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Preparation and characterization of drug delivery carriers for local administration of sodium alendronate

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Osteoporosis is often treated with the use of sodium alendronate - a drug that inhibits osteoclast-mediated bone resorption and regulates rate of bone turnover. However the disadvantage of oral administration of sodium alendronate is poor drug absorption from the gastrointestinal track and severe adverse effects. Therefore we propose local sustained drug delivery systems based on poly(lactide-co-glycolide) (PLGA) micro- and nanocarriers, which can be administered directly by simple injections to the required place in the body. In this study we encapsulated sodium alendronate into PLGA micro- and nanospheres via a double-emulsification technique. Emulsion formation in different shear rate conditions was used to optimize the size of the carriers. The prepared microspheres were observed under an inverted optical microscope which confirmed their micrometric size. The nanospheres were analyzed by atomic force microscopy, which allowed visualization of their shape and measurement of their size. Moreover the hydrodynamic diameter of the nanospheres, polydispersity index as well as zeta potential were examined by dynamic light scattering. The experiments show that drug release does not depend on the size of the carriers. Analyzed carriers do not cause cytotoxicity upon contact with osteoblast like-cells.
Rocznik
Strony
8--12
Opis fizyczny
Bibliogr. 17 poz., rys., tab., wykr.
Twórcy
  • AGH University of Science and Technology, Faculty of Materials Science and Ceramics, Department of Biomaterials, al. Mickiewicza 30, 30-059 Kraków, Poland
autor
  • AGH University of Science and Technology, Faculty of Materials Science and Ceramics, Department of Biomaterials, al. Mickiewicza 30, 30-059 Kraków, Poland
  • University of Porto, Faculty of Engineering, Rua Dr. Roberto Frias, s/n, 4200-465 Porto, Portugal
autor
  • AGH University of Science and Technology, Faculty of Materials Science and Ceramics, Department of Biomaterials, al. Mickiewicza 30, 30-059 Kraków, Poland
  • University of Porto, Faculty of Engineering, Rua Dr. Roberto Frias, s/n, 4200-465 Porto, Portugal
autor
  • AGH University of Science and Technology, Faculty of Materials Science and Ceramics, Department of Biomaterials, al. Mickiewicza 30, 30-059 Kraków, Poland
Bibliografia
  • [1] Karageorgiou V., Kaplan D.: Porosity of 3D biomaterial scaffolds and osteogenesis. Biomaterials 26(27) (2005) 5474-5491.
  • [2] Liberman U. A., Weiss S. R., Bröll J., Minne H. W., Quan H., Bell N. H., Rodriguez-Portales J., Downs R. W. Jr., Dequeker J., Favus M.: Effect of Oral Alendronate on Bone Mineral Density and the Incidence of Fractures in Postmenopausal Osteoporosis. N. Engl. J. Med. 333(22) (1995) 1437-1444.
  • [3] Ezra A., Golomb G.: Administration routes and delivery systems of bisphosphonates for the treatment of bone resorption. Adv. Drug Delivery Rev. 42(3) (2000) 175-195.
  • [4] Vallet-Regl M., Balas F., Arcos D.: Mesoporous Materials for Drug Delivery. Angew. Chem. Int. Ed. 46(40) (2007) 7548-7558.
  • [5] Choi S. W., Kim J. H.: Design of surface-modified poly(d,l-lacti- de-co-glycolide) nanoparticles for targeted drug delivery to bone. J. Controlled Release 122(1) (2007) 24-30.
  • [6] Peter B., Pioletti D. P., Ladb S., Bujoli B., Pilet P., Janvier P., Guicheux J., Zambelli P. Y., Bouler J., Gauthier O.: Calcium phosphate drug delivery system: influence of local zoledronate release on bone implant osteointegration. Bone 36(1) (2005) 52-60.
  • [7] Verron E., Khairoun I., Guicheux J., Bouler J. M.: Calcium phosphate biomaterials as bone drug delivery systems: a review. Drug Discovery Today 15(13-14) (2010) 547-552.
  • [8] Cenni E., Granchi D., Avnet S., Fotia C., Salerno M., Micieli D., Sarpietro M. G., Pignatello R., Castelli F., Baldini N.: Biocompatibility of poly(d,l-lactide-co-glycolide) nanoparticles conjugated with alendronate. Biomaterials 29(10) (2008) 1400-1411.
  • [9] Long K. A., Jackson J. K., Yang C., Chehroudi B., Brunette D. M., Burt H. M.: Controlled release of alendronate from polymeric films. J Biomater Sci Polym Ed. 20(5-6) (2009) 653-72.
  • [10] Veena H. R., Prasad D.: Evaluation of an aminobisphosphonate (alendronate) in the management of periodontal osseous defects. J. Indian Soc Periodontol 14 (2010) 40-45.
  • [11] Dobrzynski P.: Synthesis of biodegradable copolymers with low-toxicity zirconium compounds. III. Synthesis and chain-microstructure analysis of terpolymer obtained from L-lactide, glycolide, and ε-caprolactone initiated by zirconium(IV) acetylacetonate. J. Polym. Sci., Part A: Polym. Chemi. 40(18) (2002) 3129-3143.
  • [12] Miladi K., Sfar S., Fessi H., Elaissari A.: Drug carriers in osteoporosis: Preparation, drug encapsulation and applications. Int. J. Pharm. 445(1-2) (2013) 181-195.
  • [13] Taetz S., Nafee N., Beisner J., Piotrowska K., Baldes C., Mürdter T. E., Huwer H., Schneider M., Schaefer U. F., Klotz U., Lehr C. M.: The influence of chitosan content in cationic chitosan/PLGA nanoparticles on the delivery efficiency of antisense 2'-O-methyl-RNA directed against telomerase in lung cancer cells. Eur. J. Pharm. Biopharm. 72(2) (2009) 358-369.
  • [14] Lin Y., Mao S.: Z Potential and its effect on compaction of biomass fuel logs. Biomass Bioenergy 20(3) (2001) 217-222.
  • [15] Mondal T., Sunny M. C., Khastgir D., Varma H. K., Ramesh P.: Poly (l-lactide-co-ε-caprolactone) microspheres laden with bioactive glass-ceramic and alendronate sodium as bone regenerative scaffolds. Mater. Sci. Eng., C 32(4) (2012) 697-706.
  • [16] Wu L., Zhang J., Watanabe W.: Physical and chemical stability of drug nanoparticles. Adv. Drug Delivery Rev. 63(6) (2011) 456-469.
  • [17] Cruz L., Assumpęao E., Staniscuaski-Guterres S., Raffin- Pohlmann A.: High encapsulation efficiency of sodium alendronate in eudragit S100/HPMC blend microparticles. Quim. Nova 32(5) (2009) 1170-1174.
Uwagi
EN
This study was financed from the National Science Center Poland (DEC-2012/05/B/ST8/00129).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-635ed0c7-b19e-470b-b69d-9b09d726356b
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