Nalbufin

Nalbufin
(IUPAC) ime
	(–)-17-(cyclobutylmethyl)- 4,5α-epoxymorphinan- 3,6α,14-triol hydrochloride
Klinički podaci
Identifikatori
CAS broj	20594-83-6
ATC kod	N02AF02
PubChem	5311304
DrugBank	APRD01132
ChemSpider	4470813
UNII	L2T84IQI2K
ChEMBL	CHEMBL895
Hemijski podaci
Formula	C21H27NO4
Mol. masa	357.443 g/mol
SMILES	eMolekuli & PubHem
InChI
	InChI=1S/C21H27NO4/c23-14-5-4-13-10-16-21(25)7-6-15(24)19-20(21,17(13)18(14)26-19)8-9-22(16)11-12-2-1-3-12/h4-5,12,15-16,19,23-25H,1-3,6-11H2/t15-,16+,19-,20-,21+/m0/s1 ; Key: NETZHAKZCGBWSS-CEDHKZHLSA-N
Farmakokinetički podaci
Bioraspoloživost	81% @ 10 mg i 83% @ 20 mg, intramaskularno; 79% @ 10 mg i 76% @ 20 mg sabkutano
Metabolizam	3 do 6 sata
Farmakoinformacioni podaci
Trudnoća	?
Pravni status	lek na recept
Način primene	intravenozno, intramaskularno, sabkutano

Nalbufin je semi-sintetički opioid koji se koristi kao analgetik pod nizom imena, kao što je Nubain. Utvrđeno je da je niskim dozama ovaj lek efektivniji kod žena nego kod muškaraca, i da čak može da povisi bol kod muškaraca,^[5] što je dovelo do prekida njegove upotrebe u Velikoj Britaniji 2003.

Indikacije uredi

Nalbufin je indiciran za olakšanje umerenog do jakog bola. On se takođe može koristiti kao dodatak balansiranoj anesteziji, za preoperativno i postoperativno analgeziju, i za akušersku analgeziju tokom porođaja.

Mada nalbufin poseduje aktivnost narkotičnog antagonista, postoji evidencija da kod pacijenata koji nisu zavisni, on ne uzrokuje narkotični antagonizam istovremeno doziranih analgetika. Stoga, pacijenti koji primaju narkotične analgetike, generalne anestetike, fenotiazine, ili druge trankvilajzere, sedative, hipnotike, ili druge CNS depresante (uključujući alkohol) istovremeno sa nalbufinom mogu da ispolje aditivne efekte. Kad se takva kombinovana terapija koristi, doza jednog leka treba da bude umanjena.

Literatura uredi

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ Gear, RW; Miaskowski C, Gordon NC, Paul SM, Heller PH, Levine JD (November 1999). „The kappa opioid nalbuphine produces gender- and dose-dependent analgesia and antianalgesia in patients with postoperative pain”. Pain 83 (2): 339-45. DOI:10.1016/S0304-3959(99)00119-0. PMID 10534607.

Dodatna literatura uredi

Yuan-Yi Chia, Lok-Hi Chow, Chun-Chieh Hung, et al., Gender and pain upon movement are associated with the requirements for postoperative patient-controlled iv analgesia: a prospective survey of 2,298 Chinese patients, Canadian Journal of Anesthesia. 49:249-255 (2002)
Woods JR, Flynn K, Glantz JC, Pittinaro D. Sinusoidal fetal heart rate patterns. Peri-FACTS, Case #681, 2006. Retrieved from [1] Arhivirano 2011-07-15 na Wayback Machine-u, September 10, 2009.
Gear RW, Miaskowski C, Gordon NC,Paul SM, Heller PH, Levine JD. „The kappa opioid nalbuphine produces gender- and dose-dependent analgesia and antianalgesia in patients with postoperative pain”. Arhivirano iz originala na datum 2014-08-08. Pristupljeno 2014-04-05.

Spoljašnje veze uredi

	Portal Medicina
	Portal Hemija

Indeks lekova Arhivirano 2008-08-21 na Wayback Machine-u

[1] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[5] Gear, RW; Miaskowski C, Gordon NC, Paul SM, Heller PH, Levine JD (November 1999). „The kappa opioid nalbuphine produces gender- and dose-dependent analgesia and antianalgesia in patients with postoperative pain”. Pain 83 (2): 339-45. DOI:10.1016/S0304-3959(99)00119-0. PMID 10534607.

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