Academic literature on the topic 'Preclinical pharmacokinetics'

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Journal articles on the topic "Preclinical pharmacokinetics"

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Song, Wei, Meilin Liu, Junjun Wu, Hong Zhai, Yong Chen, and Zhihong Peng. "Preclinical Pharmacokinetics of Triptolide: A Potential Antitumor Drug." Current Drug Metabolism 20, no. 2 (2019): 147–54. http://dx.doi.org/10.2174/1389200219666180816141506.

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Background:Triptolide, a bioactive component in Tripterygium wilfordii extracts, possess strong antiproliferative activity on all 60-National Cancer Institute (NCI) cancer cell lines. However, the widespread use of triptolide in the clinical practice is greatly limited for its multi-organ toxicity and narrow therapeutic window. All the toxic characteristics of triptolide are associated with the pharmacokinetics especially its distribution and accumulation in the target organ.Methods:The literature review was done using PubMed search, SciFinder and Google Scholar databases with specific keyword
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Milan, Laznicek, Laznickova Alice, Cozikova Dagmar, and Velebny Vladimir. "Preclinical pharmacokinetics of radiolabelled hyaluronan." Pharmacological Reports 64, no. 2 (2012): 428–37. http://dx.doi.org/10.1016/s1734-1140(12)70784-3.

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Clarke, Stephen J., Philip J. Beale, and Laurent P. Rivory. "Clinical and Preclinical Pharmacokinetics of Raltitrexed." Clinical Pharmacokinetics 39, no. 6 (2000): 429–43. http://dx.doi.org/10.2165/00003088-200039060-00004.

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Sparreboom, Alex, Olaf van Tellingen, Willem J. Nooijen, and Jos H. Beijnen. "Preclinical pharmacokinetics of paclitaxel and docetaxel." Anti-Cancer Drugs 9, no. 1 (1998): 1–17. http://dx.doi.org/10.1097/00001813-199801000-00001.

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Tsun, Chang. "Preclinical and clinical pharmacokinetics of pirmenol." American Journal of Cardiology 59, no. 16 (1987): H15—H19. http://dx.doi.org/10.1016/0002-9149(87)90139-1.

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García-Quintanilla, Laura, Andrea Luaces-Rodríguez, María Gil-Martínez, et al. "Pharmacokinetics of Intravitreal Anti-VEGF Drugs in Age-Related Macular Degeneration." Pharmaceutics 11, no. 8 (2019): 365. http://dx.doi.org/10.3390/pharmaceutics11080365.

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Intravitreal administration of anti-vascular endothelial growth factor (VEGF) antibodies has become the standard treatment for Age-Related Macular Degeneration; however, the knowledge of their pharmacokinetics is limited. A comprehensive review of the preclinical and clinical pharmacokinetic data that were obtained in different studies with intravitreal bevacizumab, ranibizumab, and aflibercept has been conducted. Moreover, the factors that can influence the vitreous pharmacokinetics of these drugs, as well as the methods that were used in the studies for analytical determination, have been ex
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Holt, Jonathon D. S., David Cameron, Nicola Dias, et al. "The Sheep as a Model of Preclinical Safety and Pharmacokinetic Evaluations of Candidate Microbicides." Antimicrobial Agents and Chemotherapy 59, no. 7 (2015): 3761–70. http://dx.doi.org/10.1128/aac.04954-14.

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ABSTRACTWhen developing novel microbicide products for the prevention of HIV infection, the preclinical safety program must evaluate not only the active pharmaceutical ingredient but also the product itself. To that end, we applied several relatively standard toxicology study methodologies to female sheep, incorporating an assessment of the pharmacokinetics, safety, tolerability, and local toxicity of a dapivirine-containing human vaginal ring formulation (Dapivirine Vaginal Ring-004). We performed a 3-month general toxicology study, a preliminary pharmacokinetic study using drug-loaded vagina
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Pasipanodya, Jotam, and Tawanda Gumbo. "An Oracle: Antituberculosis Pharmacokinetics-Pharmacodynamics, Clinical Correlation, and Clinical Trial Simulations To Predict the Future." Antimicrobial Agents and Chemotherapy 55, no. 1 (2010): 24–34. http://dx.doi.org/10.1128/aac.00749-10.

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ABSTRACTAntimicrobial pharmacokinetic-pharmacodynamic (PK/PD) science and clinical trial simulations have not been adequately applied to the design of doses and dose schedules of antituberculosis regimens because many researchers are skeptical about their clinical applicability. We compared findings of preclinical PK/PD studies of current first-line antituberculosis drugs to findings from several clinical publications that included microbiologic outcome and pharmacokinetic data or had a dose-scheduling design. Without exception, the antimicrobial PK/PD parameters linked to optimal effect were
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Grigoleit, H. G., and P. Grigoleit. "Pharmacology and preclinical pharmacokinetics of peppermint oil." Phytomedicine 12, no. 8 (2005): 612–16. http://dx.doi.org/10.1016/j.phymed.2004.10.007.

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Heglund, I. F., Å. A. Michelet, W. F. Blazak, K. Furuhama, and E. Holtz. "Preclinical Pharmacokinetics and General Toxicology of Iodixanol." Acta Radiologica 36, no. 399_suppl (1995): 69–82. http://dx.doi.org/10.1177/0284185195036s39909.

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Dissertations / Theses on the topic "Preclinical pharmacokinetics"

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Kearbey, Jeffrey Dale. "Preclinical pharmacokinetics and skeletal pharmacology of a selective androgen receptor modulator." Connect to this title online, 2004. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1085168433.

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Thesis (Ph. D.)--Ohio State University, 2004.<br>Document formatted into pages; contains xvii, 162 p. Includes bibliographical references. Abstract available online via OhioLINK's ETD Center; full text release delayed at author's request until 2005 May 24.
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Kearbey, Jeffrey D. "Preclinical pharmacokinetics and skeletal pharmacology of a selective androgen receptor modulator." The Ohio State University, 2004. http://rave.ohiolink.edu/etdc/view?acc_num=osu1085168433.

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Dave, Nimita D. "Brain/Brain Tumor Pharmacokinetics and Pharmacodynamics of Letrozole." University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368013158.

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Tsakalozou, Eleftheria. "PRECLINICAL AND CLINICAL DEVELOPMENT OF THE LIPOPHILIC CAMPTOTHECIN ANALOGUE AR-67." UKnowledge, 2013. http://uknowledge.uky.edu/pharmacy_etds/18.

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AR-67 is a lipophilic third generation camptothecin analogue, currently under early stage clinical trials. It acts by targeting Topoisomerase 1 (Top1), a nuclear enzyme essential for DNA replication and transcription and is present in two forms, the pharmacologically active lipophilic lactone and the charged carboxylate. In oncology patients participating in a phase I clinical trial, AR-67 lactone was the predominant species in plasma. Similarly to other camptothecins, the identified dose-limiting toxicities for AR-67 were neutropenia, thrombocytopenia and fatigue. In addition, in vitro metabo
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Aimiuwu, Josephine Eki. "Modulation of Pharmacologic Effects of 5-Azacytidine by Ribonucleotide Reductase Antisense GTI-2040." The Ohio State University, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=osu1292851882.

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Hing, Jeremy P. "The application of non-linear mixed effects modelling to toxicokinetic data : population pharmacokinetics in preclinical studies." Thesis, University of Newcastle Upon Tyne, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.394740.

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Burger, A. M., Paul M. Loadman, D. E. Thurston, R. Schultz, H. H. Fiebig, and Michael C. Bibby. "Preclinical pharmacology of the pyrrolobenzodiazepine (PBD) monomer DRH-417 (NSC 709119)." Italian Society of Chemotherapy and the Italian Federation of Human and Animal Mycopathology, 2007. http://hdl.handle.net/10454/4571.

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no<br>The pyrrolobenzodiazepine monomer DRH-417 is a member of the anthramycin group of anti-tumor antibiotics that bind covalently to the N2 of guanine within the minor groove of DNA. DRH-417 emerged from the EORTC-Drug Discovery Committee and NCI 60 cell line in vitro screening programs as a potent antiproliferative agent with differential sensitivity towards certain cancer types such as melanoma, breast and renal cell carcinoma (mean IC(50) = 3 nM). DRH-417 was therefore tested for in vivo activity. The maximum tolerated dose (MTD) was established as 0.5 mg/kg given i.p. Marked anti-tumor a
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Ur-Rehman, Tofeeq. "Controlled release gel formulations and preclinical screening of drug candidates." Doctoral thesis, Umeå universitet, Kemiska institutionen, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-40489.

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Simple gel formulations may be applied to enhance the systemic and local exposure of potential compounds. The aim of this thesis is the development and characterization of controlled release formulations based on thermo-reversible poloxamer gels, which are suitable for novel drug delivery applications.  In particular co-solvents (DMSO, ethanol), mucoadhesive polymers (chitosan, alginate) and salts (sodium tripolyphosphate, CaCl2) have been used to enhance the applications of poloxamer 407 (P407) formulations in preclinical animal studies. The impact of these additives on the micellization and
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Chen, Chunli. "Pharmacokinetic-Pharmacodynamic Evaluations and Experimental Design Recommendations for Preclinical Studies of Anti-tuberculosis Drugs." Doctoral thesis, Uppsala universitet, Institutionen för farmaceutisk biovetenskap, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-318845.

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Tuberculosis is an ancient infectious disease and a leading cause of death globally. Preclinical research is important for defining drugs and regimens which should be carried forward to human studies. This thesis aims to characterize the population pharmacokinetics and exposure-response relationships of anti-tubercular drugs alone and in combinations, and to suggest experimental designs for preclinical settings. The population pharmacokinetics of rifampicin, isoniazid, ethambutol and pyrazinamide were described for the first time in two mouse models. This allowed for linking the population pha
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Jiang, Nan Verfasser], and Dieter [Akademischer Betreuer] [Willbold. "Preclinical pharmacokinetics and cerebral distribution of D-enantiomeric peptides for the treatment of Alzheimer’s disease / Nan Jiang ; Betreuer: Dieter Willbold." Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2018. http://d-nb.info/1150918845/34.

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Books on the topic "Preclinical pharmacokinetics"

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Tse, Francis L. S. Preclinical drug disposition: A laboratory handbook. M. Dekker, 1991.

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Evaluation of drug candidates for preclinical development: Pharmacokinetics, metabolism, pharmaceutics, and toxicology. John Wiley & Sons, 2010.

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Han, Chao. Evaluation of drug candidates for preclinical development: Pharmacokinetics, metabolism, pharmaceutics, and toxicology. John Wiley & Sons, 2010.

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Translational ADMET for drug therapy: Principles, methods, and pharmaceutical applications. John Wiley & Sons, Inc., 2015.

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High throughput bioanalytical sample preparation: Methods and automation strategies. Elsevier, 2003.

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Flavonoid Pharmacokinetics Methods Of Analysis Preclinical And Clinical Pharmacokinetics Safety And Toxicology. John Wiley & Sons, 2013.

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1948-, Gad Shayne C., ed. Preclinical development handbook. John Wiley & Sons, 2008.

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Wang, Binghe, Chao Han, and Charles B. Davis. Evaluation of Drug Candidates for Preclinical Development: Pharmacokinetics, Metabolism, Pharmaceutics, and Toxicology. Wiley & Sons, Incorporated, John, 2010.

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Chao, Han, Davis Charles B, and Wang Binghe PhD, eds. Evaluation of drug candidates for preclinical development: Pharmacokinetics, metabolism, pharmaceutics, and toxicology. John Wiley & Sons, 2010.

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Gad, Shayne Cox. Preclinical Development Handbook: Toxicology. Wiley & Sons, Incorporated, John, 2008.

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Book chapters on the topic "Preclinical pharmacokinetics"

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Yáñez, Jaime A., Casey L. Sayre, and Neal M. Davies. "Preclinical Pharmacokinetics of Flavonoids." In FLAVONOID PHARMACOKINETICS. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118468524.ch4.

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Caro, Carlos, M. Carmen Muñoz-Hernández, Manuel Pernia Leal, and María Luisa García-Martín. "In Vivo Pharmacokinetics of Magnetic Nanoparticles." In Preclinical MRI. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7531-0_24.

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Paxton, James W. "Interrelationship between Pharmacokinetics and Metabolism." In Preclinical Development Handbook. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470249031.ch30.

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Malik, Santosh, Ananya Ghosh, Rout George Kerry, and Jyoti Ranjan Rout. "Nanotechnology in Preclinical Pharmacokinetics." In Advances in Pharmaceutical Biotechnology. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-2195-9_30.

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El-Kattan, Ayman, and Manthena Varma. "Preclinical Pharmacokinetics: Industrial Perspective." In Mass Spectrometry Handbook. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118180730.ch5.

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Ibrahim, Mariam, and Lucila Garcia-Contreras. "Preclinical Pharmacokinetics of Antitubercular Drugs." In Drug Delivery Systems for Tuberculosis Prevention and Treatment. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118943182.ch7.

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Burger, Angelika M., and Heinz-Herbert Fiebig. "Preclinical Screening for New Anticancer Agents." In Handbook of Anticancer Pharmacokinetics and Pharmacodynamics. Humana Press, 2004. http://dx.doi.org/10.1007/978-1-59259-734-5_2.

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Branch, Robert A., and Edwin K. Jackson. "Preclinical Pharmacodynamics of Antihypertensives." In Integration of Pharmacokinetics, Pharmacodynamics, and Toxicokinetics in Rational Drug Development. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-1520-0_10.

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Levy, Gerhard. "The Case for Preclinical Pharmacodynamics." In Integration of Pharmacokinetics, Pharmacodynamics, and Toxicokinetics in Rational Drug Development. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-1520-0_2.

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Mukherjee, Asoke, Conrad Chen, Lucy Jean, and Claude B. Coutinho. "Preclinical Pharmacodynamics of Anti-Inflammatory Drugs." In Integration of Pharmacokinetics, Pharmacodynamics, and Toxicokinetics in Rational Drug Development. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4757-1520-0_13.

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Conference papers on the topic "Preclinical pharmacokinetics"

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Leal, Mauricio, Joann Wentland, Tracey Clark, et al. "Abstract C117: Preclinical pharmacokinetics of an antibody-drug conjugate targeting 5T4." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-c117.

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Casulleras, Maria Jove, Jade Spencer, Paul Loadman, et al. "Abstract 4926: Preclinical intratumoral pharmacokinetics (PK) of capecitabine (Cap) given +/- eribulin (Eri)." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-4926.

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Gu, Yi, Yang Sai, Jian Wang, et al. "Abstract 3371: Preclinical disposition and pharmacokinetics of volitinib, a novel selective cMet inhibitor ." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-3371.

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Shah, Neal, Chris E. Adkins, Afroz S. Mohammad, and Paul R. Lockman. "Abstract 1832: Bioluminescent pharmacokinetics of luciferin in preclinical brain metastases of breast cancer models." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-1832.

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Chikkanna, Dinesh, Kishore Narayanan, Sunil Panigrahi, et al. "Abstract 4086: Preclinical evaluation of pharmacokinetics, pharmacodynamics and efficacy of the dual CD73-A2AR Inhibitors." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-4086.

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Chikkanna, Dinesh, Kishore Narayanan, Sunil Panigrahi, et al. "Abstract 4086: Preclinical evaluation of pharmacokinetics, pharmacodynamics and efficacy of the dual CD73-A2AR Inhibitors." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-4086.

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Valic, Michael S., Wenlei Jiang, Lili Ding, et al. "Abstract 1947: Modelling of lipid-based nanoparticle pharmacokinetics and tumor accumulation using preclinical models of ovarian cancer." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-1947.

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Valic, Michael S., Wenlei Jiang, Lili Ding, et al. "Abstract 1947: Modelling of lipid-based nanoparticle pharmacokinetics and tumor accumulation using preclinical models of ovarian cancer." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-1947.

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Chikkanna, Dinesh, Sunil Kumar Panigrahi, Sujatha Rajagopalan, et al. "Abstract 1392: Preclinical In vivo evaluation of efficacy, pharmacokinetics and pharmacodynamics of novel PRMT5 inhibitors in multiple tumor models." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-1392.

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Feng, Ying, Yuqiao Shen, Don Musson, Huiyu Zhou, Oriane Scholler, and Leonard E. Post. "Abstract B67: Correlation of pharmacokinetics (PK), pharmacodynamics (PD) and in vivo antitumor activity of BMN 673 in preclinical models." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-b67.

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Reports on the topic "Preclinical pharmacokinetics"

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Noker, Patricia E. Preclinical Pharmacodynamic and Pharmacokinetic Studies of Investigational New Drugs. Defense Technical Information Center, 1995. http://dx.doi.org/10.21236/ada307633.

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Noker, Patricia E. Preclinical Pharmacodynamic and Pharmacokinetic Studies of Investigational New Drugs. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada425594.

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Noker, Patricia. Preclinical Pharmacodynamic and Pharmacokinetic Studies of Investigational New Drugs. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ada274309.

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