[1] Tiwari, G., Tiwari, R., Sriwastawa, B., Bhati, L., Pandey, S., Pandey, P., & Bannerjee, S. K. (2012). Drug delivery systems: An updated review. Int J Pharm Investig., 2(1), 2–11.
[2] Schaller, M., & Korting, H. C. (1996). Interaction of liposomes with human skin: The role of the stratum corneum. Adv. Drug Deliv. Rev., 18(3), 303–309.
[3] Gulati, M., Grover, M., Singh, S., & Singh, M. (1998). Lipophilic drug derivatives in liposomes. Int. J. Pharm., 165(2), 129–168.
[4] Kazi, K. M., Mandal, A. S., Biswas, N., Guha, A., Chatterjee, S., & Behera, M. (2010). Niosome : A future of targeted drug delivery systems. J. Adv. Pharm. Technol. Res., 1(4), 374–380.
[5] Azmin, M. N., Florence, a T., Handjani-Vila, R. M., Stuart, J. F., Vanlerberghe, G., & Whittaker, J. S. (1985). The effect of non-ionic surfactant vesicle (niosome) entrapment on the absorption and distribution of methotrexate in mice. J. Pharm. Pharmacol., 37(4), 237–242.
[6] Dai, C., Wang, B., Zhao, H., Li, B., & Wang, J. (2006). Preparation and characterization of liposomes-in-alginate (LIA) for protein delivery system. Colloids Surfaces B Biointerfaces., 47(2), 205–210.
[7] Masalova, O., Kulikouskaya, V., Shutava, T., & Agabekov, V. (2013). Alginate and Chitosan Gel Nanoparticles for Efficient Protein Entrapment. Phys. Procedia., 40(0), 69–75.
[8] Perez-Moral, N., Gonzalez, M. C., & Parker, R. (2013). Preparation of iron-loaded alginate gel beads and their release characteristics under simulated gastrointestinal conditions. Food Hydrocoll., 31(1), 114–120.
[9] Stojanovic, R., Belscak-Cvitanovic, A., Manojlovic, V., Komes, D., Nedovic, V., & Bugarski, B. (2012). Encapsulation of thyme (Thymus serpyllum L.) aqueous extract in calcium alginate beads. J. Sci. Food Agric., 92(3), 685–696.
[10] Lee, K. Y., & Mooney, D. J. (2012). Alginate: Properties and biomedical applications. Prog. Polym. Sci., 37(1), 106–126.
[11] Mandal, S., Basu, S. K., & Sa, B. (2009). Sustained Release of a Water-Soluble Drug from Alginate Matrix Tablets Prepared by Wet Granulation Method, 10(4), 1348–1356.
[12] Al-Mayah, A. M. R. (2012). Simulation of enzyme catalysis in calcium alginate beads. Enzyme Res., 2012.
[13] Zhang, S., Shang, W., Yang, X., Zhang, S., Zhang, X., & Chen, J. (2013). Immobilization of lipase using alginate hydrogel beads and enzymatic evaluation in hydrolysis of p-nitrophenol butyrate. Bull. Korean Chem. Soc., 34(9), 2741–2746.
[14] Suksamran, T., Opanasopit, P., Rojanarata, T., Ngawhirunpat, T., Ruktanonchai, U., & Supaphol, P. (2009). Biodegradable alginate microparticles developed by electrohydrodynamic spraying techniques for oral delivery of protein. J Microencapsul., 26(7), 563–570.
[15] Bojana, I., Verica, D., Viktor, N., & Branko, B. (2013). Liposome-in-alginate systems for encapsulation of natural antioxidants. In Insid. Symp. (pp. 9–12).
[16] Strasdat, B., & Bunjes, H. (2013). Incorporation of lipid nanoparticles into calcium alginate beads and characterization of the encapsulated particles by differential scanning calorimetry. Food Hydrocoll., 30(2), 567–575.
[17] Pjanovic, R., Bo.skovic-Vragolovic, N., Veljkovic-Giga, J., Garic-Grulovic, R., Pejanovic, S., & Bugarski, B. (2010). Diffusion of drugs from hydrogels and liposomes as drug carriers. J. Chem. Technol. Biotechnol., 85(5), 693–698.
[18] Ditizio, V., Karlgard, C., Lilge, L., Khoury, A. E., Mittelman, M. W., & Dicosmo, F. (1999). Localized drug delivery using crosslinked gelatin gels containing liposomes : Factors influencing liposome stability and drug release.
[19] Marianecci, C., Carafa, M., di Marzio, L., Rinaldi, F., di Meo, C., Alhaique, F., … Coviello, T. (2011). A new vesicle-loaded hydrogel system suitable for topical applications: Preparation and characterization. J. Pharm. Pharm. Sci., 14(3), 336–346.
[20] Bock, N., Dargaville, T. R. R., & Woodruff, M. a. A. (2012). Electrospraying of polymers with therapeutic molecules: State of the art. Prog. Polym. Sci., 37(11), 1510–1551.
[21] Jaworek, A., & Sobczyk, A. T. (2008). Electrospraying route to nanotechnology: An overview. J. Electrostat., 66(3–4), 197–219.
[22] Rayleigh, Lord. (1878). On the Instability of Jets. Proc. London Math. Soc., 10(June 1873), 4–13.
[23] Park, H., Kim, P. H., Hwang, T., Kwon, O. J., Park, T. J., Choi, S. W., … Kim, J. H. (2012). Fabrication of cross-linked alginate beads using electrospraying for adenovirus delivery. Int J Pharm., 427(2), 417–425.
[24] Lagarde, D., Batéjat, D., Sicard, B., Trocherie, S., Chassard, D., Enslen, M., & Chauffard, F. (2000). Slow-release caffeine: a new response to the effects of a limited sleep deprivation. Sleep., 23(5), 651–661.
[25] Smith, A. P., Rusted, J. M., Savory, M., Eaton-Williams, P., & Hall, S. R. (1991). The effects of caffeine, impulsivity and time of day on performance, mood and cardiovascular function. J. Psychopharmacol., 5(2), 120–128.
[26] Tan, D., Zhao, B., Moochhala, S., & Yang, Y.-Y. (2006). Sustained-release of caffeine from a polymeric tablet matrix: An in vitro and pharmacokinetic study. Mater. Sci. Eng. B., 132(1–2), 143–146.
[27] Bagheri, A., Chu, B. S., & Yaakob, H. (2014). Niosomal drug delivery systems: Formulation, preparation and applications. World Appl. Sci. J., 32(8), 1671–1685.
[28] Kavrakovski, Z., Popovska, O., Simonovska, J., Kavrakovski, Z., & Rafajlovska, V. (2013). An Overview: Methods for Preparation and Characterization of Liposomes as Drug Delivery Systems. Int. J. Pharm. Phytopharm. Res., 3(2), 13–20.
[29] Mehregan Nikoo, A., Kadkhodaee, R., Ghorani, B., Razzaq, H., & Tucker, N. (2016). Controlling the morphology and material characteristics of electrospray generated calcium alginate microhydrogels. J. Microencapsul., 2048(September), 1–28.
[30] Hadjiioannou, T. P., Christian, G. D., Koupparis, M. A., & Macheras, P. E. (1993). Quantitative Calculations in Pharmaceutical Practice and Research. VCHPublishers.
[31] Bourne, D. W. A. (2002). Modern Pharmaceutics. New York: Marcel Dekker.
[32] Higuchi, T. (1963). Mechanism of Sustained- Action Medication. J. Pharm. Sci., 52(12), 1145–1149.
[33] Jose, S., Fangueiro, J. F., Smitha, J., Cinu, T. a., Chacko, a. J., Premaletha, K., & Souto, E. B. (2013). Predictive modeling of insulin release profile from cross-linked chitosan microspheres. Eur. J. Med. Chem., 60, 249–253.
[34] J.S. Dua, Prof. A. C. Rana, D. a. K. B. (2012). Review Article LIPOSOME : METHODS OF PREPARATION AND APPLICATIONS. Int. J. Pharm. Stud. Res., III(II), 7.
[35] Woodbury, D. J., Richardson, E. S., Grigg, A. W., Welling, R. D., & Knudson, B. H. (2006). Reducing liposome size with ultrasound: bimodal size distributions. J. Liposome Res., 16(1), 57–80.
[36] Supaporn, S. (2011). Effect of Freeze-Thawing Process on the Size and Lamellarity of PEG-Lipid Liposomes. Open Colloid Sci. J., 4, 1–8.
[37] Costa, A. P., Xu, X., & Burgess, D. J. (2014). Freeze-Anneal-Thaw Cycling of Unilamellar Liposomes: Effect on Encapsulation Efficiency. Pharm. Res., 31(1), 97–103.
[38] Agashe, H., Lagisetty, P., Awasthi, S., & Awasthi, V. (2010). Improved formulation of liposome-encapsulated hemoglobin with an anionic non-phospholipid. Colloids Surfaces B Biointerfaces., 75(2), 573–583.
[39] Mehregan Nikoo, A., Kadkhodaee, R., Ghorani, B., Razzaq, H., & Tucker, N. (2016). Controlling the morphology and material characteristics of electrospray generated calcium alginate microhydrogels. J. Microencapsul., 1–28.
[40] Fadda, A. M., Baroli, B. M., Maccioni, A. M., Sinico, C., Valenti, D., & Alhaique, F. (1998). Phospholipid-detergent systems: Effects of polysorbates on the release of liposomal caffeine. Farmaco., 53(10–11), 650–654.
[41] Ram, H. N. A., Lachake, P., Kaushik, U., & Shreedhara, C. S. (2010). Formulation and evaluation of floating tablets of liquorice extract. Pharmacognosy Res., 2(5), 304–8.
)