Department of Life Sciences, University of Modena and Reggio Emilia, Via G. Campi 183, 41125 Modena, Italy.
J Pharm Biomed Anal. 2013 Oct;84:103-11. doi: 10.1016/j.jpba.2013.05.045. Epub 2013 Jun 3.
In this study, a novel and efficient method based on headspace solid-phase microextraction (HS-SPME), followed by gas chromatography-mass spectrometry (GC-MS), was developed for the analysis of propolis volatile compounds. The HS-SPME procedure, whose experimental parameters were properly optimized, was carried out using a 100 μm polydimethylsiloxane (PDMS) fiber. The GC-MS analyses were performed on a HP-5 MS cross-linked 5% diphenyl-95% dimethyl polysiloxane capillary column (30 m × 0.25 mm I.D., 1.00 μm film thickness), under programmed-temperature elution. Ninety-nine constituents were identified using this technique in the samples of raw propolis collected from different Italian regions. The main compounds detected include benzoic acid (0.87-30.13%) and its esters, such as benzyl benzoate (0.16-13.05%), benzyl salicylate (0.34-1.90%) and benzyl cinnamate (0.34-3.20%). Vanillin was detected in most of the samples analyzed in this study (0.07-5.44%). Another relevant class of volatile constituents is represented by sesquiterpene hydrocarbons, such as δ-cadinene (1.29-13.31%), γ-cadinene (1.36-8.85%) and α-muurolene (0.78-6.59%), and oxygenated sesquiterpenes, such as β-eudesmol (2.33-12.83%), T-cadinol (2.73-9.95%) and α-cadinol (4.84-9.74%). Regarding monoterpene hydrocarbons, they were found to be present at low level in the samples analyzed in this study, with the exception of one sample from Southern Italy, where α-pinene was the most abundant constituent (13.19%). The results obtained by HS-SPME-GC-MS were also compared with those of hydrodistillation (HD) coupled with GC-MS. The HS-SPME-GC-MS method developed in this study allowed us to determine the chemical fingerprint of propolis volatile constituents, thus providing a new and reliable tool for the complete characterization of this biologically active apiary product.
在这项研究中,开发了一种基于顶空固相微萃取(HS-SPME),随后是气相色谱-质谱(GC-MS)的新型高效方法,用于分析蜂胶挥发性化合物。HS-SPME 程序在适当优化的实验参数下进行,使用 100μm 聚二甲基硅氧烷(PDMS)纤维进行。GC-MS 分析在 HP-5 MS 交联 5%二苯基-95%二甲基聚硅氧烷毛细管柱(30m×0.25mm ID,1.00μm 薄膜厚度)上进行,采用程序升温洗脱。使用该技术在从意大利不同地区采集的原始蜂胶样品中鉴定出 99 种成分。检测到的主要化合物包括苯甲酸(0.87-30.13%)及其酯,如苯甲酸苄酯(0.16-13.05%)、水杨酸苄酯(0.34-1.90%)和肉桂酸苄酯(0.34-3.20%)。香草醛在本研究分析的大多数样品中均有检出(0.07-5.44%)。另一个重要的挥发性成分类是倍半萜烃,如 δ- 杜松烯(1.29-13.31%)、γ-杜松烯(1.36-8.85%)和α- 穆勒烯(0.78-6.59%),以及含氧倍半萜烯,如 β- 艾杜醇(2.33-12.83%)、T- 杜松醇(2.73-9.95%)和α- 杜松醇(4.84-9.74%)。关于单萜烃,它们在本研究分析的样品中含量较低,除了来自意大利南部的一个样品,其中α- 蒎烯是最丰富的成分(13.19%)。HS-SPME-GC-MS 法与水蒸馏(HD)与 GC-MS 耦合法的结果进行了比较。本研究中开发的 HS-SPME-GC-MS 方法使我们能够确定蜂胶挥发性成分的化学指纹图谱,从而为该生物活性蜂产品的全面表征提供了一种新的可靠工具。