Silk coating on poly(ε-caprolactone) microspheres for the delayed release of vancomycin

References

• Altman GH, Diaz F, Jakuba C, Calabro T, Horan RL, Chen JS, Lu H, Richmond J, Kaplan DL. Silk-based biomaterials. Biomaterials 2003; 24: 401–16
   PubMed Web of Science ®Google Scholar
• Baras B, Benoi MA, Gillard J. Parameters influencing the antigen release from spray-dried poly(DL-lactide) microparticles. Int J Pharm 2000; 200: 133–45
   PubMed Web of Science ®Google Scholar
• Bayraktar O, Malay O, Ozgarip Y, Batigun A. Silk fibroin as a novel coating material for controlled release of theophylline. Eur J Pharm Biopharm 2005; 60: 373–81
   PubMed Web of Science ®Google Scholar
• Billon A, Chabaud L, Gouyette A, Bouler JM, Merle C. Vancomycin biodegradable poly(lactide-co-glycolide) microparticles for bone implantation. Influence of the formulation parameters on the size, morphology, drug loading and in vitro release. J Microencapsul 2005; 22: 841–52
   Google Scholar
• Cao ZB, Chen X, Yao JR, Huang L, Shao ZZ. The preparation of regenerated silk fibroin microspheres. Soft Matter 2007; 3: 910–15
   PubMed Web of Science ®Google Scholar
• Cevher E, Orhan Z, Mulazimoglu L, Sensoy D, Alper M, Yildiz A, Ozsoy Y. Characterization of biodegradable chitosan microspheres containing vancomycin and treatment of experimental osteomyelitis caused by methicillin-resistant Staphylococcus aureus with prepared microspheres. Int J Pharm 2006; 317: 127–35
   PubMed Web of Science ®Google Scholar
• Chan LW, Liu XH, Heng PWS. Liquid phase coating to produce controlled-release alginate microspheres. J Microencapsul 2005; 22: 891–900
   PubMed Web of Science ®Google Scholar
• Gafourian T, Safari A, Adibkia K, Parviz F, Nokhodchi A. A drug release study from hydroxypropylmethylcellulose (HPMC) matrices using QSPR modeling. J Pharm Sci 2007; 96: 3334–51
   PubMed Web of Science ®Google Scholar
• Gong ZG, Yang YH, Huang L, Chen X, Shao ZZ. Formation kinetics and fractal characteristics of regenerated silk fibroin alcogel developed from nanofibrillar network. Soft Matter 2010; 6: 1217–23
   Google Scholar
• Gonzalez B, Colilla M, Vallet-Regi M. Time-delayed release of bioencapsulates: A novel controlled delivery concept for bone implant technologies. Chem Mater 2008; 20: 4826–34
   Web of Science ®Google Scholar
• Hurteaux R, Edwards-Levy F, Laurent-Maquin D, Levy MC. Coating alginate microspheres with a serum albumin-alginate membrane: application to the encapsulation of a peptide. Eur J Pharm Sci 2005; 24: 187–97
   PubMed Web of Science ®Google Scholar
• Jameela SR, Suma N, Jayakrishnan A. Protein release from poly(epsilon-caprolactone) microspheres prepared by melt encapsulation and solvent evaporation techniques: A comparative study. J Biomater Sci Polym Ed 1997; 8: 457–66
   PubMed Web of Science ®Google Scholar
• Jin HJ, Fridrikh SV, Rutledge GC, Kaplan DL. Electrospinning Bombyx mori silk with poly(ethylene oxide). Biomacromolecules 2002; 3: 1233–39
   PubMed Web of Science ®Google Scholar
• Jin HJ, Park J, Karageorgiou V, Kim UJ, Valluzzi R, Kaplan DL. Water-stable silk films with reduced beta-sheet content. Adv Funct Mater 2005; 15: 1241–47
   Web of Science ®Google Scholar
• Jin HJ, Park J, Valluzzi R, Cebe P, Kaplan DL. Biomaterial films of Bombyx mori silk fibroin with poly(ethylene oxide). Biomacromolecules 2004; 5: 711–17
   PubMed Web of Science ®Google Scholar
• Kim BK, Hwang SJ, Park JB, Park HJ. Characteristics of felodipine-located poly(epsilon-caprolactone) microspheres. J Microencapsul 2005; 22: 193–203
   PubMed Web of Science ®Google Scholar
• Kweon H, Ha HC, Um IC, Park YH. Physical properties of silk fibroin/chitosan blend films. J Appl Polym Sci 2001; 80: 928–34
   Web of Science ®Google Scholar
• Lazzarini L, Mader JT, Calhoun JH. Osteomyelitis in long bones. J Bone Joint Surg Am 2004; 86A: 2305–18
   Google Scholar
• Le Ray AM, Chiffoleau S, Iooss P, Grimandi G, Gouyette A, Daculsi G, Merle C. Vancomycin encapsulation in biodegradable poly(epsilon-caprolactone) microparticles for bone implantation. Influence of the formulation process on size, drug loading, in vitro release and cytocompatibility. Biomaterials 2003; 24: 443–49
   Google Scholar
• Lee JH, Park TG, Choi HK. Effect of formulation and processing variables on the characteristics of microspheres for water-soluble drugs prepared by w/o/o double emulsion solvent diffusion method. Int J Pharm 2000; 196: 75–83
   PubMed Web of Science ®Google Scholar
• Liu Y, Shao ZZ, Zhou P, Chen X. Thermal and crystalline behaviour of silk fiborin/nylon 66 blend films. Polymer 2004; 45: 7705–10
   Web of Science ®Google Scholar
• Liu SJ, Ueng SWN, Lin SS, Chan EC. In vivo release of vancomycin from biodegradable beads. J Biomed Mater Res 2002; 63: 807–13
   PubMed Web of Science ®Google Scholar
• Maggio RM, Castellano PM, Kaufman TS. A new principal component analysis-based approach for testing “similarity” of drug dissolution profiles. Eur J Pharm Sci 2008; 34: 66–77
   PubMed Web of Science ®Google Scholar
• Mundargi RC, Srirangarajan S, Agnihotri SA, Patil SA, Ravindra S, Setty SB, Aminabhavi TM. Development and evaluation of novel biodegradable microspheres based on poly(D,L-lactide-co-glycolide) and poly(epsilon-caprolactone) for controlled delivery of doxycycline in the treatment of human periodontal pocket: In vitro and in vivo studies. J Control Release 2007; 119: 59–68
   PubMed Web of Science ®Google Scholar
• Nafea EH, El-Massik MA, El-Khordagui LK, Marei MK, Khalafallah NM. Alendronate PLGA microspheres with high loading efficiency for dental applications. J Microencapsul 2007; 24: 525–38
   PubMed Web of Science ®Google Scholar
• Rosenberg RT, Siegel SJ, Dan N. Release of highly hydrophilic drugs from poly(epsilon-caprolactone) matrices. J Appl Polym Sci 2008; 107: 3149–56
   Web of Science ®Google Scholar
• Saito T, Takeuchi R, Hirakawa K, Nagata N, Yoshida T, Koshino T, Okuda K, Takema M, Hori T. Slow-releasing potential of vancomycin-loaded porous hydroxyapatite blocks implanted into MRSA osteomyelitis. J Biomed Mater Res 2002; 63: 245–51
   PubMed Web of Science ®Google Scholar
• Sharifpoor S, Amsden B. In vitro release of a water-soluble agent from low viscosity biodegradable, injectable oligomers. Eur J Pharm Biopharm 2007; 65: 336–45
   PubMed Web of Science ®Google Scholar
• Tanaka KSE, Dietrich E, Ciblat S, Metayer C, Arhin FF, Sarmiento I, Moeck G, Parr TR, Far AR. Synthesis and in vitro evaluation of bisphosphonated glycopeptide prodrugs for the treatment of osteomyelitis. Bioorg Med Chem Lett 2010; 20: 1355–59
   PubMed Web of Science ®Google Scholar
• Wang SB, Guo SR. Disodium norcantharidate-loaded poly(epsilon-caprolactone) microspheres II. Modification of morphology and release behavior. Int J Pharm 2008a; 353: 15–20
   Google Scholar
• Wang SB, Guo SR. Formation mechanism and release behavior of poly(epsilon-caprolactone) microspheres containing disodium norcantharidate. Eur J Pharm Biopharm 2008b; 69: 1176–81
   PubMed Web of Science ®Google Scholar
• Wang X, Kim HJ, Xu P, Matsumoto A, Kaplan DL. Biomaterial coatings by stepwise deposition of silk fibroin. Langmuir 2005; 21: 11335–41
   PubMed Web of Science ®Google Scholar
• Wang X, Wenk E, Hu X, Castro GR, Meinel L, Wang X, Li C, Merkle H, Kaplan DL. Silk coatings on PLGA and alginate microspheres for protein delivery. Biomaterials 2007; 28: 4161–69
   PubMed Web of Science ®Google Scholar
• Weidenauer U, Bodmer D, Kissel T. Microencapsulation of hydrophilic drug substances using biodegradable polyesters. Part I: Evaluation of different techniques for the encapsulation of pamidronate di-sodium salt. J Microencapsul 2003; 20: 509–24
   Google Scholar
• Zhang YT, Zhang YQ, Guo SR, Huang WL. Tyrosine kinase inhibitor loaded PCL microspheres prepared by S/O/W technique using ethanol as pretreatment agent. Int J Pharm 2009; 369: 19–23
   PubMedGoogle Scholar