Cause of bisphenol A migration from cans for drinks and assessment of improved cans

被引:25
作者
Kawamura, Y [1 ]
Inoue, K [1 ]
Nakazawa, H [1 ]
Yamada, T [1 ]
Maitani, T [1 ]
机构
[1] Natl Inst Hlth Sci, Setagaya Ku, Tokyo 1588501, Japan
来源
JOURNAL OF THE FOOD HYGIENIC SOCIETY OF JAPAN | 2001年 / 42卷 / 01期
关键词
bisphenol A; can for drink; migration; improved can; can coating; epoxy resin; polyvinyl chloride; thermal sterilization;
D O I
10.3358/shokueishi.42.13
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In the previous investigation, we found that some cans for coffee and black tea drinks released large amounts of bisphenol A (BPA) into their contents. Equivalent cans were obtained and the cause of BPA migration was investigated. Equivalent cans A, B and D contained high levels of BPA in the side seam, in the bottom, and in the bottom and the side seam, respectively, while can C contained some level of BPA in the body, which has a large area, therefore, all of them contained high amounts of BPA in their coatings. In the migration test, there was no BPA migration from the cans into water at 60 and 95 degreesC for 30 min, into 20% ethanol at 60 degreesC for 30 min, or into n-heptane at 25 degreesC for 60 min. However, at 120 degreesC for 30 min, equivalent cans released 35 similar to 124 ng/ mt BPA into the water. The total migration was similar to the total residues of BPA in the can coating and was close to the total amount of BPA in the drinks. Thus, BPA migration from the can coating requires heating to more than 105 degreesC, which is the glass transition temperature of the epoxy resin. Improved cans which contained less than 1/10 as much BPA as the equivalent cans showed very low migration levels, ie., 3 similar to6 ng/mL.
引用
收藏
页码:13 / 17
页数:5
相关论文
共 10 条
[1]   Determination of bisphenol a migrating from epoxy can coatings to infant formula liquid concentrates [J].
Biles, JE ;
McNeal, TP ;
Begley, TH .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (12) :4697-4700
[2]  
BROTONS JA, 1995, ENVIRON HEALTH PERSP, V103, P608, DOI 10.2307/3432439
[3]   Molecular structure in relation to oestrogenic activity. Compounds without a phenanthrene nucleus [J].
Dodds, EC ;
Lawson, W .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1938, 125 (839) :222-232
[4]  
Horie M, 1999, BUNSEKI KAGAKU, V48, P579
[5]  
Kawamura Y, 1999, J FOOD HYG SOC JPN, V40, P158
[6]   BISPHENOL-A - AN ESTROGENIC SUBSTANCE IS RELEASED FROM POLYCARBONATE FLASKS DURING AUTOCLAVING [J].
KRISHNAN, AV ;
STATHIS, P ;
PERMUTH, SF ;
TOKES, L ;
FELDMAN, D .
ENDOCRINOLOGY, 1993, 132 (06) :2279-2286
[7]   Chromatographic analysis of water and wine samples for phenolic compounds released from food-contact epoxy resins [J].
Lambert, C ;
Larroque, M .
JOURNAL OF CHROMATOGRAPHIC SCIENCE, 1997, 35 (02) :57-62
[8]   Relative binding affinity serum modified access (RBA-SMA) assay predicts the relative in vivo bioactivity of the xenoestrogens bisphenol A and octylphenol [J].
Nagel, SC ;
vomSaal, FS ;
Thayer, KA ;
Dhar, MG ;
Boechler, M ;
Welshons, WV .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1997, 105 (01) :70-76
[9]   Estrogenicity of resin-based composites and sealants used in dentistry [J].
Olea, N ;
Pulgar, R ;
Perez, P ;
OleaSerrano, F ;
Rivas, A ;
NovilloFertrell, A ;
Pedraza, V ;
Soto, AM ;
Sonnenschein, C .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1996, 104 (03) :298-305
[10]  
TAKINO A, 1999, SHOKUHIN EISEIGAKU Z, V40, P158