REFERENCES
- Pişkin, E., Chang, T.M.S. (1981). 5-Fluorouracil loaded chitosan microspheres for chemoembolization. J. Microencapsul. 1: 343–350, [CSA]
- Elçin, Y.M., Dixit, V., Gitnick, G. (1996). Controlled release of endothelial cell growth factor from chitosan-albumin microspheres for localized angiogenesis: In vitro and in vivo studies. Artif. Cells Blood Substit. Immobil. Biotechnol. 24(3): 257–271, [CSA]
- Gupta, K.C., Kumar, M.N.V. (2000). An overview on chitin and chitosan applications with an emphasis on controlled drug release formulations. Review. J.M.S.-Rev. Macromol. Chem. Phys. C 40(4): 273–308, [CSA]
- Muzzarelli, R.A., Mattioli-Belmonte, M., Pugnaloni, A., Biagini, G. (1999). Biochemistry, histology and clinical uses of chitins and chitosans in wound healing. Review. EXS 87: 251–264, [PUBMED], [INFOTRIEVE], [CSA]
- Elçin, A.E., Elçin, Y.M., Pappas, G.D. (1998). Neural tissue engineering: Adrenal chromaffin cell attachment and viability on chitosan scaffolds. Neurol. Res. 20: 648–654, [CSA]
- Elçin, Y.M., Dixit, V., Lewin, K., Gitnick, G. (1999). Xenotransplantation of fetal porcine hepatocytes in rats using a tissue engineering approach. Artif. Organs 23: 146–152, [CROSSREF], [CSA]
- Bodmeier, R., Paeratakul, O. (1989). Spherical agglomerates of water-insoluble drugs. J. Pharm. Sci. 78: 964–967, [PUBMED], [INFOTRIEVE], [CSA]
- Berthold, A., Cremer, K., Kreuter, J. (1996). Preparation and characterization of chitosan microspheres as drug carrier for prednisolone sodium phosphate as model for anti-inflammatory drugs. J. Control. Rel. 39: 17–25, [CROSSREF], [CSA]
- Bodmeier, R., Oh, K.H., Pramar, Y. (1989). Preparation and evaluation of drug-containing chitosan beads. Drug Dev. Ind. Pharm. 15: 1475–1494, [CSA]
- Singla, A.K., Dhawan, S. (2003). Nifedipine loaded chitosan microspheres prepared by emulsification phase separation. Biotech. Histochem. 78: 243–254, [PUBMED], [INFOTRIEVE], [CSA]
- Thanoo, B.C., Sunny, M.C., Jayakrishnan, A. (1992). Cross-linked chitosan microspheres: Preparation and evaluation as a matrix for the controlled release of pharmaceuticals. J. Pharm. Pharmacol. 44: 283–286, [PUBMED], [INFOTRIEVE], [CSA]
- Berthold, A., Cremer, K., Kreuter, J. (1996). Influence of crosslinking on the acid stability and physicochemical properties of chitosan microspheres. STP Pharm. Sci. 6: 358–364, [CSA]
- Orienti, I., Aiedeh, K., Gianasi, E., Bertasi, V., Zecchi, V. (1996). Indomethacin loaded chitosan microspheres: Correlation between the erosion process and release kinetics. J. Microencapsul. 13: 463–472, [PUBMED], [INFOTRIEVE], [CSA]
- Shu, X.Z., Zhu, K.J. (2000). A novel approach to prepare tripolyphosphate/chitosan complex beads for controlled release drug delivery. Int. J. Pharm. 201: 51–58, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Muzzarelli, R., Baldassare, V., Conti, F., Ferrara, P., Biagini, G., Gazzanelli, G., Vasi, V. (1988). Biological activity of chitosan: Ultrastructural study. Biomaterials 9: 247–252, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Jameela, S.R., Jayakrishan, A. (1995). Glutaraldehyde cross-linked chitosan microspheres as a long acting biodegradable drug delivery vehicle. Studies on the in vitro release of mitoxantrone and in vivo degradation of microspheres in rat muscle. Biomaterials 16(10): 769–775, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Lu, F., Cao, Z., Zhuang, Z., Mou, Z.X., Feng, X. (1998). Biodegradation and biocompatibility of a chitosan film. Sheng Wu Yi Xue 15(2): 183–185, [CSA]
- Pratsilp, M., Jenwithisuk, R., Kongsuwan, K., Damrongchai, N., Watts, P. (2000). Cellular responses to chitosan in vitro: The importance of deacetylation. J. Mater. Sci. Mater. Med. 11(12): 773–778, [CROSSREF], [CSA]
- Kofuji, K., Ito, T., Murata, Y., Kawashima, S. (2001). Biodegradation and drug release of chitosan gel beads in subcutaneous air pouches of mice. Biol. Pharm. Bull. 24(2): 205–208, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Vande Vord, P.J., Matthew, H.W., DeSilva, S.P., Mayton, L., Wu, B., Wooley, P.H. (2002). Evaluation of the biocompatibility of a chitosan scaffold in mice. J. Biomed. Mater. Res. 59(3): 585–590, [CROSSREF], [CSA]
- Elçin, A.E., Elçin, Y.M. (2000). Polycation-coated polyanion microspheres of urease for urea hydrolysis. Artif. Cells Blood Substit. Immobil. Biotechnol. 28(1): 95–111, [CSA]
- Kumar, M.N.V.R. (2000). Nano and microparticles as controlled drug delivery devices. J. Pharm. Pharmaceut. Sci. 3(2): 234–258, [CSA]