生物矿化的纳米空间理论。

Dentistry in Japan Pub Date : 1990-01-01
N Katsura
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引用次数: 0

摘要

从体液中析出无机晶体需要(A)消除抑制晶体形成的大分子,(B)相关离子的充分过饱和,(C)局部限制分子运动。所有这些都必须在几纳米宽的空间内完成。这种纳米空间排除了大多数多肽和寡糖(a)。水合水外层(纳秒级)在纳米空间壁上的弛豫时间是自由水(皮秒级)的1000倍。这意味着附近水的结构温度较低,从而降低了钙离子和磷酸盐离子的溶解度(B,C)。稳定的离子团簇在纳米空间中比在散装水中更容易形成。厚度为3nm的羟基磷灰石晶体能够存在的5 ~ 6nm的空间称为临界空间。临界空间的形成应根据纤维的直径和纤维的分布,或通过向细丝中展开,以及通过微管和层状结构。
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Nanospace theory for biomineralization.

The precipitation of inorganic crystals from body fluid requires (A) elimination of the macromolecules that inhibit for crystal formation, (B) sufficient supersaturation of the relevant ions, and (C) local restriction of molecular movement. All of these must be accomplished within a space of several nanometers width. Such a nanospace excludes most peptides and oligosaccharides (A). The relaxation time of the outer layer of hydration water (nano second order) on the nanospace wall is 1,000 times longer than that of free water (pico second order). This means that the structure temperature of vicinal water is low, thus the solubilities of calcium ions and phosphate ions are reduced (B,C). Stable ion clusters are formed easier in the nanospace than in the bulk water. The 5-6 nm space in which 3 nm thick hydroxyapatite crystallites can exist should be called critical space. The critical space should be formed according to the fibril diameter and disposition of the fibril or by deployment into the filaments, and by microtubular and lamellar structures.

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