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Handbook of Vitamin C Research

Handbook of Vitamin C Research

Handbook of Vitamin C Research

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208Magdalena Stevanović and Dragan Uskoković[89] Segall, A. I. Moyano, M. A. (2008). Stability <strong>of</strong> vitamin C derivatives in topicalformulations containing lipoic acid, vitamins A and E. International Journal <strong>of</strong>Cosmetic Science. 30(6), 453-458.[90] Wieland-Berghausen, S. Schote, U. Frey, M. Schmidt, F. (2002). Comparison <strong>of</strong>microencapsulation techniques for the water-soluble drugs nitenpyram andclomipramine HCl. Journal <strong>of</strong> Controlled Release, 85(1-3), 35-43.[91] Ravi Kumar, M. N. V. (2000). Nano and microparticles as controlled drug deliverydevices. Journal <strong>of</strong>. Pharmacy & Pharmaceutical Sciences, 3 (2), 234-258.[92] Miller, R. E. Anderson, J. L. Encapsulation Process and its Products, US Patent 3, 155,590, November, 1964.[93] Yoshiyuki, K. Hirata, G. Samejima, M. (1983). Studies on microcapsules II: influence<strong>of</strong> molecular weight <strong>of</strong> ethylcellulose in the microencapsulation <strong>of</strong> ascorbic acid.Chemical & Pharmaceutical Bulletin, 31, 4476–4482.[94] Benita, S. Donbrow, M. (1982). Effect <strong>of</strong> polyisobutylene on ethylcellulose-walledmicrocapsules: Wall structure and thickness <strong>of</strong> Salicylamide and Theophyllinemicrocapsules. Journal <strong>of</strong> Pharmaceutical Sciences, 71 (2), 205–210.[95] Yalabik-Kas, H. S. (1983). Microencapsulation and in vitro dissolution <strong>of</strong> oxazepamfrom ethylcellulose microcapsules. Drug Development and Industrial Pharmacy, 9 (6),1047–1060.[96] Uddin, M. S. Hawlader, M. N. A. Zhu, H. J. (2001). Microencapsulation <strong>of</strong> ascorbicacid: effect <strong>of</strong> process variables on product characteristics. Journal <strong>of</strong>Microencapsulation, 18(2), 199-209.[97] Prabha, S. Labhasetwar, V. (2004). Nanoparticle-mediated wild-type p 53 gene deliveryresults in sustained antiproliferative activity in breast cancer cells. MolecularPharmacology, 1, 211-219.[98] Sahoo, S. K. Labhasetwar, V. (2005). Enhanced antiproliferative activity <strong>of</strong> transferrinconjugatedpaclitaxel-loaded nanoparticles is mediated via sustained intracellular drugretention. Molecular Pharmacology, 2, 373-383.[99] Song, K. C. Lee, H. S. Choung, I. Y. Cho, K. I. Ahn, Y. Choi, E. J. (2006). The effecttype <strong>of</strong> organic phase solvents on the particle size <strong>of</strong> poly(D,L-lactide-co-glycolide)nanoparticles. Colloids and Surfaces A: Physicochemical and Engineering Aspects,276, 162-167.[100] Astete, C. E. Kumar, C. S. S. R. Sabliov, C. M. (2007). Size control <strong>of</strong> poly(D,Llactide-coglycolide)and poly(D,L-lactide-co-glycolide)-magnetite nanoparticlessynthesized by emulsion evaporation technique. Colloids and Surfaces A:Physicochemical and Engineering Aspects, 299, 209-216.[101] Zhang, H. Cui, W. Bei, J. Wang, S. (2006). Preparation <strong>of</strong> poly(lactide-co-glycolideco-caprolactone)nanoparticles and their degradation behaviour in aqueous solution.Polymer Degradation and Stability, 91 (9), 1929-1936.[102] Lee, S. J. Jeong, J. R. Shin, S. C. Kim, J. C. Chang, Y. H. Lee, K. H. Kim, J. D. (2005).Magnetic enhancement <strong>of</strong> iron oxide nanoparticles encapsulated with poly(D,L-lactideco-glycolide).Colloids and Surfaces A: Physicochemical and Engineering Aspects,255, 19-25.

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