生物医学用纳米颗粒来源于天然生物分子:单宁酸和精氨酸。

IF 3.9 3区 工程技术 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Biomedicines Pub Date : 2025-01-16 DOI:10.3390/biomedicines13010209
Mehtap Sahiner, Selin S Suner, Nurettin Sahiner
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引用次数: 0

摘要

背景/目的:单宁酸(tanic acid, TA)是一种众所周知的天然酚酸,由十种没食子酸通过酯键相互连接而成,除具有抗菌和抗癌特性外,还具有优异的抗氧化性能。精氨酸(ARG)是一种在生理pH值下带正电的氨基酸,因为其侧链富含氮。方法:以甲醛为连接剂,通过TA与ARG之间的曼尼希缩合反应,制备了TA:ARG = 1:1、1:2和1:3三个摩尔比的聚单宁酸-co-精氨酸(p(TA-co-ARG))颗粒。结果:获得了300 ~ 1000 nm的p(TA-co-ARG)颗粒,表面光滑。FT-IR分析证实TA和ARG成分中含有丰富的官能团-OH、-NH2和-COOH。通过增加p(TA-co-ARG)颗粒中ARG的比例,颗粒的等电点(IEP)由pH 4.98提高到pH 7.30。通过没食子酸(GA)和迷迭香酸(RA)当量测定p(TA-co- arg)颗粒的抗氧化能力表明,颗粒具有浓度依赖性,抗氧化能力随TA含量的增加而增加。p(TA-co-ARG)颗粒(2 mg/mL)摩尔比为1:1和1:2时α-葡萄糖苷酶抑制率分别为91.3±3.1%和77.6±12.0%。有趣的是,p(TA-co-ARG)(1:3比例)对大肠杆菌(ATCC 8739)和金黄色葡萄球菌(ATCC 6538)具有显著的抗菌效果。此外,1000 mg/mL浓度的p(TA-co-ARG)颗粒对L929成纤维细胞的毒性均为80%左右,并随着p(TA-co-ARG)颗粒ARG含量的增加而增加。结论:p(TA-co-ARG)作为天然生物材料具有重要的生物医学应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Nanoparticles for Biomedical Use Derived from Natural Biomolecules: Tannic Acid and Arginine.

Background/Objectives: Tannic acid (TA) is a well-known natural phenolic acid composed of ten gallic acids linked to each other with ester bonding possessing excellent antioxidant properties in addition to antimicrobial and anticancer characteristics. Arginine (ARG) is a positively charged amino acid at physiological pH because of nitrogen-rich side chain. Method: Here, poly(tannic acid-co-arginine) (p(TA-co-ARG)) particles at three mole ratios, TA:ARG = 1:1, 1:2, and 1:3, were prepared via a Mannich condensation reaction between TA and ARG by utilizing formaldehyde as a linking agent. Results: The p(TA-co-ARG) particles in 300-1000 nm size range with smooth surfaces visualized via SEM analysis were attained. Abundant numbers of functional groups, -OH, -NH2, and -COOH stemming from TA and ARG constituent confirmed by FT-IR analysis. The isoelectric point (IEP) of the particles increased from pH 4.98 to pH 7.30 by increasing the ARG ratios in p(TA-co-ARG) particles. The antioxidant capacity of p(TA-co-ARG) particles via gallic acid (GA) and rosmarinic acid (RA) equivalents tests revealed that particles possess concentration-dependent antioxidant potency and increased by TA content. The α-glucosidase inhibition of p(TA-co-ARG) particles (2 mg/mL) 1:1 and 1:2 mole ratios revealed significant enzyme inhibition ability, e.g., 91.3 ± 3.1% and 77.6 ± 12.0%. Interestingly, p(TA-co-ARG) (1:3 ratio) possessed significant antibacterial effectiveness against Escherichia coli (ATCC 8739) and Staphylococcus aureus (ATCC 6538) bacteria. Furthermore, all p(TA-co-ARG) particles at 1000 mg/mL concentration showed >80% toxicity on L929 fibroblast cells and increased as ARG content of p(TA-co-ARG) particles is increased. Conclusions: p(TA-co-ARG) showed significant potential as natural biomaterials for biomedical use.

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来源期刊
Biomedicines
Biomedicines Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
5.20
自引率
8.50%
发文量
2823
审稿时长
8 weeks
期刊介绍: Biomedicines (ISSN 2227-9059; CODEN: BIOMID) is an international, scientific, open access journal on biomedicines published quarterly online by MDPI.
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