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首页> 外文期刊>International Nano Letters >Molecular interactions between PAMAM dendrimer and some medicines that suppress the growth of hepatitis virus (Adefovir, Entecavir, Telbivudine, Lamivudine, Tenofovir): a theoretical study
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Molecular interactions between PAMAM dendrimer and some medicines that suppress the growth of hepatitis virus (Adefovir, Entecavir, Telbivudine, Lamivudine, Tenofovir): a theoretical study

机译:PAMAM树状大分子与某些抑制肝炎病毒生长的药物之间的分子相互作用(阿德福韦,恩替卡韦,替比夫定,拉米夫定,替诺福韦):一项理论研究

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Viral hepatitis is a common viral infection, can be dangerous, involves the body and leads to inflammation and destruction of tissue and normal function of the liver. Viral hepatitis is a major cause of premature death in human beings. According to the World Health Organization, it was assumed that there are more than 385 and 170 million carriers of hepatitis B and C in the world, respectively, and more than a million deaths occur due to hepatitis each year. There are a few specific drugs to treat hepatitis. To overcome some of these problems, nanoparticle systems containing organic and inorganic compounds are used for pharmaceutical purpose. One of these nanostructures is dendrimer. Dendrimers are repetitively branched nanomolecules. In this study, a theoretical study of the structural probabilities of nanostructure complex formation between polyamidoamine dendrimers (PAMAM) and some drugs that suppress the growth of hepatitis virus (Adefovir, Entecavir, Telbivudine, Lamivudine, Tenofovir: 1 – 5 ) has been carried out. The possibility of drug release, drug delivery and drug separation by PAMAM has been investigated. MMFF94 method has been used to provide results and medical solutions. In all the drug–PAMAM complexes, the relative energy levels of the complex energy have been calculated by the RHF/PM6 method. Medicine delivery, release process of drugs and separation of drugs from the in vivo and in vitro real sample were the main enforceable results obtained from this theoretical study of medicines 1 – 5 & PAMAM. This model has predicted an imaginary method to separate the medicines from real samples and study the drug release process of the discussed complexes. The imaginary separation procedure that suppresses the growth of hepatitis virus– 1 – 5 medicine mixture in in vitro samples is discussed. It is possible to collect compounds 1 and 2 by PAMAM and separate Adefovir, Telbivudine and Tenofovir ( 3 – 5 ) from the mixture of the sample of medicines 1 – 5 .
机译:病毒性肝炎是一种常见的病毒感染,可能很危险,会累及人体,并导致炎症和组织破坏以及肝脏的正常功能。病毒性肝炎是人类过早死亡的主要原因。根据世界卫生组织的估计,世界上分别有超过385和1.7亿的乙型和丙型肝炎携带者,每年因肝炎导致的死亡人数超过一百万。有几种治疗肝炎的特殊药物。为了克服这些问题中的一些问题,将包含有机和无机化合物的纳米颗粒系统用于药物目的。这些纳米结构之一是树枝状聚合物。树枝状聚合物是重复分支的纳米分子。在这项研究中,对聚酰胺酰胺树状大分子(PAMAM)和某些抑制肝炎病毒生长的药物(阿德福韦,恩替卡韦,替比夫定,拉米夫定,替诺福韦:1-5)进行了理论研究。 。已经研究了PAMAM释放药物,递送药物和分离药物的可能性。 MMFF94方法已用于提供结果和医疗解决方案。在所有药物-PAMAM复合物中,复合能的相对能级已通过RHF / PM6方法计算出。从这种药物1 – 5和PAMAM的理论研究得出的主要可执行结果是药物递送,药物释放过程以及从体内和体外真实样品中分离药物。该模型预测了一种将药物与真实样品分离并研究所讨论复合物的药物释放过程的假想方法。讨论了一种假想的分离程序,该程序可抑制体外样品中1-5种肝炎病毒混合物的生长。可以通过PAMAM收集化合物1和2,并从药物1-5的混合物中分离出阿德福韦,替比夫定和替诺福韦(3-5)。

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