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BackgroundPraziquantel remains the drug of choice for the worldwide treatment and control of schistosomiasis. The drug is synthesized and administered as a racemate. Use of the pure active enantiomer would be desirable since the inactive enantiomer is associated with side effects and is responsible for the extremely bitter taste of the pill.Methodology/principal findingsWe have identified two resolution approaches toward the production of praziquantel as a single enantiomer. One approach starts with commercially available praziquantel and involves a hydrolysis to an intermediate amine, which is resolved with a derivative of tartaric acid. This method was discovered through an open collaboration on the internet. The second method, identified by a contract research organisation, employs a different intermediate that may be resolved with tartaric acid itself.Conclusions/significanceBoth resolution procedures identified show promise for the large-scale, economically viable production of praziquantel as a single enantiomer for a low price. Additionally, they may be employed by laboratories for the production of smaller amounts of enantiopure drug for research purposes that should be useful in, for example, elucidation of the drug's mechanism of action.

Original publication

DOI

10.1371/journal.pntd.0001260

Type

Journal article

Journal

PLoS neglected tropical diseases

Publication Date

09/2011

Volume

5

Addresses

School of Chemistry, The University of Sydney, Sydney, New South Wales, Australia.

Keywords

Humans, Schistosomiasis, Praziquantel, Anthelmintics, Technology, Pharmaceutical, Stereoisomerism, Chemistry, Pharmaceutical, International Cooperation