References
- Al Zaitone, B., and Lamprecht, A., 2013. Single droplet drying step characterization in microsphere preparation. Colloids and surfaces. B, biointerfaces, 105, 328–334.
- Ali, M.E., and Lamprecht, A., 2013. Polyethylene glycol as an alternative polymer solvent for nanoparticle preparation. International journal of pharmaceutics, 456 (1), 135–142.
- Allhenn, D., and Lamprecht, A., 2011. Microsphere preparation using the untoxic solvent glycofurol. Pharmaceutical research, 28 (3), 563–571.
- Ao, Z., et al., 2011. Colloidosomes formation by controlling the solvent extraction from particle-stabilized emulsions. Colloids and surfaces A: physicochemical and engineering aspects, 384 (1–3), 592–596.
- Bapatu, H.R., Maram, R.K., and Murthy, R.S., 2015. Stability-indicating HPLC method for quantification of celecoxib and diacerein along with its impurities in capsule dosage form. Journal of chromatographic science, 53 (1), 144–153.
- Beyer, K., et al., 1987. Final report on the safety assessment of propylene carbonate. International journal of toxicology, 6 (1), 23–51.
- Birnbaum, D.T., et al., 2000. Controlled release of beta-estradiol from PLAGA microparticles: the effect of organic phase solvent on encapsulation and release. Journal of controlled release: official journal of the controlled release society, 65 (3), 375–387.
- Blanco, D., and Alonso, J., 1998. Protein encapsulation and release from poly(lactide-co-glycolide) microspheres: effect of the protein and polymer properties and of the co-encapsulation of surfactants. European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 45 (3), 285–294.
- Buske, J., et al., 2012. Influence of PEG in PEG-PLGA microspheres on particle properties and protein release. European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 81 (1), 57–63.
- Cannavà, C., et al., 2013. Celecoxib-loaded PLGA/cyclodextrin microspheres: characterization and evaluation of anti-inflammatory activity on human chondrocyte cultures. Colloids and surfaces. B, biointerfaces, 111, 289–296.
- Das, S., Mondal, A., and Balasubramanian, S., 2017. Recent advances in modeling green solvents. Current opinion in green and sustainable chemistry, 5, 37–43.
- Elkharraz, K., et al., 2011. Encapsulation of water-soluble drugs by an o/o/o-solvent extraction microencapsulation method. International journal of pharmaceutics, 409 (1–2), 89–95.
- Feczkó, T., Tóth, J., and Gyenis, J., 2008. Comparison of the preparation of PLGA-BSA nano- and microparticles by PVA, poloxamer and PVP. Colloids and surfaces A: physicochemical and engineering aspects, 319 (1-3), 188–195.
- Gao, Y., et al., 2015. Tuning microparticle porosity during single needle electrospraying synthesis via a non-solvent-based physicochemical approach. Polymers, 7 (12), 2701–2710.
- Garner, J., et al., 2018. Beyond Q1/Q2: the impact of manufacturing conditions and test methods on drug release from PLGA-based microparticle depot formulations. Journal of pharmaceutical sciences, 107 (1), 353–361.
- Grizić, D., and Lamprecht, A., 2018. Microparticle preparation by a propylene carbonate emulsification-extraction method. International journal of pharmaceutics, 544 (1), 213–221.
- Grizić, D., et al., 2016. Propylene carbonate quantification by its derivative 3,5-diacetyl-1,4-dihydro-2,6-lutidine. Talanta, 151, 75–82.
- Hales, D., et al., 2017. A quality by design (QbD) study on enoxaparin sodium loaded polymeric microspheres for colon-specific delivery. European journal of pharmaceutical sciences, 100, 249–261.
- Ito, F., Fujimori, H., and Makino, K., 2007. Incorporation of water-soluble drugs in PLGA microspheres. Colloids and surfaces. B, biointerfaces, 54 (2), 173–178.
- Katou, H., Wandrey, A.J., and Gander, B., 2008. Kinetics of solvent extraction/evaporation process for PLGA microparticle fabrication. International journal of pharmaceutics, 364 (1), 45–53.
- Kietzmann, D., et al., 2009. pH-sensitive microparticles prepared by an oil/water emulsification method using n-butanol. International journal of pharmaceutics, 375 (1–2), 61–66.
- Klose, D., et al., 2006. How porosity and size affect the drug release mechanisms from PLGA-based microparticles. International journal of pharmaceutics, 314 (2), 198–206.
- Li, W.I., et al., 1995. Prediction of solvent removal profile and effect on properties for peptide-loaded PLGA microspheres prepared by solvent extraction/evaporation method. Journal of controlled release, 37 (3), 199–214.
- Martín-Sabroso, C., et al., 2015. Critical attributes of formulation and of elaboration process of PLGA-protein microparticles. International journal of pharmaceutics, 480 (1–2), 27–36.
- Paillard-Giteau, A., et al., 2010. Effect of various additives and polymers on lysozyme release from PLGA microspheres prepared by an s/o/w emulsion technique. European journal of pharmaceutics and biopharmaceutics, 75 (2), 128–136.
- Park, C.G., et al., 2017. Nanostructured mucoadhesive microparticles to enhance oral drug bioavailability. Journal of industrial and engineering chemistry, 54, 262–269.
- Quintanar-Guerrero, D., et al., 1996. Influence of stabilizing agents and preparative variables on the formation of poly(D,L-lactic acid) nanoparticles by an emulsification-diffusion technique. International journal of pharmaceutics, 143 (2), 133–141.
- Sah, H., 1997. Microencapsulation techniques using ethyl acetate as a dispersed solvent: effects of its extraction rate on the characteristics of PLGA microspheres. Journal of controlled release, 47 (3), 233–245.
- Sah, H., 2000. Ethyl formate – Alternative dispersed solvent useful in preparing PLGA microspheres. International journal of pharmaceutics, 195 (1–2), 103–113.
- Shaikh, A.-A.G., and Sivaram, S., 1996. Organic carbonates. Chemical reviews, 96 (3), 951–976.
- Sommer, L., Ackermann, G., and Burns, D.T., 1990. Present and future status of organic analytical reagents – Part II. Inorganic chemical analysis: classical methods, molecular spectroscopy (absorption and emission) and solvent extraction. Pure and applied chemistry, 62 (12), 2323–2338.
- Takeuchi, I., et al., 2018. Effects of L-leucine on PLGA microparticles for pulmonary administration prepared using spray drying: fine particle fraction and phagocytotic ratio of alveolar macrophages. Colloids and surfaces A: physicochemical and engineering aspects, 537, 411–417.
- Wang, F.J., and Wang, C.H., 2002. Sustained release of etanidazole from spray dried microspheres prepared by non-halogenated solvents. Journal of controlled release: official journal of the controlled release society, 81 (3), 263–280.