|Systematic (IUPAC) name|
|IV, IM, inhalation|
|Biological half-life||6.4-9.4 hours|
|CAS Registry Number|
|ATC code||P01 QP51|
|Molecular mass||340.42 g/mol|
Pentamidine (formulated as a salt, pentamidine dihealth system.
Medical uses 1
- Acute PCP 1.1
- Primary and secondary prophylaxis of PCP 1.2
- Other 1.3
- Contraindications 2
- Side effects 3
- Drug Interactions 4
- Mechanism 5
- Brand names and dose forms 6
- See also 7
- References 8
Pentamidine is also used as a prophylactic against PCP in patients receiving chemotherapy, as they also have a depressed immune system as a direct side-effect of the drugs used. The mortality of untreated PCP is very high. Additionally, pentamidine has good clinical activity in treating Candida albicans. Pentamidine is also used as a prophylactic antibiotic for children undergoing treatment for leukemia.
The exact mechanism of its anti-protozoal action is unknown (though it may involve reactions with ubiquitin), despite the fact that it is a basic therapeutic modality (in concurrence with multiple antifungal medications) when treating Acanthamoeba infections in the immunocompromised patients. In the United States, pentamidine is currently designated an orphan drug by the U.S. Food and Drug Administration.
Pentamidine is taken up by purine receptors by Trypanosoma brucei gambiense.This parasite is unable to synthesise its own adenine and must uptake this nucleotide from the host. It thereby accumulates to micromolar concentrations within the parasite to kill it by inhibiting enzymes and interacting with DNA.
In the acute treatment of PCP, pentamidine is considered equally or slightly less active than co-trimoxazole (brand names Bactrim, Septrin, or Septra). Clinical evidence suggests that pentamidine is often better tolerated than co-trimoxazole because a high dose of co-trimoxazole is needed, which is associated with a high incidence and severity of side effects such as hepatitis, bone-marrow-damage, renal-damage, and life-threatening skin disease (Lyell-syndrome). Moreover, many patients are or become allergic to co-trimoxazole. For treatment of PCP, 4 milligrams of pentamidine per kilogram of body weight is given intravenously once daily for 14 to 21 days. Treatment exceeding 21 days may be necessary, but is associated with increased toxicity. Intramuscular injection is not recommended. The effect of pentamidine often becomes evident within the first 2 days of treatment, with reduction in fever and improvement of respiratory function. In any case, improvements of chest x-ray studies occur within 6 to 8 days, provided therapy is successful. Pentamidine therapy cures 50 to 70% of all patients treated.
Primary and secondary prophylaxis of PCP
Primary prophylaxis of severely immunocompromised patients can be indicated where PCP has not yet been diagnosed. Secondary prophylaxis aims to prevent recurrent infections by PCP. For both forms of prophylaxis, an aerosolized formulation of pentamidine given by nebulizer once monthly in a dose of 300 mg is used. In primary prophylaxis, this reduces the long term likelihood of PCP by 70% when compared to no prophylaxis. The aerosolized route of administration is particularly suited for pregnant women in their first trimester (when TMP-SMX is contraindicated). Aerosolized administration may lead to an atypical PCP infection involving the upper lobes.
For other indications, such as leishmaniasis or sleeping sickness, special treatment schedules developed by the WHO or CDC exist.
Use as an antitumor drug has also been proposed.
- Severe allergy; no others in PCP patients in whom a proper diagnosis has been made.
Pentamidine can cause allergic and toxic side effects, most commonly having effects on the pancreas, which in part depend on the daily and/or cumulative dose:
- Blood: Pentamidine frequently causes leukopenia and less often thrombopenia, which may cause symptomatic bleeding. Some cases of anemia, possibly related to folic acid deficiency, have been described.
- Cardiovascular: Hypotension, which may be severe, severe or fatal arrhythmias and heart failure are quite frequent
- Gastrointestinal: Nausea, vomiting, gastrointestinal discomfort, diarrhea, unpleasant taste
- Kidney: 25 percent develop signs of nephrotoxicity ranging from mild, asymptomatic azotemia (increased serum creatinine and urea) to irreversible renal failure. Ample fluids or intravenous hydration may prevent some nephrotoxicity.
- Liver: Elevated liver enzymes are associated with intravenous use of pentamidine. Hepatomegaly and hepatitis have been encountered with long term prophylactic use of pentamidine inhalation.
- Neurological: Dizziness, drowsiness, neuralgia, confusion, hallucinations, seizures and other central side effects are reported.
- Pancreas: Hypoglycemia that requires symptomatic treatment is frequently seen. On the other hand, pentamidine may cause or worsen diabetes mellitus.
- Respiratory: Cough and bronchospasm, most frequently seen with inhalation.
- Skin: Severe local reactions after extravasculation of intravenous solutions or following intramuscular injection treatment have been seen. Pentamidine itself may cause rash, or rarely Stevens–Johnson syndrome or Lyell syndrome.
- Eye discomfort, conjunctivitis, throat irritation, splenomegaly, Herxheimer reaction, electrolyte imbalances (e.g. hypocalcemia).
The additional or sequential use of other nephrotoxic drugs like aminoglycosides, amphotericin B, capreomycin, colistin, polymyxin B, vancomycin, foscarnet, or cisplatin should be closely monitored, or whenever possible completely avoided.
The mechanism is not well characterized, but there is some evidence that it may involve mitochondrial function.
Brand names and dose forms
- For oral inhalation and for nebulizer use: NebuPent Nebulizer
- For parenteral treatment: Pentacrinat, Pentam 300, and Pentamidine isethionate for injection (Abbot); all containing 300 mg of Pentamidine.
The concomitant use of Foscarnet( against CMV, or HSV) and I.V Pentamidine (against pneumocystis jiroveci) results in increased nephrotoxicities and hypocalcemia.
- "WHO Model List of EssentialMedicines" (PDF). World Health Organization. October 2013. Retrieved 22 April 2014.
- Nguewa PA, Fuertes MA, Cepeda V, et al. (2005). "Pentamidine is an antiparasitic and apoptotic drug that selectively modifies ubiquitin". Chem. Biodivers. 2 (10): 1387–400.
- "WHO | Drugs". Who.int. 2011-12-28. Retrieved 2013-03-26.
- Lee MS, Johansen L, Zhang Y, et al. (December 2007). "The novel combination of chlorpromazine and pentamidine exerts synergistic antiproliferative effects through dual mitotic action". Cancer Res. 67 (23): 11359–67.
- C. P. Thakur; et al. (1991). "Comparison of regimes of treatment of antimony-resistant kala-azar patients: a randomized study". American Journal of Tropical Medicine and Hygiene 45 (4): 435–441.
- Sun T, Zhang Y (March 2008). "Pentamidine binds to tRNA through non-specific hydrophobic interactions and inhibits aminoacylation and translation". Nucleic Acids Res. 36 (5): 1654–64.