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Titlebook: Drug Discovery and Evaluation: Safety and Pharmacokinetic Assays; Franz J. Hock,Michael K. Pugsley Living reference work 20220th edition

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樓主: 惡夢
11#
發(fā)表于 2025-3-23 10:56:34 | 只看該作者
Drug Addiction and Drug Dependency,ioned place preference, and intracranial self-stimulation. This chapter outlines approaches commonly employed in studies of abuse and dependence liability assessments and highlights recent trends and advances in the utilization of each approach over the last decade.
12#
發(fā)表于 2025-3-23 14:21:04 | 只看該作者
Side Effects of Central Analgesic Drugs,algesics. In this chapter, we describe protocols currently used to evaluate important opioid-related centrally mediated adverse effects. These include protocols for assessing respiratory depression, sedation, constipation, physical dependence, and abuse liability using rodent and non-human primate m
13#
發(fā)表于 2025-3-23 19:08:16 | 只看該作者
Drug Discovery and Evaluation: Safety and Pharmacokinetic Assays
14#
發(fā)表于 2025-3-24 01:21:51 | 只看該作者
Drug Discovery and Evaluation: Safety and Pharmacokinetic Assays978-3-030-73317-9
15#
發(fā)表于 2025-3-24 03:29:17 | 只看該作者
Denk wat meer als een journalist, recommend the realization of supplemental safety studies in order to further evaluate the risk level on specific CNS processes. We present supplemental studies in three major safety domains including dependence/abuse, cognitive functions, and electrophysiological CNS activity.
16#
發(fā)表于 2025-3-24 09:03:29 | 只看該作者
https://doi.org/10.1007/978-90-313-9159-2 this chapter. These modifications target not just the accuracy and safety but also increase the reproducibility of the original assays. We believe this approach will give examples of the thought processes from former successful studies, thus being helpful for future researchers to adjust and update
17#
發(fā)表于 2025-3-24 11:22:48 | 只看該作者
Vasculaire geneeskunde in beeldnt safety pharmacology parameters into repeat-dose toxicity studies. This chapter reviews the evolution of assessment of biopharmaceuticals using examples from approval packages of marketed agents and discusses the past, current, and new approaches and methods that can be used to generate high-quali
18#
發(fā)表于 2025-3-24 15:03:11 | 只看該作者
Jacqueline de Graaf,Anton F. H. Stalenhoefarkers identified in preclinical safety assessment studies for use in clinical drug safety studies..Imaging technologies provide powerful insights into the biological effects of pharmaceuticals and can contribute important biomarkers that aid in the development of new therapies to treat disease.
19#
發(fā)表于 2025-3-24 19:07:31 | 只看該作者
Jacqueline de Graaf,Anton F. H. Stalenhoefal-based drug delivery system is unique to the drug, peptide, or protein employed in the system. Therefore, this chapter focuses on the safety considerations along with the therapeutic efficacy offered by this evolving developing area of therapeutics.
20#
發(fā)表于 2025-3-25 01:02:35 | 只看該作者
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