|Other names||Atracurium besylate|
|Metabolism||Hofmann elimination (retro-Michael addition) and ester hydrolysis by nonspecific esterases|
|Elimination half-life||17–21 minutes|
|CompTox Dashboard (EPA)|
|Chemical and physical data|
|Molar mass||1243.49 g·mol−1|
|3D model (JSmol)|
|(what is this?)|
Atracurium besilate, also known as atracurium besylate, is a medication used in addition to other medications to provide skeletal muscle relaxation during surgery or mechanical ventilation. It can also be used to help with endotracheal intubation but suxamethonium (succinylcholine) is generally preferred if this needs to be done quickly. It is given by injection into a vein. Effects are greatest at about 4 minutes and last for up to an hour.
Common side effects include flushing of the skin and low blood pressure. Serious side effects may include allergic reactions; however, it has not been associated with malignant hyperthermia. Prolonged paralysis may occur in people with conditions like myasthenia gravis. It is unclear if use in pregnancy is safe for the baby. Atracurium is in the neuromuscular-blocker family of medications and is of the non-depolarizing type. It works by blocking the action of acetylcholine on skeletal muscles.
Atracurium was approved for medical use in the United States in 1983. It is on the World Health Organization's List of Essential Medicines, the safest and most effective medicines needed in a health system. Atracurium is available as a generic medication. The wholesale cost in the developing world is about US$1.69–1.87 per dose.
Atracurium is a medication used in addition to other medications in to provide skeletal muscle relaxation during surgery or mechanical ventilation. It can be used to help with endotracheal intubation but takes up to 2.5 minutes to result in appropriate intubating conditions.
Duration of action
Neuromuscular-blocking agents can be classified in accordance to their duration of pharmacological action, defined as follows:
|Parameter||Ultra-short Duration||Short Duration||Intermediate Duration||Long Duration|
(Time from injection to T25% recovery)
(Time from injection to T95% recovery)
|Recovery Index (T25%-T75% recovery slope)||2-3||6||
The tetrahydroisoquinolinium class of neuromuscular blocking agents, in general, is associated with histamine release upon rapid administration of a bolus intravenous injection. There are some exceptions to this rule; e.g., cisatracurium (Nimbex) is one such agent that does not elicit histamine release even up to 5xED95 doses. The liberation of histamine is a dose-dependent phenomenon such that, with increasing doses administered at the same rate, there is a greater propensity for eliciting histamine release and its ensuing sequelae. Most commonly, the histamine release following administration of these agents is associated with observable cutaneous flushing (facial face and arms, commonly), hypotension and a consequent reflex tachycardia. These sequelae are very transient effects: The total duration of the cardiovascular effects is no more than one to two minutes, while the facial flush may take around 3–4 minutes to dissipate. Because these effects are so transient, there is no reason to administer adjunctive therapy to ameliorate either the cutaneous or the cardiovascular effects.
Bronchospasm has been reported on occasion with the use of atracurium. However, this particular undesirable effect does not appear to be observed nearly as often as that seen with rapacuronium, which led to the latter's withdrawal of approval for clinical use worldwide.
The issue of bronchospasm acquired prominence in the neuromuscular-blocking agents arena after the withdrawal from clinical use of rapacuronium (Raplon - a steroidal neuromuscular-blocking agent marketed by Organon) in 2001 after several serious events of bronchospasm, including five unexplained fatalities, following its administration. Bronchospasm was not an unknown phenomenon prior to rapacuronium: occasional reports of bronchospasm have been noted also with the prototypical agents, tubocurarine and succinylcholine, as well as alcuronium, pancuronium, vecuronium, and gallamine.
Seizures rarely occur.
Because atracurium undergoes Hofmann elimination as a primary route of chemodegradation, one of the major metabolites from this process is laudanosine, a tertiary amino alkaloid reported to be a modest CNS stimulant with epileptogenic activity and cardiovascular effects such a hypotension and bradycardia. As part of the then fierce marketing battle between the competing pharmaceutical companies (Burroughs Wellcome Co. and Organon, Inc.) with their respective products, erroneous information was quickly and subtly disseminated very shortly after the clinical introduction of atracurium that the clinical use of atracurium was likely to result in a terrible tragedy because of the significant clinical hazard by way of frank seizures induced by the laudanosine by-product - the posited hypothesis being that the laudanosine produced from the chemodegradation of parent atracurium would cross the blood–brain barrier in sufficiently high enough concentrations that lead to epileptogenic foci. Fortunately, both for the public and for atracurium, rapid initial investigations irrefutably failed to find any overt or EEG evidence for a connection between atracurium administration and epileptogenic activity. Indeed, because laudanosine is cleared primarily via renal excretion, a cat study modelling anephric patients went so far as to corroborate that EEG changes, when observed, were evident only at plasma concentrations 8 to 10 times greater than those observed in humans during infusions of atracurium. Thus, the cat study predicted that, following atracurium administration in an anephric patient, laudanosine accumulation and related CNS or cardiovascular toxicity were unlikely - a prediction that correlated very well with a study in patients with kidney failure and undergoing cadaveric renal transplantation. Furthermore, almost a decade later, work by Cardone et al.. confirmed that, in fact, it is the steroidal neuromuscular-blocking agents pancuronium and vecuronium that, when introduced directly into the CNS, were likely to cause acute excitement and seizures, owing to accumulation of cytosolic calcium caused by activation of acetylcholine receptor ion channels. Unlike the two steroidal agents, neither atracurium nor laudanosine caused such accumulation of intracellular calcium. Just over two decades later with availability of atracurium, there is little doubt that laudanosine accumulation and related toxicity will likely never be seen with the doses of atracurium that are generally used.
Laudanosine is also a metabolite of cisatracurium that, because of its identical structure to atracurium, undergoes chemodegradation via Hofmann elimination in vivo. Plasma concentrations of laudanosine generated are lower when cisatracurium is used.
Atracurium is susceptible to degradation by Hofmann elimination and ester hydrolysis as components of the in vivo metabolic processes. The initial in vitro studies appeared to indicate a major role for ester hydrolysis but, with accumulation of clinical data over time, the preponderance of evidence indicated that Hofmann elimination at physiological pH is the major degradation pathway vindicating the premise for the design of atracurium to undergo an organ-independent metabolism.
Hofmann elimination is a temperature- and pH-dependent process, and therefore atracurium's rate of degradation in vivo is highly influenced by body pH and temperature: An increase in body pH favors the elimination process, whereas a decrease in temperature slows down the process. Otherwise, the breakdown process is unaffected by the level of plasma esterase activity, obesity, age, or by the status of renal or hepatic function. On the other hand, excretion of the metabolite, laudanosine, and, to a small extent, atracurium itself is dependent on hepatic and renal functions that tend to be less efficient in the elderly population. The pharmaceutical presentation is a mixture of all ten possible stereoisomers. Although there are four stereocentres, which could give 16 structures, there is a plane of symmetry running through the centre of the diester bridge, and so 6 meso structures (structures that can be superimposed by having the opposite configuration then 180° rotation) are formed. This reduces the number from sixteen to ten. There are three cis-cis isomers (an enantiomeric pair and a meso structure), four cis-trans isomers (two enantiomeric pairs), and three trans-trans isomers (an enantiomeric pair and a meso structure). The proportions of cis−cis, cis−trans, and trans−trans isomers are in the ratio of 10.5 :6.2 :1. [cis-cis isomers ≈ 58% cis-trans isomers ≈ 36% trans-trans isomers ≈ 6%]. One of the three cis-cis structures is marketed as a single-isomer preparation, cisatracurium (trade name Nimbex); it has the configuration 1R, 2R, 1′R, 2′R at the four stereocentres. The beta-blocking drug Nebivolol has ten similar structures with 4 stereocentres and a plane of symmetry, but only two are presented in the pharmaceutical preparation.
Intramuscular function parameters
- ED95: the dose of any given intramuscular-blocking agent required to produce 95% suppression of muscle twitch (e.g., the abductor pollicis) response with balanced anesthesia
- Clinical duration: difference in time between time of injection and time to 25% recovery from neuromuscular block
- Train-of-Four (TOF) response: stimulated muscle twitch response in trains of four when stimuli are applied in a burst of four as opposed to a single stimulus, equal depression in depolarizing and fading response with non-depolarizing blocker.
- 25%-75% recovery index: an indicator of the rate of skeletal muscle recovery - essentially, the difference in time between the time to recovery to 25% and time to recovery to 75% of baseline value
- T4:T1 ≥ 0.7: a 70% ratio of the fourth twitch to the first twitch in a TOF - provides a measure of the recovery of neuromuscular function
- T4:T1 ≥ 0.9: a 90% ratio of the fourth twitch to the first twitch in a TOF - provides a measure of the full recovery of neuromuscular function
Atracurium besilate was first made in 1974 by George H. Dewar, a pharmacist and a medicinal chemistry doctoral candidate in John B. Stenlake's medicinal chemistry research group in the Department of Pharmacy at Strathclyde University, Scotland. Dewar first named this compound "33A74" before its eventual emergence in the clinic as atracurium. Atracurium was the culmination of a rational approach to drug design to produce the first non-depolarizing non-steroidal skeletal muscle relaxant that undergoes chemodegradation in vivo. The term chemodegradation was coined by Roger D. Waigh, Ph.D., also a pharmacist and a postdoctoral researcher in Stenlake's research group. Atracurium was licensed by Strathclyde University to the Wellcome Foundation UK, which developed the drug (then known as BW 33A) and its introduction to first human trials in 1979, and then eventually to its first introduction (as a mixture of all ten stereoisomers) into clinical anesthetic practice in the UK, in 1983, under the tradename of Tracrium.
The premise to the design of atracurium and several of its congeners stemmed from the knowledge that a bis-quaternary structure is essential for neuromuscular-blocking activity: ideally, therefore, a chemical entity devoid of this bis-quaternary structure via susceptibility to inactive breakdown products by enzymic-independent processes would prove to be invaluable in the clinical use of a drug with a predictable onset and duration of action. Hofmann elimination provided precisely this basis: It is a chemical process in which a suitably activated quaternary ammonium compound can be degraded by the mildly alkaline conditions present at physiological pH and temperature. In effect, Hofmann elimination is a retro-Michael addition chemical process. It is important to note here that the physiological process of Hofmann elimination differs from the non-physiological Hofmann degradation process: the latter is a chemical reaction in which a quaternary ammonium hydroxide solid salt is heated to 100 °C, or an aqueous solution of the salt is boiled. Regardless of which Hofmann process is referenced, the end-products in both situations will be the same: an alkene and a tertiary amine.
The approach to utilizing Hofmann elimination as a means to promoting biodegradation had its roots in much earlier observations that the quaternary alkaloid (obtained from the Lebanese plant Leontice leontopetalum) readily underwent facile Hofmann elimination to a tertiary amine called upon passage through a basic (as opposed to an acidic) ion-exchange resin. Stenlake's research group advanced this concept by systematically synthesizing numerous quaternary ammonium β-aminoesters and β-aminoketones and evaluated them for skeletal muscle relaxant activity: one of these compounds, initially labelled as 33A74, eventually led to further clinical development, and came to be known as atracurium.
- "Atracurium Besylate". The American Society of Health-System Pharmacists. Archived from the original on 21 December 2016. Retrieved 8 December 2016.
- "Atracurium Besilate 10 mg/ml Injection - (eMC)". www.medicines.org.uk. March 2015. Archived from the original on 20 December 2016. Retrieved 16 December 2016.
- World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
- "Atracurium". International Drug Price Indicator Guide. Retrieved 8 December 2016.
- Savarese JJ, Wastila WB (1995). "The future of the benzylisoquinolinium relaxants". Acta Anaesthesiologica Scandinavica. 106 Suppl: 91–93. doi:10.1111/j.1399-6576.1995.tb04317.x. PMID 8533554.
- Ortalli GL, Tiberio I, Mammana G (Mar 1993). "A case of severe bronchospasm and laryngospasm after atracurium administration". Minerva Anestesiologica. 59 (3): 133–135. PMID 8515854.
- Siler JN, Mager JG Jr, Wyche MQ Jr (May 1985). "Atracurium: hypotension, tachycardia and bronchospasm". Anesthesiology. 62 (5): 645–646. doi:10.1097/00000542-198505000-00020. PMID 2581480.
- Woods I, Morris P, Meakin G (Feb 1985). "Severe bronchospasm following the use of atracurium in children". Anaesthesia. 40 (2): 207–208. doi:10.1111/j.1365-2044.1985.tb10733.x. PMID 3838421.
- Sale JP (May 1983). "Bronchospasm following the use of atracurium". Anaesthesia. 38 (5): 511–512. doi:10.1111/j.1365-2044.1983.tb14055.x. PMID 6687984.
- Shapse D. "Voluntary market withdrawal - Adverse Drug Reaction 27 March 2001. Raplon (rapacuronium bromide) for Injection" (PDF). Archived (PDF) from the original on 7 March 2010. Cite journal requires
- Lim R (Feb 2003). "Rapacuronium: premarket drug evaluation can be very effective for the identification of drug risks". Anesthesia & Analgesia. 96 (2): 631–632. doi:10.1213/00000539-200302000-00070. PMID 12538231.
- Goudsouzian NG. (2001). "Rapacuronium and bronchospasm". Anesthesiology. 94 (5): 727–728. doi:10.1097/00000542-200105000-00006. PMID 11388519.
- Jooste E, Klafter F, Hirshman CA, Emala CW (Apr 2003). "A mechanism for rapacuronium-induced bronchospasm: M2 muscarinic receptor antagonism". Anesthesiology. 98 (4): 906–911. doi:10.1097/00000542-200304000-00017. PMID 12657852.
- Grady D. (2001-03-31). "Anesthesia drug is removed from market after the deaths of 5 patients". The New York Times. Archived from the original on 2016-03-03.
- Harrison GA (Aug 1966). "A case of cardiac arrest associated with bronchospasm and d-tubocurarine". Australian and New Zealand Journal of Surgery. 36 (1): 40–42. doi:10.1111/j.1445-2197.1966.tb04394.x. PMID 5225576.
- Bevan DR. (1992) "Curare". In: Maltby JR, Shephard DAE (Eds.), Harold Griffith - His Life and Legacy; Suppl. to Canadian Journal of Anaesthesiology vol. 39 (1); 49-55.
- Takki S, Tammisto T (Apr 1971). "Severe bronchospasm and circulatory collapse following the administration of d-tubocurarine". Annals of Clinical Research. 3 (2): 112–115. PMID 4104054.
- Fellini AA, Bernstein RL, Zauder HL (Oct 1963). "Bronchospasm due to suxamethonium; report of a case". British Journal of Anaesthesiology. 35 (10): 657–659. doi:10.1093/bja/35.10.657. PMID 14073484.
- Bele-Binda N, Valeri F (Jan 1971). "A case of bronchospasm induced by succinylcholine". Canadian Anaesthetists' Society Journal. 18 (1): 116–119. doi:10.1007/BF03025433. PMID 5545731.
- Katz AM, Mulligan PG (Oct 1972). "Bronchospasm induced by suxamethonium. A case report". British Journal of Anaesthesiology. 44 (10): 1097–1099. doi:10.1093/bja/44.10.1097. PMID 4639831.
- Eustace BR (Oct 1967). "Suxamethonium induced bronchospasm". Anaesthesia. 22 (4): 638–641. doi:10.1111/j.1365-2044.1967.tb10161.x. PMID 4168012.
- Cardan E, Deacu E (Jan 1972). "Bronchospasm following succinyl choline". Anaesthesist. 21 (1): 27–29. PMID 4111555.
- Yeung ML, Ng LY, Koo AW (Feb 1979). "Severe bronchospasm in an asthmatic patient following alcuronium and D-tubocurarine". Anaesthesia and Intensive Care. 7 (1): 62–64. doi:10.1177/0310057X7900700111. PMID 434447.
- Heath ML (Jul 1973). "Bronchospasm in an asthmatic patient following pancuronium". Anaesthesia. 28 (4): 437–440. doi:10.1111/j.1365-2044.1973.tb00494.x. PMID 4268667.
- Kounis NG (Apr 1974). "Letter: Bronchospasm induced by althesin and pancuronium bromide". British Journal of Anaesthesiology. 46 (4): 281. doi:10.1093/bja/46.4.281-a. PMID 4451602.
- Uratsuji Y, Konishi M, Ikegaki N, Kitada H (Jan 1991). "Possible bronchospasm after administration of vecuronium". Masui. 40 (1): 109–112. PMID 1675699.
- O'Callaghan AC, Scadding G, Watkins J (Aug 1985). "Bronchospasm following the use of vecuronium". Anaesthesia. 40 (8): 801–805. doi:10.1111/j.1365-2044.1985.tb11010.x. PMID 3839980.
- Okazaki K, Saito T, Wakisaka K, Hirano T, Kozu K (Jun 1969). "Bronchospasm possible due to gallamine. A case report". Tokushima Journal of Experimental Medicine. 16 (1): 9–14. PMID 5348343.
- Standaert FG (Dec 1985). "Magic bullets, science, and medicine". Anesthesiology. 63 (6): 577–578. doi:10.1097/00000542-198512000-00002. PMID 2932980.
- Fodale V, Santamaria LB (Jul 2002). "Laudanosine, an atracurium and cisatracurium metabolite". European Journal of Anaesthesiology. 19 (7): 466–473. doi:10.1017/s0265021502000777. PMID 12113608.
- Katz Y, Weizman A, Pick CG, Pasternak GW, Liu L, Fonia O, Gavish M (May 1994). "Interactions between laudanosine, GABA, and opioid subtype receptors: implication for laudanosine seizure activity". Brain Research. 646 (2): 235–241. doi:10.1016/0006-8993(94)90084-1. PMID 8069669.
- Lanier WL, Milde JH, Michenfelder JD (Dec 1985). "The cerebral effects of pancuronium and atracurium in halothane-anesthetized dogs". Anesthesiology. 63 (6): 589–597. doi:10.1097/00000542-198512000-00007. PMID 2932982.
- Shi WZ, Fahey MR, Fisher DM, Miller RD, Canfell C, Eger EI 2nd (Dec 1985). "Laudanosine (a metabolite of atracurium) increases the minimum alveolar concentration of halothane in rabbits". Anesthesiology. 63 (6): 584–589. doi:10.1097/00000542-198512000-00006. PMID 2932981.
- Ingram MD, Sclabassi RJ, Cook DR, Stiller RL, Bennett MH (1986). "Cardiovascular and electroencephalographic effects of laudanosine in "nephrectomized" cats". British Journal of Anaesthesiology. 58 Suppl 1: 14S–18S. doi:10.1093/bja/58.suppl_1.14s. PMID 3707810.
- Fahey MR, Rupp SM, Canfell C, Fisher DM, Miller RD, Sharma M, Castagnoli K, Hennis PJ (Nov 1985). "Effect of renal failure on laudanosine excretion in man". British Journal of Anaesthesiology. 57 (11): 1049–1051. doi:10.1093/bja/57.11.1049. PMID 3840380.
- Cardone C, Szenohradszky J, Yost S, Bickler PE (May 1994). "Activation of brain acetylcholine receptors by neuromuscular blocking drugs. A possible mechanism of neurotoxicity". Anesthesiology. 80 (5): 1155–1161. doi:10.1097/00000542-199405000-00025. PMID 7912481.
- Stiller RL, Cook DR, Chakravorti S (1985). "In vitro degradation of atracurium in human plasma". British Journal of Anaesthesiology. 57 (11): 1085–1088. doi:10.1093/bja/57.11.1085. PMID 3840382.
- Nigrovic V, Fox JL (1991). "Atracurium decay and the formation of laudanosine in humans". Anesthesiology. 74 (3): 446–454. doi:10.1097/00000542-199103000-00010. PMID 2001023.
- Merrett RA, Thompson CW, Webb FW (1983). "In vitro degradation of atracurium in human plasma". British Journal of Anaesthesiology. 55 (1): 61–66. doi:10.1093/bja/55.1.61. PMID 6687375.
- Hughes R, Chapple DJ (1981). "The pharmacology of atracurium: a new competitive neuromuscular blocking agent". British Journal of Anaesthesiology. 53 (1): 31–44. doi:10.1093/bja/53.1.31. PMID 6161627.
- Payne JP, Hughes R (1981). "Evaluation of atracurium in anaesthetized man". British Journal of Anaesthesiology. 53 (1): 45–54. doi:10.1093/bja/53.1.45. PMID 7459185.
- Varin F, Ducharme J, Théorêt Y, Besner JG, Bevan DR, Donati F (1990). "Influence of extreme obesity on the body disposition and neuromuscular blocking effect of atracurium". Clinical Pharmacology and Therapeutics. 48 (1): 18–25. doi:10.1038/clpt.1990.112. PMID 2369806.
- Kent AP, Parker CJ, Hunter JM (1989). "Pharmacokinetics of atracurium and laudanosine in the elderly". British Journal of Anaesthesiology. 63 (6): 661–666. doi:10.1093/bja/63.6.661. PMID 2611066.
- Fahey MR, Rupp SM, Fisher DM, Miller RD, Sharma M, Canfell C, Castagnoli K, Hennis PJ (Dec 1984). "The pharmacokinetics and pharmacodynamics of atracurium in patients with and without renal failure". Anesthesiology. 61 (6): 699–702. doi:10.1097/00000542-198412000-00011. PMID 6239574.
- Parker CJ, Jones JE, Hunter JM (1988). "Disposition of infusions of atracurium and its metabolite, laudanosine, in patients in renal and respiratory failure in an ITU". British Journal of Anaesthesiology. 61 (5): 531–540. doi:10.1093/bja/61.5.531. PMID 3207525.
- Hunter JM. (1993). "Atracurium and laudanosine pharmacokinetics in acute renal failure". Intensive Care Medicine. 19 Suppl. 2: S91–S93. doi:10.1007/bf01708808. PMID 8106685.
- Vandenbrom RH, Wierda JM, Agoston S (1990). "Pharmacokinetics and neuromuscular blocking effects of atracurium besylate and two of its metabolites in patients with normal and impaired renal function". Clinical Pharmacokinetics. 19 (3): 230–240. doi:10.2165/00003088-199019030-00006. PMID 2394062.
- Parker CJ, Hunter JM (1989). "Pharmacokinetics of atracurium and laudanosine in patients with hepatic cirrhosis". British Journal of Anaesthesiology. 62 (2): 177–183. doi:10.1093/bja/62.2.177. PMID 2923767.
- Dewar GH (1976). "Potential short-acting neuromuscular blocking agents". Ph.D. Thesis - the Department of Pharmacy, University of Strathclyde, Scotland.
- Waigh R.D. (1986). "Atracurium". Pharmaceutical Journal. 236: 577–578.
- Basta SJ, Ali HH, Savarese JJ, Sunder N, Gionfriddo M, Cloutier G, Lineberry C, Cato AE (1982). "Clinical pharmacology of atracurium besylate (BW 33A): a new non-depolarizing muscle relaxant". Anesthesia and Analgesia. 61 (9): 723–729. doi:10.1213/00000539-198209000-00002. PMID 6213181.
- Coker GG, Dewar GH, Hughes R, Hunt TM, Payne JP, Stenlake JB, Waigh RD (1981). "A preliminary assessment of atracurium, a new competitive neuromuscular blocking agent". Acta Anaesthesiologica Scandinavica. 25 (1): 67–69. doi:10.1111/j.1399-6576.1981.tb01608.x. PMID 7293706.
- Stenlake JB, Waigh RD, Dewar GH, Dhar NC, Hughes R, Chapple DJ, Lindon JC, Ferrige AG (1984). "Biodegradable neuromuscular blocking agents. Part 6. Stereochemical studies on atracurium and related polyalkylene di-esters". European Journal of Medicinal Chemistry. 19 (5): 441–450.
- Stenlake JB, Waigh RD, Urwin J, Dewar GH, Coker GG (1983). "Atracurium: conception and inception". Br J Anaesth. 55 (Suppl. 1): 3S–10S. PMID 6688014.
- McCorkindale NJ, Magrill DS, Martin-Smith M, Smith SJ, Stenlake JB (1964). "Petaline: A 7,8-dioxygenated benzylisoquinoline". Tetrahedron Letters. 5 (51): 3841–3844. doi:10.1016/s0040-4039(01)93303-9.
- Stenlake JB, Urwin J, Waigh RD, Hughes R (1979). "Biodegradable neuromuscular blocking agents. I. Quaternary esters". European Journal of Medicinal Chemistry. 14 (1): 77–84.
- Stenlake JB, Waigh RD, Urwin J, Dewar GH, Hughes R, Chapple DJ (1981). "Biodegradable neuromuscular blocking agents. Part 3. Bis-quaternary esters". European Journal of Medicinal Chemistry. 16: 508–514.
- Stenlake JB, Waigh RD, Dewar GH, Hughes R, Chapple DJ, Coker GG (1981). "Biodegradable neuromuscular blocking agents. Part 4. Atracurium besylate and related polyalkylene di-esters". European Journal of Medicinal Chemistry. 16 (6): 515–524.
- Stenlake JB, Waigh RD, Dewar GH, Hughes R, Chapple DJ (1983). "Biodegradable neuromuscular blocking agents. Part 5. α,ω-Bisquaternary polyalkylene phenolic esters". European Journal of Medicinal Chemistry. 18: 273–276.
- Stenlake JB, Urwin J, Waigh RD, Hughes R (1979). "Biodegradable neuromuscular blocking agents. II. Quaternary ketones". European Journal of Medicinal Chemistry. 14 (1): 85–88.
- Stenlake JB. (2001). "Chance, coincidence and atracurium". Pharmaceutical Journal. 267 (7167): 430–441.
- Neuromuscular+blocking+agents at the US National Library of Medicine Medical Subject Headings (MeSH)