Smits K M, Schouten J S, Smits L J, et al. A review on the design and reporting of studies on drug-gene interaction [J]. J. Clin. Epidemiol., 2005, 58 (7):651-654.[2] Hu X, Cui S, Liu J. Fluorescence studies of interaction between flavonol p-coumaroylglucoside tiliroside and bovine serum albumin [J]. Spectrochim. Acta A, 2010, 77 (2):548-553.[3] Zhang G, Hu X, Zhao N, et al. Studies on the interaction of aminocarb with calf thymus DNA by spectroscopic methods [J]. Pestic. Biochem. Physiol., 2010, 98 (2):206-212.[4] Reinhardt C G, Krugh T R. A comparative study of ethidium bromide complexes with dinucleotides and DNA: Direct evidence for intercalation and nucleic acid sequence preferences [J]. Biochemistry, 1978, 17 (23):4845-4854.[5] Bi S, Qiao C, Song D, et al. Study of interactions of flavonoids with DNA using acridine orange as a fluorescence probe [J]. Sens. Actuators B, 2006, 119 (1):199-208.[6] Zhang G, Guo J, Pan J, et al. Spectroscopic studies on the interaction of morin-Eu(Ⅲ) complex with calf thymus DNA [J]. J. Mol. Struct., 2009, 923 (1-3):114-119.[7] Wall M E, Wani M C, Cook C Z, et al. Plant antitumor agents. Ⅰ.The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from camptotheca acuminate [J]. J. Am. Chem. Soc., 1966, 88 (16):3888-3890.[8] Hsiang Y H, Hertzberg R, Hecht S, et al. Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I [J]. J. Biol. Chem., 1985, 260 (27):14873-14878.[9] Hsiang Y H, Liu L F. Identification of mammalian DNA topoisomerase Ⅰas an intracellular target of the anticancer drug camptothecin [J]. Cancer Res., 1988, 48 (7):1722-1726.[10] Mi Z, Burke T G. Differential interactions of camptothecin lactone and carboxylate forms with human blood components [J]. Biochemistry, 1994, 33 (34):10325-10336.[11] Bi S, Zhang H, Qiao C, et al. Studies of interaction of emodin and DNA in the presence of ethidium bromide by spectroscopic method [J]. Spectrochim. Acta A, 2008, 69 (1):123-129.[12] Guo Y, Chao J, Pan J. Study on the interaction of 5-pyridine-10,15,20-tris- (p-chlorophenyl) porphyrin with cyclodextrins and DNA by spectroscopy [J]. Spectrochim. Acta A, 2007, 68 (2):231-236.[13] Bera R, Sahoo B K, Ghosh K S, et al. Studies on the interaction of isoxazolcurcumin with calf thymus DNA [J]. Int. J. Biol. Macromol., 2008, 42 (1):14-21.[14] Dey J, Warner I M. Spectroscopic and photophysical studies of the anticancer drug: Camptothecin [J]. J. Lumin., 1997, 71 (2):105-114.[15] Dey J, Warner I M. Excited state tautomerization of camptothecin in aqueous solution [J]. J. Photoch. Photobio. A, 1996, 101 (1):21-27.[16] Burke T G, Mi Z. Preferential binding of the carboxylate form of camptothecin by human serum albumin [J]. Anal. Biochem., 1993, 212 (1):285-287.[17] Liu Baosheng, Yang Chao, Wang Jing, et al. Luminescence mechanism study of the conjugation reaction between cefpirome sulfate and bovine serum albumin [J]. Chin. J. Lumin. (发光学报), 2011, 32 (3):293-299 (in Chinese).