著者

宮沢 正 中島 邦生 南 幸男 池田 昌彦

出版者

日本法科学技術学会

雑誌

日本鑑識科学技術学会誌 (ISSN:13428713)

巻号頁・発行日

vol.2, no.2, pp.95-98, 1997 (Released:2010-06-10)

参考文献数

10

---

The pinpoint condensation technique using perfluorated polymer film was applied to the identification of lysergic acid diethylamide (LSD). Rapid solvent elimination for condensation of LSD into a small single residual at room temperature was performed by solvent evaporation on perfluorated polymer film, and the residual was measured by the microscope/FTIR technique. This sample condensation method provided high sensitivity for IR analysis. The detection limit was 2ng. When interfering substances did not exist in the extracted solution from blotter paper of LSD, the extract was able to be measuered simply and rapidly by microscope/FTIR technique. If isolation by preparative TLC was needed, the best elute was ethyl acetate or isopropanol which did not elute interfering substances from TLC plate into the eluent. More than 5 μg of LSD would be detectable by this technique after preparative TLC. We were able to identify LSD by this technique with preparative TLC from blotter paper containing more than 10 μg of it. This technique was useful to identify LSD sensitively from forensic samples.

著者

西川 眞弓 中島 邦生 五十嵐 一雄 糟谷 史代 福井 巳芳 土橋 均

出版者

公益社団法人日本薬学会

雑誌

衛生化学 (ISSN:0013273X)

巻号頁・発行日

vol.38, no.2, pp.121-126, 1992-04-30

被引用文献数

8

---

An analytical procedure for morphine-3-glucuronide (M3G) and morphine (M) in the human urine was investigated by using high-performance liquid chromatography coupled with atomospheric pressure ionization mass spectrometry (LC/APCI-MS). The samples were purified with Sep-Pak C_<18> cartridges. The LC separation was carried out using a L-column ODS in 50 mM ammonium acetate-methanol (86 : 14 v/v). The calibration graphs constructed by the absolute calibration curve method showed linearity over the concentration range of 30 to 1000 ng/ml (γ=0.9965) for M3G and 30 to 2000 ng/ml (γ=0.9970) for M. The detection limits by selected ion monitoring (SIM) were 3 ng/ml for M3G and 1 ng/ml for M, and by scan mode were 350 ng/ml for M3G and 80 ng/ml for M. The coefficients of variations for M3G and M were 4.79 and 3.15% at 1 μg/ml, respectively.