Progress of albumin-polymer conjugates as efficient drug carriers

被引：3

作者：

Raveendran, Radhika ^{[1
]}

Xu, You Dan ^{[1
]}

Joshi, Nidhi ^{[1
]}

Stenzel, Martina H. ^{[1
]}

机构：

[1] Univ New South Wales, Sch Chem, Sydney, NSW 2052, Australia

来源：

PURE AND APPLIED CHEMISTRY | 2022年 / 94卷 / 08期

关键词：

albumin; drug delivery; IUPAC Distinguished Women in Chemistry and Chemical Engineering; nanoparticles; polymers; proteins; women in science; HUMAN-SERUM-ALBUMIN; DOXORUBICIN PRODRUG; CANCER-CELLS; PROTEIN; BINDING; NANOPARTICLES; DELIVERY; TUMOR; PERMEABILITY; RETENTION;

D O I：

10.1515/pac-2021-2006

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Albumin is a protein that has garnered wide attention in nanoparticle-based drug delivery of cancer therapeutics due to its natural abundance and unique cancer-targeting ability. The propensity of albumin to naturally accumulate in tumours, further augmented by the incorporation of targeting ligands, has made the field of albumin-polymer conjugate development a much pursued one. Polymerization techniques such as RAFT and ATRP have paved the path to incorporate various polymers in the design of albumin-polymer hybrids, indicating the advancement of the field since the first instance of PEGylated albumin in 1977. The synergistic combination of albumin and polymer endows manifold features to these macromolecular hybrids to evolve as next generation therapeutics. The current review is successive to our previously published review on drug delivery vehicles based on albumin-polymer conjugates and aims to provide an update on the progress of albumin-polymer conjugates. This review also highlights the alternative of exploring albumin-polymer conjugates formed via supramolecular, non-covalent interactions. Albumin-based supramolecular polymer systems provide a versatile platform for functionalization, thereby, holding great potential in enhancing cytotoxicity and controlled delivery of therapeutic agents.

引用

页码：983 / 997

页数：15

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