Hydrogel-Mediated DOX⋅HCl/PTX Delivery System for Breast Cancer Therapy
We used a hydrogel-mediated dual drug delivery approach, based on an injectable glycol chitosan (GC) hydrogel, doxorubicin hydrochloride (DOX⋅HCl), and a complex of beta-cyclodextrin (β-CD) and paclitaxel (PTX) (GDCP) for breast cancer therapy in vitro and in vivo. The hydrogel was swollen over 3 da...
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doaj-e13b7878061141cc8ea365fe7ee9ae812020-11-25T02:08:00ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-09-012019467110.3390/ijms20194671ijms20194671Hydrogel-Mediated DOX⋅HCl/PTX Delivery System for Breast Cancer TherapyHoon Hyun0Young Bum Yoo1So Yeon Kim2Hyun Sun Ko3Heung Jae Chun4Dae Hyeok Yang5Department of Biomedical Sciences, Chonnam National University Medical School, Gwangju 61469, KoreaDepartment of Surgery, School of Medicine, Konkuk University, Seoul 05030, KoreaDepartment of Dental Hygiene, College of Health Sciences, Cheongju University, Cheongju 28503, KoreaDepartment of Obstetrics & Gynecology, College of Medicine, The Catholic University of Korea, Seoul 06591, KoreaDepartment of Medical Life Sciences, College of Medicine, The Catholic University of Korea, Seoul 06591, KoreaInstitute of Cell and Tissue Engineering, College of Medicine, The Catholic University of Korea, Seoul 06591, KoreaWe used a hydrogel-mediated dual drug delivery approach, based on an injectable glycol chitosan (GC) hydrogel, doxorubicin hydrochloride (DOX⋅HCl), and a complex of beta-cyclodextrin (β-CD) and paclitaxel (PTX) (GDCP) for breast cancer therapy in vitro and in vivo. The hydrogel was swollen over 3 days and remained so thereafter. After an initial burst period of 7 hours, the two drugs were released in a sustained manner for 7 days. The in vitro cell viability test showed that GDCP had a better anticancer effect than well plate and DOX⋅HCl/PTX (DP). In addition, the in vivo tests, which evaluated the anticancer effect, systemic toxicity, and histology, proved the feasibility of GDCP as a clinical therapy for breast cancer.https://www.mdpi.com/1422-0067/20/19/4671injectable glycol chitosandoxorubicin hydrochloridebeta-cyclodextrinpaclitaxelbreast cancer therapy |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hoon Hyun Young Bum Yoo So Yeon Kim Hyun Sun Ko Heung Jae Chun Dae Hyeok Yang |
spellingShingle |
Hoon Hyun Young Bum Yoo So Yeon Kim Hyun Sun Ko Heung Jae Chun Dae Hyeok Yang Hydrogel-Mediated DOX⋅HCl/PTX Delivery System for Breast Cancer Therapy International Journal of Molecular Sciences injectable glycol chitosan doxorubicin hydrochloride beta-cyclodextrin paclitaxel breast cancer therapy |
author_facet |
Hoon Hyun Young Bum Yoo So Yeon Kim Hyun Sun Ko Heung Jae Chun Dae Hyeok Yang |
author_sort |
Hoon Hyun |
title |
Hydrogel-Mediated DOX⋅HCl/PTX Delivery System for Breast Cancer Therapy |
title_short |
Hydrogel-Mediated DOX⋅HCl/PTX Delivery System for Breast Cancer Therapy |
title_full |
Hydrogel-Mediated DOX⋅HCl/PTX Delivery System for Breast Cancer Therapy |
title_fullStr |
Hydrogel-Mediated DOX⋅HCl/PTX Delivery System for Breast Cancer Therapy |
title_full_unstemmed |
Hydrogel-Mediated DOX⋅HCl/PTX Delivery System for Breast Cancer Therapy |
title_sort |
hydrogel-mediated dox⋅hcl/ptx delivery system for breast cancer therapy |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1422-0067 |
publishDate |
2019-09-01 |
description |
We used a hydrogel-mediated dual drug delivery approach, based on an injectable glycol chitosan (GC) hydrogel, doxorubicin hydrochloride (DOX⋅HCl), and a complex of beta-cyclodextrin (β-CD) and paclitaxel (PTX) (GDCP) for breast cancer therapy in vitro and in vivo. The hydrogel was swollen over 3 days and remained so thereafter. After an initial burst period of 7 hours, the two drugs were released in a sustained manner for 7 days. The in vitro cell viability test showed that GDCP had a better anticancer effect than well plate and DOX⋅HCl/PTX (DP). In addition, the in vivo tests, which evaluated the anticancer effect, systemic toxicity, and histology, proved the feasibility of GDCP as a clinical therapy for breast cancer. |
topic |
injectable glycol chitosan doxorubicin hydrochloride beta-cyclodextrin paclitaxel breast cancer therapy |
url |
https://www.mdpi.com/1422-0067/20/19/4671 |
work_keys_str_mv |
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1724928150818783232 |