从玫瑰果提取物中合成抗hiv感染的AuNPs

Pooriya Khademi-Az, Ehi, J. Moghaddam, Roozbeh Khademi-Az, Sayed-Saeed Veradi-Esfahani, Esmaeil Shahabi-Satlsar
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Rosa canina fruit extract, can reduce initial gold salt – chloroauric acid – and produce gold colloid. The major components of this plant are Vitispiran, 5-Methyl-3-hexanone, 2-Heptanone, Hexadecanoic and Dodecanoic acid, Linolic acid, α-E-Acaridial, Myristic acid, Benzaldehyde, α-pinene, 2-pentylfuran, 2,4-Heptadienal, 1,4-Epoxy-p-menthane, Salicylaldehyde, 2-Heptenol and Linalool [6]. In this research, nanoparticles were produced via a novel green method and capped with Rosa canina fruit extract. Then, the antiretroviral effects of these nanoparticles were investigated. Size stability of AuNPs in physiological condition (pH = 7.4) is the necessary condition for their application in medicine [7]. The stability of AuNPs produced using Rosa canina fruit extract and nanoparticles produced through the conventional sodium citrate reducing agent in pH = 7.4 was thus compared. 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引用次数: 1

摘要

AuNPs因其高生物相容性和可调节的表面等离子体共振(SPR),多年来一直是研究人员关注的焦点[1]。近年来,许多研究通过绿色合成技术,即利用植物生产AuNPs[2]。绿色合成方法既环保又提高了AuNPs的生物相容性[3]。导致各种金纳米颗粒特性差异最大的一个因素是合成aunp及其表面化合物的大小[4]。Rosa canina果实提取物具有免疫调节特性,可能用于治疗免疫缺陷疾病[5]。玫瑰果提取物,可降低初始金盐-氯金酸,生成金胶体。该植物的主要成分为维地螺烷、5-甲基-3-己酮、2-庚酮、十六烷酸和十二烷酸、亚油酸、α- e -心木苷、肉豆汁酸、苯甲醛、α-蒎烯、2-戊基呋喃、2,4-庚二烯、1,4-环氧-对甲烷、水杨醛、2-庚烯醇和芳樟醇[6]。在本研究中,通过一种新颖的绿色方法制备纳米颗粒,并以犬玫瑰果实提取物覆盖。然后,研究了这些纳米颗粒的抗逆转录病毒作用。生理条件下(pH = 7.4) AuNPs的尺寸稳定性是其在医学上应用的必要条件[7]。比较了在pH = 7.4的条件下,用玫瑰果提取物和常规柠檬酸钠还原剂制备纳米颗粒制备的AuNPs的稳定性。人类免疫缺陷病毒(HIV-1)进入人体和血液循环系统后,其表面糖蛋白gp120和gp41与t淋巴细胞表面的CD4和CCR5等受体结合。通过将其衣壳送入t淋巴细胞,这种病毒将其RNA与酶(如逆转录酶、整合酶和蛋白酶)一起诱导进入细胞,允许它们开始一项操作,迫使t细胞产生新的艾滋病毒。由于这种疾病的高感染率,抗逆转录病毒药物被用于控制其发展。这些药物大多是转录酶抑制剂[8]、整合酶抑制剂[9]和蛋白酶抑制剂[10],但由于HIV对药物的耐药性,它们不能完全有效。本研究的目的是使用新的还原剂犬玫瑰果提取物第6卷第3期2017
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Creating Anti-HIV-Infection effect by Synthesis of AuNPs from Rosa canina L. Fruit Extract
AuNPs have been in the focal point of researchers’ attention for years because of high biocompatibility and adjustable surface plasmon resonance (SPR) [1]. In the recent years, many studies have been performed in producing AuNPs via green synthesis techniques, i.e. use of plants for producing AuNPs [2]. Green synthesis methods are eco-friendly and increase the biocompatibility of AuNPs [3]. A factor that gives rise to the highest difference between various gold nanoparticle characteristics is the size of synthesized AuNPs and their superficial compounds [4]. Rosa canina fruit extract has immunomodulatory characteristics with probable potential to be used in treatment of immunodeficiency diseases [5]. Rosa canina fruit extract, can reduce initial gold salt – chloroauric acid – and produce gold colloid. The major components of this plant are Vitispiran, 5-Methyl-3-hexanone, 2-Heptanone, Hexadecanoic and Dodecanoic acid, Linolic acid, α-E-Acaridial, Myristic acid, Benzaldehyde, α-pinene, 2-pentylfuran, 2,4-Heptadienal, 1,4-Epoxy-p-menthane, Salicylaldehyde, 2-Heptenol and Linalool [6]. In this research, nanoparticles were produced via a novel green method and capped with Rosa canina fruit extract. Then, the antiretroviral effects of these nanoparticles were investigated. Size stability of AuNPs in physiological condition (pH = 7.4) is the necessary condition for their application in medicine [7]. The stability of AuNPs produced using Rosa canina fruit extract and nanoparticles produced through the conventional sodium citrate reducing agent in pH = 7.4 was thus compared. After the human immunodeficiency virus (HIV-1) enters the body and the blood circulatory system, its superficial glycoproteins, gp120 and gp41, bind with receptors like CD4 and CCR5 on the surface of T-Lymphocytes. By sending its capsid into T-lymphocytes, this virus inducts its RNA together with enzymes, such as reverse transcriptase, integrase and protease into the cell, allowing them to start an operation that will force the T-cells to produce new HIVs. Because of the high infection volume of this disease, antiretroviral drugs are employed to control its advance. Most of these drugs are transcriptase inhibitors [8], integrase inhibitors [9] and protease inhibitors [10], although they cannot be completely effective, because of HIV’s resistance to drugs. The purpose of this study was to use the new reducing agent Rosa canina fruit extractto Volume 6 Issue 3 2017
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