Recent advances in paclitaxel-based self-delivery nanomedicine for cancer therapy Review


Authors: Zhou, M.; Han, S.; Aras, O.; An, F.
Review Title: Recent advances in paclitaxel-based self-delivery nanomedicine for cancer therapy
Abstract: Paclitaxel (PTX) is the first natural plant-derived chemotherapeutic drug approved by the Food and Drug Administration. However, the clinical applications of PTX are limited by some drawbacks, such as poor water solubility, rapid blood clearance, nonspecific distribution, and adverse side effects. Nanocarriers have made important contributions to drug delivery and cancer therapy in recent years. However, low drug loading capacity, nanocarrier excipients-induced toxicity or immunogenicity, and complicated synthesis technologies pose a challenge for the clinical application of nanocarriers. To address these issues, the self-delivery nanomedicine (SDNs), in which pure drug molecules directly self-assemble into nanomedicine, have been developed for drug delivery and enhancing antitumor efficacy. In this review, we comprehensively summarize the recent advances in PTX-based SDNs for cancer therapy. First, the self-assembly strategies to develop pure PTX nanodrugs are discussed. Then, the emerging strategies of co-assembly PTX and other therapeutic agents for effective combination therapy are presented, composing of combination chemotherapy, chemo-photothermal therapy, chemo-photodynamic therapy, chemo-immunotherapy, and chemo-gene therapy. Finally, the limitations and future outlook of SDNs are discussed. The rational design of these unique nanoplatforms may make a new direction to develop highly efficient drug delivery systems for cancer therapy. © 2021 Bentham Science Publishers.
Keywords: paclitaxel; cancer therapy; nanomedicine; self-assembly; carrier-free; sdns; self-delivery
Journal Title: Current Medicinal Chemistry
Volume: 28
Issue: 31
ISSN: 0929-8673
Publisher: Bentham Science Publishers  
Date Published: 2021-09-01
Start Page: 6358
End Page: 6374
Language: English
DOI: 10.2174/0929867327666201111143725
PUBMED: 33176629
PROVIDER: scopus
DOI/URL:
Notes: Review -- Source: Scopus
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  1. Omer Aras
    75 Aras