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Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity

BACKGROUND: Breast cancer is the leading cause of cancer death in women. Chemotherapy to inhibit the proliferation of cancer cells is considered to be the most important therapeutic strategy. The development of long-circulating PEG and targeting liposomes is a major advance in drug delivery. However...

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Autores principales: Han, Bing, Yang, Yue, Chen, Jinglin, Tang, Huan, Sun, Yuxin, Zhang, Zheng, Wang, Zeng, Li, Yan, Li, Yao, Luan, Xue, Li, Qianwen, Ren, Zhihui, Zhou, Xiaowei, Cong, Dengli, Liu, Zhiyi, Meng, Qin, Sun, Fei, Pei, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986409/
https://www.ncbi.nlm.nih.gov/pubmed/32158208
http://dx.doi.org/10.2147/IJN.S228715
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author Han, Bing
Yang, Yue
Chen, Jinglin
Tang, Huan
Sun, Yuxin
Zhang, Zheng
Wang, Zeng
Li, Yan
Li, Yao
Luan, Xue
Li, Qianwen
Ren, Zhihui
Zhou, Xiaowei
Cong, Dengli
Liu, Zhiyi
Meng, Qin
Sun, Fei
Pei, Jin
author_facet Han, Bing
Yang, Yue
Chen, Jinglin
Tang, Huan
Sun, Yuxin
Zhang, Zheng
Wang, Zeng
Li, Yan
Li, Yao
Luan, Xue
Li, Qianwen
Ren, Zhihui
Zhou, Xiaowei
Cong, Dengli
Liu, Zhiyi
Meng, Qin
Sun, Fei
Pei, Jin
author_sort Han, Bing
collection PubMed
description BACKGROUND: Breast cancer is the leading cause of cancer death in women. Chemotherapy to inhibit the proliferation of cancer cells is considered to be the most important therapeutic strategy. The development of long-circulating PEG and targeting liposomes is a major advance in drug delivery. However, the techniques used in liposome preparation mainly involve conventional liposomes, which have a short half-life, high concentrations in the liver and spleen reticuloendothelial system, and no active targeting. METHODS: Four kinds of paclitaxel liposomes were prepared and characterized by various analytical techniques. The long-term targeting effect of liposomes was verified by fluorescence detection methods in vivo and in vitro. Pharmacokinetic and acute toxicity tests were conducted in ICR mice to evaluate the safety of different paclitaxel preparations. The antitumor activity of ES-SSL-PTX was investigated in detail using in vitro and in vivo human breast cancer MCF-7 cell models. RESULTS: ER-targeting liposomes had a particle size of 137.93±1.22 nm and an acceptable encapsulation efficiency of 88.07±1.25%. The liposome preparation is best stored at 4°C, and is stable for up to 48 hrs. Cytotoxicity test on MCF-7 cells demonstrated the stronger cytotoxic activity of liposomes in comparison to free paclitaxel. We used the near-infrared fluorescence imaging technique to confirm that ES-SSL-PTX was effectively targeted and could quickly and specifically identify the tumor site. Pharmacokinetics and acute toxicity in vivo experiments were carried out. The results showed that ES-SSL-PTX could significantly prolong the half-life of the drug, increase its circulation time in vivo, improve its bioavailability and reduce its toxicity and side effects. ES-SSL-PTX can significantly improve the pharmacokinetic properties of paclitaxel, avoid allergic reaction of the original solvent, increase antitumor efficacy and reduce drug toxicity and side effects. CONCLUSION: ES-SSL-PTX has great potential for improving the treatment of breast cancer, thereby improving patient prognosis and quality of life.
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spelling pubmed-69864092020-03-10 Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity Han, Bing Yang, Yue Chen, Jinglin Tang, Huan Sun, Yuxin Zhang, Zheng Wang, Zeng Li, Yan Li, Yao Luan, Xue Li, Qianwen Ren, Zhihui Zhou, Xiaowei Cong, Dengli Liu, Zhiyi Meng, Qin Sun, Fei Pei, Jin Int J Nanomedicine Original Research BACKGROUND: Breast cancer is the leading cause of cancer death in women. Chemotherapy to inhibit the proliferation of cancer cells is considered to be the most important therapeutic strategy. The development of long-circulating PEG and targeting liposomes is a major advance in drug delivery. However, the techniques used in liposome preparation mainly involve conventional liposomes, which have a short half-life, high concentrations in the liver and spleen reticuloendothelial system, and no active targeting. METHODS: Four kinds of paclitaxel liposomes were prepared and characterized by various analytical techniques. The long-term targeting effect of liposomes was verified by fluorescence detection methods in vivo and in vitro. Pharmacokinetic and acute toxicity tests were conducted in ICR mice to evaluate the safety of different paclitaxel preparations. The antitumor activity of ES-SSL-PTX was investigated in detail using in vitro and in vivo human breast cancer MCF-7 cell models. RESULTS: ER-targeting liposomes had a particle size of 137.93±1.22 nm and an acceptable encapsulation efficiency of 88.07±1.25%. The liposome preparation is best stored at 4°C, and is stable for up to 48 hrs. Cytotoxicity test on MCF-7 cells demonstrated the stronger cytotoxic activity of liposomes in comparison to free paclitaxel. We used the near-infrared fluorescence imaging technique to confirm that ES-SSL-PTX was effectively targeted and could quickly and specifically identify the tumor site. Pharmacokinetics and acute toxicity in vivo experiments were carried out. The results showed that ES-SSL-PTX could significantly prolong the half-life of the drug, increase its circulation time in vivo, improve its bioavailability and reduce its toxicity and side effects. ES-SSL-PTX can significantly improve the pharmacokinetic properties of paclitaxel, avoid allergic reaction of the original solvent, increase antitumor efficacy and reduce drug toxicity and side effects. CONCLUSION: ES-SSL-PTX has great potential for improving the treatment of breast cancer, thereby improving patient prognosis and quality of life. Dove 2020-01-24 /pmc/articles/PMC6986409/ /pubmed/32158208 http://dx.doi.org/10.2147/IJN.S228715 Text en © 2020 Han et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Han, Bing
Yang, Yue
Chen, Jinglin
Tang, Huan
Sun, Yuxin
Zhang, Zheng
Wang, Zeng
Li, Yan
Li, Yao
Luan, Xue
Li, Qianwen
Ren, Zhihui
Zhou, Xiaowei
Cong, Dengli
Liu, Zhiyi
Meng, Qin
Sun, Fei
Pei, Jin
Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity
title Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity
title_full Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity
title_fullStr Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity
title_full_unstemmed Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity
title_short Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity
title_sort preparation, characterization, and pharmacokinetic study of a novel long-acting targeted paclitaxel liposome with antitumor activity
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986409/
https://www.ncbi.nlm.nih.gov/pubmed/32158208
http://dx.doi.org/10.2147/IJN.S228715
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