Sams R A, Malspeis L
J Chromatogr. 1976 Oct 13;125(2):409-20. doi: 10.1016/s0021-9673(00)83372-5.
An electron-capture gas chromatographic method is described for the determination of naloxone and naltrexone as the perfluoroalkyl esters. Each compound serves as internal standard for determination of the other. The method permits quantitation of 2-100 ng of either compound. Conditions for derivatization with heptafluorobutyric anhydride (HFBA), pentafluoropropionic anhydride (PFPA), and trifluoroacetic anhydride (TFAA) have been investigated. When catalyzed with pyridine, derivatization with HFBA and PFPA at 70 degrees gives naloxone and naltrexone triesters. Evidence for triester formation was obtained from gas chromatography-methane chemical ionization mass spectrometry and infrared spectral analysis. It was found that both the HFB and PFP triesters are suitable for quantitation of the narcotic antagonists, the HFB derivatives having greater stability than the PFP derivatives. The TFA derivatives are substantially less stable.
描述了一种电子捕获气相色谱法,用于测定全氟烷基酯形式的纳洛酮和纳曲酮。每种化合物作为测定另一种化合物的内标。该方法可对2 - 100 ng的任何一种化合物进行定量。研究了用七氟丁酸酐(HFBA)、五氟丙酸酐(PFPA)和三氟乙酸酐(TFAA)进行衍生化的条件。当用吡啶催化时,在70℃下用HFBA和PFPA进行衍生化可得到纳洛酮和纳曲酮三酯。通过气相色谱 - 甲烷化学电离质谱和红外光谱分析获得了三酯形成的证据。发现HFB和PFP三酯都适用于定量麻醉拮抗剂,HFB衍生物比PFP衍生物具有更高的稳定性。TFA衍生物的稳定性明显更低。