Intervet Innovation GmbH, Schwabenheim, Germany.
PLoS Negl Trop Dis. 2009;3(1):e357. doi: 10.1371/journal.pntd.0000357. Epub 2009 Jan 13.
Praziquantel (PZQ) is the drug compound of choice in the control and treatment of schistosomiasis. PZQ is administered as a racemate, i. e. 1ratio1 mixture of enantiomers. The schistosomicidal activity arises from one PZQ-enantiomer, whereas the other enantiomer does not contribute to the activity. The WHO's Special Programme for Research and Training in Tropical Diseases (TDR) has assigned the low-cost preparation of pure schistosomicidal (-)-PZQ a key priority for future R&D on PZQ, but so far this transition has not happened. PZQ has two major administration drawbacks, the first being the high dose needed, and its well documented bitter and disgusting taste. Attempts of taste-masking by low-cost means have not been successful. We hypothesized that the non-schistosomicidal component in PZQ would be the main contributor to the unpleasant taste of the drug. If the hypothesis was confirmed, the two major administration drawbacks of PZQ, the high dose needed and its bitter taste, could be addressed in one go by removing the component contributing to the bitter taste.
PZQ was separated into its schistosomicidal and the non-schistosomicidal component, the absolute stereochemical configuration of (-)-PZQ was determined to be (R)-PZQ by X-ray crystallography, and the extent of bitterness was determined for regular racemic PZQ and the schistosomicidal component in a taste study in humans.
The schistosomicidal component alone is significantly less bitter than regular, racemic PZQ.
Our hypothesis is confirmed. We propose to use only the pure schistosomicidal component of PZQ, offering the advantage of halving the dose and expectedly improving the compliance due to the removal of the bitter taste. Therefore, (R)-PZQ should be specifically suitable for the treatment of school-age children against schistosomiasis. With this finding, we would like to offer an additional incentive to the TDR's recommendation to switch to the pure schistosomicidal (R)-PZQ.
吡喹酮(PZQ)是控制和治疗血吸虫病的首选药物化合物。PZQ 作为外消旋体给药,即 1 对 1 混合对映异构体。杀血吸虫活性来自 PZQ 的一种对映异构体,而另一种对映异构体对活性没有贡献。世界卫生组织(WHO)热带病研究和培训特别规划署(TDR)已将低成本制备纯杀血吸虫(-)-PZQ 作为未来 PZQ 研发的关键优先事项,但到目前为止,这种转变尚未发生。PZQ 有两个主要的给药缺点,第一个是需要高剂量,以及其有记录的苦和令人恶心的味道。通过低成本手段掩盖味道的尝试尚未成功。我们假设 PZQ 中的非杀血吸虫成分将是药物不良味道的主要贡献者。如果假设得到证实,PZQ 的两个主要给药缺点,即所需的高剂量和苦味,可以通过去除导致苦味的成分一次性解决。
PZQ 被分离成其杀血吸虫和非杀血吸虫成分,通过 X 射线晶体学确定(-)-PZQ 的绝对立体化学构型为(R)-PZQ,并在人类味觉研究中确定了常规外消旋 PZQ 和杀血吸虫成分的苦味程度。
单独的杀血吸虫成分明显比常规的外消旋 PZQ 苦味小。
我们的假设得到证实。我们建议仅使用 PZQ 的纯杀血吸虫成分,由于去除了苦味,这将使剂量减半,并有望提高顺应性。因此,(R)-PZQ 特别适合治疗血吸虫病的学龄儿童。有了这个发现,我们想为 TDR 建议转向纯杀血吸虫(R)-PZQ 提供一个额外的激励。