Composite Hydrogel Embedded with Porous Microspheres for Long-Term pH-Sensitive Drug Delivery

被引:0
作者
Liu, Xifeng [1 ,2 ]
Fundora, Kevin A. [1 ]
Zhou, Zifei [1 ]
Miller, Alan Lee, II [2 ]
Lu, Lichun [1 ,2 ]
机构
[1] Mayo Clin, Coll Med, Dept Physiol & Biomed Engn, 200 First St SW, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Orthoped Surg, Rochester, MN USA
关键词
hydrogel; porous microspheres; drug delivery; osteosarcoma; cancer; POLY(PROPYLENE FUMARATE); CONTINUOUS-INFUSION; MOLECULAR-WEIGHT; PHASE-SEPARATION; DOXORUBICIN; OSTEOSARCOMA; SCAFFOLDS; BONE; CHEMOTHERAPY; THERAPY;
D O I
10.1089/ten.tea.2018.0071
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Current delivery of chemotherapy drugs to osteosarcoma is limited by the difficulties in overcoming the solid tumor microenvironment and the cardiotoxicity of doxorubicin (DOX). In previous work we found that phase separation could generate microspheres with high porosity. In this study, we applied these phase-separated porous microspheres as carriers for long-term anticancer drug delivery. Novel poly(propylene fumarate)-co-poly(l-lactic acid) microspheres incorporating DOX were fabricated by thermally induced phase separation. Following embedding into oligo(poly[ethylene glycol] fumarate) hydrogel, the composite system showed prolonged and pH-responsive release of DOX. In vitro cytotoxicity study using osteosarcoma 143B cells showed substantial long-term cytotoxic effects for up to 30 days. As a result, the DOX drug delivery hydrogel developed in this work may have significant potential as a long-term and localized chemotherapy device that would be sensitive to the acidic microenvironment of osteosarcoma and other cancers.
引用
收藏
页码:172 / 182
页数:11
相关论文
共 40 条
[1]   Doxil® - The first FDA-approved nano-drug: Lessons learned [J].
Barenholz, Yechezkel .
JOURNAL OF CONTROLLED RELEASE, 2012, 160 (02) :117-134
[2]  
Berrak SG, 2001, ONCOL REP, V8, P611
[3]   Fabrication of porous poly(L-lactide) (PLLA) scaffolds for tissue engineering using liquid-liquid phase separation and freeze extraction [J].
Budyanto, L. ;
Goh, Y. Q. ;
Ooi, C. P. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2009, 20 (01) :105-111
[4]   Thermal gelation and tissue adhesion of biomimetic hydrogels [J].
Burke, Sean A. ;
Ritter-Jones, Marsha ;
Lee, Bruce P. ;
Messersmith, Phillip B. .
BIOMEDICAL MATERIALS, 2007, 2 (04) :203-210
[5]   Doxorubicin Cardiomyopathy [J].
Chatterjee, Kanu ;
Zhang, Jianqing ;
Honbo, Norman ;
Karliner, Joel S. .
CARDIOLOGY, 2010, 115 (02) :155-162
[6]   Therapy for osteosarcoma: Where do we go from here? [J].
Chou A.J. ;
Geller D.S. ;
Gorlick R. .
Pediatric Drugs, 2008, 10 (5) :315-327
[7]  
Crenn V, 2017, AM J CANCER RES, V7, P2333
[8]   Polymeric Scaffolds in Tissue Engineering Application: A Review [J].
Dhandayuthapani, Brahatheeswaran ;
Yoshida, Yasuhiko ;
Maekawa, Toru ;
Kumar, D. Sakthi .
INTERNATIONAL JOURNAL OF POLYMER SCIENCE, 2011, 2011
[9]   Hyaluronidase induces a transcapillary pressure gradient and improves the distribution and uptake of liposomal doxorubicin (Caelyx™) in human osteosarcoma xenografts [J].
Eikenes, L ;
Tari, M ;
Tufto, I ;
Bruland, OS ;
Davies, CD .
BRITISH JOURNAL OF CANCER, 2005, 93 (01) :81-88
[10]   A mathematical model for comparison of bolus injection, continuous infusion, and liposomal delivery of doxorubicin to tumor cells [J].
El-Kareh, AW ;
Secomb, TW .
NEOPLASIA, 2000, 2 (04) :325-338