Hydrogel-PLGA delivery system prolongs 2-methoxyestradiol-mediated anti-tumor effects in osteosarcoma cells

被引:8
作者
Maran, Avudaiappan [1 ,2 ]
Dadsetan, Mahrokh [1 ,2 ]
Buenz, Colleen M. [1 ,2 ]
Shogren, Kristen L. [1 ]
Lu, Lichun [1 ,2 ]
Yaszemski, Michael J. [1 ,2 ]
机构
[1] Mayo Clin, Dept Orthoped Surg, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Biomed Engn, Rochester, MN USA
关键词
oligo(polyethylene glycol) fumarate; 2-methoxyestradiol; poly (lactic-co-glycolic acid); osteosarcoma; hydrogel; ENDOGENOUS ESTROGEN METABOLITE; GLYCOL) FUMARATE) HYDROGELS; PROSTATE-CANCER; IN-VITRO; ORAL; 2-METHOXYESTRADIOL; CYCLE PROGRESSION; MOLECULAR-WEIGHT; DRUG-DELIVERY; PEG-PLGA; APOPTOSIS;
D O I
10.1002/jbm.a.34550
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Osteosarcoma is a bone tumor that affects children and young adults. 2-Methoxyestradiol (2-ME), a naturally occurring estrogen metabolite, kills osteosarcoma cells, but does not affect normal osteoblasts. In order to effectively target osteosarcoma and improve the therapeutic index of the drug 2-ME, we have encapsulated 2-ME in a composite of oligo-(polyethylene glycol) fumarate (OPF) hydrogel and poly (lactic-co-glycolic acid) (PLGA) microspheres and investigated the effect of polymer composition on 2-ME release kinetics and osteosarcoma cell survival. The in vitro study shows that 2-ME can be released in a controlled manner over 21-days. The initial burst releases observed on day 1 were 50% and 32% for OPF and OPF/PLGA composites, respectively. The extended release kinetics show that 100% of the encapsulated 2-ME is released by day 12 from OPF, whereas the OPF/PLGA composites showed a release of 85% on day 21. 2-ME released from the polymers was biologically active and blocked osteosarcoma cell proliferation in vitro. Also, comparison of 2-ME delivery in osteosarcoma cells in culture, shows that direct treatment has no effect after 3 days, whereas polymer-mediated delivery produces anti-tumor effects that could be sustained for 21 days. These findings show that the OPF and PLGA polymeric system may prove to be useful in controlled and sustained delivery of 2-ME and could be further explored in the treatment of osteosarcoma. (c) 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 101A: 2491-2499, 2013.
引用
收藏
页码:2491 / 2499
页数:9
相关论文
共 45 条
[1]  
Bhardwaj Upkar, 2008, J Diabetes Sci Technol, V2, P1016
[2]   Evidence for vasoconstriction mediated by the endothelin-B receptor in domestic swine [J].
Burke, SE ;
Nelson, RA ;
Lubbers, NL ;
Ford, TT ;
Fu, KI ;
Padley, RJ ;
Wegner, CD ;
Cox, BF .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2000, 35 (06) :838-844
[3]   Studies on biodegradation and release of gentamicin sulphate from interpenetrating network hydrogels based on poly(acrylic acid) and gelatin: in vitro and in vivo [J].
Changez, M ;
Koul, V ;
Krishna, B ;
Dinda, AK ;
Choudhary, V .
BIOMATERIALS, 2004, 25 (01) :139-146
[4]   Hydrogel-mediated DNA delivery confers estrogenic response in nonresponsive osteoblast cells [J].
Dadsetan, M. ;
Szatkowski, J. P. ;
Shogren, K. L. ;
Yaszemski, M. J. ;
Maran, A. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2009, 91A (04) :1170-1177
[5]   Effect of hydrogel porosity on marrow stromal cell phenotypic expression [J].
Dadsetan, Mahrokh ;
Hefferan, Theresa E. ;
Szatkowski, Jan P. ;
Mishra, Prasanna K. ;
Macura, Slobodan I. ;
Lu, Lichun ;
Yaszemski, Michael J. .
BIOMATERIALS, 2008, 29 (14) :2193-2202
[6]   Characterization of photo-cross-linked oligo[poly(ethylene glycol) fumarate] hydrogels for cartilage tissue engineering [J].
Dadsetan, Mahrokh ;
Szatkowski, Jan P. ;
Yaszemski, Michael J. ;
Lu, Lichun .
BIOMACROMOLECULES, 2007, 8 (05) :1702-1709
[7]   Incorporation of phosphate group modulates bone cell attachment and differentiation on oligo(polyethylene glycol) fumarate hydrogel [J].
Dadsetan, Mahrokh ;
Giuliani, Melissa ;
Wanivenhaus, Florian ;
Runge, M. Brett ;
Charlesworth, Jon E. ;
Yaszemski, Michael J. .
ACTA BIOMATERIALIA, 2012, 8 (04) :1430-1439
[8]   A stimuli-responsive hydrogel for doxorubicin delivery [J].
Dadsetan, Mahrokh ;
Liu, Zen ;
Pumberger, Matthias ;
Giraldo, Catalina Vallejo ;
Ruesink, Terry ;
Lu, Lichun ;
Yaszemski, Michael J. .
BIOMATERIALS, 2010, 31 (31) :8051-8062
[9]   Phase I clinical trial of oral 2-methoxyestradiol, an antiangiogenic and apoptotic agent, in patients with solid tumors [J].
Dahut, WL ;
Lakhani, NJ ;
Gulley, JL ;
Arlen, PM ;
Kohn, EC ;
Kotz, H ;
McNally, D ;
Parr, A ;
Nguyen, D ;
Yang, SX ;
Steinberg, SM ;
Venitz, J ;
Sparreboom, A ;
Figg, WD .
CANCER BIOLOGY & THERAPY, 2006, 5 (01) :22-27
[10]   Effect of formulation parameters on 2-methoxyestradiol release from injectable cylindrical poly(DL-lactide-co-glycolide) implants [J].
Desai, Kashappa Goud H. ;
Mallery, Susan R. ;
Schwendeman, Steven P. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 70 (01) :187-198