Encapsulation of L-ascorbic acid via polycaprolactone-polyethylene glycol-casein bioblends

1. Chakkarapani, P., Subbiah, L., Palanisamy, S., Bibiana, A., Ahrentorp, F., Jonasson, C. & Johansson, C. (2015). Encapsulation of methotrexate loaded magnetic microcapsules for magnetic drug targeting and controlled drug release. J. Magn. Magn. Mater. 380, 285–294. DOI: 10.1016/j.jmmm.2014.11.006.10.1016/j.jmmm.2014.11.006Search in Google Scholar

2. Zhou, G., Zhao, Y., Hu, J., Shen, L., Liu, W. & Yang, X. (2013). A new drug-loading technique with high efficiency and sustained-releasing ability via the Pickering emulsion interfacial assembly of temperature/pH-sensitive nanogels. React. Funct. Polym. 73, 1537–1543. DOI: 10.1016/j.reactfunctpolym.2013.02.011.10.1016/j.reactfunctpolym.2013.02.011Search in Google Scholar

3. Ozsagiroglu, E., Iyisan, B. & Avcibasi Guvenilir, Y. (2013). Comparing the In-Vitro Biodegradation Kinetics of Commercial and Synthesized Polycaprolactone Films in Different Enzyme Solutions. Ekoloji. 86, 90–96. DOI: 10.5053/ekoloji.2013.8611.10.5053/ekoloji.2013.8611Search in Google Scholar

4. Xu, X. Khan, M.A. & Burgess, D.J. (2012). A quality by design (QbD) case study on liposomes containing hydrophilic API: II. Screening of critical variables, and establishment of design space at laboratory scale. Int. J. Pharm. 423, 543–553. DOI: 10.1016/j.ijpharm.2011.11.036.10.1016/j.ijpharm.2011.11.036Search in Google Scholar

5. Patel, A.R. & Velikov, K.P. (2011). Colloidal delivery systems in foods: A general comparison with oral drug delivery. LWT-Food Sci. Technol. 44, 1958–1964. DOI: 10.1016/j.lwt.2011.04.005.10.1016/j.lwt.2011.04.005Search in Google Scholar

6. Huang, M., Xu, Q. & Deng, X.X. (2014). L-Ascorbic acid metabolism during fruit development in an ascorbate-rich fruit crop chestnut rose (Rosa roxburghii Tratt). J. Plant Physiol. 171, 1205–1216. DOI: 10.1016/j.jplph.2014.03.010.10.1016/j.jplph.2014.03.010Search in Google Scholar

7. Khalid, N., Kobayashi, I., Neves, MA., Uemura, K., Nakajima, M. & Nabetani, H. (2014). Monodisperse W/O/W emulsions encapsulating l-ascorbic acid: Insights on their formulation using microchannel emulsification and stability studies. Colloid Surface A. 458, 69–77. DOI: 10.1016/j.colsurfa.2014.04.019.10.1016/j.colsurfa.2014.04.019Search in Google Scholar

8. Beck-Broichsitter, M., Paulus, I.E., Greiner, A. & Kissel T. (2015). Modified vibrating-mesh nozzles for advanced spray-drying applications. Eur. J. Pharm. Biopharm. 92, 96–101. DOI: 10.1016/j.ejpb.2015.03.001.10.1016/j.ejpb.2015.03.001Search in Google Scholar

9. Rassu, G., Nieddu, M., Bosi, P., Trevisi, P., Colombo, M., Priori, D., Manconi, P., Giunchedi, P. & Gavini, E. Boatto, G. (2014). Encapsulation and modified-release of thymol from oral microparticles as adjuvant or substitute to current medications. Phytomedicine. 21, 1627–1632. DOI: 10.1016/j.phymed.2014.07.017.10.1016/j.phymed.2014.07.017Search in Google Scholar

10. Carneiro, H.C.F., Tonon, R.V., Grosso, C.R.F. & Hubinger, MD (2013). Encapsulation efficiency and oxidative stability of flaxseed oil microencapsulated by spray drying using different combinations of wall materials. J. Food Eng. 115, 443–451. DOI: 10.1016/j.jfoodeng.2012.03.033.10.1016/j.jfoodeng.2012.03.033Search in Google Scholar

11. Bürki, K. Jeon, I., Arpagaus, C. & Betz, G. (2011). New insights into respirable protein powder preparation using a nano spray dryer. Int. J. Pharm. 408, 248–256. DOI: 10.1016/j.ijpharm.2011.02.012.10.1016/j.ijpharm.2011.02.012Search in Google Scholar

12. Erbay, Z. & Koca, N. (2014). Exergoeconomic performance assessment of a pilot-scale spray dryer using the specific exergy costing method. Biosyst. Eng. 122, 127–138. DOI: 10.1016/j.ijpharm.2011.02.012.10.1016/j.ijpharm.2011.02.012Search in Google Scholar

13. Paudel, A., Worku, ZA., Meeus, J., Guns, S. & Van den Mooter, G. (2013). Manufacturing of solid dispersions of poorly water soluble drugs by spray drying: Formulation and process considerations. Int. J. Pharmaceut. 453, 253–284. DOI: 10.1016/j.ijpharm.2011.02.012.10.1016/j.ijpharm.2011.02.012Search in Google Scholar

14. Van der Schueren, L., Steyaert, I., De Schoenmaker, B. & De Clerck, K. (2012). Polycaprolactone/chitosan blend nanofibres electrospun from an acetic acid/formic acid solvent system. Carbohyd. Polym. 88, 1221–1226. DOI: 10.1016/j.carbpol.2012.01.085.10.1016/j.carbpol.2012.01.085Search in Google Scholar

15. Van der Schueren, L., De Meyer, T., Steyaert, I., Ceylan, Ö., Hemelsoet, K., Van Speybroeck, V. & De Clerck, K. (2013). Polycaprolactone and polycaprolactone/chitosan nanofibres functionalised with the pH-sensitive dye Nitrazine Yellow. Carbohyd. Polym. 91, 284–293. DOI: 10.1016/j.carbpol.2012.08.003.10.1016/j.carbpol.2012.08.003Search in Google Scholar

16. Horton, D.C., Derveer, D.V., Krzystek, J., Telser, J., Pittman, T., Crans, D.C. & Holder, A.A. (2014). Spectroscopic Characterization of L-ascorbic Acid-induced Reduction of Vanadium(V) Dipicolinates: Formation of Vanadium(III) and Vanadium(IV) Complexes from Vanadium(V) Dipicolinate Derivatives. Inorg. Chim. Acta. 420, 112–119. DOI: 10.1016/j.ica.2013.12.001.10.1016/j.ica.2013.12.001Search in Google Scholar

17. Porras-Saavedra, J., Palacios-González, E., Lartundo-Rojas, L., Garibay-Febles, V., Yáñez-Fernández, J., Hernández-Sánchez, H., Gutiérrez-López, G. & Alamilla-Beltrán, L. (2015). Microstructural properties and distribution of components in microparticles obtained by spray-drying. J. Food Eng. 152,105–112. DOI: 10.1016/j.jfoodeng.2014.11.014.10.1016/j.jfoodeng.2014.11.014Search in Google Scholar

18. Grund, J., Koerber, M., Walther, M. & Bodmeier, R. (2014). The effect of polymer properties on direct compression and drug release from water-insoluble controlled release matrix tablets. Int. J. Pharmaceut. 469, 94–101. DOI: 10.1016/j.ijpharm.2014.04.033.10.1016/j.ijpharm.2014.04.033Search in Google Scholar

19. Kadajji, V.G. & Betageri, G.V. (2011). Water Soluble Polymers for Pharmaceutical Applications. Polymers. 3(4), 1972–2009. DOI: 10.3390/polym3041972.10.3390/polym3041972Search in Google Scholar

20. Li, F., Li, X. & Li, B. (2011). Preparation of magnetic polylactic acid microspheres and investigation of its releasing property for loading curcumin. J. Magn. Magn. Mater. 323, 2770–2775. DOI: 10.1016/j.jmmm.2011.05.045.10.1016/j.jmmm.2011.05.045Search in Google Scholar

21. Orellana, B.R. & Puleo, D.A. (2014). Cyanide induced self-assembly and copper recognition in human blood serum by a new carbazole AIEE active material. Mater. Sci. Eng. C 43, 418–423. DOI: 10.1016/j.msec.2014.07.041.10.1016/j.msec.2014.07.041Search in Google Scholar

22. Alexa, I.F., Ignat, M., Popovici, R.F., Timpu, D. & Popovici, E. (2012). In vitro controlled release of antihypertensive drugs intercalated into unmodified SBA-15 and MgO modified SBA-15 matrices. Int. J. Pharmaceut. 436, 111–119. DOI: 10.1016/j.ijpharm.2012.06.036.10.1016/j.ijpharm.2012.06.036Search in Google Scholar

23. Moribe, K. Makishima, T., Higashi, K., Liu, N., Limwikrant, W., Ding, W., Masuda, M., Shimizu, T. & Yamamoto, K. (2014). Encapsulation of poorly water-soluble drugs into organic nanotubes for improving drug dissolution. Int. J. Pharmaceut. 469, 190–196. DOI: 10.1016/j.ijpharm.2014.04.005.10.1016/j.ijpharm.2014.04.005Search in Google Scholar

24. Jensen, D.M., Cun, D., Maltesen, M.J., Frokjaer, S., Nielsen, H.M. & Foged, C. (2010). Spray drying of siRNA-containing PLGA nanoparticles intended for inhalation. J. Control Release 142, 138–145. DOI: 10.1016/j.jconrel.2009.10.010.10.1016/j.jconrel.2009.10.010Search in Google Scholar

25. Wu, Y., Zou, L., Mao, J., Huang, J. & Liu, S. (2014). Stability and encapsulation efficiency of sulforaphane micro-encapsulated by spray drying. Carbohyd. Polym. 102, 497–503. DOI: 10.1016/j.carbpol.2013.11.057.10.1016/j.carbpol.2013.11.057Search in Google Scholar

26. Yuzbasi, N.S. & Selçuk, N. (2011). Air and oxy-fuel combustion characteristics of biomass/lignite blends in TGA-FTIR. Fuel Process. Technol. 92, 1101–1108. DOI: 10.1016/j.fuproc.2011.01.005.10.1016/j.fuproc.2011.01.005Search in Google Scholar

27. Wang, H., Helwa, Y. & Rempel, G.L. (2013). Preparation of polyacrylamide based microgels with different charges for drug encapsulation. Eur. Polym. J. 49(6), 1479–1486. DOI: 10.1016/j.eurpolymj.2013.04.003.10.1016/j.eurpolymj.2013.04.003Search in Google Scholar

28. Kalhapure, R.S., Mocktar, C., Sikwal, D.R., Sonawane, S.J., Kathiravan, M.K., Skelton, A. & Govender, T. (2014). Ion pairing with linoleic acid simultaneously enhances encapsulation efficiency and antibacterial activity of vancomycin in solid lipid nanoparticle. Colloid. Surface B. 117, 303–311. DOI: 10.1016/j.colsurfb.2014.02.045.10.1016/j.colsurfb.2014.02.045Search in Google Scholar

29. Post, A.E., Arnold, B., Weiss, J. & Hinrichs, J. (2012). Effect of temperature and pH on the solubility of caseins: Environmental influences on the dissociation of αS- and β-casein. J. Dairy. Sci. 95, 1603–1616. DOI: 10.3168/jds.2011-4641.10.3168/jds.2011-4641Search in Google Scholar

30. Zhou, Y., Song, F., Li, Y.S., Liu, J.Q., Lu, S.Y., Ren, H.L., Liu, Z.S., Zhang, Y.Y., Yang, L., Li, Z.H., Zhang, J.H. & Wang, X.R. (2013). Double-antibody based immunoassay for the detection of β-casein in bovine milk samples. Food Chem. 141(1), 167–173. DOI: 10.1016/j.foodchem.2013.03.010.10.1016/j.foodchem.2013.03.010Search in Google Scholar

31. de Almeida, R.R., Magalhães, H.S., de Souza, J.R.R., Trevisan, M.T.S., Vieira, I.G.P., Feitosa, J.P.A., Araújo, T.G. & Ricardo, N.M.P.S. (2015). Exploring the potential of Dimorphandra gardneriana galactomannans as drug delivery systems. Ind. Crop. Prod. 69, 284–289. DOI: 10.1016/j.indcrop.2015.02.041.10.1016/j.indcrop.2015.02.041Search in Google Scholar

32. England, C.G., Miller, M.C., Kuttan, A., Trent, J.O. & Frieboes, H.B. (2015). Release kinetics of paclitaxel and cisplatin from two and three layered gold nanoparticles. Eur. J. Pharm. Biopharm. 92, 120–129. DOI: 10.1016/j.ejpb.2015.02.017.10.1016/j.ejpb.2015.02.017Search in Google Scholar

33. Ozsagiroglu, E., Hayta, E.N. & Avcibasi Guvenilir, Y. (2015). Preparation of bioblends using spray dryer and their applications in drug delivery systems. Asian J. Chem. 27(10), 3734–3738. DOI: 10.14233/ajchem.2015.18958.10.14233/ajchem.2015.18958Search in Google Scholar