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新型磷结合剂PA21与其他磷结合剂在体内外的磷结合能力比较

Comparison of Phosphate Binding Capacities of PA21, A Novel Phosphate Binder, with those of other Phosphate Binders in vitro and in vivo.

作者信息

Yaguchi A, Yonekubo S, Maruyama I, Tatemichi S, Maruyama K, Kobayashi M

机构信息

Pharmacology Research Laboratory, R&D, Kissei Pharmaceutical Co., Ltd., Nagano, Japan.

出版信息

Drug Res (Stuttg). 2016 May;66(5):262-9. doi: 10.1055/s-0035-1569328. Epub 2016 Jan 13.

Abstract

PURPOSE

The phosphate binding capacity of PA21, a novel phosphate binder, was compared with those of other phosphate binders in vitro and in vivo.

METHODS

  1. For in vitro studies, PA21, sevelamer hydrochloride, lanthanum carbonate hydrate, calcium carbonate, and ferric citrate hydrate were incubated with a phosphate solution at 37°C for 2 h. Phosphate binding capacity was assessed at simulated gastrointestinal tract pH levels of 2, 5, and 8 for estimation of clinical effects, and the quantity of phosphate adsorbed by each phosphate binder was determined. 2) For in vivo studies, rats were orally administered various phosphate binders after the oral administration of phosphate solution (100 mg/kg) adjusted to pH 2, 5, or 8, and the effects of PA21 and other phosphate binders on the serum phosphorus level of the rats were investigated.

RESULTS

  1. The in vitro studies revealed that PA21 and sevelamer hydrochloride adsorbed phosphate better at all tested pH levels than lanthanum carbonate hydrate, calcium carbonate, and ferric citrate hydrate, and PA21 showed the most potent phosphate binding capacity among the tested compounds. 2) The in vivo studies showed that PA21 dose-dependently inhibited the increase in the serum phosphorus level after the administration of phosphate solution and no difference in the extent of inhibition by PA21 was observed at the different pH levels (in contrast to other phosphate binders).

CONCLUSION

These results indicated that PA21 has a phosphate binding capacity over the entire pH range of the GI tract.

摘要

目的

在体外和体内将新型磷酸盐结合剂PA21的磷酸盐结合能力与其他磷酸盐结合剂进行比较。

方法

1)体外研究中,将PA21、碳酸司维拉姆、水合碳酸镧、碳酸钙和水合柠檬酸铁与磷酸盐溶液在37°C孵育2小时。在模拟胃肠道pH值2、5和8的条件下评估磷酸盐结合能力以估计临床效果,并测定每种磷酸盐结合剂吸附的磷酸盐量。2)体内研究中,在口服pH值调至2、5或8的磷酸盐溶液(100mg/kg)后,给大鼠口服各种磷酸盐结合剂,研究PA21和其他磷酸盐结合剂对大鼠血清磷水平的影响。

结果

1)体外研究表明,在所有测试的pH水平下,PA21和碳酸司维拉姆比水合碳酸镧、碳酸钙和水合柠檬酸铁更能吸附磷酸盐,并且PA21在测试化合物中显示出最强的磷酸盐结合能力。2)体内研究表明,PA21剂量依赖性地抑制磷酸盐溶液给药后血清磷水平的升高,并且在不同pH水平下未观察到PA21的抑制程度有差异(与其他磷酸盐结合剂相反)。

结论

这些结果表明PA21在胃肠道的整个pH范围内都具有磷酸盐结合能力。

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