Literature DB >> 23727910

Current status and prospects of polyethyleneglycol-modified medicines.

Hiroshi Ishihara1.   

Abstract

Polyethyleneglycol (PEG) compounds have a large hydrogen bonding capability and possess various functions that depend on the length of the chain and conformational diversity. Modification of a drug with PEG is a well-known technology for improving the physicochemical properties and biological responses of a drug. There are many reports about the modification of small molecules with PEG, however, there are no modified small molecule products currently on the market. Several protein products for medical use are commercially available. In this review, the effects of modification with PEG on biopharmaceuticals are described through the comparison of two interferon-α products modified with PEG, one with 12 kDa linear PEG and the other 40 kDa branched PEG. There is one original drug delivery system product, Doxil(®)/Caelyx(®), on the market in which liposomes modified with PEG and encapsulating doxorubicin are stabilized sterically and invisible to the reticuloendothelial system. The benefits of modification with PEG are described here with examples of modified products on the market and used in clinical trials.

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Year:  2013        PMID: 23727910     DOI: 10.1248/bpb.b13-00087

Source DB:  PubMed          Journal:  Biol Pharm Bull        ISSN: 0918-6158            Impact factor:   2.233


  4 in total

1.  Curc-mPEG454, a PEGylated Curcumin Derivative, Improves Anti-inflammatory and Antioxidant Activities: a Comparative Study.

Authors:  Fei Cheng; Yuhe Chen; Zhu Zhan; Yu Liu; Peng Hu; Hong Ren; Huadong Tang; Mingli Peng
Journal:  Inflammation       Date:  2018-03       Impact factor: 4.092

2.  Polyethylene glycol submucosal irrigation: a novel approach to improve visibility during endoscopic submucosal dissection.

Authors:  Vitor Arantes; Takashi Toyonaga; Elias Alfonso Forero Piñeros
Journal:  Endosc Int Open       Date:  2014-07-16

3.  PEGylated Curcumin Derivative Attenuates Hepatic Steatosis via CREB/PPAR-γ/CD36 Pathway.

Authors:  Yu Liu; Fei Cheng; Yuxuan Luo; Zhu Zhan; Peng Hu; Hong Ren; Huadong Tang; Mingli Peng
Journal:  Biomed Res Int       Date:  2017-07-09       Impact factor: 3.411

4.  Intratracheal Administration of siRNA Triggers mRNA Silencing in the Lung to Modulate T Cell Immune Response and Lung Inflammation.

Authors:  Bruce Ng; Tanesha Cash-Mason; Yi Wang; Jessica Seitzer; Julja Burchard; Duncan Brown; Vadim Dudkin; Joseph Davide; Vasant Jadhav; Laura Sepp-Lorenzino; Pedro J Cejas
Journal:  Mol Ther Nucleic Acids       Date:  2019-02-26
  4 in total

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