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Microwave-Assisted versus Conventional Isolation of Glucosinolate Degradation Products from Lunaria annua L. and Their Cytotoxic Activity

机译:微波辅助常规分离芥子油中芥子油苷降解产物及其细胞毒活性

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摘要

Glucosinolates (GSLs) from L. seeds were analyzed qualitatively and quantitatively by their desulfo counterparts using UHPLC-DAD-MS/MS technique and by their volatile breakdown products, isothiocyanates (ITCs), using GC-MS technique. GSL breakdown products were obtained by conventional techniques (hydrodistillation in a Clevenger type apparatus (HD), CH Cl extraction after myrosinase hydrolysis (EXT) for 24 h) as well as by modern techniques, microwave-assisted distillation (MAD) and microwave hydrodiffusion and gravity (MHG). Seven GSLs were identified as follows: isopropyl GSL ( ), -butyl GSL ( ), 5-(methylsulfinyl)pentyl GSL ( ), 6-(methylsulfinyl)hexyl GSL ( ), 5-(methylsulfanyl)pentyl GSL ( ), 6-(methylsulfanyl)hexyl GSL ( ), and benzyl GSL ( ). Additionally, pent-4-enyl- and hex-5-enyl ITCs were detected in the volatile extracts. However, their corresponding GSLs were not detected using UHPLC-DAD-MS/MS. Thus, they are suggested to be formed during GC-MS analysis via thermolysis of 5-(methylsulfinyl)pentyl- and 6-(methylsulfinyl)hexyl ITCs, respectively. Volatile isolates were tested for their cytotoxic activity using MTT assay. EXT and MHG showed the best cytotoxic activity against human lung cancer cell line A549 during an incubation time of 72 h (IC 18.8, and 33.5 μg/mL, respectively), and against breast cancer cell line MDA-MB-231 after 48 h (IC 6.0 and 11.8 μg/mL, respectively). These activities can be attributed to the ITCs originating from and .
机译:使用UHPLC-DAD-MS / MS技术通过脱硫对应物的定硫和定性定量分析L.种子中的葡糖苷(GSL),使用GC-MS技术通过挥发性分解产物异硫氰酸酯(ITC)进行定性和定量分析。 GSL分解产物可通过常规技术(在Clevenger型仪器中进行加氢蒸馏(HD),黑芥子酶水解(EXT)24小时后提取CH Cl)以及现代技术,微波辅助蒸馏(MAD)和微波加氢扩散和重力(MHG)。鉴定出七个GSL,如下所示:异丙基GSL(),-丁基GSL(),5-(甲基亚磺酰基)戊基GSL(),6-(甲基亚磺酰基)己基GSL(),5-(甲基亚硫酰基)戊基GSL(),6- (甲基硫烷基)己基GSL()和苄基GSL()。此外,在挥发性提取物中还检测到了戊-4-烯基和六-5-烯基ITC。但是,使用UHPLC-DAD-MS / MS未检测到其相应的GSL。因此,建议它们在GC-MS分析过程中分别通过热分解5-(甲基亚磺酰基)戊基和6-(甲基亚磺酰基)己基ITC形成。使用MTT测定法测试挥发性分离物的细胞毒性活性。 EXT和MHG在72 h的孵育时间(分别为IC 18.8和33.5μg/ mL)中对人肺癌细胞A549表现出最佳的细胞毒性活性,在48 h的孵育时间中对乳腺癌细胞MDA-MB-231表现出最佳的细胞毒性活性( IC 6.0和11.8μg/ mL)。这些活动可以归因于和起源的ITC。

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