cleaner to evade anti-drug laws.[2]
The term poppers comes from the popping sound made when glass vials of the substance were crushed to release the vapors for inhalation. Amyl nitrite was originally prescribed in the late 1800s for the medical management of angina.[2] Many analogues exist, such as isoamyl nitrite, isopentyl nitrite, isopropyl nitrite, and isobutyl nitrite. These substances are subject to different regulations; for example, isobutyl nitrite is banned in the European Union.
Poppers act as muscle relaxants, causing the relaxation of involuntary smooth muscles such as the throat and anus.[5][6] Such physiological effects, along with others (such as mild euphoria), have resulted in poppers being used as recreational drugs, sometimes during sexual intercourse, as the effects can heighten arousal and help facilitate acts such as anal intercourse.[7] Poppers were a part of the club culture which began during the mid-1970s disco scene, and surged in popularity during the rave scene of the 1980s and 1990s.[8][9]
- ^ Therapeutic Goods (Poisons Standard—October 2024) Instrument 2024 (Cth). Amyl nitrite also classified in Schedule 3 (Pharmacist only) in certain preparations. Isopropyl nitrite classified in Schedule 10 (Dangerous substance).
- ^ a b c Romanelli F, Smith KM, Thornton AC, Pomeroy C (January 2004). "Poppers: epidemiology and clinical management of inhaled nitrite abuse". Pharmacotherapy. 24 (1): 69–78. doi:10.1592/phco.24.1.69.34801. PMID 14740789. S2CID 44991387.
- ^ Davies AJ, Kelly SP, Naylor SG, Bhatt PR, Mathews JP, Sahni J, et al. (November 2012). "Adverse ophthalmic reaction in poppers users: case series of 'poppers maculopathy'". Eye. 26 (11): 1479–1486. doi:10.1038/eye.2012.191. PMC 3496104. PMID 23079752.
- ^ Vignal-Clermont C, Audo I, Sahel JA, Paques M (October 2010). "Poppers-associated retinal toxicity". The New England Journal of Medicine. 363 (16): 1583–1585. doi:10.1056/NEJMc1005118. PMID 20942681.
- ^ Zhao P, Tang S, Wang C, Zhang Y, Best J, Tangthanasup TM, et al. (20 January 2017). "Recreational Drug Use among Chinese MSM and Transgender Individuals: Results from a National Online Cross-Sectional Study". PLOS ONE. 12 (1): e0170024. Bibcode:2017PLoSO..1270024Z. doi:10.1371/journal.pone.0170024. PMC 5249205. PMID 28107391.
- ^ Schmidt AJ, Bourne A, Weatherburn P, Reid D, Marcus U, Hickson F (December 2016). "Illicit drug use among gay and bisexual men in 44 cities: Findings from the European MSM Internet Survey (EMIS)". The International Journal on Drug Policy. 38: 4–12. doi:10.1016/j.drugpo.2016.09.007. PMID 27788450.
- ^ "Sex and Poppers". SexInfo Online. 28 November 2017. Archived from the original on 2019-12-26. Retrieved 2020-05-01.
- ^ "Nitrites". Drugscope. Archived from the original on 2007-04-05. Retrieved 2007-04-24.
- ^ Nickerson M (1979). Isobutyl nitrite and related compounds. Pharmex. OCLC 4790673.