Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga, 2752, 90610-000 Porto Alegre, RS, Brazil.
Nat Prod Res. 2013;27(10):907-10. doi: 10.1080/14786419.2012.666751. Epub 2012 Mar 12.
An LC method was developed and validated in order to quantify the saponin purified fraction named QB-90 obtained from the aqueous extracts of Quillaja brasiliensis leaves. Previously, QB-90 was shown to be active as adjuvant in an experimental vaccine for herpesvirus bovine type 1 in mice. The analysis was performed using an RP-8 column with acetonitrile:water isocratic elution at 214 nm. The standard curve for QB-90 was linear over the range of 0.8-10 µg mL(-1) (r = 0.9996). The aqueous extract showed linear response in the range of 50-1000 µg mL(-1) (r = 0.9996). The proposed method showed adequate repeatability and intermediary precision. The limits of detection (LOD) and quantification (LOQ) were 0.074 and 0.248 µg mL(-1), respectively. This method was applied successfully to analyse QB-90 organ-specific distribution in field stands of Q. brasiliensis and in laboratory-grown seedlings. Leaves from young plants accumulated higher QB-90 amounts than leaves from adult trees.
建立并验证了一种 LC 方法,用于对从 Quillaja brasiliensis 叶的水提物中得到的名为 QB-90 的皂苷纯化物进行定量分析。此前,QB-90 已被证明在用于牛疱疹病毒 1 型的实验性疫苗中具有佐剂活性。采用 RP-8 柱,在 214nm 处进行乙腈:水等度洗脱进行分析。QB-90 的标准曲线在 0.8-10μg mL(-1)(r = 0.9996)范围内呈线性。水提物在 50-1000μg mL(-1)(r = 0.9996)范围内呈线性响应。所提出的方法具有良好的重复性和中间精密度。检测限(LOD)和定量限(LOQ)分别为 0.074 和 0.248μg mL(-1)。该方法成功地应用于分析 Q. brasiliensis 田间植株和实验室培养的幼苗中 QB-90 的器官特异性分布。幼树叶片积累的 QB-90 量高于成年树木叶片。