Emerging nanomedicines of paclitaxel for cancer treatment
Malignant tumor is still a leading threat to human health. Despite the rapid development of targeted therapeutic strategies, any treatment specifically acting on single target would inevitably suffer from tumor resistance, largely due to the genetic instability and variability of tumor cells. Thus,...
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Veröffentlicht in: | Journal of controlled release 2022-02, Vol.342, p.280-294 |
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Sprache: | eng |
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Zusammenfassung: | Malignant tumor is still a leading threat to human health. Despite the rapid development of targeted therapeutic strategies, any treatment specifically acting on single target would inevitably suffer from tumor resistance, largely due to the genetic instability and variability of tumor cells. Thus, traditional therapies such as broad-spectrum chemotherapy would certainly occupy an important position in clinical cancer therapy. Nevertheless, most chemotherapeutic drugs have long been criticized for unsatisfactory therapeutic efficacy with severe off-target toxicity. Although several chemotherapeutic nanomedicines with improved therapeutic safety have been applied in clinics, the therapeutic outcomes still do not fulfill expectation. To address this challenge, enormous efforts have been devoted to developing novel nano-formulations for efficient delivery of chemotherapeutic drugs. Herein, we aim to outline the latest progression in the emerging nanomedicines of paclitaxel (PTX), with special attention to the functional nanocarriers, self-delivering prodrug-nanoassemblies and combination nanotherapeutics of PTX. Finally, the challenges and opportunities of these functional PTX nanomedicines in clinical translation are spotlighted.
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•Biomedical nanotechnology significantly facilitates PTX delivery.•Smart PTX delivery can be realized by designing functional nanocarriers.•Emerging prodrug-nanoassemblies of PTX shows promising application prospects.•Combination nanotherapeutics of PTX boost multimodal cancer treatment. |
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ISSN: | 0168-3659 1873-4995 |
DOI: | 10.1016/j.jconrel.2022.01.010 |