Sulfur hexafluoride

DB11104

small molecule approved

Deskripsi

Sulfur hexafluoride is an ultrasound contrast agent indicated for use
•in echocardiography to opacify the left ventricular chamber and to improve the delineation of the left ventricular endocardial border in adult patients with suboptimal echocardiograms
•in ultrasonography of the liver for characterization of focal liver lesions in adult and pediatric patients

Struktur Molekul 2D

Berat 146.05
Wujud -

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) The terminal half-life of SF6 in blood was approximately 10 minutes for the 0.3 mL/kg dose. (At the 0.03 mL/kg dose, terminal half-life could not be estimated.)
Volume Distribusi In a study of healthy subjects, the mean values for the apparent steady-state volume of distribution of SF6 were 341 L and 710 L for Lumason doses of 0.03 mL/kg and 0.3 mL/kg, respectively. Preferential distribution to the lung is likely responsible for these values.
Klirens (Clearance) -

Absorpsi

The pharmacokinetic of the SF6 gas component of Lumason was evaluated in 12 healthy adult subjects (7 men and 5 women). After intravenous bolus injections of 0.03 mL/kg and 0.3 mL/kg of Lumason, corresponding to approximately 1 and 10 times the recommended doses, concentrations of SF6 in blood peaked within 1 to 2 minutes for both doses.

Metabolisme

SF6 undergoes little or no biotransformation; 88% of an administered dose is recovered unchanged in expired air.

Rute Eliminasi

The SF6 component of Lumason is eliminated via the lungs.

Interaksi Obat

0 Data
Tidak ada data.

Referensi & Sumber

Link

Contoh Produk & Brand

Produk: 5 • International brands: 0
Produk
  • LumaSon
    Kit • - • Intravenous; Intravesical • US • Approved
  • LumaSon
    Injection, powder, lyophilized, for suspension; Kit • - • Intravenous; Intravesical • US • Approved
  • Lumason
    Injection, powder, lyophilized, for suspension • - • Intravenous; Intravesical • US • Approved
  • Sonovue
    Powder, for suspension • 8 mcL / mL • Intravenous; Intravesical • Canada • Approved
  • Sonovue
    Injection, powder, for solution • 8 μl/ml • Intravenous • EU • Approved

Sekuens Gen/Protein (FASTA)

Sekuens dimuat saat dibutuhkan agar halaman tetap ringan.
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