Sodium stibogluconate

Sodium stibogluconate
Names
Trade namesPentostam, Stiboson, others[1]
IUPAC name
  • 2,4:2',4'-O-(oxydistibylidyne)bis[D-gluconic acid]
Clinical data
Drug classPentavalent antimonial[2]
Main usesLeishmaniasis[3]
Side effectsLoss of appetite, nausea, muscle pains, headache, feeling tired[4]
Routes of
use		Intravenous, intramusclar[4]
Defined daily dose0.85 gram[5]
External links
AHFS/Drugs.comInternational Drug Names
US NLMSodium stibogluconate
Legal
Legal status
  • UK: POM (Prescription only)
Chemical and physical data
FormulaC12H38Na3O26Sb2
Molar mass910.899 g·mol−1
3D model (JSmol)
SMILES
  • [Na+].[Na+].[Na+].O=[Sb]2(O[Sb]1(=O)OC([C@H](O)CO)[C@H](O)[C@@H](O1)C([O-])=O)O[C@@H]([C@H](O)[C@@H](O2)C([O-])=O)[C@H](O)CO
InChI
  • InChI=1S/2C6H10O7.3Na.3O.2Sb/c2*7-1-2(8)3(9)4(10)5(11)6(12)13;;;;;;;;/h2*2-5,7-8,10H,1H2,(H,12,13);;;;;;;;/q2*-2;3*+1;;;;2*+2/p-2/t2-,3?,4+,5-;2-,3-,4+,5-;;;;;;;;/m11......../s1 checkY
  • Key:RTLKTTNTVTVWPV-UQCYVGCHSA-L checkY

Sodium stibogluconate, sold under the brand name Pentostam among others, is a medication used to treat leishmaniasis.[3] This includes leishmaniasis of the cutaneous, visceral, and mucosal types.[6] Some combination of miltefosine, paramycin and liposomal amphotericin B, however, may be recommended due to issues with resistance.[4][2] It is given by injection.[7]

Side effects are common and include loss of appetite, nausea, muscle pains, headache, and feeling tired.[4][2] Serious side effect may include an irregular heartbeat or pancreatitis.[2] Sodium stibogluconate is less safe than some other options during pregnancy.[4] It is not believed to result in any problems if used during breastfeeding.[8] Sodium stibogluconate is in the pentavalent antimonials class of medication.[2]

Sodium stibogluconate has been studied as early as 1937 and has been in medical use since the 1940s.[9][10] It is on the World Health Organization's List of Essential Medicines.[11] The wholesale price in the developing world is about 10 USD per vial.[7] This gives the cost for a course of treatment at between 12 and 56 USD.[4] In the United States it is available from the Center for Disease Control.[3]

Medical uses

Sodium stibogluconate is used to treats leishmaniasis.[3]

Dosage

(a) Erythematous and edematous plaque of cutaneous leishmaniasis with crusting. (b) Clearance of the lesion with little atrophy and milia formation 3 weeks after treatment

The defined daily dose is 0.85 gram by injection.[5]

Sodium stibogluconate is available in the United Kingdom as Pentostam, where it is manufactured by GlaxoSmithKline. It is available in the United States on a named-patient basis from the Centers for Disease Control and Prevention (CDC).

As dosage regimens for treating leishmaniasis have evolved, the daily dose of antimony and the duration of therapy have been progressively increased to combat unresponsiveness to therapy. In the 1980s, the use of 20 mg/kg/day (instead of 10 mg/kg/day) of antimony was recommended, but only to a maximum daily dose of 850 mg. Recent research has suggested on the basis of recent efficacy and toxicity data that this 850-mg restriction should be removed. The evidence to date, which is in their research, suggests that a regimen of 20 mg/kg/day of pentavalent antimony, without an upper limit on the daily dose, is more efficacious and is not substantially more toxic than regimens with lower daily doses. It is recommend treating all forms of leishmaniasis with a full 20 mg/kg/day of pentavalent antimony. Treatment of cutaneous leishmaniasis usually lasts for 20 days and visceral and mucosal leishmaniasis for 28 days.[12]

The dose of sodium stibogluconate is by slow intravenous infusion (at least five minutes with cardiac monitoring). The injection are stopped if there is coughing or central chest pain. The chemotherapeutic index was established by Leonard Goodwin during the Second World War when a treatment was urgently required for Allied troops during the invasion of Sicily.[13]

The duration of treatment is usually 10 to 21 days and depends on the species of Leishmania and the type of infection (cutaneous or visceral).

Side effects

Sodium stibogluconate is exceedingly toxic to veins. One of the practical problems is that after a few doses it can become exceedingly difficult to find a vein in which to inject the drug. The insertion of a PICC does not prevent the problem and can instead exacerbate it: the entire vein along the course of the PICC line can become inflamed and thrombose. Large doses of sodium stibogluconate are often administered as dilute solutions.

Pancreatitis is a common deleterious effect of the drug, and the serum amylase or lipase should be monitored twice weekly; there is no need to stop treatment if the amylase remains less than four times the upper limit of normal; if the amylase rises above the cut-off, then treatment should be interrupted until the amylase falls to less than twice the upper limit of normal, whereupon treatment can be resumed. Cardiac conduction disturbances are less common, but ECG monitoring while the medicine is injected is advisable and changes quickly reverse after the drug is stopped or the infusion rate is decreased.

The drug can be given intramuscularly but is exceedingly painful when given by this route. It can also be given intralesionally when treating cutaneous leishmaniasis (i.e., injected directly into the area of infected skin) and again, this is exceedingly painful and does not give results superior to intravenous administration.

Sodium stibogluconate can also cause a reduced appetite, metallic taste in mouth, nausea, vomiting, diarrhoea, headache, tiredness, joint pains, muscle aches, dizziness, and anaphylaxis.

Mechanism of action

The mechanism of sodium stibogluconate is poorly understood, but is thought to stem from the inhibition of macromolecular synthesis via a reduction in available ATP and GTP, likely secondary to inhibition of the citric acid cycle and glycolysis. Bermann et al. studied the effects of stibogluconate on Leishmaniasis mexicana and demonstrated a 56-65% reduction in incorporation of a label into purine nucleoside triphosphates (ATP and GTP) as well as between a 34-60% increase of label incorporation into purine nucleoside mono and di phosphates (AMP, GMP, ADP, and GDP) following 4 hour exposure to stibogluconate.[14]

Chemical structure

It is a pentavalent antimonials class medication.[15] The chemical structure of sodium stibogluconate is somewhat ambiguous, and the structure shown above is idealized. Its solutions may contain multiple antimony compounds, although this heterogeneity may be unimportant. It has been speculated that the active species contains only a single antimony centre.[16]

Pharmacokinetics

Although antimony itself is a cause of heavy metal poisoning, stibogluconate does not appear to accumulate in the body and is excreted by the kidneys.[17]

References

  1. ↑ "Sodium Stibogluconate - Drugs.com". www.drugs.com. Archived from the original on 20 December 2016. Retrieved 7 December 2016.
  2. 1 2 3 4 5 Oryan, A; Akbari, M (October 2016). "Worldwide risk factors in leishmaniasis". Asian Pacific Journal of Tropical Medicine. 9 (10): 925–932. doi:10.1016/j.apjtm.2016.06.021. PMID 27794384.
  3. 1 2 3 4 "Our Formulary Infectious Diseases Laboratories CDC". www.cdc.gov. 22 September 2016. Archived from the original on 16 December 2016. Retrieved 7 December 2016.
  4. 1 2 3 4 5 6 Control of the leishmaniasis: report of a meeting of the WHO Expert Committee on the Control of Leishmaniases (PDF). World Health Organization. March 2010. p. 55,186. hdl:10665/44412. ISBN 9789241209496. Archived (PDF) from the original on 2016-06-08.
  5. 1 2 "WHOCC - ATC/DDD Index". www.whocc.no. Archived from the original on 9 August 2020. Retrieved 21 September 2020.
  6. ↑ Herwaldt, BL; Berman, JD (March 1992). "Recommendations for treating leishmaniasis with sodium stibogluconate (Pentostam) and review of pertinent clinical studies". The American Journal of Tropical Medicine and Hygiene. 46 (3): 296–306. doi:10.4269/ajtmh.1992.46.296. PMID 1313656.
  7. 1 2 "Sodium Stibogluconate". International Drug Price Indicator Guide. Archived from the original on 22 January 2018. Retrieved 6 December 2016.
  8. ↑ "Sodium Stibogluconate use while Breastfeeding | Drugs.com". www.drugs.com. Archived from the original on 20 December 2016. Retrieved 7 December 2016.
  9. ↑ Sneader, Walter (2005). Drug Discovery: A History. John Wiley & Sons. p. 58. ISBN 9780470015520. Archived from the original on 2016-12-20.
  10. ↑ Jäger, Timo; Koch, Oliver; Flohé, Leopold (2013). Trypanosomatid Diseases: Molecular Routes to Drug Discovery. John Wiley & Sons. p. 17. ISBN 9783527670406. Archived from the original on 2016-12-20.
  11. ↑ 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.
  12. ↑ Herwaldt, Barbara L.; Berman, Jonathan D. (1992-03-01). "Recommendations for Treating Leishmaniasis with Sodium Stibogluconate (Pentostam) and Review of Pertinent Clinical Studies". The American Journal of Tropical Medicine and Hygiene. 46 (3): 296–306. doi:10.4269/ajtmh.1992.46.296. ISSN 0002-9637. PMID 1313656.
  13. ↑ "Leonard Goodwin - Telegraph". The Daily Telegraph. 14 January 2009. Archived from the original on 20 April 2009. Retrieved 2009-01-18.
  14. ↑ Berman, J. D.; Waddell, D.; Hanson, B. D. (1985-06-01). "Biochemical mechanisms of the antileishmanial activity of sodium stibogluconate". Antimicrobial Agents and Chemotherapy. 27 (6): 916–920. doi:10.1128/aac.27.6.916. ISSN 0066-4804. PMC 180186. PMID 2411217.
  15. ↑ "Sodium stibogluconate". go.drugbank.com. Archived from the original on 29 September 2021. Retrieved 8 October 2021.
  16. ↑ Frézard F, Demicheli C, Ribeiro PR (2009). "Pentavalent Antimonials: New Perspectives for Old Drugs". Molecules. 14 (7): 2317–2336. doi:10.3390/molecules14072317. PMC 6254722. PMID 19633606.
  17. ↑ Rees PH, Keating MI, Kager PA, Hockmeyer WT (1980). "Renal clearance of pentavalent antimony (sodium stibogluconate)". Lancet. 2 (8188): 226–9. doi:10.1016/s0140-6736(80)90120-8. PMID 6105394.
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