Matsuoka T
Criminal Investigation Laboratory, Aichi Prefectural Police Headquarters, Nagoya, Japan.
Biol Pharm Bull. 1997 Nov;20(11):1208-11. doi: 10.1248/bpb.20.1208.
A sensitive and rapid colorimetry for determination of methemoglobin (MetHb) in hemolysate of the test blood was devised by measurement of absorbance at 563 nm, the isosbestic point of spectra of cyanomethemoglobin and oxyhemoglobin, at pH 6.8. MetHb was determined as the difference in absorption caused by cyanide in the absence of potassium ferricyanide divided by the difference in absorption caused by cyanide in the presence of the ferricyanide. Carboxyhemoglobin (COHb) in the blood was also estimated from the absorbance values of the hemolysates with or without potassium ferricyanide after the addition of cyanide. The method requires only 3 microliters of test blood and 10 min for determinations of MetHb and COHb in blood. Results obtained by the method were in satisfactory agreement with theoretical results for mixture of MetHb, COHb, and oxyhemoglobin. The method was compared with two other methods using 55 forensic blood samples containing various amounts of MetHb and COHb, and proved to be suitable for practical samples.
通过在pH 6.8条件下测量563 nm处的吸光度(氰化高铁血红蛋白和氧合血红蛋白光谱的等吸收点),设计了一种灵敏且快速的比色法,用于测定受试血液溶血产物中的高铁血红蛋白(MetHb)。MetHb的测定方法为:在没有铁氰化钾的情况下,由氰化物引起的吸光度差异除以在有铁氰化钾存在时由氰化物引起的吸光度差异。在加入氰化物后,还可根据有无铁氰化钾的溶血产物的吸光度值估算血液中的碳氧血红蛋白(COHb)。该方法测定血液中的MetHb和COHb仅需3微升受试血液,耗时10分钟。该方法所得结果与MetHb、COHb和氧合血红蛋白混合物的理论结果吻合良好。使用55份含有不同量MetHb和COHb的法医血液样本,将该方法与其他两种方法进行比较,结果证明该方法适用于实际样本。