参考文献
[1] 肖小河, 苏中武, 乔传卓, 等. 姜黄属药用植物研究进展[J]. 中草药, 1997, 28(2): 114-119.
[2] Govindarajan V S. Turmeric-chemistry, technology and quanlity [J]. Critical Reviews in Food Science and Nutrition, 1980, 12(3): 199-301.
[3] 旷春桃. 姜黄素的包合、结构修饰及姜黄饲料添加剂研究[D]. 长沙: 中南林业科技大学, 2012.
[4] 韩刚, 霍文, 李秋影, 等. 姜黄素的稳定性研究[J]. 中成药, 2007, 29(2): 291-293.
[5] Natarajan C P, Lewis Y S. Technology of Ginger and Turmeric-In Status Papers and Abstracts[C].National Seminar on Ginger and Turmeric, Central Plantation Crops Research Institute, Calicut, India, 1980, 8: 83-89.
[6] 汤敏燕, 汪洪武, 孙凌峰. 中药姜黄挥发油化学成分研究[J]. 江西师范大学学报(自然科学版), 2000, 24(3): 274-276.
[7] 杭太俊, 张正行, 相秉仁, 等. 姜黄挥发油毛细管气相色谱指纹谱的标准化和数字化研究[J]. 中草药, 2003, 34(9): 793-797.
[8] 李瑞敏. 鲜姜黄中姜黄素的提取分离及纯化工艺研究[D]. 长沙: 中南林业科技大学, 2013.
[9] Ramachandraiah O S, Azeemoddin G, Charyulu J K, et al. Isolation, characteristics, chemical composition andmicrobial activity of turmeric(Curcuma longa Syn. C. domestica valeton) leaf oil[J]. Indian Perfumer, 2002, 46(3): 211-216.
[10] Singh R, Chandra R, Bose M, et al. Antibacterial activity of Curcuma longa rhizome extract on pathogenic bacteria [J]. Curr Sci, 2002 , 83(6): 737-740.
[11] Giang T S. Study on chemical components and separation of curcumin from rhizome Curcuma longa [J]. Tap Chi Duoc Hoc, 2002, 1: 15-17.
[12] Apisariyakul A, Vanittanakom N, Buddhasukh D. Antifungal activity of turmeric oil extractedfrom Curcuma longa(Zingiberaceae)[J]. J Ethnopharmacol, 1995, 49: 163-169.
[13] Singh G, OmPrakash Maurya S. Chemical and biocidal investigations on essential oils of some Indian Curcuma species [J]. Progress in Crystal Growth and Characterization of Materials, 2002,45(1-2): 75-81.
[14] Chandra D, Gupta S S. Anti-inflammatory and antiarthritic activity of volatile oil of Curcuma longa(Haldi) [J]. Indian J Med Res, 1972 , 60: 138-142.
[15] 石雪蓉, 顾健, 谭睿. 姜黄挥发油抗肿瘤作用机制研究[J]. 中药药理与临床, 2003, 19(6): 15-16.
[16] Tawatsin A, Wratten S D, Scott R R, et al. Repellency of volatile oils from plants against three mosquito vectors [J]. J Vector Ecol, 2001, 26: 76-82.
[17] Tripathi A K, Prajapati V, Verma N, et al. Bioactivities of the leaf essential oil of Curcuma Longa(var. Ch-66) on three stored-product beetles(Coleoptera) [J]. J Economic Entomology,2002, 95(1): 183-189.
[18] 赵泽贞, 温登瑰, 魏丽珍, 等. 姜黄油抗突变作用机理进一步试验研究[J]. 癌变·畸变·突变, 1999, 11(2): 75-77.
[19] 李诚秀, 李玲, 罗俊, 等. 姜黄挥发油对呼吸道作用的研究[J]. 中国中药杂志, 1998, 23(10): 624-626.
[20] 凌关庭. 抗氧化食品与健康[M]. 北京:化学工业出版社, 2004: 22-23.
[21] Mara M Braga, Patriaciaf Leal, Joae Carvalho, et al. Comparison of Yield, Composition, and Antioxidant Activity of Turmeric(Curcuma longa L. ) Extracts Obtained Using Various Techniques [J]. J Agric Food Chem, 2003, 51: 6604-6611.
[22] Jeng-Leun Mau,Eric Y C Lai, Wang N P, et al. Composition and antioxidant activity of the essential oil from curcuma zedoaria[J]. Food Chem, 2003, 82(4): 583-591.
[23] 江琰, 陈训. 四种植物挥发油对食用油脂抗氧化作用的研究[J]. 贵州科学, 2006, 24(2): 20-23.
[24] Priyanka Rathore,Preeti Dohare,Saurabh Varma, et al. Curcuma Oil: Reduces Early Accumulation of Oxidative Product and is Anti-apoptogenic in Transient Focal Ischemia in Rat Brain [J]. Neurochem Res, 2008 , 33(11) : 2376.
[25] 赵心宇, 孟秀香, 贾莉, 等. 姜黄素抗肿瘤机制实用药物与临床[J]. 2006, 9(1): 51-52.
[26] Kuttan R, Bhanumathy P, Nirmala K, et al. Potential anticancer activity of turmeric(curcuma-longa) [J]. Cancer Letters, 1985, 29(2): 197-202.
[27] Kawamori T, Lubet R, Steele V E, et al. Chemopreventive effect of curcumin, a naturally occurring anti-inflammatory agent, during the promotion/progression stages of colon cancer [J]. Cancer Research, 1999, 59(3): 597-601.
[28] Rao T S, Basu N, Siddiqui H H. Anti-inflammatory activity of curcumin analogs [J]. Indian Journal of Medical Research, 1982, 75(4): 574-578.
[29] 赵保路, 马学海. 氧自由基和天然抗氧化剂[M]. 北京: 科学出版社, 2002.
[30] Masuda T, Isobe J, Jitoe A, et al. Antioxidative curcuminoids from rhizomes of curcuma-xanthorrhiza [J]. Phytochemistry, 1992, 31(10): 3645-3647.
[31] Okada K, Wangpoengtrakul C, Tanaka T, et al. Curcumin and especially tetra-hydrocurcumin ameliorate oxidative stress-induced renal injury in mice [J]. Journal of Nutrition, 2001, 131(8): 2090-2095.
[32] Su H C F, Horvat R, Jilani G. Isolation, purification, and characterization of insect repellents from curcuma-longa l [J]. Journal of Agricultural and Food Chemistry, 1982, 30(2): 290-292.
[33] Jilani G, Su H C F. Laboratory studies on several plant materials as insect repellants for protection of cereal-grains [J]. Journal of Economic Entomology, 1983, 76(1): 154-157.
[34] 丁伟. 14种中药植物杀虫活性的初步研究[J]. 西南农业大学学报(自然科学版), 2003, 25(5): 417-420.
[35] 张永强, 丁伟, 赵志模. 姜黄素类化合物对朱砂叶螨的生物活性[J]. 昆虫学报, 2007(12): 1304-1308.
[36] Kim M K, Choi G J, Lee H S. Fungicidal property of curcuma longa l. Rhizome-derived curcumin against phytopathogenic fungi in a greenhouse [J]. Journal of Agricultural and Food Chemistry, 2003, 51(6): 1578-1581.
[37] 杨帮. 美洲商陆和姜黄提取物抑菌活性的研究[J]. 西南农业大学学报(自然科学版), 2005, 27(3): 297-300.
[38] Asai A, Miyazawa T. Dietary curcuminoids prevent high-fat diet-induced lipid accumulation in rat liver and epididymal adipose tissue [J]. Journal of Nutrition, 2001, 131(11): 2932-2935.
[39] Suresh Babu P, Srinivasan K. Influence of dietary curcumin and cholesterol on the progression of experimentally induced diabetes in albino rat [J]. Molecular and Cellular Biochemistry, 1995, 152(1): 13-21.
[40] Reddy A C P, Lokesh B R. Effect of curcumin and eugenol on iron-induced hepatic toxicity in rats[J]. Toxicology, 1996, 107(1): 39-45.
[41] Oetari S, Sudibyo M, Commandeur J N M, et al. Effects of curcumin on cytochrome p450 and glutathione s-transferase activities in rat liver[J]. Biochemical Pharmacology, 1996, 51(1): 39-45.
[42] 刘永刚, 陈厚昌, 蒋毅萍. 姜黄素抗肝纤维化的实验研究[J]. 时珍国医国药, 2002(5): 273-275.
[43] 杨伟峰, 陈厚昌. 联用阿米洛利与姜黄素预防大鼠肝纤维化的实验研究[J]. 胃肠病学和肝病学杂志, 2003(05): 424-426.
[44] 杨伟峰, 陈厚昌, 蒋毅萍. 姜黄素与阿米洛利联用对大鼠肝星状细胞氧应激所致纤维化的抑制作用[J]. 中药材, 2003(11): 795-798.
[45] 胡小军. 正交法优化姜黄油提取工艺的研究[J]. 食品与药品, 2007, 9(5): 4-6.
[46] 葛发欢, 史庆龙, 谭晓华, 等. 超临界CO2萃取姜黄油的工艺研究[J]. 中药, 1997, 20(7): 345-350.
[47] 李湘洲, 张炎强. 超临界CO2静动态结合萃取姜黄油的工艺[J]. 北京理工大学学报, 2007, 27(4): 366-369.
[48] 刘树兴, 胡小军. 超临界二氧化碳萃取姜黄油的工艺研究[J]. 中国油脂, 2004, 29(4): 18-20.
[49] 冉启良, 周显荣. 姜黄素制取新工艺的研究[J]. 食品科学, 1988, (5): 12-15.
[50] 熊国华, 李稳宏. 食用天然色素姜黄素的提取[J]. 精细化工, 1991, 8(5): 26.
[51] 王贤纯. 姜黄的综合利用[J]. 食品研究与开发, 1992, (3): 1-6, 17.
[52] 董海丽, 纵伟. 酶法提取姜黄素的研究[J]. 纯碱工业, 2000, (6): 55-57.
[53] 张有林, 韩军岐, 卢琛慧, 等. 姜黄色素提取及防腐效果研究[J]. 农业工程学报, 2005, 21(2): 144 -148.
[54] 唐课文, 易健民, 李立. 微波萃取吸附分离法提取姜黄素的研究[J]. 化工进展, 2005, 24(6): 647-650.
[55] 张炎强. 姜黄活性成分的提取、分离纯化及鉴定分析[D]. 长沙: 中南林业科技大学, 2007.
[56] 李湘洲, 张炎强, 刘艳华, 等. 不同方法提取姜黄色素的研究[J]. 林产化学与工业, 2006, 26(4): 83-86.
[57] 秦炜, 郑涛, 原永辉. 超声场对姜黄素提取过程的强化[J]. 清华大学学报(自然科学版), 1998, 38(6): 46-48.
[58] 刘树兴, 胡小军, 张薇, 等. 超声强化提取姜黄色素的研究[J]. 食品科学, 2004, (2): 53-55.
[59] 宿树兰, 吴启南, 欧阳臻, 等. 超临界CO2萃取测定姜黄中姜黄素的实验研究[J]. 中国中药杂志, 2004, 29(9): 857-860.
[60] 彭永芳, 马银海, 李维莉. 水溶性姜黄色素提取工艺的优化[J]. 食品科学, 2001, 22(9): 40-42.
[61] 张建超, 肖琪, 程光明, 等. 分离纯化姜黄素的大孔树脂筛选[J]. 湖北中医杂志, 2009, 31(4): 56-58.
[62] 刘硕谦, 刘仲华, 田娜, 等. 柱色谱法分离制备姜黄素的研究[J]. 色谱, 2004, 22(4): 457-458.
[63] 张玉领, 陈培, 王季茹, 等. 姜黄素提取条件的正交设计及硅胶柱色谱纯化的研究[J]. 价值工程, 2010, 29(16): 241-242.
[64] 王贤纯. 活性炭柱层析法分离姜黄素[J]. 生物学杂志, 2000, 17(5): 8-10.
[65] 段正康, 曾志丁, 罗爱文, 等. 活性白土柱层析法分离提纯姜黄素[J]. 湘潭大学学报(自然科学版), 2011,33(1): 78-83.
[66] 戴汉松, 单堂云, 高艳,等. 姜黄素的提取及其甲基化研究[J]. 天然产物研究与开发, 2008(20): 254-256.
[67] 袁利佳. 姜黄素静脉注射乳剂的制备[D]. 长春:吉林大学, 2007.
[68] 刘保启, 胡孝忠, 王玉春, 等. 姜黄素的提取、分离和测定[J]. 中华国际医学杂志, 2003, 3(2): 183-184.
[69] Tønnesen H H, Karlsen J. Studies on curcumin and curcuminoids. Ⅵ. Kinetics of curcumin degradation in aqueous solution [J]. Z Lebensm-Unters Forsch,1985, 180(5): 402-404.
[70] Tønnesen H H, Karlsen J. Studies on curcumin and curcuminoids. Ⅴ. Alkaline degradation of curcumin [J]. Z Lebensm-Unters Forsch, 1985, 180(2): 132-134.
[71] Tønnesen H H, Karlsen J, Beijersbergen van Henegouwen G. Studies on curcumin and curcuminoids. Ⅷ. Photochemical stability of curcumin [J]. Z Lebensm-Unters Forsch, 1986, 183(2): 116-122.
[72] Sharma R A, Mc Lelland H R, Hill K A, et al. Pharmacodynamic and pharmacokinetic study of oral Curcuma extract in patients with colorectal cancer[J]. Clinical Cancer Research, 2001, 7(7): 1894-1900.
[73] 高振珅, 王兰. 姜黄素-羟丙基-β-环糊精包合物的制备及其理化性质研究[J]. 中国药房, 2007, 18(13): 999-1000.
[74] 李剑明. 水溶性姜黄色素的制备及其抗肺癌转移作用的实验研究[D]. 重庆: 第三军医大学西南医院, 2005.
[75] 李剑明, 杨和平, 白中红, 等. 姜黄素可溶性制剂对小鼠结肠癌C26细胞在体诱导血管生成的抑制作用[J]. 中国肿瘤生物治疗杂志, 2008, 15(1): 56-59.
[76] 李香, 林秀丽. β-环糊精及其衍生物对姜黄素的增溶和荧光增强作用[J]. 中国医药工业杂志, 2008, 39(3): 194-198.
[77] 许东晖, 王胜, 梅雪婷, 等. 聚乙烯吡咯烷酮K30对姜黄素的增溶作用研究[J]. 中药材, 2008, 31(3): 438-442.
[78] 黄秀旺, 许建华, 吴国华, 等. 姜黄素固体分散体的制备及体外溶出特性[J]. 福建中医学院学报, 2008, 18(5): 30-33.
[79] 刘钰, 栾立标. 姜黄素固体分散体的制备及体外溶出度测定[J]. 药学进展, 2006, 30(1): 40-42.
[80] 关辉, 欧阳梅, 梁娇旸, 等. 姜黄素固体分散体的制备和溶出度考察[J]. 沈阳药科大学学报, 2009, 26(12): 945-950.
[81] 刘延敏, 王传胜, 韩刚, 等. 姜黄素固体分散体的制备及体外溶出度测定[J]. 哈尔滨医科大学学报, 2006, 40(4): 327-328.
[82] 韩刚, 孙广利, 孔晶晶, 等. 姜黄素增溶方法的比较研究[J]. 时珍国医国药, 2009, 20(2): 416-417.
[83] 高群玉, 黄立新, 周俊侠, 等. 姜黄色素及其微胶囊化的应用研究[J]. 食品科技, 2000, (3): 35-37.
[84] 许汉林, 孙芸, 邵继征, 等. 姜黄素脂质体在大鼠体内药代动力学研究[J]. 湖北中医学院学报, 2007, 9(1): 42-43.
[85] 许汉林, 孙芸, 邵继征, 等. 不同方法制备姜黄素脂质体的研究[J]. 中国中医药信息杂志, 2006, 13(7): 51-52.
[86] 孙芸. 姜黄素脂质体的制备及其药代动力学研究[D]. 武汉: 湖北中医学院, 2006.
[87] 许汉林, 张念, 程光明, 等. 姜黄素脂质体制备工艺的研究[J]. 湖北中医学院学报, 2009, 11(1): 36-39.
[88] 王云红, 汪圣华, 杨荣平, 等. 姜黄素自乳化制剂的设计、优化及质量评价[J]. 中药材, 2010, 33(12): 1933-1937.
[89] 吴雪梅. 姜黄素新剂型:自乳化和亚微乳给药系统的研究[D]. 福州: 福建医科大学, 2010.
[90] 吴雪梅, 张晶, 许建华, 等. 姜黄素自微乳化给药系统的体内外评价[J]. 福建医科大学学报, 2010, 44(3): 172-177.
[91] Conover C D, Zhao H, Longley C B, et al. Utility of poly(ethylene glycol) conjugation to create prodrugs of amphotericin B[J]. Bioconjugate Chemistry, 2003, 14(3): 661-666.
[92] Conover C D, Greenwald R B, Pendri A, et al. Camptothecin delivery systems: enhanced efficacy and tumor accumulation of camptothecin following its conjugation to polyethylene glycol via a glycine linker[J]. Cancer Chemotherapy and Pharmacology, 1998, 42(5): 407-414.
[93] Karen M, Caroline M P. Oseltamivir: a review of its use in in-fluenza [J]. Drugs, 2001, 61(2): 263-283.
[94] 厉凤霞, 李晓丽, 李斌. 葡萄糖-聚乙二醇-姜黄素的合成及其对姜黄素性能的改善[J]. 合成化学, 2011, 19(1): 15-18.
[95] 刘占军, 韩刚, 于九皋, 等. 姜黄素纳米粒的制备和释药性能[J]. 中药材, 2009, 32(2): 277-279.
[96] 陈德, 刘意, 范凯燕, 等. 姜黄素微球中药物存在形式与释药行为的关系研究[J]. 药学学报, 2016, 51(1): 140-146.
[97] Majhi A, Rahman G M, Panchal S, et al. Binding of curcumin and its long chain derivatives to the activator binding domain of novel protein kinase[J]. Bioorganic & Medicinal Chemistry, 2010, 18(4): 1591-1598.
[98] Tanaka R, Tsujii H, Yamada T, et al. Novel 3α-methoxyserrat-14-en-21β-ol(pj-1) and 3β-methoxyserrat-14-en-21β-ol(pj-2)-curcumin, kojic acid, quercetin, and baicalein conjugates as hiv agents [J]. Bioorganic & Medicinal Chemistry, 2009, 17(14): 5238-5246.
[99] Ligeret H, Barthelemy S, Doulakas G B, et al. Fluoride curcumin derivatives: New mitochondrial uncoupling agents [J]. FEBS Letters, 2004, 569(1-3): 37-42.
[100] Jankun J, Aleem A M, Malgorzewicz S, et al. Synthetic curcuminoids modulate the arachidonic acid metabolism of human platelet 12-lipoxygenase and reduce sprout formation of human endothelial cells [J]. Molecular cancer therapeutics, 2006, 5(5): 1371-1382.
[101] Fuchs J R, Pandit B, Bhasin D, et al. Structure-activity relationship studies of curcumin analogues[J]. Bioorganic & Medicinal Chemistry Letters, 2009, 19(7): 2065-2069.
[102] Tong Q S, Zheng L D, Lu P, et al. Apoptosis-inducing effects of curcumin derivatives in human bladder cancer cells [J]. Anti-Cancer Drugs, 2006, 17(3): 279-287.
[103] Dubey S K, Sharma A K, Narain U, et al. Design, synthesis and characterization of some bioactive conjugates of curcumin with glycine, glutamic acid, valine and demethylenated piperic acid and study of their antimicrobial and antiproliferative properties [J]. European Journal of Medicinal Chemistry, 2008, 43(9): 1837-1846.
[104] Singh R K, Rai D, Yadav D, et al. Synthesis, antibacterial and antiviral properties of curcumin bioconjugates bearing dipeptide, fatty acids and folic acid [J]. European Journal of Medicinal Chemistry, 2010, 45(3): 1078-1086.
[105] Shi W, Dolai S, Rizk S, et al. Synthesis of monofunctional curcumin derivatives, clicked curcumin dimer, and a pamam dendrimer curcumin conjugate for therapeutic applications [J]. Organic Letters, 2007, 9(26): 5461-5464.
[106] Changtam C, De Koning H P, Ibrahim H, et al. Curcuminoid analogs with potent activity against trypanosoma and leishmania species[J]. European Journal of Medicinal Chemistry, 2010, 45(3): 941-956.
[107] Simoni D, Rizzi M, Rondanin R, et al. Antitumor effects of curcumin and structurally [beta]-diketone modified analogs on multidrug resistant cancer cells[J]. Bioorganic & Medicinal Chemistry Letters, 2008, 18(2): 845-849.
[108] Kumar S, Narain U, Tripathi S, et al. Syntheses of curcumin bioconjugates and study of their antibacterial activities against beta-lactamase-producing microorganisms[J]. Bioconjugate Chemistry, 2001, 12(4): 464-469.
[109] Robinson T P, Hubbard R B, Ehlers T J, et al. Synthesis and biological evaluation of aromatic enones related to curcumin[J]. Bioorganic & Medicinal Chemistry, 2005, 13(12): 4007-4013.
[110] Woo H B, Shin W S, Lee S, et al. Synthesis of novel curcumin mimics with asymmetrical units and their anti-angiogenic activity[J]. Bioorganic & Medicinal Chemistry Letters, 2005, 15(16): 3782-3786.
[111] Ahn C M, Park B G, Woo H B, et al. Synthesis of sulfonyl curcumin mimics exerting a vasodilatation effect on the basilar artery of rabbits[J]. Bioorganic & Medicinal Chemistry Letters, 2009, 19(5): 1481-1483.
[112] 赵振坤, 王淑玲, 丁刘涛, 等. 中药药渣再利用研究进展[J]. 杭州师范大学学报(自然科学版), 2012, 11(1): 38-42.
[113] 张旭, 蒋桂韬, 王向荣, 等. 姜黄渣对蛋鸡生产性能、蛋品质及蛋黄胆固醇和丙二醛含量的影响[J]. 动物营养学报, 2016, 28(9): 2795-2801.
[114] Chen Y, Zhang Y F, Qian H C, et al. Supplementation with turmeric residue increased survival of the Chinese soft-shelled turtle(Pelodiscus sinensis) under high ambient temperatures[J]. Journal of Zhejiang University-SCIENCE B(Biomedicine & Biotechnology), 2018,19(3): 245-252.