Biodegradable thermosensitive hydrogel for SAHA and DDP delivery: therapeutic effects on oral squamous cell carcinoma xenografts.

<h4>Background</h4>OSCC is one of the most common malignancies and numerous clinical agents currently applied in combinative chemotherapy. Here we reported a novel therapeutic strategy, SAHA and DDP-loaded PECE (SAHA-DDP/PECE), can improve the therapeutic effects of intratumorally chemot...

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Autores principales: Jing Li, Changyang Gong, Xiaodong Feng, Xikun Zhou, Xiaoping Xu, Liang Xie, Ruinan Wang, Dunfang Zhang, Hui Wang, Peng Deng, Min Zhou, Ning Ji, Yu Zhou, Yun Wang, Zhiyong Wang, Ga Liao, Ning Geng, Liangyin Chu, Zhiyong Qian, Zhi Wang, Qianming Chen
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:71301349b8af4b8fad62443dbb9413fc2021-11-18T07:21:52ZBiodegradable thermosensitive hydrogel for SAHA and DDP delivery: therapeutic effects on oral squamous cell carcinoma xenografts.1932-620310.1371/journal.pone.0033860https://doaj.org/article/71301349b8af4b8fad62443dbb9413fc2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22529899/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>OSCC is one of the most common malignancies and numerous clinical agents currently applied in combinative chemotherapy. Here we reported a novel therapeutic strategy, SAHA and DDP-loaded PECE (SAHA-DDP/PECE), can improve the therapeutic effects of intratumorally chemotherapy on OSCC cell xenografts.<h4>Objective/purpose</h4>The objective of this study was to evaluate the therapeutic efficacy of the SAHA-DDP/PECE in situ controlled drug delivery system on OSCC cell xenografts.<h4>Methods</h4>A biodegradable and thermosensitive hydrogel was successfully developed to load SAHA and DDP. Tumor-beared mice were intratumorally administered with SAHA-DDP/PECE at 50 mg/kg (SAHA) +2 mg/kg (DDP) in 100 ul PECE hydrogel every two weeks, SAHA-DDP at 50 mg/kg(SAHA) +2 mg/kg(DDP) in NS, 2 mg/kg DDP solution, 50 mg/kg SAHA solution, equal volume of PECE hydrogel, or equal volume of NS on the same schedule, respectively. The antineoplastic actions of SAHA and DDP alone and in combination were evaluated using the determination of tumor volume, immunohistochemistry, western blot, and TUNEL analysis.<h4>Results</h4>The hydrogel system was a free-flowing sol at 10 °C, become gel at body temperature, and could sustain more than 14 days in situ. SAHA-DDP/PECE was subsequently injected into tumor OSCC tumor-beared mice. The results demonstrated that such a strategy as this allows the carrier system to show a sustained release of SAHA and DDP in vivo, and could improved therapeutic effects compared with a simple additive therapeutic effect of SAHA and DDP on mouse model.<h4>Conclusions</h4>Our research indicated that the novel SAHA-DDP/PECE system based on biodegradable PECE copolymer enhanced the therapeutic effects and could diminished the side effects of SAHA/DDP. The present work might be of great importance to the further exploration of the potential application of SAHA/DDP-hydrogel controlled drug release system in the treatment of OSCC.Jing LiChangyang GongXiaodong FengXikun ZhouXiaoping XuLiang XieRuinan WangDunfang ZhangHui WangPeng DengMin ZhouNing JiYu ZhouYun WangZhiyong WangGa LiaoNing GengLiangyin ChuZhiyong QianZhi WangQianming ChenPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 4, p e33860 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Jing Li
Changyang Gong
Xiaodong Feng
Xikun Zhou
Xiaoping Xu
Liang Xie
Ruinan Wang
Dunfang Zhang
Hui Wang
Peng Deng
Min Zhou
Ning Ji
Yu Zhou
Yun Wang
Zhiyong Wang
Ga Liao
Ning Geng
Liangyin Chu
Zhiyong Qian
Zhi Wang
Qianming Chen
Biodegradable thermosensitive hydrogel for SAHA and DDP delivery: therapeutic effects on oral squamous cell carcinoma xenografts.
description <h4>Background</h4>OSCC is one of the most common malignancies and numerous clinical agents currently applied in combinative chemotherapy. Here we reported a novel therapeutic strategy, SAHA and DDP-loaded PECE (SAHA-DDP/PECE), can improve the therapeutic effects of intratumorally chemotherapy on OSCC cell xenografts.<h4>Objective/purpose</h4>The objective of this study was to evaluate the therapeutic efficacy of the SAHA-DDP/PECE in situ controlled drug delivery system on OSCC cell xenografts.<h4>Methods</h4>A biodegradable and thermosensitive hydrogel was successfully developed to load SAHA and DDP. Tumor-beared mice were intratumorally administered with SAHA-DDP/PECE at 50 mg/kg (SAHA) +2 mg/kg (DDP) in 100 ul PECE hydrogel every two weeks, SAHA-DDP at 50 mg/kg(SAHA) +2 mg/kg(DDP) in NS, 2 mg/kg DDP solution, 50 mg/kg SAHA solution, equal volume of PECE hydrogel, or equal volume of NS on the same schedule, respectively. The antineoplastic actions of SAHA and DDP alone and in combination were evaluated using the determination of tumor volume, immunohistochemistry, western blot, and TUNEL analysis.<h4>Results</h4>The hydrogel system was a free-flowing sol at 10 °C, become gel at body temperature, and could sustain more than 14 days in situ. SAHA-DDP/PECE was subsequently injected into tumor OSCC tumor-beared mice. The results demonstrated that such a strategy as this allows the carrier system to show a sustained release of SAHA and DDP in vivo, and could improved therapeutic effects compared with a simple additive therapeutic effect of SAHA and DDP on mouse model.<h4>Conclusions</h4>Our research indicated that the novel SAHA-DDP/PECE system based on biodegradable PECE copolymer enhanced the therapeutic effects and could diminished the side effects of SAHA/DDP. The present work might be of great importance to the further exploration of the potential application of SAHA/DDP-hydrogel controlled drug release system in the treatment of OSCC.
format article
author Jing Li
Changyang Gong
Xiaodong Feng
Xikun Zhou
Xiaoping Xu
Liang Xie
Ruinan Wang
Dunfang Zhang
Hui Wang
Peng Deng
Min Zhou
Ning Ji
Yu Zhou
Yun Wang
Zhiyong Wang
Ga Liao
Ning Geng
Liangyin Chu
Zhiyong Qian
Zhi Wang
Qianming Chen
author_facet Jing Li
Changyang Gong
Xiaodong Feng
Xikun Zhou
Xiaoping Xu
Liang Xie
Ruinan Wang
Dunfang Zhang
Hui Wang
Peng Deng
Min Zhou
Ning Ji
Yu Zhou
Yun Wang
Zhiyong Wang
Ga Liao
Ning Geng
Liangyin Chu
Zhiyong Qian
Zhi Wang
Qianming Chen
author_sort Jing Li
title Biodegradable thermosensitive hydrogel for SAHA and DDP delivery: therapeutic effects on oral squamous cell carcinoma xenografts.
title_short Biodegradable thermosensitive hydrogel for SAHA and DDP delivery: therapeutic effects on oral squamous cell carcinoma xenografts.
title_full Biodegradable thermosensitive hydrogel for SAHA and DDP delivery: therapeutic effects on oral squamous cell carcinoma xenografts.
title_fullStr Biodegradable thermosensitive hydrogel for SAHA and DDP delivery: therapeutic effects on oral squamous cell carcinoma xenografts.
title_full_unstemmed Biodegradable thermosensitive hydrogel for SAHA and DDP delivery: therapeutic effects on oral squamous cell carcinoma xenografts.
title_sort biodegradable thermosensitive hydrogel for saha and ddp delivery: therapeutic effects on oral squamous cell carcinoma xenografts.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/71301349b8af4b8fad62443dbb9413fc
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