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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Volumetric absorptive microsampling for the therapeutic drug monitoring of psychiatric patients treated with cariprazine</dc:title><dc:creator>Millán-Santiago,	Jaime	(Avtor)
	</dc:creator><dc:creator>Vitagliano,	Rosalba	(Avtor)
	</dc:creator><dc:creator>Mondella,	Fortunata	(Avtor)
	</dc:creator><dc:creator>Mandrioli,	Roberto	(Avtor)
	</dc:creator><dc:creator>Sardella,	Roccaldo	(Avtor)
	</dc:creator><dc:creator>Vovk,	Tomaž	(Avtor)
	</dc:creator><dc:creator>Lucena,	Rafael	(Avtor)
	</dc:creator><dc:creator>Cárdenas,	Soledad	(Avtor)
	</dc:creator><dc:creator>Boaron,	Federico	(Avtor)
	</dc:creator><dc:creator>Mercolini,	Laura	(Avtor)
	</dc:creator><dc:subject>cariprazine</dc:subject><dc:subject>microsampling</dc:subject><dc:subject>therapeutic drug monitoring (TDM)</dc:subject><dc:subject>volumetric absorptive microsampling (VAMS)</dc:subject><dc:subject>microsampling (VAMS)</dc:subject><dc:description>Psychiatric disorders are usually treated with antipsychotic agents belonging to different pharmacological and chemical classes, the most recent ones collectively known as “third-generation antipsychotics”, such as cariprazine, approved in 2015 for the treatment of patients affected by schizophrenia. For these patients, a frequent therapeutic drug monitoring (TDM) becomes essential to assess compliance and to optimise and personalise their therapy, also due to cariprazine interindividual variability and narrow therapeutic range. In this study, a bioanalytical method featuring miniaturised sampling and pretreatment was developed, based on volumetric absorptive microsampling (VAMS) for TDM of psychiatric patients under cariprazine treatment and compared to a classic, reference method based on fluid plasma analysis. Minimally invasive whole blood VAMS was coupled to an original instrumental method based on ultra-high performance liquid chromatography hyphenated to mass spectrometry (UHPLC-MS). A feasible and streamlined, yet reliable VAMS pretreatment protocol was carefully optimised and the VAMS-UHPLC-MS methodology was validated with satisfactory results in terms of linearity ($r^2$ &gt; 0.9970 in the 1.5-100 ng/mL range), precision (%RSD ≤ 11.7), extraction yield (&gt; 90.0%) and matrix effect (8.2≤ RE% ≤ 10.9%). Finally, the microsampling approach coupled to UHPLC-MS was successfully applied to the TDM of psychiatric patients treated with cariprazine and compared with standard fluid plasma analysis, providing reliable quali-quantitative results, and proving to be readily applicable to the clinical practice in TDM programs as a useful alternative to cariprazine plasma analysis. This is the first report of a successful microsampling application, and in particular the first report of VAMS application, for the TDM of cariprazine.</dc:description><dc:date>2023</dc:date><dc:date>2023-10-10 09:55:51</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>151577</dc:identifier><dc:identifier>UDK: 615.214:616.89</dc:identifier><dc:identifier>ISSN pri članku: 0731-7085</dc:identifier><dc:identifier>DOI: 10.1016/j.jpba.2023.115740</dc:identifier><dc:identifier>COBISS_ID: 165592835</dc:identifier><dc:language>sl</dc:language></metadata>
