全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Preparation of Polysaccharide-Based Microspheres by a Water-in-Oil Emulsion Solvent Diffusion Method for Drug Carriers

DOI: 10.1155/2013/761870

Full-Text   Cite this paper   Add to My Lib

Abstract:

Polysaccharide-based microspheres of chitosan, starch, and alginate were prepared by the water-in-oil emulsion solvent diffusion method for use as drug carriers. Blue dextran was used as a water-soluble biomacromolecular drug model. Scanning electron microscopy showed sizes of the resultant microspheres that were approximately 100? m or less. They were spherical in shape with a rough surface and good dispersibility. Microsphere matrices were shown as a sponge. Drug loading efficiencies of all the microspheres were higher than 80%, which suggested that this method has potential to prepare polysaccharide-based microspheres containing a biomacromolecular drug model for drug delivery applications. 1. Introduction During the past few decades, research interest in biodegradable polymeric microspheres has increased steadily as their potential in a wide range of biomedical applications has been realized [1]. Research related to encapsulation of water-soluble biomacromolecular active agents with hydrophilic polymeric microspheres for drug delivery has been widely investigated. The specific requirements, such as swelling and dissolution, of these hydrophilic microspheres can be tailored by the polymer blending and cross-linking methods [2, 3]. Polysaccharides are common and cheap biopolymers that have been widely investigated as a microsphere matrix to carry water-soluble model drugs. Polysaccharide-based microspheres of chitosan [4–12], starch [13], and alginate [2, 14, 15] have been used as biodegradable matrices for controlled release drug delivery. Several methods have been reported for preparing the polysaccharide-based microspheres, such as spray-drying, emulsification-precipitation, and emulsification-cross-linking methods [4, 13, 16, 17]. However, a suitable method for fabricating polysaccharide-based microspheres remains a major challenge in the field of microencapsulation, especially a method that can be used for various polysaccharide types. Moreover, drug loading efficiency is also an important factor for consideration. Recently, a water-in-oil (W/O) emulsion solvent diffusion method used to prepare water-soluble polymeric microspheres has been reported by our group [18, 19]. This method is simple, rapid, and low in cost. Heat, high-energy and high-cost apparatus, and the surfactant can be avoided, while the time is also reduced. Thus, it is suitable for larger-scale microsphere production. In this work, we report that this single-step W/O emulsion solvent diffusion method can be used to prepare various polysaccharide-based microspheres with and

References

[1]  K. Z. Gumargalieva, D. Horak, and G. E. Zaikov, “Biodegradable polymeric microparticles in biomedical applications,” International Journal of Polymeric Materials, vol. 42, no. 1-2, pp. 83–117, 1998.
[2]  Y. Xu, C. Zhan, L. Fan, L. Wang, and H. Zheng, “Preparation of dual crosslinked alginate-chitosan blend gel beads and in vitro controlled release in oral site-specific drug delivery system,” International Journal of Pharmaceutics, vol. 336, no. 2, pp. 329–337, 2007.
[3]  A. Roy, J. Bajpai, and A. K. Bajpai, “Dynamics of controlled release of chlorpyrifos from swelling and eroding biopolymeric microspheres of calcium alginate and starch,” Carbohydrate Polymers, vol. 76, no. 2, pp. 222–231, 2009.
[4]  S. A. Agnihotri, N. N. Mallikarjuna, and T. M. Aminabhavi, “Recent advances on chitosan-based micro- and nanoparticles in drug delivery,” Journal of Controlled Release, vol. 100, no. 1, pp. 5–28, 2004.
[5]  S. G. Kumbar and T. M. Aminabhavi, “Synthesis and characterization of modified chitosan microspheres: effect of the grafting ratio on the controlled release of nifedipine through microspheres,” Journal of Applied Polymer Science, vol. 89, no. 11, pp. 2940–2949, 2003.
[6]  S. A. Agnihotri and T. M. Aminabhavi, “Controlled release of clozapine through chitosan microparticles prepared by a novel method,” Journal of Controlled Release, vol. 96, no. 2, pp. 245–259, 2004.
[7]  K. S. V. Krishna Rao, B. Vijaya Kumar Naidu, M. C. S. Subha, M. Sairam, and T. M. Aminabhavi, “Novel chitosan-based pH-sensitive interpenetrating network microgels for the controlled release of cefadroxil,” Carbohydrate Polymers, vol. 66, no. 3, pp. 333–344, 2006.
[8]  A. Rokhade, N. Shelke, S. Patil, and T. Aminabhavi, “Novel hydrogel microspheres of chitosan and pluronic F-127 for controlled release of 5-fluorouracil,” Journal of Microencapsulation, vol. 24, no. 3, pp. 274–288, 2007.
[9]  A. P. Rokhade, P. V. Kulkarni, N. N. Mallikarjuna, and T. M. Aminabhavi, “Preparation and characterization of novel semi-interpenetrating polymer network hydrogel microspheres of chitosan and hydroxypropyl cellulose for controlled release of chlorothiazide,” Journal of Microencapsulation, vol. 26, no. 1, pp. 27–36, 2009.
[10]  S. C. Angadi, L. S. Manjeshwar, and T. M. Aminabhavi, “Interpenetrating polymer network blend microspheres of chitosan and hydroxyethyl cellulose for controlled release of isoniazid,” International Journal of Biological Macromolecules, vol. 47, no. 2, pp. 171–179, 2010.
[11]  W. E. Rudzinski and T. M. Aminabhavi, “Chitosan as a carrier for targeted delivery of small interfering RNA,” International Journal of Pharmaceutics, vol. 399, no. 1-2, pp. 1–11, 2010.
[12]  K. Ganguly, T. M. Aminabhavi, and A. R. Kulkarni, “Colon targeting of 5-fluorouracil using polyethylene glycol cross-linked chitosan microspheres enteric coated with cellulose acetate phthalate,” Industrial and Engineering Chemistry Research, vol. 50, no. 21, pp. 11797–11807, 2011.
[13]  Y.-Y. Fang, L.-J. Wang, D. Li et al., “Preparation of crosslinked starch microspheres and their drug loading and releasing properties,” Carbohydrate Polymers, vol. 74, no. 3, pp. 379–384, 2008.
[14]  M. D. Kurkuri, A. R. Kulkarni, M. Y. Kariduraganavar, and T. M. Aminabhavi, “In vitro release study of verapamil hydrochloride through sodium alginate interpenetrating monolithic membranes,” Drug Development and Industrial Pharmacy, vol. 27, no. 10, pp. 1107–1114, 2001.
[15]  X. Zhang, Z. Hui, D. Wan et al., “Alginate microsphere filled with carbon nanotube as drug carrier,” International Journal of Biological Macromolecules, vol. 47, no. 3, pp. 389–395, 2010.
[16]  R. C. Mundargi, N. B. Shelke, A. P. Rokhade, S. A. Patil, and T. M. Aminabhavi, “Formulation and in-vitro evaluation of novel starch-based tableted microspheres for controlled release of ampicillin,” Carbohydrate Polymers, vol. 71, no. 1, pp. 42–53, 2008.
[17]  B.-Z. Li, L.-J. Wang, D. Li et al., “Fabrication of starch-based microparticles by an emulsification-crosslinking method,” Journal of Food Engineering, vol. 92, no. 3, pp. 250–254, 2009.
[18]  N. Kotsaeng, J. Karnchanajindanun, and Y. Baimark, “Chitosan microparticles prepared by the simple emulsification-diffusion method,” Particulate Science and Technology, vol. 28, no. 4, pp. 369–378, 2010.
[19]  J. Karnchanajindanun, M. Srisa-Ard, and Y. Baimark, “Genipin-cross-linked chitosan microspheres prepared by a water-in-oil emulsion solvent diffusion method for protein delivery,” Carbohydrate Polymers, vol. 85, no. 3, pp. 674–680, 2011.
[20]  D. P. Chattopadhyay and M. S. Inamdar, “Aqueous behaviour of chitosan,” International Journal of Polymer Science, vol. 2010, Article ID 939536, 7 pages, 2010.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413