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本文引用的文献

1
Twenty-six week toxicity study with KASAL® (basic sodium aluminum phosphate) in beagle dogs.用KASAL®(碱式磷酸铝钠)对比格犬进行的26周毒性研究。
Environ Geochem Health. 1990 Mar;12(1-2):121-3. doi: 10.1007/BF01734061.
2
The influence of citrate, maltolate and fluoride on the gastrointestinal absorption of aluminum at a drinking water-relevant concentration: A 26Al and 14C study.柠檬酸盐、麦芽酚和氟化物在与饮用水相关浓度下对铝胃肠道吸收的影响:一项26Al和14C研究。
J Inorg Biochem. 2008 Apr;102(4):798-808. doi: 10.1016/j.jinorgbio.2007.11.019. Epub 2007 Dec 14.
3
Human health risk assessment for aluminium, aluminium oxide, and aluminium hydroxide.铝、氧化铝和氢氧化铝的人体健康风险评估。
J Toxicol Environ Health B Crit Rev. 2007;10 Suppl 1(Suppl 1):1-269. doi: 10.1080/10937400701597766.
4
Elevated urinary aluminium in current and past users of illicit heroin.当前及既往非法海洛因使用者尿铝水平升高。
Addict Biol. 2007 Jun;12(2):197-9. doi: 10.1111/j.1369-1600.2007.00055.x.
5
Aluminum bioavailability from the approved food additive leavening agent acidic sodium aluminum phosphate, incorporated into a baked good, is lower than from water.烘焙食品中添加的已获批准的食品添加剂膨松剂酸性磷酸铝钠的铝生物利用度低于水中的铝生物利用度。
Toxicology. 2006 Oct 3;227(1-2):86-93. doi: 10.1016/j.tox.2006.07.014. Epub 2006 Jul 21.
6
Aluminum toxicity following IV use of oral methadone solution.静脉注射口服美沙酮溶液后的铝中毒
Clin Toxicol (Phila). 2006;44(3):307-14. doi: 10.1080/15563650600637077.
7
Aluminum toxicity due to intravenous injection of boiled methadone.静脉注射煮沸的美沙酮导致铝中毒。
N Engl J Med. 2006 Mar 16;354(11):1210-1. doi: 10.1056/NEJMc053341.
8
Aluminum in tobacco and cannabis and smoking-related disease.烟草和大麻中的铝与吸烟相关疾病
Am J Med. 2006 Mar;119(3):276.e9-11. doi: 10.1016/j.amjmed.2005.08.004.
9
Aluminium content of some foods and food products in the USA, with aluminium food additives.美国一些含有铝制食品添加剂的食品和食品产品中的铝含量。
Food Addit Contam. 2005 Mar;22(3):234-44. doi: 10.1080/02652030500073584.
10
Comparative in situ study of the intestinal absorption of aluminum, manganese, nickel, and lead in rats.大鼠肠道对铝、锰、镍和铅吸收的比较原位研究。
Biol Trace Elem Res. 2004 Summer;99(1-3):157-71. doi: 10.1385/BTER:99:1-3:157.

来自磷酸铝钠(一种已获批准的食品添加剂乳化剂)的铝生物利用度,该乳化剂添加于奶酪中。

Aluminum bioavailability from basic sodium aluminum phosphate, an approved food additive emulsifying agent, incorporated in cheese.

作者信息

Yokel Robert A, Hicks Clair L, Florence Rebecca L

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky Academic Medical Center, 511C Pharmacy Building, 725 Rose Street, Lexington, KY 40536-0082, USA.

出版信息

Food Chem Toxicol. 2008 Jun;46(6):2261-6. doi: 10.1016/j.fct.2008.03.004. Epub 2008 Mar 10.

DOI:10.1016/j.fct.2008.03.004
PMID:18436363
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2449821/
Abstract

Oral aluminum (Al) bioavailability from drinking water has been previously estimated, but there is little information on Al bioavailability from foods. It was suggested that oral Al bioavailability from drinking water is much greater than from foods. The objective was to further test this hypothesis. Oral Al bioavailability was determined in the rat from basic [26Al]-sodium aluminum phosphate (basic SALP) in a process cheese. Consumption of approximately 1g cheese containing 1.5% or 3% basic SALP resulted in oral Al bioavailability (F) of approximately 0.1% and 0.3%, respectively, and time to maximum serum 26Al concentration (Tmax) of 8-9h. These Al bioavailability results were intermediate to previously reported results from drinking water (F approximately 0.3%) and acidic-SALP incorporated into a biscuit (F approximately 0.1%), using the same methods. Considering the similar oral bioavailability of Al from food vs. water, and their contribution to the typical human's daily Al intake ( approximately 95% and 1.5%, respectively), these results suggest food contributes much more Al to systemic circulation, and potential Al body burden, than does drinking water. These results do not support the hypothesis that drinking water provides a disproportionate contribution to total Al absorbed from the gastrointestinal tract.

摘要

此前已对饮用水中铝(Al)的口服生物利用度进行了估算,但关于食物中铝生物利用度的信息却很少。有人认为,饮用水中铝的口服生物利用度远高于食物中的。目的是进一步验证这一假设。通过大鼠食用含碱性[26Al] - 磷酸铝钠(碱性SALP)的加工干酪来测定铝的口服生物利用度。食用约1克含1.5%或3%碱性SALP的干酪,铝的口服生物利用度(F)分别约为0.1%和0.3%,血清26Al浓度达到峰值的时间(Tmax)为8 - 9小时。采用相同方法,这些铝生物利用度结果介于先前报道的饮用水(F约为0.3%)和添加到饼干中的酸性SALP(F约为0.1%)的结果之间。考虑到食物和水中铝的口服生物利用度相似,以及它们对典型人类每日铝摄入量的贡献(分别约为95%和1.5%),这些结果表明,与饮用水相比,食物对全身循环及潜在铝体内负荷的贡献要大得多。这些结果并不支持饮用水对胃肠道吸收的总铝贡献不成比例这一假设。