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Nanoparticles Loaded with Docetaxel and Resveratrol as an Advanced Tool for Cancer Therapy.

作者信息

Jurczyk Magdalena, Kasperczyk Janusz, Wrześniok Dorota, Beberok Artur, Jelonek Katarzyna

机构信息

Centre of Polymer and Carbon Materials, Polish Academy of Sciences, Curie-Skłodowska 34 St., 41-819 Zabrze, Poland.

Department of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia, Jagiellońska 4, 41-200 Sosnowiec, Poland.

出版信息

Biomedicines. 2022 May 20;10(5):1187. doi: 10.3390/biomedicines10051187.


DOI:10.3390/biomedicines10051187
PMID:35625921
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9138983/
Abstract

A growing interest in the use of a combination of chemosensitizers and cytostatics for overcoming cancer resistance to treatment and the development of their delivery systems has been observed. Resveratrol (Res) presents antioxidant, anti-inflammatory and chemopreventive properties but also limits multidrug resistance against docetaxel (Dtx), which is one of the main causes of failure in cancer therapy with this drug. However, the use of both drugs presents challenges, including poor bioavailability, the unfavourable pharmacokinetics and chemical instability of Res and the poor water solubility and dose-limiting toxicity of Dtx. In order to overcome these difficulties, attempts have been made to create different forms of delivery for both agents. This review is focused on the latest developments in nanoparticles for the delivery of Dtx, Res and for the combined delivery of those two drugs. The aim of this review was also to summarize the synergistic mechanism of action of Dtx and Res on cancer cells. According to recent reports, Dtx and Res loaded in a nano-delivery system exhibit better efficiency in cancer treatment compared to free drugs. Also, the co-delivery of Dtx and Res in one actively targeted delivery system providing the simultaneous release of both drugs in cancer cells has a chance to fulfil the requirements of effective anticancer therapy and reduce limitations in therapy caused by multidrug resistance (MDR).

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/af41e5935181/biomedicines-10-01187-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/c93285948fb9/biomedicines-10-01187-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/5ded58f7f0fe/biomedicines-10-01187-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/ac81ce5e035b/biomedicines-10-01187-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/028417e8207b/biomedicines-10-01187-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/df57a28c1e70/biomedicines-10-01187-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/aa493c2c950a/biomedicines-10-01187-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/af41e5935181/biomedicines-10-01187-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/c93285948fb9/biomedicines-10-01187-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/5ded58f7f0fe/biomedicines-10-01187-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/ac81ce5e035b/biomedicines-10-01187-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/028417e8207b/biomedicines-10-01187-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/df57a28c1e70/biomedicines-10-01187-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/aa493c2c950a/biomedicines-10-01187-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b9/9138983/af41e5935181/biomedicines-10-01187-g007.jpg

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引用本文的文献

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[2]
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[3]
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[4]
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[5]
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[6]
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Int J Nanomedicine. 2025-1-31

[7]
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[8]
Extracellular Signal-Regulated Kinase Inhibitor SCH772984 Augments the Anti-Cancer Effects of Gemcitabine in Nanoparticle Form in Pancreatic Cancer Models.

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[9]
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[10]
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Int J Nanomedicine. 2024

本文引用的文献

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Nutr Res Pract. 2021-2

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Adv Drug Deliv Rev. 2021-7

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