생물학적 반감기 (Korean Wikipedia)

Analysis of information sources in references of the Wikipedia article "생물학적 반감기" in Korean language version.

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  • Curry, Stephen H. (1993). 〈PHARMACOKINETICS OF ANTIPSYCHOTIC DRUGS〉. 《Antipsychotic Drugs and their Side-Effects》. Elsevier. 127–144쪽. doi:10.1016/b978-0-12-079035-7.50015-4. ISBN 978-0-12-079035-7. The elimination half-life measures the kinetics of loss of drug from the body as a whole once all distribution equilibria have been achieved. 
  • Dasgupta, Amitava; Krasowski, Matthew D. (2020). 〈Pharmacokinetics and therapeutic drug monitoring〉. 《Therapeutic Drug Monitoring Data》. Elsevier. 1–17쪽. doi:10.1016/b978-0-12-815849-4.00001-3. ISBN 978-0-12-815849-4. The half-life of a drug is the time required for the serum concentration to be reduced by 50%. Once the half-life of the drug is known, the time required for clearance can be estimated. Approximately 97% of the drug is eliminated by 5 halflives, while ~99% is eliminated by 7 half-lives. 
  • Toutain, P. L.; Bousquet-Melou, A. (2004). “Plasma terminal half-life” (PDF). 《Journal of Veterinary Pharmacology and Therapeutics》 27 (6): 427–439. doi:10.1111/j.1365-2885.2004.00600.x. PMID 15601438. 2020년 2월 20일에 원본 문서 (PDF)에서 보존된 문서. Following i.v. administration, the terminal half-life is the time required for plasma/blood concentration to decrease by 50% after pseudo-equilibrium of distribution has been reached; then, terminal half-life is computed when the decrease in drug plasma concentration is due only to drug elimination, and the term ‘elimination half-life’ is applicable. Therefore, it is not the time necessary for the amount of the administered drug to fall by one half. 
  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). 온라인 수정 버전: (2006–) "Biological Half Life". doi 10.1351/goldbook.B00658
  • Ehrsson, Hans; 외. (Winter 2002). “Pharmacokinetics of oxaliplatin in humans”. 《Medical Oncology》 19 (4): 261–5. doi:10.1385/MO:19:4:261. PMID 12512920. S2CID 1068099. 2007년 9월 28일에 원본 문서에서 보존된 문서. 2007년 3월 28일에 확인함. 
  • Asiri, Yousif A.; Mostafa, Gamal A.E. (2010). 〈Donepezil〉. 《Profiles of Drug Substances, Excipients and Related Methodology》 35. Elsevier. 117–150쪽. doi:10.1016/s1871-5125(10)35003-5. ISBN 978-0-12-380884-4. ISSN 1871-5125. PMID 22469221. Plasma donepezil concentrations decline with a half-life of approximately 70 h. Sex, race, and smoking history have no clinically significant influence on plasma concentrations of donepezil [46–51]. 

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  • Toutain, P. L.; Bousquet-Melou, A. (2004). “Plasma terminal half-life” (PDF). 《Journal of Veterinary Pharmacology and Therapeutics》 27 (6): 427–439. doi:10.1111/j.1365-2885.2004.00600.x. PMID 15601438. 2020년 2월 20일에 원본 문서 (PDF)에서 보존된 문서. Following i.v. administration, the terminal half-life is the time required for plasma/blood concentration to decrease by 50% after pseudo-equilibrium of distribution has been reached; then, terminal half-life is computed when the decrease in drug plasma concentration is due only to drug elimination, and the term ‘elimination half-life’ is applicable. Therefore, it is not the time necessary for the amount of the administered drug to fall by one half. 

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  • Asiri, Yousif A.; Mostafa, Gamal A.E. (2010). 〈Donepezil〉. 《Profiles of Drug Substances, Excipients and Related Methodology》 35. Elsevier. 117–150쪽. doi:10.1016/s1871-5125(10)35003-5. ISBN 978-0-12-380884-4. ISSN 1871-5125. PMID 22469221. Plasma donepezil concentrations decline with a half-life of approximately 70 h. Sex, race, and smoking history have no clinically significant influence on plasma concentrations of donepezil [46–51].