Moors M, Massart D L
Vrije Universiteit Brussels, Pharmaceutical Institute, Belgium.
J Pharm Biomed Anal. 1991;9(2):129-39. doi: 10.1016/0731-7085(91)80136-w.
This article evaluates the use of commercially available cyanopropyl and octadecyl sorbents for the extraction of basic drugs from breast milk. Twenty drugs were selected from different pharmacological groups (beta-blocking agents, antidepressants, anxiolytic sedatives and neuroleptics, antihistamines, alkaloids and an anthelmintic) and subjected to a general solid-phase extraction (SPE) procedure described earlier for plasma samples. This SPE method was developed on a cyanopropyl cartridge and consisted of a conditioning step with methanol and water, the adsorption of the deproteinized matrix, washing with water and/or methanol, and finally the elution of the basic compounds with 0.1% propylamine in methanol. The extracts were further analysed by reversed-phase liquid chromatography (RP-LC). The application of SPE to human milk samples utilized cyanopropyl and octadecyl cartridges. The latter can be applied more generally because it better retains the basic compounds. For 14 out of 17 drugs extracted from breast milk, recoveries of greater than 70% were obtained. Standard deviations were, with the exception of three drugs, in the same range as those observed for plasma samples, i.e. 2-8%. The development of a strategy for SPE of drugs from human milk was difficult. For a number of drugs, in particular those present in human milk at low concentrations and/or detected in a non-selective way, matrix compounds interfered with the subsequent LC analysis. Therefore, SPE on CN or C18-sorbent for the analysis of basic compounds in breast milk was found to be useful as one of the steps in an extraction procedure, but not as a single technique. A major drawback of SPE is the batch-to-batch variation of the sorbents.
本文评估了市售氰丙基和十八烷基吸附剂用于从母乳中提取碱性药物的效果。从不同药理组(β受体阻滞剂、抗抑郁药、抗焦虑镇静药和抗精神病药、抗组胺药、生物碱和一种驱虫药)中选择了20种药物,并按照先前针对血浆样本描述的通用固相萃取(SPE)程序进行处理。这种SPE方法是在氰丙基柱上开发的,包括用甲醇和水进行预处理步骤、吸附脱蛋白后的基质、用水和/或甲醇洗涤,最后用0.1%丙胺的甲醇溶液洗脱碱性化合物。提取物进一步通过反相液相色谱(RP-LC)进行分析。将SPE应用于母乳样本时使用了氰丙基柱和十八烷基柱。后者的应用更广泛,因为它能更好地保留碱性化合物。从母乳中提取的17种药物中有14种的回收率大于70%。除了三种药物外,标准偏差与血浆样本中观察到的值处于相同范围,即2-8%。开发从母乳中提取药物的SPE策略很困难。对于许多药物,特别是那些在母乳中浓度较低和/或以非选择性方式检测到的药物,基质化合物会干扰后续的LC分析。因此,发现用于分析母乳中碱性化合物的CN或C18吸附剂SPE作为提取程序中的一个步骤是有用的,但不能作为单一技术。SPE的一个主要缺点是吸附剂的批次间差异。