含5-氟尿嘧啶和氯喹纳米颗粒对卡斯特兰棘阿米巴活性的评价

IF 1.4 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Balsam Qubais Saeed , Mutasem Rawas Qalaji , Noor Akbar , Ruqaiyyah Siddiqui , Cagliani Roberta , Shaista Manzoor , Jibran Sualeh Muhammad , Ahmed Omar Adrees , Rula Al-Shahrabi , Naveed Ahmed Khan
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引用次数: 4

摘要

棘阿米巴是一种机会致病菌,可引起威胁视力的棘阿米巴角膜炎(AK)。以往的研究建议使用氯喹(CQ)和5-氟尿嘧啶(5FU)作为抗棘阿米巴药物。本研究的目的是确定使用5FU和CQ纳米颗粒(NP)制剂对属于T4基因型的castellanii的益处,并评估它们的抗棘阿米巴特性。采用改进的纳米沉淀法合成了三批5FU纳米颗粒(5FU- np),采用改进的双乳法合成了CQ纳米颗粒(CQ- np)。对合成的纳米颗粒进行了生物测定,以研究其对castellanii的杀阿米巴、抑制阿米巴、抗胞囊和抗胞囊作用以及细胞毒性。使用人角质细胞(HaCaT)进行细胞毒性试验,以确定CQ和5FU纳米制剂对宿主细胞的影响。浓度为60µM的5FU-NP对变形虫与人细胞系的结合具有明显的抑制作用,且主要在成囊期具有显著的预防作用。此外,与游离5FU相比,5FU- np的细胞毒性和致病性更低。另一方面,在相同浓度下,CQ和CQ- np对阿米巴结合人细胞的抑制作用较差,对成囊期的抑制作用不明显。用CQ和CQ- np治疗后,出现了中度的人体细胞损伤。综上所述,5FU有潜力作为抗棘阿米巴原虫的抗阿米巴药物,最好是作为纳米制剂来增强其活性并降低其细胞毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of nanoparticles with 5-fluorouracil and chloroquine on Acanthamoeba castellanii activity

Acanthamoeba is opportunistic pathogens that cause vision-threatening Acanthamoeba keratitis (AK). Previous studies proposed the use of chloroquine (CQ) and 5-fluorouracil (5FU) as anti-Acanthamoeba agents. The objective of this study was to determine the benefit of using 5FU and CQ nanoparticles (NP) formulations against A. castellanii that belonging to the T4 genotype and evaluate their anti-Acanthamoebic characteristic. Triplicate batches of 5FU nanoparticles (5FU-NP) were synthesized by using a modified nanoprecipitation method, while CQ nanoparticles (CQ-NP) synthesized using a modified double emulsion method. The synthesized nanoparticles were subjected to biological assays to investigate their amoebicidal, amoebistatic, anti-encystation, and anti-excystation effects against A. castellanii, as well as cell cytotoxicity. Cytotoxicity assays were performed using human keratinocyte cells (HaCaT) to determine the effect of CQ and 5FU nanoformulations on host cells. 5FU-NP with a concentration of 60 µM showed significant inhibition to amoeba binding into human cell lines and remarkable prevention mainly during the encystation stage. Moreover, 5FU-NP resulted in less cytotoxicity and pathogenicity when compared with the free 5FU. On the other hand, CQ and CQ-NP, at the same concentration, showed poor inhibition to amoeba binding into human cells and insignificant prevention to encystation stage. Moderate human cells damage was resulted following their treatment with CQ and CQ-NP. In conclusion, 5FU may have the potential as an antiamoebic agent against Acanthamoeba spp. preferably as a nanoformulation to enhance its activity and reduce its cytoxicity.

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来源期刊
CiteScore
2.90
自引率
0.00%
发文量
51
审稿时长
63 days
期刊介绍: The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are: • the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances • intermediary metabolism and bioenergetics • drug target characterization and the mode of action of antiparasitic drugs • molecular and biochemical aspects of membrane structure and function • host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules. • analysis of genes and genome structure, function and expression • analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance. • parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules • parasite programmed cell death, development, and cell division at the molecular level.
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