Cargando…
A Novel Diosgenin-Based Liposome Delivery System Combined with Doxorubicin for Liver Cancer Therapy
As a malignant tumor, liver cancer is mainly treated with chemotherapy, while chemotherapeutic drugs, such as doxorubicin (DOX), may lead to toxicity, drug resistance and poor prognosis. The targeted delivery systems of combining natural products and chemotherapeutic drugs are useful to eliminate ca...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416271/ https://www.ncbi.nlm.nih.gov/pubmed/36015311 http://dx.doi.org/10.3390/pharmaceutics14081685 |
_version_ | 1784776439277551616 |
---|---|
author | Chen, Lixia Lan, Jinshuai Li, Zhe Zeng, Ruifeng Wang, Yu Zhen, Lu Jin, Haojieyin Ding, Yue Zhang, Tong |
author_facet | Chen, Lixia Lan, Jinshuai Li, Zhe Zeng, Ruifeng Wang, Yu Zhen, Lu Jin, Haojieyin Ding, Yue Zhang, Tong |
author_sort | Chen, Lixia |
collection | PubMed |
description | As a malignant tumor, liver cancer is mainly treated with chemotherapy, while chemotherapeutic drugs, such as doxorubicin (DOX), may lead to toxicity, drug resistance and poor prognosis. The targeted delivery systems of combining natural products and chemotherapeutic drugs are useful to eliminate cancers with reduced toxicity and increased efficiency. In this study, a diosgenin-based liposome loaded with DOX (Dios-DOX-LP) was developed for synergistic treatment of liver cancer, in which Dios not only replaced cholesterol as the membrane regulator to keep stability of liposomes, but also became the chemotherapy adjuvant of DOX for synergistic treatment. Dios-DOX-LP was characterized by particle size (99.4 ± 6.2 nm), zeta potential (−33.3 ± 2.5 mV), and entrapment efficiency (DOX: 98.77 ± 2.04%, Dios: 87.75 ± 2.93%), which had a good stability and slow-release effect. Compared with commercial DOX liposome (CHOL-DOX-LP), Dios-DOX-LP had an improved anti-tumor effect in vitro and in vivo by inducing the apoptosis and inhibiting the proliferation of the tumor cell, which was 1.6 times better than CHOL-DOX-LP in cytotoxicity, and had 78% of the tumor inhibition rate on tumor-bearing nude mice. Dios-DOX-LP provided a novel idea to achieve synergistic tumor treatment using diosgenin as a liposome material. |
format | Online Article Text |
id | pubmed-9416271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94162712022-08-27 A Novel Diosgenin-Based Liposome Delivery System Combined with Doxorubicin for Liver Cancer Therapy Chen, Lixia Lan, Jinshuai Li, Zhe Zeng, Ruifeng Wang, Yu Zhen, Lu Jin, Haojieyin Ding, Yue Zhang, Tong Pharmaceutics Article As a malignant tumor, liver cancer is mainly treated with chemotherapy, while chemotherapeutic drugs, such as doxorubicin (DOX), may lead to toxicity, drug resistance and poor prognosis. The targeted delivery systems of combining natural products and chemotherapeutic drugs are useful to eliminate cancers with reduced toxicity and increased efficiency. In this study, a diosgenin-based liposome loaded with DOX (Dios-DOX-LP) was developed for synergistic treatment of liver cancer, in which Dios not only replaced cholesterol as the membrane regulator to keep stability of liposomes, but also became the chemotherapy adjuvant of DOX for synergistic treatment. Dios-DOX-LP was characterized by particle size (99.4 ± 6.2 nm), zeta potential (−33.3 ± 2.5 mV), and entrapment efficiency (DOX: 98.77 ± 2.04%, Dios: 87.75 ± 2.93%), which had a good stability and slow-release effect. Compared with commercial DOX liposome (CHOL-DOX-LP), Dios-DOX-LP had an improved anti-tumor effect in vitro and in vivo by inducing the apoptosis and inhibiting the proliferation of the tumor cell, which was 1.6 times better than CHOL-DOX-LP in cytotoxicity, and had 78% of the tumor inhibition rate on tumor-bearing nude mice. Dios-DOX-LP provided a novel idea to achieve synergistic tumor treatment using diosgenin as a liposome material. MDPI 2022-08-12 /pmc/articles/PMC9416271/ /pubmed/36015311 http://dx.doi.org/10.3390/pharmaceutics14081685 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chen, Lixia Lan, Jinshuai Li, Zhe Zeng, Ruifeng Wang, Yu Zhen, Lu Jin, Haojieyin Ding, Yue Zhang, Tong A Novel Diosgenin-Based Liposome Delivery System Combined with Doxorubicin for Liver Cancer Therapy |
title | A Novel Diosgenin-Based Liposome Delivery System Combined with Doxorubicin for Liver Cancer Therapy |
title_full | A Novel Diosgenin-Based Liposome Delivery System Combined with Doxorubicin for Liver Cancer Therapy |
title_fullStr | A Novel Diosgenin-Based Liposome Delivery System Combined with Doxorubicin for Liver Cancer Therapy |
title_full_unstemmed | A Novel Diosgenin-Based Liposome Delivery System Combined with Doxorubicin for Liver Cancer Therapy |
title_short | A Novel Diosgenin-Based Liposome Delivery System Combined with Doxorubicin for Liver Cancer Therapy |
title_sort | novel diosgenin-based liposome delivery system combined with doxorubicin for liver cancer therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416271/ https://www.ncbi.nlm.nih.gov/pubmed/36015311 http://dx.doi.org/10.3390/pharmaceutics14081685 |
work_keys_str_mv | AT chenlixia anoveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT lanjinshuai anoveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT lizhe anoveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT zengruifeng anoveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT wangyu anoveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT zhenlu anoveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT jinhaojieyin anoveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT dingyue anoveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT zhangtong anoveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT chenlixia noveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT lanjinshuai noveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT lizhe noveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT zengruifeng noveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT wangyu noveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT zhenlu noveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT jinhaojieyin noveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT dingyue noveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy AT zhangtong noveldiosgeninbasedliposomedeliverysystemcombinedwithdoxorubicinforlivercancertherapy |