Nhận Dạng Quốc Tế & Đặc Tính Hóa Học
Monoisotopic mass
200.007212153
InChI
InChI=1S/C4H3F7O/c5-1-12-2(3(6,7)8)4(9,10)11/h2H,1H2
InChI Key
InChIKey=DFEYYRMXOJXZRJ-UHFFFAOYSA-N
IUPAC Name
1,1,1,3,3,3-hexafluoro-2-(fluoromethoxy)propane
Traditional IUPAC Name
sevoflurane
SMILES
FCOC(C(F)(F)F)C(F)(F)F
Độ hòa tan
Very slightly soluble
pKa (strongest acidic)
15.07
pKa (Strongest Basic)
-4.5
Refractivity
23.3 m3·mol-1
Dược Lực Học :
Sevoflurane (also called fluoromethyl) is a halogenated ether used for induction and maintenance of general anesthesia. Together with desflurane, it is replacing isoflurane and halothane in modern anesthesiology. It is often administered in nitrous oxide and pure oxygen. After desflurane it is the volatile anesthetic with the fastest onset and offset. It induces muscle relaxation and reduces pains sensitivity by altering tissue excitability. It does so by decreasing the extent of gap junction mediated cell-cell coupling and altering the activity of the channels that underlie the action potential.
Cơ Chế Tác Dụng :
Sevoflurane (2,2,2-trifluoro-1-[trifluoromethyl]ethyl fluoromethyl ether), also called fluoromethyl, is a sweet-smelling, non-flammable, highly fluorinated methyl isopropyl ether used for induction and maintenance of general anesthesia. Together with desflurane, it is replacing isoflurane and halothane in modern anesthesiology. [Wikipedia]
Sevoflurane induces a reduction in junctional conductance by decreasing gap junction channel opening times and increasing gap junction channel closing times. Sevoflurane also activates calcium dependent ATPase in the sarcoplasmic reticulum by increasing the fluidity of the lipid membrane. It also appears to bind the D subunit of ATP synthase and NADH dehydogenase and also binds to the GABA receptor, the large conductance Ca2+ activated potassium channel, the glutamate receptor, and the glycine receptor.
Dược Động Học :
▧ Absorption :
Rapidly absorbed into circulation via the lungs, however solubility in the blood is low.
▧ Metabolism :
Relatively little biotransformation, only 5% is metabolized by cytochrome P450 CYP2E1 to hexafluoroisopropanol (HFIP) with release of inorganic fluoride and CO2. No other metabolic pathways have been identified for sevoflurane.
▧ Route of Elimination :
The low solubility of sevoflurane facilitates rapid elimination via the lungs. In vivo metabolism studies suggest that approximately 5% of the sevoflurane dose may be metabolized. Up to 3.5% of the sevoflurane dose appears in the urine as inorganic fluoride.
▧ Half Life :
15-23 hours
Độc Tính :
LC50=49881 ppm/hr (rat), LD50=10.8 g/kg (rat)
Chỉ Định :
Used for induction and maintenance of general anesthesia in adult and pediatric patients for inpatient and outpatient surgery.
Liều Lượng & Cách Dùng :
Liquid - Respiratory (inhalation)
Dữ Kiện Thương Mại
Giá thị trường
-
Giá bán buôn : USD >1.16
Đơn vị tính : ml
-
Giá bán buôn : USD >0.89
Đơn vị tính : ml
-
Giá bán buôn : USD >0.99
Đơn vị tính : ml
Nhà Sản Xuất
-
Sản phẩm biệt dược : Sevorane
-
Sản phẩm biệt dược : Sojourn
-
Sản phẩm biệt dược : Ultane
Tài Liệu Tham Khảo Thêm
National Drug Code Directory