Farmakokinetika — разлика између измена

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[[ImageДатотека:Gráfica Km.png|thumb|250px|Grafikon koji demonstrira [[Михаелис-Ментенина кинетика|Mihaelis-Menteninov kinetčki]] model odnosa između enzima i supstrata]]
 
Farmakokinetika opisuje kako telo deluje na specifični lek nakon doziranja putem mehanizama apsorpcije i distribucije, kao i hemijske promene supstane u telu (e.g. posredstvom metaboličkih enzima kao što su [[enzim]]i [[citohrom P450]] ili [[glukuronoziltransferaza]]), i efekte i puteve izlučivanja metabolita leka.<ref>-{Pharmacokinetics. (2006). In ''Mosby's Dictionary of Medicine, Nursing, & Health Professions''. Philadelphia, PA: Elsevier Health Sciences. Retrieved December 11, 2008, from http://www.credoreference.com/entry/6686418 }-</ref> Farmakokinetička svojstva leka mogu da budu uslovljena faktorima poput mesta administriranja i doze leka. Ti faktori mogu da utiču na brzinu apsorpcije.<ref>{{Cite book |author=Kathleen Knights; Bronwen Bryant |title=Pharmacology for Health Professionals |publisher=Elsevier |location=Amsterdam |year=2002 |pages= |isbn=0-7295-3664-5 |oclc= |doi= |accessdate=}}</ref> Farmakokinetika se često studira zajedno sa [[farmakodinamika|farmakodinamikom]].
 
== Reference ==
{{reflist|2}}
 
== Literatura ==
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* {{Cite book |ref= harv|editor = Horning MG, Mitchell J | title = Drug metabolism and drug toxicity | publisher = Raven Press | location = New York | year = 1984 | isbn = 0-89004-997-1 | chapter = Pharmacokinetics: Basic Principles and Its Use as a Tool in Drug Metabolism | chapterurl = http://bts.ucsf.edu/benet_lab/index.php?page=benet | author = Benet LZ | ref = harv}}
* {{Cite book |ref= harv|author=Kathleen Knights; Bronwen Bryant |title=Pharmacology for Health Professionals |publisher=Elsevier |location=Amsterdam |year=2002 |isbn=0-7295-3664-5 |oclc= |doi= |accessdate=| ref = harv}}
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* Cooper, ''La célula'', pág 470-471, 2ª edición, Ed. Marbán
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* Hsieh Y, Korfmacher WA "Increasing speed and throughput when using HPLC-MS/MS systems for drug metabolism and pharmacokinetic screening". Current Drug Metabolism 7 (5): 479–89.(June 2006). PMID 16787157. Disponible en [http://www.bentham-direct.org/pages/content.php?CDM/2006/00000007/00000005/0004F.SGM.]
* Janssen D, Dinkla I, Poelarends G, Terpstra P (2005). "Bacterial degradation of xenobiotic compounds: evolution and distribution of novel enzyme activities". Environ Microbiol 7 (12): 1868-82. PMID 16309386.
* Kathleen Knights; Bronwen Bryant (2002). ''Pharmacology for Health Professionals''. Amsterdam: Elsevier. ISBN 0-7295-3664-5.
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* Sheehan D, Meade G, Foley V, Dowd C (2001). "Structure, function and evolution of glutathione transferases: implications for classification of non-mammalian members of an ancient enzyme superfamily". Biochem J 360 (Pt 1): 1-16. PMID 11695986.
* Sheiner, L.B.; Beal, S.L., Rosenberg, B. Marathe, V.V. "Forecasting Individual Pharmacokinetics". Clin. Pharmacol. Ther. 26: 294–305. (1979). PMID 466923.
* Sheiner, L.B.; Rosenberg, B., Marathe, V.V. "Estimation of Population Characteristics of Pharmacokinetic Parameters from Routine Clinical Data". J. Pharmacokin. Biopharm. 5: 445–79. 1.997 doi:10.1007/BF01061728.
* Sies H (1997). "Oxidative stress: oxidants and antioxidants". Exp Physiol 82 (2): 291-5. PMID 9129943.
* Singh SS., ''Preclinical pharmacokinetics: an approach towards safer and efficacious drugs'', Curr Drug Metab. 2006 Feb;7(2):165-82.