INFORMAZIONI SU QUESTO ARTICOLO

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Fig. 1

Illustration of Mitra tip (A) and workflow of blood sampling (B – D)
Illustration of Mitra tip (A) and workflow of blood sampling (B – D)

Fig. 2

Chemical structures of direct oral anticoagulants
Chemical structures of direct oral anticoagulants

Examples of drugs applicable for monitoring using the volumetric absorptive microsampling technique [17]

Drug class Analytes
Antibiotics cefepime, fosfomycin, linezolid, meropenem, tazobactam, vancomycin
Anticonvulsants brivaracetam, carbamezpine, ethosuximide, lamotrigine, levetiracetam, phenytoin, rufinamide, topiramate, valproic acid
Immunosuppressants cyclosporin A, everolimus, mycophenolic acid, tacrolimus, sirolimus
Cardiovascular drugs acetylsalicylic acid, atenolol, lisinopril, simvastatin, valsartan
Endogenous compounds HbA1c, gamma-hydroxybutyric acid

Selected pharmacokinetics characteristic of direct oral anticoagulants

Dabigatran Apixaban Edoxaban Rivaroxaban
Target free and clot-bound thrombin factor Xa factor Xa factor Xa
Prodrug yes no no no
Bioavability 3 – 7% 50% 60% 80 – 100%
Protein binding 35% 85% 55% 90–95%
Dominant clearance renal hepatobiliary hepatobiliary hepatobiliary
Tmax 1.5 – 3 hrs 3 – 4 hrs 1 – 2 hrs 2 – 3 hrs
Dosing frequency twice daily twice daily once daily once daily

Physiochemical properties of direct oral anticoagulants

Molecular mass (Da) Lipophilicity (LogP) pKa PSA (Å)
Apixaban 459.49 2.33 pKaa = 13.12 110.77
Dabigatran 471.52 2.37 pKaa = 11.51pKab = 4.24 150.22
Edoxaban 548.06 1.61 pKaa = 11.08pKab = 7.23 136.62
Rivaroxaban 435.88 1.74 pKaa = 13.6 88.18
eISSN:
1338-4139
Lingua:
Inglese
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3 volte all'anno
Argomenti della rivista:
Medicine, Clinical Medicine, Internal Medicine, Cardiology