Cargando…
Long-Circulating Thermosensitive Liposomes for the Targeted Drug Delivery of Oxaliplatin
INTRODUCTION: Oxaliplatin (L-OHP) is a well-known third-generation platinum anticancer drug with severe systemic- and neuro-toxicity. The main objective of the current research was to develop a targeted long-circulating thermosensitive smart-release liposome (LCTL) system for better therapeutic effi...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494235/ https://www.ncbi.nlm.nih.gov/pubmed/32982229 http://dx.doi.org/10.2147/IJN.S250773 |
_version_ | 1783582706569838592 |
---|---|
author | Li, Yanan Xu, Pengcheng He, Dongsheng Xu, Bohui Tu, Jiasheng Shen, Yan |
author_facet | Li, Yanan Xu, Pengcheng He, Dongsheng Xu, Bohui Tu, Jiasheng Shen, Yan |
author_sort | Li, Yanan |
collection | PubMed |
description | INTRODUCTION: Oxaliplatin (L-OHP) is a well-known third-generation platinum anticancer drug with severe systemic- and neuro-toxicity. The main objective of the current research was to develop a targeted long-circulating thermosensitive smart-release liposome (LCTL) system for better therapeutic efficacy and less toxicity. METHODS: The reverse-phase evaporation method (REV) was used to prepare L-OHP loaded LCTL (L-OHP/LCTL). The physical characteristics were evaluated including encapsulation efficiency (EE), size, zeta potential and stability. The release behavior, cytotoxicity and in vivo evaluation were also carried out. RESULTS: EE of LCTL was around 25% with a uniform size distribution, and LCTL achieved almost complete release at 42°C while it was only 10% at 37°C. Moreover, the LCTL showed significantly higher cytotoxicity at 42°C than that at 37°C. The in vivo results indicated LCTL could target tumors and enhance retention for more than 24 h, thereby enhancing anti-tumor efficacy on 4T1-bearing mice. DISCUSSION: These results indicated that LCTL not only possessed a prolonged circulation time but it also enhanced accumulation and achieved selective release at the tumor sites. Conclusively, LCTL could serve as a promising carrier for oxaliplatin delivery to treat solid tumors. |
format | Online Article Text |
id | pubmed-7494235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-74942352020-09-24 Long-Circulating Thermosensitive Liposomes for the Targeted Drug Delivery of Oxaliplatin Li, Yanan Xu, Pengcheng He, Dongsheng Xu, Bohui Tu, Jiasheng Shen, Yan Int J Nanomedicine Original Research INTRODUCTION: Oxaliplatin (L-OHP) is a well-known third-generation platinum anticancer drug with severe systemic- and neuro-toxicity. The main objective of the current research was to develop a targeted long-circulating thermosensitive smart-release liposome (LCTL) system for better therapeutic efficacy and less toxicity. METHODS: The reverse-phase evaporation method (REV) was used to prepare L-OHP loaded LCTL (L-OHP/LCTL). The physical characteristics were evaluated including encapsulation efficiency (EE), size, zeta potential and stability. The release behavior, cytotoxicity and in vivo evaluation were also carried out. RESULTS: EE of LCTL was around 25% with a uniform size distribution, and LCTL achieved almost complete release at 42°C while it was only 10% at 37°C. Moreover, the LCTL showed significantly higher cytotoxicity at 42°C than that at 37°C. The in vivo results indicated LCTL could target tumors and enhance retention for more than 24 h, thereby enhancing anti-tumor efficacy on 4T1-bearing mice. DISCUSSION: These results indicated that LCTL not only possessed a prolonged circulation time but it also enhanced accumulation and achieved selective release at the tumor sites. Conclusively, LCTL could serve as a promising carrier for oxaliplatin delivery to treat solid tumors. Dove 2020-09-11 /pmc/articles/PMC7494235/ /pubmed/32982229 http://dx.doi.org/10.2147/IJN.S250773 Text en © 2020 Li 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 Li, Yanan Xu, Pengcheng He, Dongsheng Xu, Bohui Tu, Jiasheng Shen, Yan Long-Circulating Thermosensitive Liposomes for the Targeted Drug Delivery of Oxaliplatin |
title | Long-Circulating Thermosensitive Liposomes for the Targeted Drug Delivery of Oxaliplatin |
title_full | Long-Circulating Thermosensitive Liposomes for the Targeted Drug Delivery of Oxaliplatin |
title_fullStr | Long-Circulating Thermosensitive Liposomes for the Targeted Drug Delivery of Oxaliplatin |
title_full_unstemmed | Long-Circulating Thermosensitive Liposomes for the Targeted Drug Delivery of Oxaliplatin |
title_short | Long-Circulating Thermosensitive Liposomes for the Targeted Drug Delivery of Oxaliplatin |
title_sort | long-circulating thermosensitive liposomes for the targeted drug delivery of oxaliplatin |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494235/ https://www.ncbi.nlm.nih.gov/pubmed/32982229 http://dx.doi.org/10.2147/IJN.S250773 |
work_keys_str_mv | AT liyanan longcirculatingthermosensitiveliposomesforthetargeteddrugdeliveryofoxaliplatin AT xupengcheng longcirculatingthermosensitiveliposomesforthetargeteddrugdeliveryofoxaliplatin AT hedongsheng longcirculatingthermosensitiveliposomesforthetargeteddrugdeliveryofoxaliplatin AT xubohui longcirculatingthermosensitiveliposomesforthetargeteddrugdeliveryofoxaliplatin AT tujiasheng longcirculatingthermosensitiveliposomesforthetargeteddrugdeliveryofoxaliplatin AT shenyan longcirculatingthermosensitiveliposomesforthetargeteddrugdeliveryofoxaliplatin |