Doxorubicin Conjugates: An Efficient Approach for Enhanced Therapeutic Efficacy with Reduced Side Effects.

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Assay and drug development technologies Pub Date : 2023-05-01 Epub Date: 2023-04-20 DOI:10.1089/adt.2022.102
Pallavi Sandal, Lakshmi Kumari, Preeti Patel, Amrinder Singh, Dilpreet Singh, Ghanshyam Das Gupta, Balak Das Kurmi
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引用次数: 0

Abstract

Continuous drug delivery modification is the scientific approach and is a basic need for the efficient therapeutic efficacy of active drug molecules. Polymer-drug conjugates have long been a hallmark of the drug delivery sector, with various conjugates on the market or in clinical trials. Improved drug solubilization, extended blood circulation, decreased immunogenicity, controlled release behavior, and increased safety are the advantages of conjugating drugs to the polymeric carrier like polyethylene glycol (PEG). Polymer therapies have evolved over the last decade, resulting in polymer-drug conjugates with diverse topologies and chemical properties. Traditional nondegradable polymeric carriers like PEG and hydroxy propyl methacrylate have been clinically employed to fabricate polymer-drug conjugates. Still, functionalized polymer-drug conjugates are increasingly being used to increase localized drug delivery and ease of removal. Researchers have developed multifunctional carriers that can "see and treat" patients using medicinal and diagnostic chemicals. This review focused on the various conjugation approaches for attaching the doxorubicin to different polymers to achieve enhanced therapeutic efficacy, that is, increased bioavailability and reduced adverse effects.

多柔比星共轭物:提高疗效、减少副作用的有效方法。
连续给药改性是一种科学方法,也是活性药物分子发挥高效疗效的基本需要。聚合物-药物共轭物一直以来都是给药领域的标志性产品,各种共轭物已经上市或正在进行临床试验。将药物与聚乙二醇(PEG)等聚合物载体共轭可提高药物溶解度、延长血液循环、降低免疫原性、控制释放行为以及增加安全性。在过去的十年中,聚合物疗法不断发展,产生了具有不同拓扑结构和化学性质的聚合物-药物共轭物。传统的不可降解聚合物载体,如 PEG 和甲基丙烯酸羟丙酯,已被临床用于制造聚合物-药物共轭物。不过,功能化聚合物-药物共轭物正被越来越多地用于增加局部给药和易于清除。研究人员已开发出多功能载体,可利用药用和诊断化学品 "看病治病"。本综述重点介绍将多柔比星附着在不同聚合物上的各种共轭方法,以达到增强疗效的目的,即提高生物利用度和减少不良反应。
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来源期刊
Assay and drug development technologies
Assay and drug development technologies 医学-生化研究方法
CiteScore
3.60
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: ASSAY and Drug Development Technologies provides access to novel techniques and robust tools that enable critical advances in early-stage screening. This research published in the Journal leads to important therapeutics and platforms for drug discovery and development. This reputable peer-reviewed journal features original papers application-oriented technology reviews, topical issues on novel and burgeoning areas of research, and reports in methodology and technology application. ASSAY and Drug Development Technologies coverage includes: -Assay design, target development, and high-throughput technologies- Hit to Lead optimization and medicinal chemistry through preclinical candidate selection- Lab automation, sample management, bioinformatics, data mining, virtual screening, and data analysis- Approaches to assays configured for gene families, inherited, and infectious diseases- Assays and strategies for adapting model organisms to drug discovery- The use of stem cells as models of disease- Translation of phenotypic outputs to target identification- Exploration and mechanistic studies of the technical basis for assay and screening artifacts
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