Preparation and evaluation of double-walled microparticles prepared with a modified water-in-oil-in-oil-in-water (w₁/o/o/w₃) method

References

• Aubert-Pouessel A, Venier-Julienne M-C, Clavreul A, Sergent M, Jollivet C, Montero-Menei CN, Garcion E, Bibby DC, Menei P, Benoit J-P. In vitro study of GDNF release from biodegradable PLGA microspheres. J Control Release, 2004;95:463–75
   PubMed Web of Science ®Google Scholar
• Barakat NS, Radwan MA. In vitro performance of carbamazepine loaded to various molecular weights of poly(d, l-lactide-co-glycolide). Drug Deliv, 2006;13:9–18
   PubMed Web of Science ®Google Scholar
• Berkland C, Cox A, Kim K, Pack DW. Three-month, zero-order piroxicam release from monodispersed double-walled microspheres of controlled shell thickness. J Biomed Mater Res A, 2004;70(4):576–84
   PubMed Web of Science ®Google Scholar
• Blanco MD, Alonso MJ. Development and characterization of protein-loaded poly(lactide-co-glycolide) nanospheres. Eur J Pharm Biopharm, 1997;43:287–94
   Web of Science ®Google Scholar
• Blasi P, Schoubben A, Giovagnoli S, Perioli L, Ricci M, Rossi C. Ketoprofen poly(lactide-co-glycolide) physical interaction. AAPS PharmSciTech, 2007;8(2):Article 37
   PubMed Web of Science ®Google Scholar
• Chen H, Yang W, Chen H, Liu L, Gao F, Yang X, Jiang Q, Zhang Q, Wang Y. Surface modification of mitoxantrone-loaded PLGA nanospheres with chitosan. Colloids Surf B: Biointerfaces, 2009;73:212–18
   PubMed Web of Science ®Google Scholar
• Chen X, Ooi CP. Hydrolytic degradation and drug release properties of ganciclovir-loaded biodegradable microspheres. Acta Biomaterialia, 2008;4:1046–56
   PubMed Web of Science ®Google Scholar
• Choi DH, Park CH, Kim IH, Chun HJ, Park K, Han DK. Fabrication of core-shell microcapsules using PLGA and alginate for dual growth factor delivery system. J Control Release, 2010;147:193–201
   PubMed Web of Science ®Google Scholar
• Cui F, Cun D, Tao A, Yang M, Shi K, Zhao M, Guan Y. Preparation and characterization of melittin-loaded poly(dl-lactic acid) or poly (dl-lactic-co-glycolic acid) microspheres made by the double emulsion method. J Control Release, 2005;107:310–19
   PubMed Web of Science ®Google Scholar
• D’Souza SS, Faraj JA, DeLuca PP. Model dependent approach to correlate accelerated with real-time release from biodegradable microspheres. AAPS Pharm Sci Tech, 2005;6:article 70
   Web of Science ®Google Scholar
• Devrim B, Bozkır A, Canefe K. Preparation and evaluation of PLGA microparticles as carrier for the pulmonary delivery of rhIL-2: I. Effects of some formulation parameters on microparticle characteristics. J Microencapsulation, 2011;28(6):582–94
   PubMed Web of Science ®Google Scholar
• Feng L, Qi XR, Zhou XJ, Maitani Y, Wang SC, Jiang Y, Nagai T. Pharmaceutical and immunological evaluation of a single-dose hepatitis B vaccine using PLGA microspheres. J Control Release, 2006;112:35–42
   PubMed Web of Science ®Google Scholar
• Ferrero C, Massuelle D, Doelker E. Towards elucidation of the drug release mechanism from compressed hydrophilic matrices made of cellulose ethers. II. Evaluation of a possible swelling-controlled drug release mechanism using dimensionless analysis. J Control Release, 2010;141:223–33
   PubMed Web of Science ®Google Scholar
• Florindo HF, Pandit S, Lacerda L, Goncalves LMD, Alpar HO, Almeida AJ. The enhancement of the immune response against S. equi antigens through the intranasal administration of poly-3-caprolactone-based nanoparticles. Biomaterials, 2009;30:879–91
   PubMed Web of Science ®Google Scholar
• Fredenberg S, Wahlgren M, Reslow M, Axelsson A. The mechanisms of drug release in poly(lactic-co-glycolic acid)-based drug delivery systems-A review. Int J Pharm, 2011;415:34–52
   PubMed Web of Science ®Google Scholar
• Giunchedi P, Alpar HO, Conte U. PDLLA microspheres containing steroids: spray-drying, o/w and w/o/w emulsifications as preparation methods. J Microencapsulation, 1998;15(2):185–95
   PubMed Web of Science ®Google Scholar
• Gopferich A. Mechanisms of polymer degradation and erosion. Biomaterials, 1996;17(2):103–14
   PubMed Web of Science ®Google Scholar
• Hickey T, Kreutzer D, Burgess DJ, Moussy F. Dexamethasone/PLGA microspheres for continuous delivery of an anti-inflammatory drug for implantable medical devices. Biomaterials, 2002;23:1649–56
   PubMed Web of Science ®Google Scholar
• Homayoun P, Mandal T, Landry D, Komiskey H. Controlled release of anti-cocaine catalytic antibody from biodegradable polymer microspheres. J Pharm Pharmacol, 2003;55:933–8
   PubMed Web of Science ®Google Scholar
• Ichikawa H, Fukumori Y, Adeyeye CM. Design of prolonged-release microcapsules containing diclofenac sodium for oral suspension and their preparation by the wurster process. Int J Pharm, 1997;156:39–48
   Web of Science ®Google Scholar
• Jaganathan KS, Vyas SP. Strong systemic and mucosal immune responses to surface-modified PLGA microspheres containing recombinant Hepatitis B antigen administered intranasally. Vaccine, 2006;24:4201–11
   PubMed Web of Science ®Google Scholar
• Jain RA. The manufacturing techniques of various drug loaded biodegradable poly(lactide-co-glycolide) (PLGA) devices. Biomaterials, 2000;21(23):2475–90
   PubMed Web of Science ®Google Scholar
• Jeon H-J, Jeong Y-I, Jang M-K, Park Y-H, Nah J-W. Effect of solvent on the preparation of surfactant-free poly(lactide-co-glycolide) nanoparticles and norfloxacin release characteristics. Int J Pharm, 2000;207:99–108
   PubMed Web of Science ®Google Scholar
• Kepmen DHR, Lu L, Zhu X, Kim C, Jabbari E, Dhert WAJ, Currier BL, Yaszemski MJ. Development of biodegradable poly(propylene fumarate)/poly(lactic-co-glycolic acid) blend microspheres. II. Controlled drug release and microsphere degradation. J Biomed Mater Res A, 2004;70(2):293–302
   PubMedGoogle Scholar
• Kokai LE, Tan H, Jhunjhunwala S, Little SR, Frank JW, Marra KG. Protein bioactivity and polymer orientation is affected by stabilizer incorporation for double-walled microspheres. J Control Release, 2010;141:168–76
   PubMed Web of Science ®Google Scholar
• Kumar G, Sharma S, Shafiq N, Khuller GK, Malhotra S. Optimization, in vitro–in vivo evaluation, and short-term tolerability of novel levofloxacin-loaded PLGA nanoparticle formulation. J Pharm Sci, 2012;101(6):2165–76
   PubMed Web of Science ®Google Scholar
• Leach K, Noh K, Mathiowitz E. Effect of manufacturing conditions on the formation of double-walled polymer microspheres. J Microencapsulation, 1999;16(2):153–67
   PubMed Web of Science ®Google Scholar
• Lee TH, Wang J, Wang CH. Double-walled microspheres for the sustained release of a highly water soluble drug: Characterization and irradiation studies. J Control Release, 2002;83:437–52
   PubMed Web of Science ®Google Scholar
• Lee WL, Loei C, Widjaja E, Loo SC. Altering the drug release profiles of double layered ternary-phase microparticles. J Control Release, 2011;151:229–38
   PubMed Web of Science ®Google Scholar
• Leonardi D, Salomón CJ, Lamas MC, Olivieri AC. Development of novel formulations for Chagas’ disease: Optimization of benznidazole chitosan microparticles based on artificial neural networks. Int J Pharm, 2009;367:140–7
   PubMed Web of Science ®Google Scholar
• Li M, Rouaud O, Poncelet D. Microencapsulation by solvent evaporation: State of the art for process engineering approaches. Int J Pharm, 2008a;363:26–39
   PubMed Web of Science ®Google Scholar
• Li X, Xu Y, Chen G, Wei P, Ping Q. PLGA nanoparticles for the oral delivery of 5-Fluorouracil using high pressure homogenization-emulsification as the preparation method and in vitro/in vivo studies. Drug Dev Ind Pharm, 2008b;34(1):107–15
   PubMed Web of Science ®Google Scholar
• Mainardes RM, Daflon Gremião MP, Evangelista RC. Thermoanalytical study of praziquantel-loaded PLGA nanoparticles. Brazilian J Pharm Sci, 2006;42(4):523–30
   Google Scholar
• Malik DK, Baboota S, Ahuja A, Hasan S, Ali J. Recent advances in protein and peptide drug delivery systems. Curr Drug Deliv, 2007;4(2):141–51
   PubMedGoogle Scholar
• Manca ML, Mourtas S, Dracopoulos V, Fadda AM, Antimisiaris SG. PLGA, chitosan or citosan-coated PLGA microparticles for alveoler delivery? A comparative study of particle stability during nebulization. Colloids Surf B: Biointerfaces, 2008;62:220–31
   PubMed Web of Science ®Google Scholar
• Mao S, Xu J, Cai C, Germershaus O, Schaper A, Kissel T. Effect of wow process parameters on morphology and burst release of FITC-dextran loaded PLGA microspheres. Int J Pharm, 2007;334:137–48
   PubMed Web of Science ®Google Scholar
• Mathiowitz E, Kreitz M. 1999. Microencapsulation. In: Mathiowitz E, ed. Encyclopedia of controlled drug delivery, vol. 2. New York: Wiley, pp. 493–553
   Google Scholar
• Matsumoto A, Matsukawa Y, Horikiri Y, Suzuki T. Rupture and drug release characteristics of multi-reservoir type microspheres with poly(dl-lactide-co-glycolide) and poly(dl-lactide). Int J Pharm, 2006;327:110–16
   PubMedGoogle Scholar
• Meng FT, Ma GH, Qiu W, Su ZG. W/O/W double emulsion technique using ethyl acetate as organic solvent: Effects of its diffusion rate on the characteristics of microparticles. J Control Release, 2003;91:407–16
   PubMed Web of Science ®Google Scholar
• Mollo AR, Corrigan OI. Effect of poly-hydroxy aliphatic ester polymer type on amoxicillin release from cylindrical compacts. Int J Pharm, 2003;268:71–9
   PubMed Web of Science ®Google Scholar
• Nie H, Dong Z, Arifin DY, Hu Y, Wang CH. Core/shell microspheres via coaxial electrohydrodynamic atomization for sequential and parallel release of drugs. J Biomed Mater Res A, 2010;95:709–16
   PubMed Web of Science ®Google Scholar
• Okada H, Toguchi H. Biodegradable microspheres in drug delivery. Crit Rev Ther Drug Carrier Syst, 1995;12(1):1–99
   PubMed Web of Science ®Google Scholar
• Patel RS, Cho DY, Tian C, Chang A, Estrellas KM, Lavin D, Furtado S, Mathiowitz E. Doxycycline delivery from PLGA microspheres prepared by a modified solvent removal method. J Microencapsulation, 2012;29(4):344–52
   PubMed Web of Science ®Google Scholar
• Pekarek KJ, Jacob JS, Mathiowitz E. Double-walled polymer microspheres for controlled drug-release. Lett Nat, 1994;367:258–60
   PubMed Web of Science ®Google Scholar
• Pollauf EJ, Kim KK, Pack DW. Small-molecule release from poly(d,l-lactide)/poly(d,l-lactide-co-glycolide) composite microparticles. J Pharm Sci, 2005;94:2013–22
   PubMed Web of Science ®Google Scholar
• Rahman NA, Mathiowitz E. Localization of bovine serum albumin in double-walled microspheres. J Control Release, 2004;94:163–75
   PubMed Web of Science ®Google Scholar
• Rouse JJ, Mohamed F, van der Walle CF. Physical ageing and thermal analysis of PLGA microspheres encapsulating protein or DNA. Int J Pharm, 2007;339:112–20
   PubMed Web of Science ®Google Scholar
• Ruan G, Feng SS, Li QT. Effects of material hydrophobicity on physical properties of polymeric microspheres formed by double emulsion process. J Control Release, 2002;84(3):151–60
   PubMed Web of Science ®Google Scholar
• Sharma G, van der Walle CF, Ravi Kumar MNV. Antacid co-encapsulated polyester nanoparticles for peroral delivery of insulin: Development, pharmacokinetics, biodistribution and pharmacodynamics. Int J Pharm, 2013;440:99–110
   PubMedGoogle Scholar
• Song X, Song S-K, Zhao P, Wei L-M, Jiao H-S. β-methasone-containing biodegradable poly(lactide-coglycolide) acid microspheres for intraarticular injection: Effect of formulation parameters on characteristics and in vitro release. Pharm Dev Technol, 2012;1–10, Early Online
   Web of Science ®Google Scholar
• Soppimath KS, Aminabhavi TM, Kulkarni AR, Rudzinski WE. Biodegradable polymeric nanoparticles as drug delivery devices. J Control Rel, 2001;70:1–20
   PubMed Web of Science ®Google Scholar
• Spiers ID, Alpar HO, Eyles JE, Bozkir A, Miller J, Williamson ED. Studies on the co-encapsulation, release and integrity of two subunit antigens: rV and rF1 from Yersinia pestis. J Pharm Pharmacol, 1999;51:991–7
   PubMed Web of Science ®Google Scholar
• Tan EC, Lin R, Wang C-H. Fabrication of double-walled microspheres for the sustained release of doxorubicin. J Colloid Interface Sci, 2005;291:135–43
   PubMed Web of Science ®Google Scholar
• Vladisavljevi’c GT, Schubert H. Influence of process parameters on droplet size distribution in SPG membrane emulsification and stability of prepared emulsion droplets. J Membr Sci, 2003;225:15–23
   Web of Science ®Google Scholar
• Wang J, Wang BM, Schwendeman SP. Characterization of the initial burst release of a model peptide from poly(d,l-lactideco-glycolide) microspheres. J Control Release, 2002;82:289–307
   PubMed Web of Science ®Google Scholar
• Yang YY, Chung TS, Ng NP. Morphology, drug distribution, and in vitro release profiles of biodegradable polymeric microspheres containing protein fabricated by double-emulsion solvent extraction/evaporation method. Biomaterials, 2001;22:231–41
   PubMed Web of Science ®Google Scholar
• Yeh MK, Chen JL, Chiang CH. In vivo and in vitro characteristics for insulin-loaded PLA microparticles prepared by w/o/w solvent evaporation method with electrolytes in the continuous phase. J Microencapsulation, 2004;21(7):719–28
   PubMed Web of Science ®Google Scholar
• Yeo Y, Park K. Control of encapsulation efficiency and initial burst in polymeric microparticle systems. Arch Pharm Res, 2004;27(1):1–12
   PubMed Web of Science ®Google Scholar
• Zhao J, Liu C-S, Yuan Y, Tao X-Y, Shan X-Q, Sheng Y, Wu F. Preparation of hemoglobin-loaded nano-sized particles with porous structure as oxygen carriers. Biomaterials, 2007;28:1414–22
   PubMed Web of Science ®Google Scholar
• Zheng W. A water-in-oil-in-oil-in-water (W/O/O/W) method for producing drug-releasing, double-walled microspheres. Int J Pharm, 2009;374:90–5
   PubMed Web of Science ®Google Scholar