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Drug Monograph on Rifampicin - page 8

Keywords: rifampicin, drug monograph, pharmacology, efficay, therapeutic uses, pharmacodynamics, Prophylaxis of meningococcal meningitis rifampin rifadin SA infections tuberculosis essay on rifampicin pharmacokinetics absorption distribution matabolism excretion bmj referecing

By Einstein10 on 30/12/2009

Level: Foundation Degree

Page Number: 8 of 11   pages: 1 2 3 4 5 6 7 8 9 10 11

and The Oral Contraceptive Pill

Rifampicin can potentially reduce the efficacy of the oral contraceptive pill because estradiol levels can be reduced by rifampicin-mediated CYP3A induction. Rifampicin is a potent inducer of estrogen-metablolising enzymes in the endoplasmic reticulum of the liver. When patients are treated with Rifampicin with a usual dose of 60mg/day, hepatic cytochrome-p450 3A4 (oestrogen-metaboliser) increases by 2-3 folds. Therefore, this shows that rifampicin induces the estrogen-2-hydroxylase in the endoplasmic reticulum of human liver, and explains the markedly reduced effectiveness of estrogens in contraceptives, if the patients are treated with rifampicin. Taking Rifampicin with a contraceptive pill could lead to unintentional conception. 44


Summary

Rifampicin is considered first line treatment for tuberculosis (TB) and should be prescribed as part of a multi drug regime for the treatment of the disease. The drug should not be prescribed as a single agent due to the increased resistance associated with the drug. 21
Research into the delivery system of rifampicin has shown that encapsulation of the drug within a lung specific stealth liposome showed to be more effective against Mycobacterium than the free drug 5.
Further research has shown that administering ant tuberculosis drugs in combination via a liposomal drug carrier system at one third of the therapeutic dose results in a greater reduction in the number of bacteria opposed o administering free drug 5

From this it can be concluded that delivering rifampicin as well other antituberculosis drugs via a drug liposomal carrier system could prove beneficial in improving compliance of patients, a reduction in the dose required resulting in decreased side effects of the therapy and a reduction in the cost of the treatment.


Bibliography

1. Dollery, C. Therapeutic drugs. Second edition. Edinburgh: Churchill Livingstone, 1999

2. Katzung, BG. Basic and clinical pharmacology. Eighth edition international edition. USA: McGraw Hill companies, 2001

3. Campbell A, Korzheva N, Mustaev A, Murakami K, Nair S, Goldfarb A, Darst A S. Structural Mechanism for Rifampicin Inhibition of Bacterial RNA Polymerase. Cell Press.2001;104:901-12

4. Hartmann R G, Heinrich P, Kollenda C M, Skrobranek B, Tropschug M, Weid W. Molecular Mechanism of Action of the Antibiotic Rifampicin. Angewandte Cheme. 1985; 24: 1009-74

5. Thomen P, Lopez J P, Heslot C F. Unravelling the mechanism of RNA-polymerase forward motion by using mechanical force. Laboratoire Pierre Aigrain.2004; 1: 1-4


6. British National Formulary. London: Pharmaceutical press, 2008

7. Sweetman, SC. Martindale: The complete drug reference. 35 edition. London: Pharmaceutical press, 2007

8. Tuberculosis.2007.http://www.dh.gov.uk/en/Publichealth/Communicablediseases/Tuberculosis/index.htm (accessed March 2009)

9. Petrie G.Tuberculosis. 2005. http://www.netdoctor.co.uk/diseases/facts/tuberculosis.htm (accessed March 2009)

10. Electronic Medicines Compendium. 2009. http://emc.medicines.org.uk/medicine/21221/SPC/Rifadin+150mg+Capsules/ (accessed March

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Drug Monograph on Rifampicin- page 8