Preparation and characterization of three types of cefquinome-loaded microspheres

References

• Kutmalge, M., M. Ratnaparkhi, M. Wattamwar, and S. Chaudhari. 2014. A review on microsphere. Pharm. Sci. Moni. 5:180–190.
   Google Scholar
• Dumka, V. K., V. Dinakaran, B. Ranjan, and S. Rampal. 2013. Comparative pharmacokinetics of cefquinome following intravenous and intramuscular administration in goats. Small. Rumi. Res. 113:273–277.
   Web of Science ®Google Scholar
• Zonca, A., M. Gallo, C. Locatelli, S. Carli, P. Moroni, and R. Villa. 2011. Cefquinome sulfate behavior after intramammary administration in healthy and infected cows. J. Dairy. Sci. 94:3455–3461.
   PubMed Web of Science ®Google Scholar
• Vasseur, M. V., M. Laurentie, J-G. Rolland, A. Perrin-Guyomard, J. Henri, and A. A. Ferran. 2014. Low or high doses of cefquinome targeting low or high bacterial inocula cure Klebsiella pneumoniae lung infections but differentially impact the levels of antibiotic resistance in fecal flora. Antimicrob. Agents Chem. 58:1744–1748.
   PubMed Web of Science ®Google Scholar
• Wan, L., P. Heng, and L. Chan. 1992. Drug encapsulation in alginate microspheres by emulsification. J. Microencapsul. 9:309–316.
   PubMed Web of Science ®Google Scholar
• Dinarvand, R., S. Mahmoodi, and E. Farboud. 2005. Effect of process variables on particle size of gelatin microspheres containing lactic acid. Pharm. Dev. Technol. 9:291–299.
   Web of Science ®Google Scholar
• Tabata, Y., and Y. Ikada. 1989. Synthesis of gelatin microspheres containing interferon. Pharm. Res. 6:422–427.
   PubMed Web of Science ®Google Scholar
• de Jalón, E. G., M. Blanco-Prıeto, P. Ygartua, and S. Santoyo. 2001. PLGA microparticles: Possible vehicles for topical drug delivery. Int. J. Pharm. 226:181–194.
   PubMed Web of Science ®Google Scholar
• Freiberg, S., and X. Zhu. 2004. Polymer microspheres for controlled drug release. Int. J. Pharm. 282:1–18.
   PubMed Web of Science ®Google Scholar
• Fan, H., and A. K. Dash. 2001. Effect of cross-linking on the in vitro release kinetics of doxorubicin from gelatin implants. Int. J. Pharm. 213:103–116.
   PubMed Web of Science ®Google Scholar
• Vandelli, M., F. Rivasi, P. Guerra, F. Forni, and R. Arletti. 2001. Gelatin microspheres crosslinked with D,L-glyceraldehyde as a potential drug delivery system: Preparation, characterisation, in vitro and in vivo studies. Int. J. Pharm. 215:175–184.
   PubMed Web of Science ®Google Scholar
• Brime, B., M. Ballesteros, and P. Frutos. 2000. Preparation and in vitro characterization of gelatin microspheres containing Levodopa for nasal administration. J. Microencapsul. 17:777–784.
   PubMed Web of Science ®Google Scholar
• Digenis, G. A., T. B. Gold, and V. P. Shah. 1994. Cross‐linking of gelatin capsules and its relevance to their in vitro–in vivo performance. J. Pharm. Sci. 83:915–921.
   PubMed Web of Science ®Google Scholar
• Liang, H. C., W. H. Chang, K. J. Lin, and H. W. Sung. 2003. Genipin‐crosslinked gelatin microspheres as a drug carrier for intramuscular administration: In vitro and in vivo studies. J. Biomed. Mater. Res. A. 65:271–282.
   PubMed Web of Science ®Google Scholar
• Hausberger, A. G., P. P. DeLuca. 1995. Characterization of biodegradable poly(D,L-lactide-co-glycolide) polymers and microspheres. J. Pharm. Biomed. Anal. 6:747–760.
   Web of Science ®Google Scholar
• Jeyanthib, R., R. C. Mehtac, B. C. Thanooa, and P. P. Deluca. 1997. Effect of processing parameters on the properties of peptide-containing PLGA microspheres. J. Microencapsul. 2:163–174.
   Google Scholar
• Kangarlou, S., I. Haririan, and Y. Gholipour. 2008. Physico-mechanical analysis of free ethyl cellulose films comprised with novel plasticizers of vitamin resources. Int. J. Pharm. 2:153–166.
   Web of Science ®Google Scholar
• Lai, H. L., K. Pitt, and D. Q. M. Craig. 2010. Characterisation of the thermal properties of ethylcellulose using differential scanning and quasi-isothermal calorimetric approaches. Int. J. Pharm. 2:178–184.
   Web of Science ®Google Scholar
• Sogol, K., and H. Ismaeil. 2011. Mechanical influence of static versus dynamic loadings on parametrical analysis of plasticized ethyl cellulose films. Int J Pharm. 2:1–8.
   Web of Science ®Google Scholar
• Wang, Y., B. Gu, and D. J. Burgess. 2014. Microspheres prepared with PLGA blends for delivery of dexamethasone for implantable medical devices. Pharm. Res. 31:373–381.
   PubMed Web of Science ®Google Scholar
• Sengel-Turk, C. T., C. Hascicek, and N. Gonul. 2011. Ethylcellulose-based matrix-type microspheres: Influence of plasticizer ratio as pore-forming agent. AAPS Pharm. Sci. Technol. 12:1127–1135.
   PubMed Web of Science ®Google Scholar
• Quaglia, F., G. de Rosa, E. Granata, F. Ungaro, E. Fattal, and M. I. La Rotonda. 2003. Feeding liquid, non-ionic surfactant and cyclodextrin affect the properties of insulin-loaded poly(lactide-co-glycolide) microspheres prepared by spray-drying. J. Control. Release 86:267–278.
   PubMed Web of Science ®Google Scholar
• Samein, L. H. 2014. Preparation, characterization, and in-vivo evaluation of daptomycin poly(D,L-lactide-co-glycolide) microspheres. Iraqi. J. Pharm. Sci. 23:42–52.
   Google Scholar
• Roh, H-S., J-S. Chang, and S-E. Park. 1999. Synthesis of mesoporous silica in acidic condition by solvent evaporation method. Korean J. Chem. Eng. 16:331–337.
   Web of Science ®Google Scholar
• Torrado, J., L. Illum, and S. Davis. 1989. Particle size and size distribution of albumin microspheres produced by heat and chemical stabilization. Int. J. Pharm. 51:85–93.
   Web of Science ®Google Scholar
• Hao, Z., H. Wu, L. Hao, Y. Zhao, Z. Ding, and F. Yang. 2013. Preparation, characterization, and release behavior of ceftiofur‐loaded gelatin‐based microspheres. J. Appl. Polym. Sci. 130:2369–2376.
   Web of Science ®Google Scholar
• Gu, B., X. Sun, F. Papadimitrakopoulos, and D. J. Burgess. 2016. Seeing is believing, PLGA microsphere degradation revealed in PLGA microsphere/PVA hydrogel composites. J. Control. Release 228:170–178.
   PubMed Web of Science ®Google Scholar
• Ghorab, M. M., H. Zia, and L. A. Luzzi. 1990. Preparation of controlled release anticancer agents I: 5-Fluorouracil-ethyl cellulose microspheres. J. Microencapsul. 7(4): 447–454.
   PubMed Web of Science ®Google Scholar
• Huang, H-P., and I. Ghebre-Sellassie. 1989. Preparation of microspheres of water-soluble pharmaceuticals. J. Microencapsul. 6:219–225.
   PubMed Web of Science ®Google Scholar
• Crotts, G., H. Sah, and T. G. Park. 1997. Adsorption determines in-vitro protein release rate from biodegradable microspheres: Quantitative analysis of surface area during degradation. J. Control. Release 1:101–111.
   Web of Science ®Google Scholar