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聚乙二醇替代物在克服药物递送和生物偶联中聚乙二醇免疫原性方面的重要性。

The Importance of Poly(ethylene glycol) Alternatives for Overcoming PEG Immunogenicity in Drug Delivery and Bioconjugation.

作者信息

Hoang Thi Thai Thanh, Pilkington Emily H, Nguyen Dai Hai, Lee Jung Seok, Park Ki Dong, Truong Nghia P

机构信息

Biomaterials and Nanotechnology Research Group, Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City 758307, Vietnam.

Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria 3052, Australia.

出版信息

Polymers (Basel). 2020 Feb 2;12(2):298. doi: 10.3390/polym12020298.

Abstract

Poly(ethylene glycol) (PEG) is widely used as a gold standard in bioconjugation and nanomedicine to prolong blood circulation time and improve drug efficacy. The conjugation of PEG to proteins, peptides, oligonucleotides (DNA, small interfering RNA (siRNA), microRNA (miRNA)) and nanoparticles is a well-established technique known as PEGylation, with PEGylated products have been using in clinics for the last few decades. However, it is increasingly recognized that treating patients with PEGylated drugs can lead to the formation of antibodies that specifically recognize and bind to PEG (i.e., anti-PEG antibodies). Anti-PEG antibodies are also found in patients who have never been treated with PEGylated drugs but have consumed products containing PEG. Consequently, treating patients who have acquired anti-PEG antibodies with PEGylated drugs results in accelerated blood clearance, low drug efficacy, hypersensitivity, and, in some cases, life-threatening side effects. In this succinct review, we collate recent literature to draw the attention of polymer chemists to the issue of PEG immunogenicity in drug delivery and bioconjugation, thereby highlighting the importance of developing alternative polymers to replace PEG. Several promising yet imperfect alternatives to PEG are also discussed. To achieve asatisfactory alternative, further joint efforts of polymer chemists and scientists in related fields are urgently needed to design, synthesize and evaluate new alternatives to PEG.

摘要

聚乙二醇(PEG)在生物偶联和纳米医学中被广泛用作金标准,以延长血液循环时间并提高药物疗效。将PEG与蛋白质、肽、寡核苷酸(DNA、小干扰RNA(siRNA)、微小RNA(miRNA))和纳米颗粒进行偶联是一种成熟的技术,称为聚乙二醇化,聚乙二醇化产品在过去几十年中一直在临床中使用。然而,越来越多的人认识到,用聚乙二醇化药物治疗患者会导致形成特异性识别并结合PEG的抗体(即抗PEG抗体)。在从未接受过聚乙二醇化药物治疗但食用过含PEG产品的患者中也发现了抗PEG抗体。因此,用聚乙二醇化药物治疗已产生抗PEG抗体的患者会导致血液清除加速、药物疗效降低、过敏反应,在某些情况下还会出现危及生命的副作用。在这篇简要综述中,我们整理了近期文献,以引起聚合物化学家对药物递送和生物偶联中PEG免疫原性问题的关注,从而突出开发替代聚合物以取代PEG的重要性。还讨论了几种有前景但并不完美的PEG替代品。为了获得令人满意的替代品,迫切需要聚合物化学家和相关领域的科学家进一步共同努力,设计、合成和评估PEG的新替代品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2353/7077443/65c89835e1b9/polymers-12-00298-g001.jpg

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