By E. W. McChesney, C. D. Fitch (auth.), Wallace Peters M.D., DSc, FRCP, DTM & H, William H. G. Richards BSc, Ph. D. (eds.)

ISBN-10: 3642692540

ISBN-13: 9783642692543

ISBN-10: 3642692567

ISBN-13: 9783642692567

The development of this quantity has been guided via own convictions. adventure within the box of experimental chemotherapy, either within the pharmaceutical and academia, has confident us that fresh quantum technological advances in biochemistry, molecular biology, and immunology will let and, certainly, necessitate an more and more higher use of rational drug improvement sooner or later than has been the customized prior to now. partially l, consequently, we requested our individuals to supply distinct experiences protecting the biology of the malaria parasites and their relation with their hosts, the experimental methods together with tradition ideas which are essential to take a drug from fundamental screening to scientific trial, and an account of antimalarial drug resistance. Our moment conviction is that many study staff are all too loath to profit from the teachings of the prior. accordingly we requested the participants to half 2 of this quantity to check very completely the generally scattered yet voluminous literature on these few chemical teams that experience supplied the antimalarial medications in medical use this day. a lot may be discovered from the background in their improvement and the issues that experience arisen with them in guy. a few certainly should still have a lot to provide in the event that they will be deployed in higher methods than they're at the moment. this question has been taken up through numerous authors.

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Extra resources for Antimalarial Drug II: Current Antimalarial and New Drug Developments

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In the albino rats, in spite of an intake of more than twice that of the pigmented animals, CQ was found only in retina and sclera, the concentration in the former being about the same as that in liver and hair. The strong affinity of CQ for the iris and choroid, of the pigmented animals only, was very evident. General confirmation of these findings has been reported by other investigators (MCCHESNEY et al. 1965 a, 1967 a; GRUNDMANN et al. 1970) in the sense that the eyes of pigmented rats and rabbits accumulate large amounts of CQ relative to those of albinos and release these deposits very slowly on cessation of medication.

Pituitary gland does not appear to have been studied otherwise as a repository for CQ in the rat, but its strong affinity for the drug has been demonstrated in the rhesus monkey (see Table 3, line 18). Hair has been identified as a repository for CQ by BERNSTEIN et al. (1963). z) Discussion. At numerous points in Table 3 cognisance has been taken of the fact that, although the mean concentrations given in the literature for two or more tissues in the increasing order may have differed numerically, the differences were not statistically significant.

Obviously (MCCHESNEY et al. 1967b), a biological sample such as urine, which exhibits no absorption at 3,430 A, cannot contain more than traces of compounds in which the 4-amino-7-chloroquinoline nucleus remains intact. D. Metabolism I. General Considerations Complete information on the metabolism of any xenobiotic includes data on its absorption, tissue distribution, biotransformation, and rate, and routes of excretion. At least 57 publications listed in the bibliography of this review deal with one or more aspects of this problem.

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Antimalarial Drug II: Current Antimalarial and New Drug Developments by E. W. McChesney, C. D. Fitch (auth.), Wallace Peters M.D., DSc, FRCP, DTM & H, William H. G. Richards BSc, Ph. D. (eds.)


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