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通过改变pH值和P(CO₂)来测定钙盐溶解度,模拟不同的胃肠道环境。

Determination of calcium salt solubility with changes in pH and P(CO(2)), simulating varying gastrointestinal environments.

作者信息

Goss Sandra L, Lemons Karen A, Kerstetter Jane E, Bogner Robin H

机构信息

University of Connecticut, School of Pharmacy, Box 2092, Storrs, CT 0626, USA.

出版信息

J Pharm Pharmacol. 2007 Nov;59(11):1485-92. doi: 10.1211/jpp.59.11.0004.

Abstract

The amount of calcium available for absorption is dependent, in part, on its sustained solubility in the gastrointestinal (GI) tract. Many calcium salts, which are the calcium sources in supplements and food, have pH-dependent solubility and may have limited availability in the small intestine, the major site of absorption. The equilibrium solubility of four calcium salts (calcium oxalate hydrate, calcium citrate tetrahydrate, calcium phosphate, calcium glycerophosphate) were determined at controlled pH values (7.5, 6.0, 4.5 and < or = 3.0) and in distilled water. The solubility of calcium carbonate was also measured at pH 7.5, 6.0 and 4.5 with two CO(2) environments (0.3 and 152 mmHg) above the solution. The precipitation profile of CaCO(3) was calculated using in-vivo data for bicarbonate and pH from literature and equilibrium calculations. As pH increased, the solubility of each calcium salt increased. However, in distilled water each salt produced a different pH, affecting its solubility value. Although calcium citrate does have a higher solubility than CaCO(3) in water, there is little difference when the pH is controlled at pH 7.5. The partial pressure of CO(2) also played a role in calcium carbonate solubility, depressing the solubility at pH 7.5. The calculations of soluble calcium resulted in profiles of available calcium, which agreed with previously published in-vivo data on absorbed calcium. The experimental data illustrate the impact of pH and CO(2) on the solubility of many calcium salts in the presence of bicarbonate secretions in the intestine. Calculated profiles using in-vivo calcium and bicarbonate concentrations demonstrate that large calcium doses may not further increase intestinal calcium absorption once the calcium carbonate solubility product has been reached.

摘要

可吸收的钙量部分取决于其在胃肠道(GI)中的持续溶解度。许多钙盐是补充剂和食物中的钙来源,它们具有pH依赖性溶解度,在小肠(主要吸收部位)中的可利用性可能有限。在控制的pH值(7.5、6.0、4.5和≤3.0)以及蒸馏水中测定了四种钙盐(水合草酸钙、四水合柠檬酸钙、磷酸钙、甘油磷酸钙)的平衡溶解度。还在溶液上方有两种CO₂环境(0.3和152 mmHg)的情况下,于pH 7.5、6.0和4.5下测量了碳酸钙的溶解度。使用文献中的体内碳酸氢盐和pH数据以及平衡计算来计算CaCO₃的沉淀曲线。随着pH升高,每种钙盐的溶解度增加。然而,在蒸馏水中,每种盐产生不同的pH值,影响其溶解度值。尽管柠檬酸钙在水中的溶解度确实高于CaCO₃,但在pH控制为7.5时差异不大。CO₂的分压也对碳酸钙的溶解度有影响,在pH 7.5时降低了溶解度。可溶性钙的计算得出了可用钙的曲线,这与先前发表的关于吸收钙的体内数据一致。实验数据说明了pH和CO₂对许多钙盐在肠道中存在碳酸氢盐分泌时溶解度的影响。使用体内钙和碳酸氢盐浓度计算得出的曲线表明,一旦达到碳酸钙的溶解度积,大剂量的钙可能不会进一步增加肠道钙吸收。

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