Nanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy

Xin Li,1 Xiaoqian Jia,2 Hu Niu2 1Department of Breast and Thyroid Surgery, Heze Municipal Hospital, Heze, Shandong, China; 2Department of General Surgery 2, The Fourth People’s Hospital of Jinan, Jinan, Shandong, China Background: Multidrug resistance is responsible for the poor outcome...

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Autores principales: Li X, Jia X, Niu H
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Publicado: Dove Medical Press 2018
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spelling oai:doaj.org-article:c729af607cab47ebb3abc5a25878ee1d2021-12-02T00:20:35ZNanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy1178-2013https://doaj.org/article/c729af607cab47ebb3abc5a25878ee1d2018-07-01T00:00:00Zhttps://www.dovepress.com/nanostructured-lipid-carriers-co-delivering-lapachone-and-doxorubicin--peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Xin Li,1 Xiaoqian Jia,2 Hu Niu2 1Department of Breast and Thyroid Surgery, Heze Municipal Hospital, Heze, Shandong, China; 2Department of General Surgery 2, The Fourth People’s Hospital of Jinan, Jinan, Shandong, China Background: Multidrug resistance is responsible for the poor outcome in breast cancer therapy. Lapa is a novel therapeutic agent that generates ROS through the catalysis of the NAD(P)H:quinone oxidoreductase-1 (NQO1) enzyme which significantly facilitate the intracellular accumulation of the co-delivered DOX to overcome MDR in cancer cells. Purpose: Herein, in our study, nanostructured lipid carrier (NLC) co-delivering β-lapachone (Lapa) and doxorubicin (DOX) was developed (LDNLC) with the aim to overcome the multidrug resistance (MDR) in breast cancer therapy. Patients and methods: Lapa and DOX were loaded into NLC to prepare LDNLC using melted ultrasonic dispersion method. Results: The well designed LDNLC was nanoscaled particles that exhibited preferable stability in physiological environment. In vitro cell experiments on MCF-7 ADR cells showed increased DOX retention as compared to DOX mono-delivery NLC (DNLC). In vivo anti-cancer assays on MCF-7 ADR tumor bearing mice model also revealed significantly enhanced efficacy of LDNLC than mono-delivery NLCs (DNLC and LNLC). Conclusion: LDNLC might be a promising platform for effective breast cancer therapy. Keywords: β-lapachone, doxorubicin, nanostructured lipid carriers, multidrug resistance, breast cancerLi XJia XNiu HDove Medical Pressarticleβ-lapachonedoxorubicinnanostructured lipid carriersmultidrug resistancebreast cancerMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 13, Pp 4107-4119 (2018)
institution DOAJ
collection DOAJ
language EN
topic β-lapachone
doxorubicin
nanostructured lipid carriers
multidrug resistance
breast cancer
Medicine (General)
R5-920
spellingShingle β-lapachone
doxorubicin
nanostructured lipid carriers
multidrug resistance
breast cancer
Medicine (General)
R5-920
Li X
Jia X
Niu H
Nanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy
description Xin Li,1 Xiaoqian Jia,2 Hu Niu2 1Department of Breast and Thyroid Surgery, Heze Municipal Hospital, Heze, Shandong, China; 2Department of General Surgery 2, The Fourth People’s Hospital of Jinan, Jinan, Shandong, China Background: Multidrug resistance is responsible for the poor outcome in breast cancer therapy. Lapa is a novel therapeutic agent that generates ROS through the catalysis of the NAD(P)H:quinone oxidoreductase-1 (NQO1) enzyme which significantly facilitate the intracellular accumulation of the co-delivered DOX to overcome MDR in cancer cells. Purpose: Herein, in our study, nanostructured lipid carrier (NLC) co-delivering β-lapachone (Lapa) and doxorubicin (DOX) was developed (LDNLC) with the aim to overcome the multidrug resistance (MDR) in breast cancer therapy. Patients and methods: Lapa and DOX were loaded into NLC to prepare LDNLC using melted ultrasonic dispersion method. Results: The well designed LDNLC was nanoscaled particles that exhibited preferable stability in physiological environment. In vitro cell experiments on MCF-7 ADR cells showed increased DOX retention as compared to DOX mono-delivery NLC (DNLC). In vivo anti-cancer assays on MCF-7 ADR tumor bearing mice model also revealed significantly enhanced efficacy of LDNLC than mono-delivery NLCs (DNLC and LNLC). Conclusion: LDNLC might be a promising platform for effective breast cancer therapy. Keywords: β-lapachone, doxorubicin, nanostructured lipid carriers, multidrug resistance, breast cancer
format article
author Li X
Jia X
Niu H
author_facet Li X
Jia X
Niu H
author_sort Li X
title Nanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy
title_short Nanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy
title_full Nanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy
title_fullStr Nanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy
title_full_unstemmed Nanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy
title_sort nanostructured lipid carriers co-delivering lapachone and doxorubicin for overcoming multidrug resistance in breast cancer therapy
publisher Dove Medical Press
publishDate 2018
url https://doaj.org/article/c729af607cab47ebb3abc5a25878ee1d
work_keys_str_mv AT lix nanostructuredlipidcarrierscodeliveringlapachoneanddoxorubicinforovercomingmultidrugresistanceinbreastcancertherapy
AT jiax nanostructuredlipidcarrierscodeliveringlapachoneanddoxorubicinforovercomingmultidrugresistanceinbreastcancertherapy
AT niuh nanostructuredlipidcarrierscodeliveringlapachoneanddoxorubicinforovercomingmultidrugresistanceinbreastcancertherapy
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