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The protocols described here may be used in the future for comparing experimental groups when new technologies for parasite control are tested.
Herbal extracts have been investigated as an alternative for parasite control, aiming to slow the development of resistance and to obtain low-cost biodegradable parasiticides.
This review article provides integrated pharmacokinetic/pharmacodynamic and clinical pharmacology information pertinent to preserve the traditional and modern active ingredients as practical tools for parasite control.
Characterisation of ivermectin kinetics can be used to predict and optimise the value of the parasiticide effects and to design programmes for parasite control.
Overall, the outcome from integrated pharmaco-parasitological research approaches has greatly contributed to optimize drug activity, which seems relevant to preserve existing and particularly novel active ingredients as useful tools for parasite control in livestock animals.
None of the non-chemical methods for parasite control, i.e. nutrition, vaccines, parasite resistant breeds, is sufficiently effective without anthelmintic support and thus do not offer a practical option.
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The correct use of pharmacology-based information is critical to design successful strategies for the future of parasite control in livestock animals.
Considering the increasing concern for the development of anthelmintic resistance, the use of pharmacology-based information is critical to design successful strategies for the future of parasite control in livestock.
The need for new methods of parasite control is fully recognized by the industry, authorities and society.
A natural method of parasite control is breeding for host resistance.
The second tactic may be to avoid focusing solely on meeting the objective of uncertain elimination and exploit the ability of even a relatively poor model to give fairly good guidance to promote good parasite system transitions (for example, parasite control or even elimination) and prevent bad transitions (for example, infection re-emergence following control) [ 9].
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