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[top]Introduction to Atropine


Atropine is an alkaloid produced by the perennial Atropa belladonna, family Solanaceae. Commonly known as belladonna or deadly nightshade. Belladonna is a small shrub that produces bell-shaped flowers and shiny round black fruit.


[top]Using Atropine

[top]Ways of administration


Can be administered orally, intraocularly, intravenously or intramuscularly.

[top]Effects of Atropine


Two mnemonics, which apply to all anticholinergic drugs, from professors of mine include:

"Can't spit, shit, see or pee."
"Blind as a bat, hot as a hare, dry as a bone, mad as a hatter, red as a beet."

Through its anticholinergic activity, atropine:
  • Increases heart rate
  • Dries nasal and oral mucosa, as well as other secretions throughout the body, including preventing perspiration.
  • Dilates pupils and increases intraocular pressure
  • Slows the movement of food through the gastrointestinal tract
  • Constricts smooth muscle around the urethra
  • Causes hallucinations

[top]Combinations with Atropine


Belladonna combined with opium is still used in suppositories to control diarrhea. This is one of the few remaining examples of whole herbs used in mainstream Western medicine.

[top]Different Uses for Atropine


Most often used for its effects on the heart, eyes, gastrointestinal tract. When administered as eyedrops, atropine causes mydriasis. The eyedrops may also be used sublingually to prevent drooling in terminally ill patients. To stop diarrhea, atropine may be taken orally or as a rectal suppository. To increase heart rate in an emergency situation, it is given intravenously.

Atropine is also used intravenously or intramuscularly as an antidote to organophosphate neurotoxins such as the insecticide Malathion and the chemical weapons VX and Sarin.

Rarely used recreationally (see below).


[top]Pharmacology of Atropine


LD50 (mg/kg) :
Rat : 750 orally (freebase), 622 orally (sulfate monohydrate)


[top]Chemistry of Atropine

Systematic (IUPAC) name:[alpha]-(hydroxylmethyl)benzeneacetic acid (3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester
Synonyms:1[alpha]H,5[alpha]H-tropan-3[alpha]-ol ()-tropate (ester), dl-hyoscyamine, tropic acid ester with tropine, dl-tropine tropate, tropine tropate; Methylatropine bromide, Tropin (methylbromide); Methylatropine nitrate, Eumydrin (methylnitrate); Atropisol, Atropt (Sulfate monohydrate); atropine aminoxide, aminoxytropine tropate, genatropine (N-Oxide)
Molecular Formula:C17H27NO3
Molar mass: 289.38 g/mol, 384.31 g/mol (methylbromide), 366.41 g/mol (methylnitrate), 694.84 g/mol (sulfate monohydrate), 305.37 g/mol (N-Oxide)
CAS Registry Number:51-55-8, 2870-71-5 (methylbromide), 52-88-0 (methylnitrate), 5908-99-6 (sulfate monohydrate), 55-48-1 (anhydrous sulfate), 4438-22-6 (N-Oxide)
Melting Point:114-116C, 222-223C (methylbromide), 163C (methylnitrate), 190-194C (sulfate monohydrate), 127-128C (N-Oxide)
Boiling Point:no data
Flash Point:no data
Solubility:Freebase : 1 g dissolves in 455 mL water (@ room temperature), 90 mL water (@ 80C), 2 mL alcohol (@ room temperature), 1.2 mL alcohol (@ 60C), 27 mL glycerol, 25 mL ether, 1 mL; soluble in benzene, dilute acids. Methylbromide : soluble in 1 part water, slightly soluble in alcohol; almost insoluble in chloroform, ether. Methylnitrate : freely soluble in water, alcohol; very slightly soluble in chloroform, ether. Sulfate monohydrate : 1 g dissolves in 0.4 mL water, 5 mL cold alcohol, 2.4 mL boiling alcohol, 2.5 mL glycerol, 420 mL chloroform, 3000 mL ether. N-Oxide : Soluble in alcohol, chloroform; practically insoluble in ether
Additionnal data:Freebase : pK 4.35, pH of 0.0015 molar solution 10.0, sublimes in ahigh vacuum at 93-110C. Sulfate monohydrate : bitterness threshold 1/10000, pKa ~5.4. N-Oxide : decomposes at 135C
Notes:Freebase : aspect long orthorhombic prisms from acetone. Sulfate monohydrate : very bitter; incompatible with alkalies, tannin salt of mercury or gold, vegetable decoctions or infusions, borax, bromides, iodides, benzoates. N-Oxide : very hygroscopic
[3]


[top]The dangers of Atropine


Small amounts of the plant can quickly cause death by respiratory or cardiac failure.
Potential symptoms of overexposure include : blurred vision, suppressed salivation, vasodilatation, hyperpyrexia, excitement, agitation and delirium.


[top]Producing Atropine


A. belladonna is native to Europe, and is hardy in U.S. zones 6-9. Needs well-drained, alkaline soil in sun or partial shade. (2)


[top]Forms of Atropine




[top]Legal status of Atropine

[top]United Nations

[top]USA


By prescription only, not a controlled substance.

[top]EU



[top]History of Atropine


Used by women in the Middle Ages to dilate pupils. "Bella donna" is Italian and translates to "beautiful woman." Used supposedly by witches in Europe for its hallucinogenic properties, and in surgery for its sedative properties before modern anesthetics.




[top]The latest Atropine threads


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[top]References


1. Foster, S. and Johnson, R. L., eds. (2006) National Geographic Desk Reference to Nature's Medicine. Washington, DC: National Geographic Press.

2. Bown, D. (2001) Encyclopedia of Herbs. New York, NY: DK Publishing, Inc.

[3] Merck Index, fifteenth edition (2013)


Created by chibi curmudgeon Gold member, 08-12-2009 at 18:15
Last edited by John_bob, 21-04-2014 at 21:29
0 Comments, 18,317 Views

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