スルファダイアジン 化學特性,用途語,生産方法
外観
白色～わずかにうすい黃色, 結(jié)晶性粉末～粉末
溶解性
希塩酸, 水酸化ナトリウム試液, アンモニア試液に可溶, アセトン, エタノールに難溶, 水に不溶水酸化ナトリウム溶液に溶けやすく、水にほとんど溶けない。
解説
スルファダイアジンは，サルファ剤の一種。ぶどう球菌?大腸菌などに抗菌力を持ち、皮膚の細菌感染癥や肺炎?赤痢などに用いる。小學館 デジタル大辭泉について 情報 | 凡例
用途
スルファジアジン（Sulfadiazine）は、サルファ薬の一つ。感染源の細菌細胞內(nèi)での葉酸の合成を阻害することによって殺す効果があり、尿路感染癥（UTIs）の治療に使われる。
スルファジアジンとピリメタミンとの組み合わせは、トキソプラズマ（Toxoplasma gondii）が原因のトキソプラズマ癥の治療に使われる。
用途
細菌性下痢癥、ヘモフィルス感染癥 (豚) 。
効能
抗菌薬, 葉酸合成阻害薬
化學的特性
White to slightly yellow crystalline pow
使用
It is used in the form of silver salts (sulfadiazine silver) as an external antibacterial
agent, primarily for treating burns. It is believed that the presence of the silver ion in the
molecule facilitates increased antimicrobial and wound-healing action.
定義
ChEBI: A sulfonamide consisting of pyrimidine with a 4-aminobenzenesulfonamido group at the 2-position.
抗菌性
Sulfadiazine is somewhat more active than other sulphonamides.
一般的な説明
Sulfadiazine’s plasma half-life is 17 hours. It is a white,odorless crystalline powder soluble in water to the extentof 1:8,100 at 37°C and 1:13,000 at 25°C, in human serumto the extent of 1:620 at 37°C, and sparingly soluble in alcoholand acetone. It is readily soluble in dilute mineralacids and bases. Its pKa is 6.3.
応用例（製薬）
Sulfadiazine is almost insoluble in water and unstable on
exposure to light. It is administered orally or, as the sodium
salt, by intravenous injection. It is a component of several
multi-ingredient preparations. Its low solubility in urine led
to its general replacement by other compounds. The intravenous
solution is highly alkaline and should not be given by
any other route.
薬物動態(tài)學
Oral absorption： Very good
C
max 3 g oral： c. 50 mg/L after 3–4 h
Plasma half-life ：7–12 h
Volume of distribution： 0.36 L/kg
Plasma protein binding： c. 40%
Absorption and distribution
Adequate blood concentrations are easily achieved and
maintained after oral administration. It is well distributed
and penetrates in therapeutic concentrations into
the CSF, but because of resistance it is no longer the
drug of choice in meningitis. It crosses the placenta and
enters breast milk to achieve concentrations around 20%
of plasma levels.
Metabolism and excretion
Sulfadiazine is subject to acetylation in the liver. The acetyl
derivative lacks antibacterial activity and is excreted more
slowly (half-life 8–18 h). Parent compound and metabolite
are both excreted mainly by glomerular filtration.
臨床応用
Urinary tract infection
Nocardiasis
Chancroid
Toxoplasmosis (in combination with pyrimethamine)
Meningococcal infections
Prophylaxis of rheumatic fever
副作用
In addition to side effects common to the group, sulfadiazine
inhibits the metabolism of phenytoin. The risk of crystalluria
can be reduced by high fluid intake and alkalization of
the urine.
安全性プロファイル
Poison by intravenous route. Moderately toxic by ingestion and intraperitoneal routes. Human systemic
effects by ingestion: hematuria, anuria, general anesthesia, gastrointestinal effects. Experimental teratogenic and reproductive effects. When heated to decomposition it emits very toxic fumes of NOx and SOx.
スルファダイアジン 上流と下流の製品情報
原材料
準備製品