Biomedical Engineering Reference
In-Depth Information
50. Tikhonov, V. E., Stepnova, E. A., Babak, V. G., Krayukhina, M. A., Berezin. B. B., and Yamskov,
I. A. 2008. Amphiphilic
N
-[2(3)-(dodec-2′-en-1′-yl)succinoyl]chitosan: Synthesis and properties.
React Funct Polym
68: 436-445.
51. Zhu, A., Yuan, L., and Dai, S. 2008. Preparation of well-dispersed superparamagnetic iron oxide
nanoparticles in aqueous solution with biocompatible
N
-succinyl-
O
-carboxymethylchitosan.
J Phys Chem C
112: 5432-5438.
52. Nandanan, E., Jana, N. R., and Ying, J. Y. 2008. Functionalization of gold nanospheres and
nanorods by chitosan oligosaccharide derivatives.
Adv Mater
20: 2068-2073.
53. Félix, L., Hernández, J., Argüelles, W. M., and Goycoolea, F. M. 2005. Kinetics of gelation and
thermal sensitivity of
N
-isobutyryl chitosan hydrogels.
Biomacromolecules
6: 2408-2415.
54. You, J., Hu, F. Q., Du, Y. Z., and Yuan, H. 2007. Polymeric micelles with glycolipidlike structure
and multiple hydrophobic domains for mediating molecular target delivery of paclitaxel.
Biomacromolecules
8: 2450-2456.
55. You, J., Hu, F. Q., Du, Y. Z., Yuan, H., and Ye, B. F. 2007. High cytotoxicity and resistant-cell
reversal of novel paclitaxel loaded micelles by enhancing the molecular-target delivery of the
drug.
Nanotechnology
18: 495101.
56. You, J., Hu, F. Q., Du, Y. Z., and Yuan, H. 2008. Improved cytotoxicity of doxorubicin by enhanc-
ing its nuclear delivery mediated via nanosized micelles.
Nanotechnology
19: 255103.
57. Uygun, D. A., Uygun, M., Karagözler, A., Öztürk, N., Akgöl, S., and Denizli, A. 2009. A novel
support for antibody purification: Fatty acid attached chitosan beads.
Colloid Surf B
70: 266-270.
58. Tong, Y., Wang, S., Xu, J., Chua, B., and He, C. 2005. Synthesis of
O
,
O
′-dipalmitoyl chitosan and
its amphiphilic properties and capability of cholesterol absorption.
Carbohydr Polym
60:
229-233.
59. Wu, Y., Hisada, K., Maeda, S., Sasaki, T., and Sakurai, K. 2007. Fabrication and structural char-
acterization of the Langmuir-Blodgett films from a new chitosan derivative containing cinna-
mate chromophores.
Carbohydr Polym
68: 766-772.
60. Shigemasa, Y., Usui, H., Morimoto, M., Saimoto, H., Okamoto, Y., Minami, S., and Sashiwa, H.
1999. Chemical modification of chitin and chitosan 1: Preparation of partially deacetylated chi-
tin derivatives via a ring-opening reaction with cyclic acid anhydrides in lithium
chloride/
N
,
N
-dimethylacetamide.
Carbohydr Polym
39: 237.
61. Hirano, S., Yamaguchi, Y., and Kamiya, M. 2002. Novel N-saturated-fatty-acyl derivatives of
chitosan soluble in water and in aqueous acid and alkaline solutions.
Carbohydr Polym
48: 203.
62. Seo, T., Hagura, S., Kanbara, T., and Iijima, T. 1989. Interaction of dyes with chitosan deriva-
tives.
J Appl Polym Sci
37: 3011-3027.
63. Tien, C. L., Lacroix, M., Ispas-Szabo, P., and Mateescu, M. A. 2003. N-acylated chitosan:
Hydrophobic matrices for controlled drug release.
J Controlled Release
93: 1-13.
64. Sashiwa, H., Kawasaki, N., Nakayama, A., Muraki, E., Yamamoto, N., and Zhu, H. 2002.
Chemical modification of chitosan. 13.1: Synthesis of organosoluble, palladium adsorbable,
and biodegradable chitosan derivatives toward the chemical plating on plastics.
Biomacro-
molecules
3: 1120-1125.
65. Grant, S., Blair, H. S., and Mckay, G. 1990. Deacetylation effects on the dodecanoyl substitution.
Polym Commun
31: 267-268.
66. Seo, T., Ikeda, Y., Torada, Y., Nakata, Y., and Shimomura, Y. 2001. Synthesis of N,O-acylated
chitosan and its sorptivity.
Chitin Chitosan Res
7: 212-213.
67. Wu, Y., Seo, T., Maeda, S., Sasaki, T., Irie, S., and Sakurai, K. 2005. Circular dichroism induced
by the helical conformations of acylated chitosan derivatives bearing cinnamate chromophores.
J Polym Sci Part B: Polym Phys
43: 1354-1364.
68. Zong, Z., Kimura, Y., Takahashi, M., and Yamane, H. 2000. Characterization of chemical and
solid state structures of acylated chitosans.
Polymer
41: 899-906.
69. Martin, L., Wilson, C. G., Koosha, F., Tetley, L., Gray, A. I., Senel, S., and Uchegbu, I. F. 2002.
The release of model macromolecules may be controlled by the hydrophobicity of palmitoyl
glycol chitosan hydrogels.
J Controlled Release
80: 87-100.
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