有前途的合成双(芳基甲基)丙酮-聚合PCL乳化纳米颗粒具有增强的抗菌/抗氧化功效:体外和体内评价

Q2 Pharmacology, Toxicology and Pharmaceutics
Sally A. Abou Taleb , Shaymaa Abdalla Ismail , Marwan Mohamed , Reda M. Mourad , Hadeer A. El-Hashemy
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引用次数: 2

摘要

近年来,被称为c5 -姜黄素的双(芳基甲基)丙酮药物被公认为姜黄素的新合成替代品,具有强大的生物学效应,可有效地用于治疗多种疾病。方法采用新型的聚合物乳化纳米颗粒(PENS),在其框架内携带可生物降解的聚己内酯(PCL)聚合物基团,作为现代合成的双芳基亚甲基丙酮(1E,4E)-1,5-二(噻吩-2-基)五-1,4二烯-3 -1”(TPO)的载体,具有较高的生物利用度。这些系统是通过研究它们的;包封效率,释放行为,理化评价,TEM和SEM测量,细胞毒性,以及体外和体内生物学研究筛选。结果本品包封率为99.31±2.15% ~ 99.55±2.03%,具有纳米级缓释24 h的性能。TPO乳化纳米颗粒(TPO- enps)对白色念珠菌和巴西曲霉具有良好的抑菌活性和抗氧化活性,对2,2-二苯基-1-苯基水合肼(DPPH)自由基的清除率为177.6μg TE/ mg,高于对照药。F1 '和F2 ' TPO-ENPs对vero细胞是安全的,并且在对照组中证明肝细胞改变和血清ALT水平显著降低。结论新合成的TPO-ENPs具有明显的抗菌/抗氧化/抗炎/镇痛/保肝治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Promising synthesized bis (arylmethylidene) acetone -polymeric PCL emulsified nanoparticles with enhanced antimicrobial/antioxidant efficacy: in-vitro and in-vivo evaluation

Introduction

Recently, bis(arylmethylidene)acetone drugs known as C5-curcumin, were acknowledged for their potent biological effects as a neoteric synthetic alternative to curcumin effectively used to treat many diseases.

Methods

In this study, new polymeric emulsified nanoparticles (PENS) carrying biodegradable polycaprolactone (PCL) polymer moieties within their framework were developed as promising carriers for a modern synthesized bis(arylmethylidene)acetone “(1E,4E)-1,5-di(thiophen-2-yl) penta-1,4dien-3-one” (TPO) with improved bioavailability. Such systems were evaluated by studying their; encapsulation efficiency, release behavior, physicochemical evaluations, TEM and SEM measurements and cytotoxicity, besides the in-vitro and in-vivo biological studies screening.

Results

The results revealed high encapsulation efficiency ranging between 99.31± 2.15 and 99.55 ± 2.03 %, and a sustained release behavior for up to 24 h with nanosized particle size. TPO emulsified nanoparticles (TPO-ENPs) showed effective antimicrobial activity against Candida albicans and Aspergillus brasiliensis as well as antioxidant efficacy with a higher scavenging activity of 177.6μg TE/ mg against free radicals of 2,2-diphenyl-1-picrylhydrazyl hydrate (DPPH) relatively to the control drug. F1’ and F2’ TPO-ENPs were safe on Vero-cells and proved a significant reduction of hepatocellular alterations and serum ALT levels in control groups.

Conclusion

In conclusion, these novel synthesized TPO-ENPs showed pronounced efficacy as antimicrobial/ antioxidant/ anti-inflammatory/ analgesic/ hepatoprotective therapeutic vehicles.

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来源期刊
OpenNano
OpenNano Medicine-Pharmacology (medical)
CiteScore
4.10
自引率
0.00%
发文量
63
审稿时长
50 days
期刊介绍: OpenNano is an internationally peer-reviewed and open access journal publishing high-quality review articles and original research papers on the burgeoning area of nanopharmaceutics and nanosized delivery systems for drugs, genes, and imaging agents. The Journal publishes basic, translational and clinical research as well as methodological papers and aims to bring together chemists, biochemists, cell biologists, material scientists, pharmaceutical scientists, pharmacologists, clinicians and all others working in this exciting and challenging area.
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