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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Aqueous Poly(amidoamine) Dendrimer G3 and G4 Generations with Several Interior Cores at pHs 5 and 7: A Molecular Dynamics Simulation Study
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Aqueous Poly(amidoamine) Dendrimer G3 and G4 Generations with Several Interior Cores at pHs 5 and 7: A Molecular Dynamics Simulation Study

机译:在pH 5和7下具有多个内芯的含水聚(酰胺基胺)树状聚合物G3和G4世代:分子动力学模拟研究

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摘要

Poly(amidoamine) (PAMAM) dendrimers play an important role in drug delivery systems, because the dendrimers are susceptible to gain unique features with modification of their structure such as changing their terminals or improving their interior core. To investigate the core improvement and the effect of core nature on PAMAM dendrimers, we studied two generations G3 and G4 PAMAM dendrimers with the interior cores of commonly used ethylendiamine (EDA), 1,5-diaminohexane (DAH), and bis(3-aminopropyl) ether (BAPE) solvated in water, as an aqueous dendrimer system, by using molecular dynamics simulation and applying a coarsegrained (CG) dendrimer force field. To consider the electrostatic interactions, the simulations were performed at two protonation states, pHs 5 and 7. The results indicated that the core improvement of PAMAM dendrimers with DAH produces the largest size for G3 and G4 dendrimers at both pHs 5 and 7. The increase in the size was also observed for BAPE core but it was not so significant as that for DAH core. By considering the internal structure of dendrimers, it was found that PAMAM dendrimer shell with DAH core had more cavities than with BAPE core at both pHs 5 and 7. Also the moment of inertia calculations showed that the generation G3 is more open-shaped and has higher structural asymmetry than the generation G4. Possessing these properties by G3, specially due to its structural asymmetry, make penetration of water beads into the dendrimer feasible. But for higher generation G4 with its relatively structural symmetry, the encapsulation efficiency for water molecules can be enhanced by changing its core to DAH or BAPE. It is also observed that for the higher generation G4 the effect of core modification is more profound than G3 because the core modification promotes the structural asymmetry development of G4 more significantly. Comparing the number of water beads that penetrate into the PAMAM dendrimers for EDA, DAH, and BAPE cores indicates a significant increase when their cores have been modified with DAH or BAPE and substantiates the effective influence of the core nature in the dendrimer encapsulation efficiency.
机译:聚(酰胺基胺)(PAMAM)树状聚合物在药物递送系统中起着重要作用,因为树状聚合物易于通过改变其结构(例如改变其末端或改善其内部核心)而获得独特的功能。为了研究核心改进和核心性质对PAMAM树状聚合物的影响,我们研究了两代G3和G4 PAMAM树状聚合物,它们的内部核心为常用的乙二胺(EDA),1,5-二氨基己烷(DAH)和bis(3-通过使用分子动力学模拟并施加粗粒(CG)树枝状聚合物力场,将氨基丙基)醚(BAPE)溶解在水中,作为水性树枝状聚合物系统。为了考虑静电相互作用,在pH值为5和7的两个质子化状态下进行了模拟。结果表明,带有DAH的PAMAM树枝状聚合物的核心改进在pH值为5和7时产生最大的G3和G4树枝状聚合物。 BAPE磁芯的尺寸也有所减小,但没有DAH磁芯的尺寸显着。通过考虑树枝状聚合物的内部结构,发现在pH值为5和7时,带有DAH核的PAMAM树枝状聚合物壳比带有BAPE核的树突壳具有更多的空洞。另外,惯性矩计算表明,G3代更开放,并且具有比G4代更高的结构不对称性。特别是由于G3的结构不对称性,它们具有这些特性,使水珠渗入树枝状聚合物成为可能。但是对于具有相对结构对称性的更高代G4,可以通过将其核心更改为DAH或BAPE来提高水分子的封装效率。还观察到,对于更高代的G4,核心修饰的作用比G3更为深刻,因为核心修饰更显着地促进了G4的结构不对称性发展。比较渗透入PAMAM树枝状聚合物以形成EDA,DAH和BAPE核心的水珠的数量,表明当用DAH或BAPE修饰其核心后,水珠的数量显着增加,并证实了核心性质对树枝状聚合物封装效率的有效影响。

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