Safety pharmacology screening: Practical problems in drug development

被引:3
|
作者
Mortin, LI
Horvath, CJ
Wyand, MS
机构
[1] Dept. of Exp. Medicine and Surgery, GTC/TSI Mason Laboratories, Worcester, MA
[2] Dept. of Exp. Medicine and Surgery, T.S.I. Mason Laboratories, Worcester, MA 01608
关键词
cardiovascular; central nervous system; disease models; drug development; general pharmacology; gastrointestinal; safety pharmacology;
D O I
10.1080/109158197227350
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Undesired pharmacologic activities of novel drugs or biologics may limit development of a therapeutic prior to the characterization of any toxicologic effects. In rodent species, general pharmacology assays have traditionally been used to screen new agents for pharmacologic effects on the central and peripheral nervous systems, the autonomic nervous system and smooth muscles, the respiratory and cardiovascular systems, the digestive system, and the physiologic mechanisms of water and electrolyte balance. In large animal species, such as dogs and nonhuman primates, smaller numbers of animals per study limit their we for screening assays, but these species may play an important role in. more detailed mechanistic studies. For drugs and biologics that must be tested in. nonhuman primates because of species-specific action of the test agent, functional pharmacologic data are often collected during acute or subacute toxicity studies. This requires careful experimental design to minimize any impact pharmacologic effects or instrumentation may have on the assessment of toxicity. In addition, with many new therapies targeted at immunologic diseases, the pharmacologic effect of therapeutics on the immune system presents new challenges for pharmacologic profiling. The application of pharmacology assays by organ system in both rodent and large animal species are discussed, as well as practical issues in assessing pharmacology endpoints in the context of toxicity studies.
引用
收藏
页码:41 / 65
页数:25
相关论文
共 50 条
  • [41] Practical guide to urine drug screening clarified
    Reisfield, Gary M.
    Bertholf, Roger L.
    MAYO CLINIC PROCEEDINGS, 2008, 83 (07) : 848 - 849
  • [42] Problems of Safety Codes Evaluation in Practical Applications
    Franekova, Maria
    Rastocny, Karol
    TRANSPORT SYSTEM TELEMATICS, 2010, 104 : 232 - 242
  • [43] Virtual modelling of safety helmets: practical problems
    Cernicchi, A.
    Galvanetto, U.
    Iannucci, L.
    INTERNATIONAL JOURNAL OF CRASHWORTHINESS, 2008, 13 (04) : 451 - 467
  • [44] The Journal of Clinical Pharmacology, Clinical Pharmacology in Drug Development, and the Impact Factor
    Bertino, Joseph S., Jr.
    Greenblatt, David J.
    JOURNAL OF CLINICAL PHARMACOLOGY, 2017, 57 (05): : 545 - 546
  • [45] The Journal of Clinical Pharmacology, Clinical Pharmacology in Drug Development, and the Impact Factor
    Bertino, Joseph S., Jr.
    Greenblatt, David J.
    CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT, 2017, 6 (03): : 218 - 219
  • [46] PROBLEMS OF DRUG DEVELOPMENT
    LASAGNA, L
    SCIENCE, 1964, 145 (363) : 362 - &
  • [47] Safety pharmacology in 2022: Taking one small step for cardiovascular safety assay development but one giant leap for regulatory drug safety assessment
    Pugsley, Michael K.
    Koshman, Yevgeniya E.
    de Korte, Tessa
    Authier, Simon
    Winters, Brett R.
    Curtis, Michael J.
    JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 2022, 117
  • [48] PRACTICAL PHARMACOLOGY
    Ihle-Hansen, Hakon
    TIDSSKRIFT FOR DEN NORSKE LAEGEFORENING, 2018, 138 (11) : 1064 - 1064
  • [49] COMET and the challenge of drug safety screening
    Nicholson, Jeremy
    Keun, Hector
    Ebbels, Tim
    JOURNAL OF PROTEOME RESEARCH, 2007, 6 (11) : 4098 - 4099
  • [50] Pharmacovigilance and Drug Safety: Practical Difficulty and Challenges
    Sud, S. S.
    Sud, K. S.
    DRUG SAFETY, 2016, 39 (10) : 1023 - 1024