Novel Strategies Enhancing Bioavailability and Therapeutical Potential of Silibinin for Treatment of Liver Disorders.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2024-10-19 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S483140
Michal Selc, Radka Macova, Andrea Babelova
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引用次数: 0

Abstract

Silibinin, a bioactive component found in milk thistle extract (Silybum marianum), is known to have significant therapeutic potential in the treatment of various liver diseases. It is considered a key element of silymarin, which is traditionally used to support liver function. The main mechanisms of action of silibinin are attributed to its antioxidant properties protecting liver cells from damage caused by free radicals. Experimental studies conducted in vitro and in vivo have confirmed its ability to inhibit inflammatory and fibrotic processes, as well as promote the regeneration of damaged liver tissue. Therefore, silibinin represents a promising tool for the treatment of liver diseases. Since the silibinin molecule is insoluble in water and has poor bioavailability in vivo, new perspectives on solving this problem are being sought. The two most promising approaches are the water-soluble derivative silibinin-C-2',3-dihydrogen succinate, disodium salt, and the silibinin-phosphatidylcholine complex. Both drugs are currently under evaluation in liver disease clinical trials. Nevertheless, the mechanism underlying silibinin biological activity is still elusive and its more detailed understanding would undoubtedly increase its potential in the development of effective therapeutic strategies against liver diseases. This review is focused on the therapeutic potential of silibinin and its derivates, approaches to increase the bioavailability and the benefits in the treatment of liver diseases that have been achieved so far. The review discusses the relevant in vitro and in vivo studies that investigated the protective effects of silibinin in various forms of liver damage.

提高治疗肝脏疾病的西利宾生物利用度和治疗潜力的新策略。
水飞蓟素是奶蓟提取物(Silybum marianum)中的一种生物活性成分,在治疗各种肝病方面具有显著的治疗潜力。它被认为是水飞蓟素的关键成分,而水飞蓟素传统上用于支持肝功能。水飞蓟素的主要作用机制是其抗氧化特性,可保护肝细胞免受自由基的损害。体外和体内的实验研究证实,它能够抑制炎症和纤维化过程,并促进受损肝组织的再生。因此,丝利比宁是一种治疗肝脏疾病的有前途的工具。由于丝利比宁分子不溶于水,在体内的生物利用度较低,因此人们正在寻找解决这一问题的新视角。最有前景的两种方法是水溶性衍生物丝利宾-C-2',3-二氢琥珀酸二钠盐和丝利宾-磷脂酰胆碱复合物。这两种药物目前正在肝病临床试验中进行评估。然而,丝利宾素生物活性的机理仍然难以捉摸,对其进行更详细的了解无疑将提高其在开发有效肝病治疗策略方面的潜力。本综述的重点是丝核苷及其衍生物的治疗潜力、提高生物利用度的方法以及迄今为止在治疗肝病方面取得的疗效。综述讨论了调查丝利宾对各种形式肝损伤的保护作用的相关体外和体内研究。
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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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