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Volumn 23, Issue 7, 2012, Pages 1663-1674

In vitro evaluation of polymeric micelles based on hydrophobically-modified sulfated chitosan as a carrier of doxorubicin

Author keywords

[No Author keywords available]

Indexed keywords

CELL CULTURE MEDIA; CHOLIC ACIDS; DEGREE OF SUBSTITUTION; DOXORUBICIN; HYDROPHOBIC GROUPS; IN-VITRO EVALUATION; LONG-TERM STORAGE; POLYMERIC MICELLE; PROTEIN SOLUTION; SULFATE GROUPS; SULFATED CHITOSAN;

EID: 84863325095     PISSN: 09574530     EISSN: 15734838     Source Type: Journal    
DOI: 10.1007/s10856-012-4627-1     Document Type: Article
Times cited : (45)

References (46)
  • 2
    • 0004434395 scopus 로고
    • Adriamycin - Thoughts for the future
    • Carter SK. Adriamycin - thoughts for the future. Cancer Chemother Rep. 1975;63:1833-77.
    • (1975) Cancer Chemother Rep , vol.63 , pp. 1833-1877
    • Carter, S.K.1
  • 3
    • 0025642721 scopus 로고
    • Studies on the myelosuppressive activity of doxorubicin entrapped in liposomes
    • Bally MB, Nayar R, Masin D, Cullis PR, Mayer LD. Studies on the myelosuppressive activity of doxorubicin entrapped in liposomes. Cancer Chemother Pharm. 1990;27(1):13-9.
    • (1990) Cancer Chemother Pharm , vol.27 , Issue.1 , pp. 13-19
    • Bally, M.B.1    Nayar, R.2    Masin, D.3    Cullis, P.R.4    Mayer, L.D.5
  • 4
    • 1542349909 scopus 로고    scopus 로고
    • 99mTc Labeling of Pegylated Liposomal Doxorubicin (Doxil) for Pharmacokinetic and Non-Invasive Imaging Studies
    • DOI 10.1124/jpet.103.059535
    • Bao A, Goins B, Klipper R, Negrete G, Phillips WT. Direct 99mTc labeling of PEGylated liposomal doxorubicin (Doxil) for pharmacokinetic and non-invasive imaging studies. J Pharmacol Exp Ther. 2004;308(2):419-25. (Pubitemid 38134199)
    • (2004) Journal of Pharmacology and Experimental Therapeutics , vol.308 , Issue.2 , pp. 419-425
    • Bao, A.1    Goins, B.2    Klipper, R.3    Negrete, G.4    Phillips, W.T.5
  • 5
    • 0030579707 scopus 로고    scopus 로고
    • Doxorubicin in sterically stabilized liposomes
    • Lasic DD. Doxorubicin in sterically stabilized liposomes. Nature. 1996;380(6574):561-2.
    • (1996) Nature , vol.380 , Issue.6574 , pp. 561-562
    • Lasic, D.D.1
  • 6
    • 0033802643 scopus 로고    scopus 로고
    • Pegylated liposomal doxorubicin (doxil): Reduced clinical cardiotoxicity in patients reaching or exceeding cumulative doses of 500 mg/m(2)
    • Safra T, Muggia F, Jeffers S, Tsao-Wei DD, Groshen S, Lyass O, Henderson R, Berry G, Gabizon A. Pegylated liposomal doxorubicin (doxil): reduced clinical cardiotoxicity in patients reaching or exceeding cumulative doses of 500 mg/m(2). Ann Oncol. 2000;11(8):1029-33.
    • (2000) Ann Oncol , vol.11 , Issue.8 , pp. 1029-1033
    • Safra, T.1    Muggia, F.2    Jeffers, S.3    Tsao-Wei, D.D.4    Groshen, S.5    Lyass, O.6    Henderson, R.7    Berry, G.8    Gabizon, A.9
  • 7
    • 70149092937 scopus 로고    scopus 로고
    • Folatebearing doxorubicin-loaded magnetic poly(N-isopropylacrylamide) microspheres as a new strategy for cancer therapy
    • Sun Y, Chen L, Yu J, Zhi X, Tang S, Zhou P, Wang C. Folatebearing doxorubicin-loaded magnetic poly(N-isopropylacrylamide) microspheres as a new strategy for cancer therapy. Anti-Cancer Drug. 2009;20(7):607-15.
    • (2009) Anti-Cancer Drug , vol.20 , Issue.7 , pp. 607-615
    • Sun, Y.1    Chen, L.2    Yu, J.3    Zhi, X.4    Tang, S.5    Zhou, P.6    Wang, C.7
  • 8
    • 67650022001 scopus 로고    scopus 로고
    • Synthesis of pH-sensitive hollow polymer microspheres and their application as drug carriers
    • Yang X, Chen L, Huang B, Bai F, Yang X. Synthesis of pH-sensitive hollow polymer microspheres and their application as drug carriers. Polymer. 2009;50(15):3556-63.
    • (2009) Polymer , vol.50 , Issue.15 , pp. 3556-3563
    • Yang, X.1    Chen, L.2    Huang, B.3    Bai, F.4    Yang, X.5
  • 11
  • 12
    • 44749092859 scopus 로고    scopus 로고
    • Glycyrrhizin surface-modified chitosan nanoparticles for hepatocytetargeted delivery
    • Lin A, Liu Y, Huang Y, Sun J, Wu Z, Zhang X, Ping Q. Glycyrrhizin surface-modified chitosan nanoparticles for hepatocytetargeted delivery. Int J Pharm. 2008;359(1-2):247-53.
    • (2008) Int J Pharm , vol.359 , Issue.1-2 , pp. 247-253
    • Lin, A.1    Liu, Y.2    Huang, Y.3    Sun, J.4    Wu, Z.5    Zhang, X.6    Ping, Q.7
  • 15
    • 77950819407 scopus 로고    scopus 로고
    • Polymeric micelles with ionic cores containing biodegradable cross-links for delivery of chemotherapeutic agents
    • Kim JO, Sahay G, Kabanov AV, Bronich TK. Polymeric micelles with ionic cores containing biodegradable cross-links for delivery of chemotherapeutic agents. Biomacromolecules. 2010;11(4): 919-26.
    • (2010) Biomacromolecules , vol.11 , Issue.4 , pp. 919-926
    • Kim, J.O.1    Sahay, G.2    Kabanov, A.V.3    Bronich, T.K.4
  • 16
    • 77954301085 scopus 로고    scopus 로고
    • Self-assembled micelles from an amphiphilic hyperbranched copolymer with polyphosphate arms for drug delivery
    • Liu J, Huang W, Pang Y, Zhu X, Zhou Y, Yan D. Self-assembled micelles from an amphiphilic hyperbranched copolymer with polyphosphate arms for drug delivery. Langmuir. 2010;26(13): 10585-92.
    • (2010) Langmuir , vol.26 , Issue.13 , pp. 10585-10592
    • Liu, J.1    Huang, W.2    Pang, Y.3    Zhu, X.4    Zhou, Y.5    Yan, D.6
  • 17
    • 16344390189 scopus 로고    scopus 로고
    • Formation of core-shell type biodegradable polymeric micelles from amphiphilic poly(aspartic acid)-block-polylactide diblock copolymer
    • DOI 10.1021/bm0494491
    • Arimura H, Ohya Y, Ouchi T. Formation of core-shell type biodegradable polymeric micelles from amphiphilic poly(aspartic acid)-block-polylactide diblock copolymer. Biomacromolecules. 2005;6(2):720-5. (Pubitemid 40467813)
    • (2005) Biomacromolecules , vol.6 , Issue.2 , pp. 720-725
    • Arimura, H.1    Ohya, Y.2    Ouchi, T.3
  • 18
    • 69849089755 scopus 로고    scopus 로고
    • Biodegradable micelles with sheddable poly(ethylene glycol) shells for triggered intracellular release of doxorubicin
    • Sun H, Guo B, Cheng R, Meng F, Liu H, Zhong Z. Biodegradable micelles with sheddable poly(ethylene glycol) shells for triggered intracellular release of doxorubicin. Biomaterials. 2009;30(31): 6358-66.
    • (2009) Biomaterials , vol.30 , Issue.31 , pp. 6358-6366
    • Sun, H.1    Guo, B.2    Cheng, R.3    Meng, F.4    Liu, H.5    Zhong, Z.6
  • 19
    • 1842638560 scopus 로고    scopus 로고
    • Folate receptor targeted biodegradable polymeric doxorubicin micelles
    • DOI 10.1016/j.jconrel.2004.02.003, PII S0168365904000811
    • Yoo HS, Park TG. Folate receptor targeted biodegradable polymeric doxorubicin micelles. J Control Release. 2004;96(2): 273-83. (Pubitemid 38481509)
    • (2004) Journal of Controlled Release , vol.96 , Issue.2 , pp. 273-283
    • Yoo, H.S.1    Park, T.G.2
  • 20
    • 76249092854 scopus 로고    scopus 로고
    • Cholic acid micellesa - Controlling the size of the aqueous cavity by PEGylation
    • Despa F, Luo JT, Li J, Duan Y, Lam KS. Cholic acid micellesa - controlling the size of the aqueous cavity by PEGylation. Phys Chem Chem Phys. 2010;12(7):1589-94.
    • (2010) Phys Chem Chem Phys , vol.12 , Issue.7 , pp. 1589-1594
    • Despa, F.1    Luo, J.T.2    Li, J.3    Duan, Y.4    Lam, K.S.5
  • 21
    • 0033740505 scopus 로고    scopus 로고
    • Synthesis and the micellar characteristics of poly(ethylene oxide)-deoxycholic acid conjugates
    • Kim C, Lee SC, Kang SW, Kwon IC, Kim Y-H, Jeong SY. Synthesis and the micellar characteristics of poly(ethylene oxide)-deoxycholic acid conjugates. Langmuir. 2000;16(11): 4792-7.
    • (2000) Langmuir , vol.16 , Issue.11 , pp. 4792-4797
    • Kim, C.1    Lee, S.C.2    Kang, S.W.3    Kwon, I.C.4    Kim, Y.-H.5    Jeong, S.Y.6
  • 22
    • 33751418300 scopus 로고    scopus 로고
    • In vivo tumor targeting and radionuclide imaging with self-assembled nanoparticles: Mechanisms, key factors, and their implications
    • DOI 10.1016/j.biomaterials.2006.10.002, PII S0142961206008908
    • Cho YW, Park SA, Han TH, Son DH, Park JS, Oh SJ, Moon DH, Cho K-J, Ahn C-H, Byun Y, Kim I-S, Kwon IC, Kim SY. In vivo tumor targeting and radionuclide imaging with self-assembled nanoparticles: mechanisms, key factors, and their implications. Biomaterials. 2007;28(6):1236-47. (Pubitemid 44816372)
    • (2007) Biomaterials , vol.28 , Issue.6 , pp. 1236-1247
    • Cho, Y.W.1    Park, S.A.2    Han, T.H.3    Son, D.H.4    Park, J.S.5    Oh, S.J.6    Moon, D.H.7    Cho, K.-J.8    Ahn, C.-H.9    Byun, Y.10    Kim, I.-S.11    Kwon, I.C.12    Kim, S.Y.13
  • 24
    • 0033204185 scopus 로고    scopus 로고
    • Aggregation in water of dextran hydrophobically modified with bile acids
    • DOI 10.1021/ma990408k
    • Nichifor M, Lopes A, Carpov A, Melo E. Aggregation in water of dextran hydrophobically modified with bile acids. Macromolecules. 1999;32(21):7078-85. (Pubitemid 32079732)
    • (1999) Macromolecules , vol.32 , Issue.21 , pp. 7078-7085
    • Nichifor, M.1    Lopes, A.2    Carpov, A.3    Melo, E.4
  • 26
    • 62649086512 scopus 로고    scopus 로고
    • PEG conjugated N-octyl-O-sulfate chitosan micelles for delivery of paclitaxel: In vitro characterization and in vivo evaluation
    • Qu G, Yao Z, Zhang C, Wu X, Ping Q. PEG conjugated N-octyl-O-sulfate chitosan micelles for delivery of paclitaxel: in vitro characterization and in vivo evaluation. Eur J Pharm Sci. 2009;37(2):98-105.
    • (2009) Eur J Pharm Sci , vol.37 , Issue.2 , pp. 98-105
    • Qu, G.1    Yao, Z.2    Zhang, C.3    Wu, X.4    Ping, Q.5
  • 27
    • 33947172648 scopus 로고    scopus 로고
    • A series of novel chitosan derivatives: Synthesis, characterization and micellar solubilization of paclitaxel
    • DOI 10.1016/j.carbpol.2006.08.023, PII S0144861706004140
    • Yao Z, Zhang C, Ping Q, Yu L. A series of novel chitosan derivatives: synthesis, characterization and micellar solubilization of paclitaxel. Carbohydr Polym. 2007;68(4):781-92. (Pubitemid 46412476)
    • (2007) Carbohydrate Polymers , vol.68 , Issue.4 , pp. 781-792
    • Yao, Z.1    Zhang, C.2    Ping, Q.3    Yu, L.4
  • 28
    • 33847336085 scopus 로고    scopus 로고
    • Hydrophobically modified hydroxyethyl starch: Synthesis, characterization, and aqueous self-assembly into nano-sized polymeric micelles and vesicles
    • DOI 10.1021/bm0609487
    • Besheer A, Hause G, Kressler J, Mäder K. Hydrophobically modified hydroxyethyl starch: synthesis, characterization, and aqueous self-assembly into nano-sized polymeric micelles and vesicles. Biomacromolecules. 2007;8(2):359-67. (Pubitemid 46323248)
    • (2007) Biomacromolecules , vol.8 , Issue.2 , pp. 359-367
    • Besheer, A.1    Hause, G.2    Kressler, J.3    Mader, K.4
  • 30
    • 39549108475 scopus 로고    scopus 로고
    • Coremodified chitosan-based polymeric micelles for controlled release of doxorubicin
    • Ye Y-Q, Yang F-L, Hu F-Q, Du Y-Z, Yuan H, Yu H-Y. Coremodified chitosan-based polymeric micelles for controlled release of doxorubicin. Int J Pharm. 2008;352(1-2):294-301.
    • (2008) Int J Pharm , vol.352 , Issue.1-2 , pp. 294-301
    • Ye, Y.-Q.1    Yang, F.-L.2    Hu, F.-Q.3    Du, Y.-Z.4    Yuan, H.5    Yu, H.-Y.6
  • 32
    • 60449087425 scopus 로고    scopus 로고
    • Preparation and characteristics of linoleic acid-grafted chitosan oligosaccharide micelles as a carrier for doxorubicin
    • Du Y-Z, Wang L, Yuan H, Wei X-H, Hu F-Q. Preparation and characteristics of linoleic acid-grafted chitosan oligosaccharide micelles as a carrier for doxorubicin. Colloid Surf B. 2009;69(2): 257-63.
    • (2009) Colloid Surf B , vol.69 , Issue.2 , pp. 257-263
    • Du, Y.-Z.1    Wang, L.2    Yuan, H.3    Wei, X.-H.4    Hu, F.-Q.5
  • 33
    • 33745346800 scopus 로고    scopus 로고
    • Shell cross-linked stearic acid grafted chitosan oligosaccharide self-aggregated micelles for controlled release of paclitaxel
    • DOI 10.1016/j.colsurfb.2006.04.009, PII S092777650600141X
    • Hu F-Q, Ren G-F, Yuan H, Du Y-Z, Zeng S. Shell cross-linked stearic acid grafted chitosan oligosaccharide self-aggregated micelles for controlled release of paclitaxel. Colloid Surf B. 2006;50(2):97-103. (Pubitemid 43946659)
    • (2006) Colloids and Surfaces B: Biointerfaces , vol.50 , Issue.2 , pp. 97-103
    • Hu, F.-Q.1    Ren, G.-F.2    Yuan, H.3    Du, Y.-Z.4    Zeng, S.5
  • 35
    • 33746739461 scopus 로고    scopus 로고
    • Preparation of cholesterol-modified chitosan self-aggregated nanoparticles for delivery of drugs to ocular surface
    • DOI 10.1016/j.carbpol.2006.01.020, PII S0144861706000336
    • Yuan X-B, Li H, Yuan Y-B. Preparation of cholesterol-modified chitosan self-aggregated nanoparticles for delivery of drugs to ocular surface. Carbohydr Polym. 2006;65(3):337-45. (Pubitemid 44160627)
    • (2006) Carbohydrate Polymers , vol.65 , Issue.3 , pp. 337-345
    • Yuan, X.-b.1    Li, H.2    Yuan, Y.-b.3
  • 36
    • 41549123975 scopus 로고    scopus 로고
    • Nanoparticles for drug delivery: The need for precision in reporting particle size parameters
    • DOI 10.1016/j.ejpb.2007.08.001, PII S0939641107002895
    • Gaumet M, Vargas A, Gurny R, Delie F. Nanoparticles for drug delivery: the need for precision in reporting particle size parameters. Eur J Pharm Biopharm. 2008;69(1):1-9. (Pubitemid 351467152)
    • (2008) European Journal of Pharmaceutics and Biopharmaceutics , vol.69 , Issue.1 , pp. 1-9
    • Gaumet, M.1    Vargas, A.2    Gurny, R.3    Delie, F.4
  • 38
    • 77549083832 scopus 로고    scopus 로고
    • Dual drug loaded superparamagnetic iron oxide nanoparticles for targeted cancer therapy
    • Dilnawaz F, Singh A, Mohanty C, Sahoo SK. Dual drug loaded superparamagnetic iron oxide nanoparticles for targeted cancer therapy. Biomaterials. 2010;31(13):3694-706.
    • (2010) Biomaterials , vol.31 , Issue.13 , pp. 3694-3706
    • Dilnawaz, F.1    Singh, A.2    Mohanty, C.3    Sahoo, S.K.4
  • 39
    • 33748307496 scopus 로고    scopus 로고
    • Doxorubicin encapsulation and diffusional release from stable, polymeric, hydrogel nanoparticles
    • DOI 10.1016/j.ejps.2006.06.003, PII S0928098706001680
    • Missirlis D, Kawamura R, Tirelli N, Hubbell JA. Doxorubicin encapsulation and diffusional release from stable, polymeric, hydrogel nanoparticles. Eur J Pharm Sci. 2006;29(2):120-9. (Pubitemid 44332885)
    • (2006) European Journal of Pharmaceutical Sciences , vol.29 , Issue.2 , pp. 120-129
    • Missirlis, D.1    Kawamura, R.2    Tirelli, N.3    Hubbell, J.A.4
  • 40
    • 77956189395 scopus 로고    scopus 로고
    • Glycyrrhetinic acid-modified poly(ethylene glycol)-b-poly([gamma]-benzyl l-glutamate) micelles for liver targeting therapy
    • Huang W, Wang W, Wang P, Tian Q, Zhang C, Wang C, Yuan Z, Liu M, Wan H, Tang H. Glycyrrhetinic acid-modified poly(ethylene glycol)-b-poly([gamma]-benzyl l-glutamate) micelles for liver targeting therapy. Acta Biomater. 2010;6(10):3927-35.
    • (2010) Acta Biomater , vol.6 , Issue.10 , pp. 3927-3935
    • Huang, W.1    Wang, W.2    Wang, P.3    Tian, Q.4    Zhang, C.5    Wang, C.6    Yuan, Z.7    Liu, M.8    Wan, H.9    Tang, H.10
  • 41
    • 84855739069 scopus 로고    scopus 로고
    • Doxorubicin-loaded glycyrrhetinic acid-modified alginate nanoparticles for liver tumor chemotherapy
    • Zhang C-N, Wang W, Liu T, Wu Y-K, Guo H, Wang P, Tian Q, Wang Y-M, Yuan Z. Doxorubicin-loaded glycyrrhetinic acid-modified alginate nanoparticles for liver tumor chemotherapy. Biomaterials. 2012;33(7):2187-96.
    • (2012) Biomaterials , vol.33 , Issue.7 , pp. 2187-2196
    • Zhang, C.-N.1    Wang, W.2    Liu, T.3    Wu, Y.-K.4    Guo, H.5    Wang, P.6    Tian, Q.7    Wang, Y.-M.8    Yuan, Z.9
  • 42
    • 70350542589 scopus 로고    scopus 로고
    • Biodegradable nanoparticles modified by branched polyethylenimine for plasmid DNA delivery
    • Son S, Kim WJ. Biodegradable nanoparticles modified by branched polyethylenimine for plasmid DNA delivery. Biomaterials. 2010;31(1):133-43.
    • (2010) Biomaterials , vol.31 , Issue.1 , pp. 133-143
    • Son, S.1    Kim, W.J.2
  • 43
    • 68749103243 scopus 로고    scopus 로고
    • Polymer micelles with crosslinked polyanion core for delivery of a cationic drug doxorubicin
    • Kim JO, Kabanov AV, Bronich TK. Polymer micelles with crosslinked polyanion core for delivery of a cationic drug doxorubicin. J Control Release. 2009;138(3):197-204.
    • (2009) J Control Release , vol.138 , Issue.3 , pp. 197-204
    • Kim, J.O.1    Kabanov, A.V.2    Bronich, T.K.3
  • 44
    • 34548226035 scopus 로고    scopus 로고
    • Preparation, characterization and uptake by primary cultured rat hepatocytes of liposomes surface-modified with glycyrrhetinic acid
    • Mao SJ, Bi YQ, Jin H, Wei DP, He R, Hou SX. Preparation, characterization and uptake by primary cultured rat hepatocytes of liposomes surface-modified with glycyrrhetinic acid. Pharmazie. 2007;62(8):614-9.
    • (2007) Pharmazie , vol.62 , Issue.8 , pp. 614-619
    • Mao, S.J.1    Bi, Y.Q.2    Jin, H.3    Wei, D.P.4    He, R.5    Hou, S.X.6
  • 46
    • 84864109937 scopus 로고    scopus 로고
    • Selfassembly and liver targeting of sulfated chitosan nanoparticles functionalized with glycyrrhetinic acid
    • doi:10.1016/j.nano.2011.11.002
    • Tian Q, Wang X-H, Wang W, Zhang C-N, Wang P, Yuan Z. Selfassembly and liver targeting of sulfated chitosan nanoparticles functionalized with glycyrrhetinic acid. Nanomed Nanotechnol Biol Med. doi:10.1016/j.nano.2011.11. 002.
    • Nanomed Nanotechnol Biol Med
    • Tian, Q.1    Wang, X.-H.2    Wang, W.3    Zhang, C.-N.4    Wang, P.5    Yuan, Z.6


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