参考文献/References:
[1]杨暹,刘厚诚. 白子菜的特征特性及栽培技术[J]. 广东农业科学, 1998(5):16-17.
[2]WANG Z Z, ZHANG Q Q, HAO X, et al. Isolation, purification and identification of polysaccharides from Gynura divaricata.[J]. China Journal of Chinese Materia Medica, 2015, 40(8):1497-1502.
[3]ROEDER E, ECKERT A, WIEDENFELD H. Pyrrolizidine alkaloids from Gynura divaricata[J]. Planta Medica, 1996, 62(4):386-386.
[4]WAN C, YU Y, ZHOU S, et al. Isolation and identification of phenolic compounds from Gynura divaricata leaves[J]. Pharmacognosy Magazine, 2011, 7(26):101-108.
[5]LEE C H, YANG L, XU J Z, et al. Relative antioxidant activity of soybean isoflavones and their glycosides[J]. Food Chemistry, 2005, 90(4):735-741.
[6]王波,张晓艳,黄攀,等. 响应面法优化马齿苋黄酮超声波提取工艺[J].江苏农业学报,2018,34(1):166-171.
[7]刘微微,刘旭,曹学丽,等. 白背三七多糖的结构表征及α葡萄糖苷酶的抑制活性[J]. 食品科学, 2013, 34(7):115-120.
[8]王永立, 袁浩, 樊淑华. 七叶一枝花总黄酮提取工艺优化[J]. 南方农业学报,2017,48(4):698-703.
[9]陈贤兴. 白背三七草的诱变及抗诱变作用的初步研究[J]. 河南科学, 2002, 20(3):260-262.
[10]古丽巴哈尔·卡吾力,高晓黎,常占瑛,等.黑果枸杞总黄酮提取工艺优化及抗氧化活性[J].江苏农业科学,2017,45(22):213-217.
[11]陈磊. 白背三七降血糖物质基础研究[D]. 上海:第二军医大学, 2009.
[12]俞浩,毛斌斌,周国梁,等. 白背三七总黄酮对糖尿病大鼠的降血糖作用[J]. 食品科学, 2013, 34(15):295-298.
[13]姜曼花. 白背三七多糖及黄酮的提取测定与降血糖作用研究[D]. 长沙:湖南师范大学, 2009.
[14]TAN C, WANG Q, LUO C, et al. Yeast αglucosidase inhibitory phenolic compounds isolated from gynura medica leaf[J]. International Journal of Molecular Sciences, 2013, 14(2):2551-2558.
[15]刘璐,付明哲,王侠,等. 植物黄酮类化合物提取及测定方法研究进展[J]. 动物医学进展, 2011, 32(6):151-155.
[16]李辉,卜晓英,陈功锡,等. 超声辅助提取白背三七总黄酮[J]. 食品科学, 2011, 32(14):144-146.
[17]何晋浙,汪钊,金再宿. 柚皮中生物类黄酮提取优化工艺研究[J]. 食品工业科技, 2002(3):39-40.
[18]袁尔东,王菊芳,刘本国,等. 亮叶杨桐叶类黄酮的提取及其抗氧化活性研究[J]. 食品科学, 2009, 30(14):105-109.
[19]RAJHA H N, DARRA N E, HOBAIKA Z, et al. Extraction of total phenolic compounds, flavonoids, anthocyanins and tannins from grape byproducts by response surface methodology. influence of solidliquid ratio, particle size, time, temperature and solvent mixtures on the optimization process[J]. Food & Nutrition Sciences, 2014, 5(4):397-409.
[20]ALMAJANO M P, DELGADO M E, GORDON M H. Changes in the antioxidant properties of protein solutions in the presence of epigallocatechin gallate[J]. Food Chemistry, 2007, 101(1):126-130.
[21]HEO S J, PARK E J, LEE K W, et al. Antioxidant activities of enzymatic extracts from brown seaweeds.[J]. European Food Research & Technology, 2005, 221(1/2):41-47.
[22]CAMPOS A M, LISSI E A. Kinetics of the reaction between 2,2′azinobis (3ethylbenzothiazoline6sulfonic acid (ABTS) derived radical cations and phenols[J]. International Journal of Chemical Kinetics, 2015, 29(3):219-224.
[23]刘洁,江连洲,张景亮,等. 响应面法对Protamex酶解醇法大豆浓缩蛋白的优化[J]. 食品科学, 2009, 30(13):163-167.
[24]SANMARTNSUREZ C, SOTOOTERO R, SNCHEZSELLERO I, et al. Antioxidant properties of dimethyl sulfoxide and its viability as a solvent in the evaluation of neuroprotective antioxidants[J]. Journal of Pharmacological & Toxicological Methods, 2011, 63(2):209-215.
[25]DARGEL R. Lipid peroxidationa common pathogenetic mechanism?[J]. Experimental & Toxicologic Pathology Official Journal of the Gesellschaft Für Toxikologische Pathologie, 1992, 44(4):169.
[26]YAO Y, YANG X, TIAN J, et al. Antioxidant and antidiabetic activities of black mung bean (Vigna radiata L.)[J]. Journal of Agricultural & Food Chemistry, 2013, 61(34):8104-8109.
[27]OZGEN M, REESE R N, TULIO A Z, et al. Modified 2,2Azinobis3ethylbenzothiazoline6sulfonic Acid (ABTS) method to measure antioxidant capacity of selected small fruits and comparison to ferric reducing antioxidant power (FRAP) and 2,2’Diphenyl1picrylhydrazyl (DPPH) methods[J]. Journal of Agricultural & Food Chemistry, 2006, 54(4):1151.
[28]ALIAGA C, LISSI E A. Reaction of 2,2’AzinoBis(3Ethylbenzothiazoline6Sulfonic Acid) (ABTS) derived radicals with hydroperoxides. Kinetics and mechanism[J]. International Journal of Chemical Kinetics, 2015, 30(8):565-570.
[29]YU S H, HSIEH H Y, PANG J C, et al. Active films from watersoluble chitosan/cellulose composites incorporating releasable caffeic acid for inhibition of lipid oxidation in fish oil emulsions[J]. Food Hydrocolloids, 2013, 32(1):9-19.
[30]SINGANUSONG R, NIPORNRAM S, TOCHAMPA W, et al. Low power ultrasoundassisted extraction of phenolic compounds from mandarin ( Citrus reticulata, Blanco cv. Sainampueng) and Lime ( Citrus aurantifolia ) peels and the antioxidant[J]. Food Analytical Methods, 2015, 8(5):1112-1123.
[31]MA Y Q, YE X Q, FANG Z X, et al. Phenolic compounds and antioxidant activity of extracts from ultrasonic treatment of Satsuma Mandarin (Citrus unshiu Marc.) peels[J]. Journal of Agricultural & Food Chemistry, 2008, 56(14):5682-5690.