메뉴 건너뛰기




Volumn 83, Issue 3, 2011, Pages 1153-1161

Oligoamines conjugated chitosan derivatives: Synthesis, characterization, in vitro and in vivo biocompatibility evaluations

Author keywords

Biocompatibility; Chitosan; Drug delivery; Gene therapy; Low cytotoxicity

Indexed keywords

AMINE FUNCTIONALITY; BIOMEDICAL APPLICATIONS; CANDIDATE MATERIALS; CELL LINES; CHITOSAN DERIVATIVES; ETHYLENE DIAMINE; FUNCTIONALIZED; GOOD COMPATIBILITY; H NMR SPECTRA; HEMOLYSIS TEST; HIGH WATER; IN-VITRO; IN-VIVO; INTRAMUSCULAR INJECTIONS; LOW CYTOTOXICITY; ORDER OF MAGNITUDE; POLYETHYLENEIMINE; POLYMER STRUCTURE; TUMOR CELL LINES; WATER-SOLUBLE CHITOSAN;

EID: 78650287162     PISSN: 01448617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carbpol.2010.09.046     Document Type: Article
Times cited : (39)

References (43)
  • 1
    • 33749858852 scopus 로고    scopus 로고
    • Synthesis of various chitosan derivatives bearing cyclodextrin moieties and their adsorption behavior
    • Polymer Preprints, Japan - 55th SPSJ Annual Meeting
    • N. Aoki, M. Nishikawa, and K. Hattori Synthesis of chitosan derivatives bearing cyclodextrin and adsorption of p-nonylphenyl and bisphenol A Carbohydrate Polymers 52 3 2003 219 223 (Pubitemid 44559345)
    • (2006) Polymer Preprints, Japan , vol.55 , Issue.1 , pp. 2277
    • Aoki, N.1    Kinoshita, K.2    Hattori, K.3
  • 3
    • 0346094228 scopus 로고    scopus 로고
    • Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications
    • DOI 10.1016/S0939-6411(03)00161-9
    • J. Berger, M. Reist, J.M. Mayer, O. Felt, N.A. Peppas, and R. Gurny Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications European Journal of Pharmaceutics and Biopharmaceutics 57 1 2004 19 34 (Pubitemid 38058801)
    • (2004) European Journal of Pharmaceutics and Biopharmaceutics , vol.57 , Issue.1 , pp. 19-34
    • Berger, J.1    Reist, M.2    Mayer, J.M.3    Felt, O.4    Peppas, N.A.5    Gurny, R.6
  • 4
    • 60549084795 scopus 로고    scopus 로고
    • Uniform chitosan microspheres for potential application to colon-specific drug delivery
    • C.Y. Bin, F. Cheng, H. Choi, and K. Kim Uniform chitosan microspheres for potential application to colon-specific drug delivery Macromolecular Bioscience 8 12 2008 1173 1181
    • (2008) Macromolecular Bioscience , vol.8 , Issue.12 , pp. 1173-1181
    • Bin, C.Y.1    Cheng, F.2    Choi, H.3    Kim, K.4
  • 5
    • 65149098527 scopus 로고    scopus 로고
    • Synthesis, characterization and self-assemble behavior of chitosan-O-poly(epsilon-caprolactone)
    • G.Q. Cai, H.L. Jiang, Z.J. Chen, K.H. Tu, L.Q. Wang, and K.J. Zhu Synthesis, characterization and self-assemble behavior of chitosan-O- poly(epsilon-caprolactone) European Polymer Journal 45 6 2009 1674 1680
    • (2009) European Polymer Journal , vol.45 , Issue.6 , pp. 1674-1680
    • Cai, G.Q.1    Jiang, H.L.2    Chen, Z.J.3    Tu, K.H.4    Wang, L.Q.5    Zhu, K.J.6
  • 6
    • 65149090527 scopus 로고    scopus 로고
    • A facile route for regioselective conjugation of organo-soluble polymers onto chitosan
    • G.Q. Cai, H.L. Jiang, K.H. Tu, L.Q. Wang, and K.J. Zhu A facile route for regioselective conjugation of organo-soluble polymers onto chitosan Macromolecular Bioscience 9 3 2009 256 261
    • (2009) Macromolecular Bioscience , vol.9 , Issue.3 , pp. 256-261
    • Cai, G.Q.1    Jiang, H.L.2    Tu, K.H.3    Wang, L.Q.4    Zhu, K.J.5
  • 7
    • 28444451851 scopus 로고    scopus 로고
    • Deoxycholic acid-conjugated chitosan oligosaccharide nanoparticles for efficient gene carrier
    • DOI 10.1016/j.jconrel.2005.09.040, PII S0168365905005006
    • S.Y. Chae, S. Son, M. Lee, M.K. Jang, and J.W. Nah Deoxycholic acid-conjugated chitosan oligosaccharide nanoparticles for efficient gene carrier Journal of Controlled Release 109 1-3 2005 330 344 (Pubitemid 41737274)
    • (2005) Journal of Controlled Release , vol.109 , Issue.1-3 , pp. 330-344
    • Chae, S.Y.1    Son, S.2    Lee, M.3    Jang, M.-K.4    Nah, J.-W.5
  • 8
    • 58149229478 scopus 로고    scopus 로고
    • Preparation of chitosan scaffolds loaded with dexamethasone for tissue engineering applications using supercritical fluid technology
    • A.R.C. Duarte, J.F. Mano, and R.L. Reis Preparation of chitosan scaffolds loaded with dexamethasone for tissue engineering applications using supercritical fluid technology European Polymer Journal 45 1 2009 141 148
    • (2009) European Polymer Journal , vol.45 , Issue.1 , pp. 141-148
    • Duarte, A.R.C.1    Mano, J.F.2    Reis, R.L.3
  • 10
    • 33646349221 scopus 로고    scopus 로고
    • A novel chitosan oligosaccharide-stearic acid micelles for gene delivery: Properties and in vitro transfection studies
    • DOI 10.1016/j.micromeso.2006.02.019, PII S0378517306001384
    • F. Hu, M. Zhao, H. Yuan, J. You, Y. Du, and S. Zeng A novel chitosan oligosaccharide-stearic acid micelles for gene delivery: Properties and in vitro transfection studies International Journal of Pharmaceutics 315 1-2 2006 158 166 (Pubitemid 43674116)
    • (2006) International Journal of Pharmaceutics , vol.315 , Issue.1-2 , pp. 158-166
    • Hu, F.-Q.1    Zhao, M.-D.2    Yuan, H.3    You, J.4    Du, Y.-Z.5    Zeng, S.6
  • 14
    • 33749578243 scopus 로고    scopus 로고
    • A PEG-based biocompatible block catiomer with high buffering capacity for the construction of polyplex micelles showing efficient gene transfer toward primary cells
    • N. Kanayama, S. Fukushima, N. Nishiyama, K. Itaka, W.D. Jang, and K. Miyata A PEG-based biocompatible block catiomer with high buffering capacity for the construction of polyplex micelles showing efficient gene transfer toward primary cells ChemMedChem 1 4 2006 439 444
    • (2006) ChemMedChem , vol.1 , Issue.4 , pp. 439-444
    • Kanayama, N.1    Fukushima, S.2    Nishiyama, N.3    Itaka, K.4    Jang, W.D.5    Miyata, K.6
  • 17
    • 0036158678 scopus 로고    scopus 로고
    • Graft copolymerization of methyl methacrylate onto mercaptochitin and some properties of the resulting hybrid materials
    • DOI 10.1021/bm0101320
    • K. Kurita, M. Inoue, and M. Harata Graft copolymerization of methyl methacrylate onto mercaptochitin and some properties of the resulting hybrid materials Biomacromolecules 3 1 2002 147 152 (Pubitemid 34121169)
    • (2002) Biomacromolecules , vol.3 , Issue.1 , pp. 147-152
    • Kurita, K.1    Inoue, M.2    Harata, M.3
  • 18
    • 0037384149 scopus 로고    scopus 로고
    • Preparation of water-soluble chitosan/heparin complex and its application as wound healing accelerator
    • D.K. Kweon, S.B. Song, and Y.Y. Park Preparation of water-soluble chitosan/heparin complex and its application as wound healing accelerator Biomaterials 24 9 2003 1595 1601
    • (2003) Biomaterials , vol.24 , Issue.9 , pp. 1595-1601
    • Kweon, D.K.1    Song, S.B.2    Park, Y.Y.3
  • 19
    • 33751195735 scopus 로고    scopus 로고
    • Hydrogels in controlled release formulations: Network design and mathematical modeling
    • C.C. Lin, and A.T. Metters Hydrogels in controlled release formulations: Network design and mathematical modeling Advanced Drug Delivery Reviews 58 12-13 2006 1379 1408
    • (2006) Advanced Drug Delivery Reviews , vol.58 , Issue.1213 , pp. 1379-1408
    • Lin, C.C.1    Metters, A.T.2
  • 22
    • 59249098389 scopus 로고    scopus 로고
    • Chitins and chitosans for the repair of wounded skin, nerve, cartilage and bone
    • R.A.A. Muzzarelli Chitins and chitosans for the repair of wounded skin, nerve, cartilage and bone Carbohydrate Polymers 76 2009 167 182
    • (2009) Carbohydrate Polymers , vol.76 , pp. 167-182
    • Muzzarelli, R.A.A.1
  • 23
  • 24
    • 63649092083 scopus 로고    scopus 로고
    • Cellular uptake mechanism and intracellular fate of hydrophobically modified glycol chitosan nanoparticles
    • H.Y. Nam, S.M. Kwon, H. Chung, S.Y. Lee, S.H. Kwon, and H. Jeon Cellular uptake mechanism and intracellular fate of hydrophobically modified glycol chitosan nanoparticles Journal of Controlled Release 135 3 2009 259 267
    • (2009) Journal of Controlled Release , vol.135 , Issue.3 , pp. 259-267
    • Nam, H.Y.1    Kwon, S.M.2    Chung, H.3    Lee, S.Y.4    Kwon, S.H.5    Jeon, H.6
  • 26
    • 63349092889 scopus 로고    scopus 로고
    • Chitosan: An option for development of essential oil delivery systems for oral cavity care?
    • A.S. Pedro, E. Cabral-Albuquerque, D. Ferreita, and B. Sarmento Chitosan: An option for development of essential oil delivery systems for oral cavity care? Carbohydrate Polymers 76 2009 501 508
    • (2009) Carbohydrate Polymers , vol.76 , pp. 501-508
    • Pedro, A.S.1    Cabral-Albuquerque, E.2    Ferreita, D.3    Sarmento, B.4
  • 27
    • 0142184041 scopus 로고    scopus 로고
    • Chitosan: An Attractive Biocompatible Polymer for Microencapsulation
    • DOI 10.1002/mabi.200300019
    • C. Peniche, W. Arguelles-Monal, H. Peniche, and N. Acosta Chitosan: An attractive biocompatible polymer for microencapsulation Macromolecular Bioscience 3 10 2003 511 520 (Pubitemid 37309674)
    • (2003) Macromolecular Bioscience , vol.3 , Issue.10 , pp. 511-520
    • Peniche, C.1    Arguelles-Monal, W.2    Peniche, H.3    Acosta, N.4
  • 29
    • 0342656709 scopus 로고    scopus 로고
    • Synthesis and characterization of pH-sensitive hydrogels based on chitosan and D,L-lactic acid
    • DOI 10.1002/(SICI)1097-4628(19991220)74:13<3193::AID-APP23>3.0. CO;2-V
    • X. Qu, A. Wirsen, and A.C. Albertsson Synthesis and characterization of pH-sensitive hydrogels based on chitosan and d,l-lactic acid Journal of Applied Polymer Science 74 13 1999 3193 3202 (Pubitemid 30538329)
    • (1999) Journal of Applied Polymer Science , vol.74 , Issue.13 , pp. 3193-3202
    • Xin, Q.1    Wirsen, A.2    Albertsson, A.-C.3
  • 30
    • 58149271115 scopus 로고    scopus 로고
    • In vitro assessment of N-(benzyl)chitosan derivatives against some plant pathogenic bacteria and fungi
    • E.I. Rabea, M.E.I. Badawy, W. Steurbaut, and C.V. Stevens In vitro assessment of N-(benzyl)chitosan derivatives against some plant pathogenic bacteria and fungi European Polymer Journal 45 1 2009 237 245
    • (2009) European Polymer Journal , vol.45 , Issue.1 , pp. 237-245
    • Rabea, E.I.1    Badawy, M.E.I.2    Steurbaut, W.3    Stevens, C.V.4
  • 31
    • 33747846583 scopus 로고    scopus 로고
    • Chitin and chitosan: Properties and applications
    • DOI 10.1016/j.progpolymsci.2006.06.001, PII S0079670006000530
    • M. Rinaudo Chitin and chitosan: Properties and applications Progress in Polymer Science 31 7 2006 603 632 (Pubitemid 44287019)
    • (2006) Progress in Polymer Science (Oxford) , vol.31 , Issue.7 , pp. 603-632
    • Rinaudo, M.1
  • 32
    • 77949655108 scopus 로고    scopus 로고
    • Synthetic methods and applications of chitosan containing pyridylmethyl moiety and its quaternized derivatives: A review
    • W. Sajomsang Synthetic methods and applications of chitosan containing pyridylmethyl moiety and its quaternized derivatives: A review Carbohydrate Polymers 80 2010 631 647
    • (2010) Carbohydrate Polymers , vol.80 , pp. 631-647
    • Sajomsang, W.1
  • 33
    • 67650514070 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of methylated N-(4-N,N- dimethylaminocinnamyl) chitosan chloride
    • W. Sajomsang, P. Gonil, and S. Saesoo Synthesis and antibacterial activity of methylated N-(4-N,N-dimethylaminocinnamyl) chitosan chloride European Polymer Journal 45 8 2009 2319 2328
    • (2009) European Polymer Journal , vol.45 , Issue.8 , pp. 2319-2328
    • Sajomsang, W.1    Gonil, P.2    Saesoo, S.3
  • 34
    • 4444246205 scopus 로고    scopus 로고
    • Chemically modified chitin and chitosan as biomaterials
    • H. Sashiwa, and S.I. Aiba Chemically modified chitin and chitosan as biomaterials Progress in Polymer Science 29 9 2004 887 908
    • (2004) Progress in Polymer Science , vol.29 , Issue.9 , pp. 887-908
    • Sashiwa, H.1    Aiba, S.I.2
  • 35
    • 0036740534 scopus 로고    scopus 로고
    • Chemical modification of chitosan. 14: Synthesis of water-soluble chitosan derivatives by simple acetylation
    • H. Sashiwa, N. Kawasaki, A. Nakayama, E. Muraki, N. Yamamoto, and S.I. Aiba Chemical modification of chitosan. 14: Synthesis of water-soluble chitosan derivatives by simple acetylation Biomacromolecules 3 5 2002 1126 1128
    • (2002) Biomacromolecules , vol.3 , Issue.5 , pp. 1126-1128
    • Sashiwa, H.1    Kawasaki, N.2    Nakayama, A.3    Muraki, E.4    Yamamoto, N.5    Aiba, S.I.6
  • 36
    • 0002639407 scopus 로고    scopus 로고
    • 1: Synthesis of organo-soluble chitosan derivatives toward palladium absorbent for chemical plating
    • H. Sashiwa, N. Kawasaki, A. Nakayama, E. Muraki, N. Yamamoto, and H. Zhu Chemical modification of chitosan. 13. Synthesis of organosoluble, palladium adsorbable, and biodegradable chitosan derivatives toward the chemical plating on plastics Biomacromolecules 3 5 2002 1120 1125 (Pubitemid 36930498)
    • (2002) Chemistry Letters , Issue.6 , pp. 598-599
    • Sashiwa, H.1    Kawasaki, N.2    Nakayama, A.3    Muraki, E.4    Yamamoto, N.5    Arvanitoyannis, I.6    Zhu, H.7    Aiba, S.-I.8
  • 37
    • 0034354601 scopus 로고    scopus 로고
    • Novel N-alkylation of chitosan via michael type reaction
    • H. Sashiwa, Y. Shigemasa, and R. Roy Novel N-alkylation of chitosan via michael type reaction Chemistry Letters 8 2000 862 863
    • (2000) Chemistry Letters , vol.8 , pp. 862-863
    • Sashiwa, H.1    Shigemasa, Y.2    Roy, R.3
  • 38
    • 0036462647 scopus 로고    scopus 로고
    • Chemical modification of chitosan 8: Preparation of chitosan-dendrimer hybrids via short spacer
    • DOI 10.1016/S0144-8617(01)00166-7, PII S0144861701001667
    • H. Sashiwa, Y. Shigemasa, and R. Roy Chemical modification of chitosan 8: Preparation of chitosan-dendrimer hybrids via short spacer Carbohydrate Polymers 47 2 2002 191 199 (Pubitemid 33018660)
    • (2002) Carbohydrate Polymers , vol.47 , Issue.2 , pp. 191-199
    • Sashiwa, H.1    Shigemasa, Y.2    Roy, R.3
  • 39
    • 0038617569 scopus 로고    scopus 로고
    • Chemical modification of chitosan, 17: Michael reaction of chitosan with acrylic acid in water
    • DOI 10.1002/mabi.200390029
    • H. Sashiwa, N. Yamamori, Y. Ichinose, J. Sunamoto, and S.I. Aiba Chemical modification of chitosan, 17 Michael reaction of chitosan with acrylic acid in water Macromolecular Bioscience 3 5 2003 231 233 (Pubitemid 36676084)
    • (2003) Macromolecular Bioscience , vol.3 , Issue.5 , pp. 231-233
    • Sashiwa, H.1    Yamamori, N.2    Ichinose, Y.3    Sunamoto, J.4    Aiba, S.-I.5
  • 40
    • 0032066826 scopus 로고    scopus 로고
    • Preparation and characterization of water-soluble chitin and chitosan derivatives
    • PII S014486179700235X
    • M. Sugimoto, M. Morimoto, H. Sashiwa, H. Saimoto, and Y. Shigemasa Preparation and characterization of water-soluble chitin and chitosan derivatives Carbohydrate Polymers 36 1 1998 49 59 (Pubitemid 128431739)
    • (1998) Carbohydrate Polymers , vol.36 , Issue.1 , pp. 49-59
    • Sugimoto, M.1    Morimoto, M.2    Sashiwa, H.3    Saimoto, H.4    Shigemasa, Y.5
  • 41
    • 0037186243 scopus 로고    scopus 로고
    • Study of the synthesis of chitosan derivatives containing benzo-21-crown-7 and their adsorption properties for metal ions
    • DOI 10.1002/app.2316
    • X.H. Tang, S.Y. Tan, and Y.T. Wang Study of the synthesis of chitosan derivatives containing benzo-21-crown-7 and their adsorption properties for metal ions Journal of Applied Polymer Science 83 9 2002 1886 1891 (Pubitemid 34063925)
    • (2002) Journal of Applied Polymer Science , vol.83 , Issue.9 , pp. 1886-1891
    • Tang, X.-H.1    Tan, S.-Y.2    Wang, Y.-T.3
  • 42
    • 13844308942 scopus 로고    scopus 로고
    • Periodate oxidation of chitosans with different chemical compositions
    • I.M.N. Vold, and B.E. Christensen Periodate oxidation of chitosans with different chemical compositions Carbohydrate Research 340 4 2005 679 684
    • (2005) Carbohydrate Research , vol.340 , Issue.4 , pp. 679-684
    • Vold, I.M.N.1    Christensen, B.E.2
  • 43
    • 63749113575 scopus 로고    scopus 로고
    • Polyaspartamide-based oligo-ethylenimine brushes with high buffer capacity and low cytotoxicity for highly efficient gene delivery
    • M. Zhang, M. Liu, Y.N. Xue, S.W. Huang, and R.X. Zhuo Polyaspartamide-based oligo-ethylenimine brushes with high buffer capacity and low cytotoxicity for highly efficient gene delivery Bioconjugate Chemistry 20 3 2009 440 446
    • (2009) Bioconjugate Chemistry , vol.20 , Issue.3 , pp. 440-446
    • Zhang, M.1    Liu, M.2    Xue, Y.N.3    Huang, S.W.4    Zhuo, R.X.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.