Enhancing Alendronate Release from a Novel PLGA/Hydroxyapatite Microspheric System for Bone Repairing Applications

被引:164
作者
Shi, Xuetao [1 ,2 ,3 ]
Wang, Yingjun [2 ,3 ]
Ren, Li [2 ,3 ]
Gong, Yihong [1 ]
Wang, Dong-An [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Div Bioengn, Singapore 637457, Singapore
[2] S China Univ Technol, Sch Mat Sci & Engn, Guangzhou 510641, Peoples R China
[3] S China Univ Technol, Minist Educ, Key Lab Specially Funct Mat & Adv Mfg Technol, Guangzhou 510641, Peoples R China
基金
中国国家自然科学基金;
关键词
alendronate; bone repair; drug delivery; hydroxyapatite; microspheres; PLGA; OSTEOBLAST-LIKE CELLS; IN-VITRO; MESOPOROUS SILICA; RESORBING CELLS; BISPHOSPHONATES; HYDROXYAPATITE; DIFFERENTIATION; OSTEOCLASTS; RESORPTION; DELIVERY;
D O I
10.1007/s11095-008-9759-0
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Purpose. The goal of this study was to exploit the multifunction of PLGA based microsphere as efficient alendronate delivery and also as potential injectable cell carrier for bone-repairing therapeutics. Materials and Methods. Novel poly (lactic-co-glycolic acid) (PLGA)-hybridizing-hydroxyapatite (HA) microspheres loaded with bisphosphonate-based osteoporosis preventing drugs, alendronate (AL), are prepared with solid/oil/water (s/o/w) or water/oil/water (w/o/w) technique. Macrophage resistance was evaluated by MTT [3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay, DNA assay and Live/dead staining, and osteoblast proliferation and maturation was assessed by MTT assay, Alkaline phosphatase (ALP) activity assay and Real time-PCR. Results. In such fabricated AL laden PLGA/HA microspheric composites (abbreviated "PLGA/HA-AL"), the introduction of HA component has been proven capable of largely enhancing drug encapsulation efficiency especially when the single emulsion protocol is adopted. The in-vitro drug (AL) releasing profile of PLGA/HA-AL system was plotted basing over 30 days' data collection. It indicates a sustained releasing tendency despite a minimal burst at the very beginning. The in-vitro bone-repairing efficacy of PLGA/HA-AL system was first tested with macrophages that are identified as precursors of osteoclasts and potentially responsible for osteoporosis. The results indicated that the AL release significantly inhibited the growth of macrophages. Additionally, as a central executor for osteogenesis, osteoblasts were also treated with PLGA/HA-AL system in vitro. The outcomes confirmed that this controlled release system functions to improve osteoblast proliferation and also enables upregulation of a key osteogenic enzyme ALP. Conclusions. By pre-resisting osteoclastic commitment and promoting osteoblastic development in vitro, this newly designed PLGA/HA-AL controlled release system is promoting for bone-repairing therapeutics.
引用
收藏
页码:422 / 430
页数:9
相关论文
共 45 条
[1]
Plasma-sprayed carbon nanotube reinforced hydroxyapatite coatings and their interaction with human osteoblasts in vitro [J].
Balani, Kantesh ;
Anderson, Rebecca ;
Laha, Tapas ;
Andara, Melanie ;
Tercero, Jorge ;
Crumpler, Eric ;
Agarwal, Arvind .
BIOMATERIALS, 2007, 28 (04) :618-624
[2]
Confinement and controlled release of bisphosphonates on ordered mesoporous silica-based materials [J].
Balas, Francisco ;
Manzano, Miguel ;
Horcajada, Patricia ;
Vallet-Regi, Maria .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (25) :8116-8117
[3]
Alendronate-hydroxyapatite nanocomposites and their interaction with osteoclasts and osteoblast-like cells [J].
Boanini, Elisa ;
Torricelli, Paola ;
Gazzano, Massimo ;
Giardino, Roberto ;
Bigi, Adriana .
BIOMATERIALS, 2008, 29 (07) :790-796
[4]
Tissue engineered microsphere-based matrices for bone repair: design and evaluation [J].
Borden, M ;
Attawia, M ;
Khan, Y ;
Laurencin, CT .
BIOMATERIALS, 2002, 23 (02) :551-559
[5]
Alendronate-loaded nanoparticles deplete monocytes and attenuate restenosis [J].
Cohen-Sela, Einat ;
Rosenzweig, Ohad ;
Gao, Jianchuan ;
Epstein, Hila ;
Gati, Irith ;
Reich, Reuven ;
Danenberg, Haim D. ;
Golomb, Gershon .
JOURNAL OF CONTROLLED RELEASE, 2006, 113 (01) :23-30
[6]
Administration routes and delivery systems of bisphosphonates for the treatment of bone resorption [J].
Ezra, A ;
Golomb, G .
ADVANCED DRUG DELIVERY REVIEWS, 2000, 42 (03) :175-195
[7]
Osteonecrosis of the jaws in periodontal patients with a history of bisphosphonates treatment [J].
Ficarra, G ;
Beninati, F ;
Rubino, I ;
Vannucchi, A ;
Longo, G ;
Tonelli, P ;
Pini Prato, G .
JOURNAL OF CLINICAL PERIODONTOLOGY, 2005, 32 (11) :1123-1128
[8]
Alendronate mechanism of action:: geranylgeraniol, an intermediate in the mevalonate pathway, prevents inhibition of osteoclast formation, bone resorption, and kinase activation in vitro [J].
Fisher, JE ;
Rogers, MJ ;
Halasy, JM ;
Luckman, SP ;
Hughes, DE ;
Masarachia, PJ ;
Wesolowski, G ;
Russell, RGG ;
Rodan, GA ;
Reszka, AA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (01) :133-138
[9]
Bisphosphonates: Mechanisms of action [J].
Fleisch, H .
ENDOCRINE REVIEWS, 1998, 19 (01) :80-100
[10]
Selective protein adsorption property and characterization of nano-crystalline zinc-containing hydroxyapatite [J].
Fujii, E ;
Ohkubo, M ;
Tsuru, K ;
Hayakawa, S ;
Osaka, A ;
Kawabata, K ;
Bonhomme, C ;
Babonneau, F .
ACTA BIOMATERIALIA, 2006, 2 (01) :69-74