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生理条件下完全可分散的聚乙二醇化金纳米颗粒:用精确控制的聚乙二醇- b -聚胺修饰金纳米颗粒

Completely dispersible PEGylated gold nanoparticles under physiological conditions: modification of gold nanoparticles with precisely controlled PEG-b-polyamine.

作者信息

Miyamoto Daisuke, Oishi Motoi, Kojima Keiji, Yoshimoto Keitaro, Nagasaki Yukio

机构信息

Graduate School of Pure and Applied Sciences, University of Tsukuba.

出版信息

Langmuir. 2008 May 6;24(9):5010-7. doi: 10.1021/la703813f. Epub 2008 Apr 4.

Abstract

A novel water-soluble, biocompatible polymer, poly(ethylene glycol)-block-poly((2-N,N-dimethylamino)ethyl methacrylate) (PEG-b-PAMA), possessing controlled molecular weight with a narrow molecular weight distribution, was synthesized by the atom-transfer radical polymerization (ATRP) method. PEG-b-PAMA having a short PAMA chain length was successfully synthesized under suitable polymerization conditions. Gold nanoparticles (GNPs) were modified using PEG-b-PAMA prepared under a variety of PEGylation conditions. Under alkaline conditions (pH >10) and an [N]/[GNP] ratio of more than 3300, the PEGylated GNPs (PEG-GNPs) showed complete dispersion stability, avoiding coagulation. The amino groups of the PAMA segment of the block copolymers were completely deprotonated above pH 10. This means that PEG-b-PAMA interacted with the GNP surface via multipoint coordination of the tertiary amino groups of PAMA, not electrostatically. The effect of the number of amino groups in the PAMA segment on GNP surface modifications was investigated by zeta potential and dynamic light scattering (DLS) measurements. When the PEG-GNPs were prepared in excess polymer solution, almost the same diameter was observed regardless of the PAMA chain length. After the PEG-GNPs were purified by centrifugation, the zeta potentials of all PEG-GNPs were shielded to almost 0 mV, indicating the effective modifications of the GNP surface by PEG-b-PAMA regardless of the chain length. However, the particle size and particle size distribution of the purified PEG-GNPs were strongly affected by the PAMA chain length. PEG-GNPs with longer PAMA segments underwent coagulation after purification, whereas PEG-GNPs with shorter PAMA segments increased their dispersion stability. The experimental results of the thermal gravimetric analysis confirmed that the PEG density on the GNP surface increased as the AMA units decreased to 3. Thus, the dispersion stability depended significantly on the PEG density on the GNP surface. GNPs modified with PEG-b-PAMA having short AMA units showed excellent dispersion stability under a variety of pH conditions. The excellent dispersion stability of the obtained PEG-GNP was also confirmed both in bovine serum albumin (BSA) solution and 95% human serum.

摘要

通过原子转移自由基聚合(ATRP)方法合成了一种新型的水溶性、生物相容性聚合物,聚(乙二醇)-嵌段-聚(甲基丙烯酸(2-N,N-二甲基氨基)乙酯)(PEG-b-PAMA),其分子量可控且分子量分布窄。在合适的聚合条件下成功合成了PAMA链长较短的PEG-b-PAMA。使用在各种聚乙二醇化条件下制备的PEG-b-PAMA对金纳米颗粒(GNP)进行修饰。在碱性条件(pH>10)且[N]/[GNP]比大于3300时,聚乙二醇化的GNP(PEG-GNP)表现出完全的分散稳定性,避免了凝聚。在pH 10以上,嵌段共聚物PAMA链段的氨基完全去质子化。这意味着PEG-b-PAMA通过PAMA叔氨基的多点配位与GNP表面相互作用,而非静电作用。通过zeta电位和动态光散射(DLS)测量研究了PAMA链段中氨基数量对GNP表面修饰的影响影响。当在过量聚合物溶液中制备PEG-GNP时,无论PAMA链长如何,观察到的直径几乎相同。通过离心纯化PEG-GNP后,所有PEG-GNP的zeta电位都被屏蔽到几乎0 mV,表明无论链长如何,PEG-b-PAMA都有效地修饰了GNP表面。然而,纯化后的PEG-GNP的粒径和粒径分布受PAMA链长的强烈影响。PAMA链段较长的PEG-GNP在纯化后发生凝聚,而PAMA链段较短的PEG-GNP则提高了其分散稳定性。热重分析的实验结果证实,随着AMA单元减少到3,GNP表面的PEG密度增加。因此,分散稳定性显著取决于GNP表面的PEG密度。用具有短AMA单元的PEG-b-PAMA修饰的GNP在各种pH条件下均表现出优异的分散稳定性。在牛血清白蛋白(BSA)溶液和95%人血清中也证实了所得PEG-GNP具有优异的分散稳定性。

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