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Naslov:An LC-MS/MS method for quantification of lamotrigine and its main metabolite in dried blood spots
Avtorji:ID Milosheska, Daniela (Avtor)
ID Roškar, Robert (Avtor)
ID Vovk, Tomaž (Avtor)
ID Lorber, Bogdan (Avtor)
ID Grabnar, Iztok (Avtor)
ID Trontelj, Jurij (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (2,87 MB)
MD5: CA6DA12A4BC76D6FD2F8E3C8F133899F
 
URL URL - Izvorni URL, za dostop obiščite https://www.mdpi.com/1424-8247/17/4/449
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek:Background: The antiepileptic drug lamotrigine (LTG) shows high pharmacokinetic variability due to genotype influence and concomitant use of glucuronidation inducers and inhibitors, both of which may be frequently taken by elderly patients. Our goal was to develop a reliable quantification method for lamotrigine and its main glucuronide metabolite lamotrigine-N2-glucuronide (LTG-N2-GLU) in dried blood spots (DBS) to enable routine therapeutic drug monitoring and to identify altered metabolic activity for early detection of drug interactions possibly leading to suboptimal drug response. Results: The analytical method was validated in terms of selectivity, accuracy, precision, matrix effects, haematocrit, blood spot volume influence, and stability. It was applied to a clinical study, and the DBS results were compared to the concentrations determined in plasma samples. A good correlation was established for both analytes in DBS and plasma samples, taking into account the haematocrit and blood cell-to-plasma partition coefficients. It was demonstrated that the method is suitable for the determination of the metabolite-to-parent ratio to reveal the metabolic status of individual patients. Conclusions: The clinical validation performed confirmed that the DBS technique is a reliable alternative for plasma lamotrigine and its glucuronide determination.
Ključne besede:dried blood spot, lamotrigine, lamotrigine glucuronide, therapeutic drug monitoring, clinical validation, haematocrit effect
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2024
Št. strani:16 str.
Številčenje:Vol. 17, no. 4, [Article no.] 449
PID:20.500.12556/DiRROS-30161 Novo okno
UDK:615.015:616.853
ISSN pri članku:1424-8247
DOI:10.3390/ph17040449 Novo okno
COBISS.SI-ID:191424771 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 4. 4. 2024;
Datum objave v DiRROS:16.06.2026
Število ogledov:39
Število prenosov:15
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Pharmaceuticals
Skrajšan naslov:Pharmaceuticals
Založnik:MDPI, Molecular Diversity Preservation International
ISSN:1424-8247
COBISS.SI-ID:517582617 Novo okno

Gradivo je financirano iz projekta

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P1-0189-2018
Naslov:Farmacevtska tehnologija: od dostavnih sistemov učinkovin do terapijskih izidov zdravil pri otrocih in starostnikih

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:posušena krvna lisa, lamotrigin, lamotrigin glukuronid, terapevtsko spremljanje zdravil, klinična validacija, učinek hematokrita


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