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Ti(IV) 取代对羟基磷灰石颗粒表面蛋白质吸附行为的影响。

Effects of Ti(IV) substitution on protein adsorption behaviors of calcium hydroxyapatite particles.

机构信息

School of Chemistry, Osaka University of Education, Kashiwara-shi, Osaka, Japan.

出版信息

Colloids Surf B Biointerfaces. 2013 Jan 1;101:68-73. doi: 10.1016/j.colsurfb.2012.06.017. Epub 2012 Jul 3.

Abstract

The fundamental experiments on the adsorption behaviors of proteins onto photocatalytic Ti(IV)-doped calcium hydroxyapatite (TiHap) particles with varied amounts of Ti(IV) ions doped (called as original particle) were examined comparing to those onto the calcium hydroxyapatite (CaHap) ones. The heat treated TiHaps and CaHap particles at 650°C for 1h were also examined (called as heat treated particle). The Ti/(Ca+Ti) atomic ratio (X(Ti)) of the TiHap particles was varied between 0 and 0.20. Since the surface acidity of the particles was increased by increase in X(Ti) value, the negative zeta potential (zp) of the particles was increased. All the adsorption isotherms of bovine serum albumin (BSA), myoglobin (MGB) and lysozyme (LSZ) from 1×10(-4)mol/dm(3) KCl solution were the pseudo-Langmuirian type. The saturated amounts of adsorbed LSZ (n(S)(LSZ)) values onto the original particles were increased with increase in the negative zp of the particles. However, the saturated amounts of adsorbed BSA (n(S)(BSA)) values were decreased by increase in the negative zp except at X(Ti)=0.05 where n(S)(BSA) value exhibited a maximum. In the case of MGB, the saturated amounts of adsorbed MGB (n(s)(MGB)) values were less dependent on the zp of the particles. These results were explained by changing the electrostatic forces between protein molecules and TiHap particles by doping Ti(IV) ions. On the other hand, n(S)(BSA), n(S)(LSZ) and n(s)(MGB) values onto the heat treated particles were larger than the original particles in each particle system, though no relationship to the X(Ti) value was recognized in each protein system. This result was interpreted to the formation of β-TCP crystal phase in both the CaHap and TiHap particles by the heat treatment. The Ca(2+) ions produced by dissolution from β-TCP phase may exert as binders between BSA and surfaces of the heat treated particles. The weak binder effects of Ca(2+) and PO(4)(3-) ions were observed for the adsorptions of LSZ and MGB.

摘要

将不同量 Ti(IV) 掺杂的(称为原始颗粒)光催化 Ti(IV) 掺杂的羟基磷灰石(TiHap)颗粒与羟基磷灰石(CaHap)颗粒对蛋白质吸附行为的基础实验进行了比较。还对在 650°C 下热处理 1 小时的 TiHap 和 CaHap 颗粒(称为热处理颗粒)进行了研究。TiHap 颗粒的 Ti/(Ca+Ti)原子比(X(Ti))在 0 到 0.20 之间变化。由于颗粒表面酸度随 X(Ti) 值的增加而增加,因此颗粒的负 ζ 电位(zp)也随之增加。从 1×10(-4)mol/dm(3) KCl 溶液中,所有牛血清白蛋白(BSA)、肌红蛋白(MGB)和溶菌酶(LSZ)的吸附等温线均为拟 Langmuir 型。原始颗粒上吸附的 LSZ 的饱和量(n(S)(LSZ))随着颗粒负 zp 的增加而增加。然而,除了 X(Ti)=0.05 时,BSA 的饱和吸附量(n(S)(BSA))随负 zp 的增加而减少,此时 n(S)(BSA)值达到最大值。对于 MGB,吸附的 MGB 的饱和量(n(s)(MGB))值不太依赖于颗粒的 zp。这些结果可以通过掺杂 Ti(IV) 离子来改变蛋白质分子和 TiHap 颗粒之间的静电力来解释。另一方面,在每个颗粒体系中,热处理后的 n(S)(BSA)、n(S)(LSZ)和 n(s)(MGB)值均大于原始颗粒的值,尽管在每个蛋白质体系中都没有与 X(Ti) 值的关系。这一结果可以解释为 CaHap 和 TiHap 颗粒在热处理过程中形成了β-TCP 晶相。β-TCP 相溶解产生的 Ca(2+)离子可能作为 BSA 和热处理后颗粒表面之间的粘结剂。对于 LSZ 和 MGB 的吸附,观察到 Ca(2+)和 PO(4)(3-)离子的弱结合效应。

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