The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
PEGylated chitosan derivatives: Synthesis, characterizations and pharmaceutical applications
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“PEGylation is a suitable method for introducing new physicochemical properties to chitosan such as the solubility at wide range of pH values.188”
From Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment (2022) · cites this paper as [188]
Citations
Cites
Poly(ethylene glycol) in Drug Delivery: Pros and Cons as Well as Potential Alternatives
Knop, K., Hoogenboom, R., Fischer, D., & Schubert, U. S. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200902672 · Cited by 3,533
Jeong, Y.-I., Kim, S.-H., Jung, T.-Y., Kim, I.-Y., Kang, S.-S., Jin, Y.-H., Ryu, H.-H., Sun, H.-S., Jin, S., Kim, K.-K., et al. (2006) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.20586 · Cited by 90
Research works printed but not linked: 235
- Dodane, 1998, Pharmaceutical applications of chitosan, Pharm Sci Technol Today, 1, 246, 10.1016/S1461-5347(98)00059-5 · DOI
- Rinaudo, 2006, Chitin and chitosan—properties and applications, Prog Polym Sci, 31, 603, 10.1016/j.progpolymsci.2006.06.001 · DOI
- Prabaharan, 2008, Review paper: chitosan derivatives as promising materials for controlled drug delivery, J Biomater Appl, 23, 5, 10.1177/0885328208091562 · DOI
- Felt, 1998, Chitosan: a unique polysaccharide for drug delivery, Drug Dev Ind Pharm, 24, 979, 10.3109/03639049809089942 · DOI
- Illum, 1998, Chitosan and its use as a pharmaceutical excipient, Pharm Res, 15, 1326, 10.1023/A:1011929016601 · DOI
- Lehr, 1992, In vitro evaluation of mucoadhesive properties of chitosan and some other natural polymers, Int J Pharm, 78, 43, 10.1016/0378-5173(92)90353-4 · DOI
- Dash, 2011, Chitosan—a versatile semi-synthetic polymer in biomedical applications, Prog Polym Sci, 36, 981, 10.1016/j.progpolymsci.2011.02.001 · DOI
- Fiebrig, 1995, Transmission electron microscopy studies on pig gastric mucin and its interactions with chitosan, Carbohydr Polym, 28, 239, 10.1016/0144-8617(95)00105-0 · DOI
- Fiebrig, 1997, Colloidal gold and colloidal gold labelled wheat germ agglutinin as molecular probes for identification in mucin/chitosan complexes, Carbohydr Polym, 33, 91, 10.1016/S0144-8617(97)00028-3 · DOI
- Deacon, 1999, Are chitosan-mucin interactions specific to different regions of the stomach? Velocity ultracentrifugation offers a clue, Carbohydr Polym, 38, 235, 10.1016/S0144-8617(98)00097-6 · DOI
- He, 1998, In vitro evaluation of the mucoadhesive properties of chitosan microspheres, Int J Pharm, 166, 75, 10.1016/S0378-5173(98)00027-1 · DOI
- Senel, 2000, Enhancing effect of chitosan on peptide drug delivery across buccal mucosa, Biomaterials, 21, 2067, 10.1016/S0142-9612(00)00134-4 · DOI
- Ramdas, 1999, Alginate encapsulated bioadhesive chitosan microspheres for intestinal drug delivery, J Biomater Appl, 13, 290, 10.1177/088532829901300402 · DOI
- Bugamelli, 1998, Controlled insulin release from chitosan microparticles, Arch Pharm, 331, 133, 10.1002/(SICI)1521-4184(199804)331:4<133::AID-ARDP133>3.0.CO;2-H · DOI
- Iqbal, 2003, Nasal delivery of chitosan-DNA plasmid expressing epitopes of respiratory syncytial virus (RSV) induces protective CTL responses in BALB/c mice, Vaccine, 21, 1478, 10.1016/S0264-410X(02)00662-X · DOI
- Roy, 1999, Oral gene delivery with chitosan–DNA nanoparticles generates immunologic protection in a murine model of peanut allergy, Nat Med, 5, 387, 10.1038/7385 · DOI
- Illum, 2001, Chitosan as a novel nasal delivery system for vaccines, Adv Drug Del Rev, 51, 81, 10.1016/S0169-409X(01)00171-5 · DOI
- Smart, 1984, An in-vitro investigation of mucosa-adhesive materials for use in controlled drug delivery, J Pharm Pharmacol, 36, 295, 10.1111/j.2042-7158.1984.tb04377.x · DOI
- Peppas, 1985, Surface, interfacial and molecular aspects of polymer bioadhesion on soft tissues, J Controlled Release, 2, 257, 10.1016/0168-3659(85)90050-1 · DOI
- Robinson, 1995, Bioadhesive and phase-change polymers for ocular drug delivery, Adv Drug Del Rev, 16, 45, 10.1016/0169-409X(95)00013-W · DOI
- Robinson, 1987, Bioadhesive polymers for controlled drug delivery, Ann NY Acad Sci, 507, 307, 10.1111/j.1749-6632.1987.tb45810.x · DOI
- Illum, 1994, Chitosan as a novel nasal delivery system for peptide drugs, Pharm Res, 11, 1186, 10.1023/A:1018901302450 · DOI
- Luessen, 1994, Bioadhesive polymers for the peroral delivery of peptide drugs, J Controlled Release, 29, 329, 10.1016/0168-3659(94)90078-7 · DOI
- Aspden, 1996, Chitosan as a nasal delivery system: evaluation of insulin absorption enhancement and effect on nasal membrane integrity using rat models, Eur J Pharm Sci, 4, 23, 10.1016/0928-0987(95)00026-7 · DOI
- Srinivasa, 2007, Chitin/chitosan—safe, ecofriendly packaging materials with multiple potential uses, Food Rev Int, 23, 53, 10.1080/87559120600998163 · DOI
- Mei, 2008, Effect of chitosan structure properties and molecular weight on the intranasal absorption of tetramethylpyrazine phosphate in rats, Eur J Pharm Biopharm, 70, 874, 10.1016/j.ejpb.2008.06.031 · DOI
- Kasaai, 2009, Various methods for determination of the degree of N-acetylation of chitin and chitosan: a review, J Agric Food Chem, 57, 1667, 10.1021/jf803001m · DOI
- Heux, 2000, Solid state NMR for determination of degree of acetylation of chitin and chitosan, Biomacromolecules, 1, 746, 10.1021/bm000070y · DOI
- Vårum, 1991, Determination of the degree of N-acetylation and the distribution of N-acetyl groups in partially N-deacetylated chitins (chitosans) by high-field n. m. r. spectroscopy, Carbohydr Res, 211, 17, 10.1016/0008-6215(91)84142-2 · DOI
- Lavertu, 2003, A validated 1H NMR method for the determination of the degree of deacetylation of chitosan, J Pharm Biomed Anal, 32, 1149, 10.1016/S0731-7085(03)00155-9 · DOI
- Hirai, 1991, Determination of degree of deacetylation of chitosan by 1H NMR spectroscopy, Polym Bull, 26, 87, 10.1007/BF00299352 · DOI
- Hwang, 2002, Controlling molecular weight and degree of deacetylation of chitosan by response surface methodology, J Agric Food Chem, 50, 1876, 10.1021/jf011167u · DOI
- Duarte, 2002, An optimised method to determine the degree of acetylation of chitin and chitosan by FTIR spectroscopy, Int J Biol Macromol, 31, 1, 10.1016/S0141-8130(02)00039-9 · DOI
- Sabnis, 1997, Improved infrared spectroscopic method for the analysis of degree of N-deacetylation of chitosan, Polym Bull, 39, 67, 10.1007/s002890050121 · DOI
- Khan, 2002, Reporting degree of deacetylation values of chitosan: the influence of analytical methods, J Pharm Pharm Sci, 5, 205
- Kasaai, 2008, A review of several reported procedures to determine the degree of N-acetylation for chitin and chitosan using infrared spectroscopy, Carbohydr Polym, 71, 497, 10.1016/j.carbpol.2007.07.009 · DOI
- Vårum, 1995, Characterization of partially N-acetylated chitosans by near infra-red spectroscopy, Carbohydr Polym, 28, 187, 10.1016/0144-8617(95)00130-1 · DOI
- Rathke, 1993, Determination of the degree of N-deacetylation in chitin and chitosan as well as their monomer sugar ratios by near infrared spectroscopy, J Polym Sci, Part A Polym Chem, 31, 749, 10.1002/pola.1993.080310320 · DOI
- Tan, 1998, The degree of deacetylation of chitosan: advocating the first derivative UV-spectrophotometry method of determination, Talanta, 45, 713, 10.1016/S0039-9140(97)00288-9 · DOI
- Jiang, 2003, A new linear potentiometric titration method for the determination of deacetylation degree of chitosan, Carbohydr Polym, 54, 457, 10.1016/j.carbpol.2003.05.004 · DOI
- Prochazkova, 1999, Quantitative determination of chitosans by ninhydrin, Carbohydr Polym, 38, 115, 10.1016/S0144-8617(98)00108-8 · DOI
- Aiba, 1986, Studies on chitosan: 1. Determination of the degree of N-acetylation of chitosan by ultraviolet spectrophotometry and gel permeation chromatography, Int J Biol Macromol, 8, 173, 10.1016/0141-8130(86)90022-X · DOI
- Zhang, 2005, Determination of the degree of deacetylation of chitin and chitosan by X-ray powder diffraction, Carbohydr Res, 340, 1914, 10.1016/j.carres.2005.05.005 · DOI
- Ottey, 1996, Compositional heterogeneity of heterogeneously deacetylated chitosans, Carbohydr Polym, 29, 17, 10.1016/0144-8617(95)00154-9 · DOI
- Nanjo, 1991, Enzymatic method for determination of the degree of deacetylation of chitosan, Anal Biochem, 193, 164, 10.1016/0003-2697(91)90002-B · DOI
- Alonso, 1983, Determination of the degree of acetylation of chitin and chitosan by thermal analysis, J Therm Anal Calorim, 28, 189, 10.1007/BF02105290 · DOI
- Lal, 1984, Determination of the amine content of chitosan by pyrolysis-gas chromatography, J Anal Appl Pyrolysis, 6, 183, 10.1016/0165-2370(84)80012-1 · DOI
- Sato, 1998, Determination of the degree of acetylation of chitin/chitosan by pyrolysis-gas chromatography in the presence of oxalic acid, Anal Chem, 70, 7, 10.1021/ac9706685 · DOI
- Terbojevich, 1993, High-performance gel-permeation chromatography of chitosan samples, Carbohydr Res, 250, 301, 10.1016/0008-6215(93)84008-T · DOI
- Fee, 2003, Correlation of SEC/MALLS with ultracentrifuge and viscometric data for chitosans, Eur Biophys J, 32, 457, 10.1007/s00249-003-0317-8 · DOI
- Beri, 1993, Characterization of chitosans via coupled size-exclusion chromatography and multiple-angle laser light-scattering technique, Carbohydr Res, 238, 11, 10.1016/0008-6215(93)87002-A · DOI
- Nguyen, 2009, Improved reproducibility in the determination of the molecular weight of chitosan by analytical size exclusion chromatography, Carbohydr Polym, 75, 528, 10.1016/j.carbpol.2008.08.013 · DOI
- Illum, 1996, Nasal administration of morphine-6-glucuronide in sheep—a pharmacokinetic study, Biopharm Drug Dispos, 17, 717, 10.1002/(SICI)1099-081X(199611)17:8<717::AID-BDD985>3.0.CO;2-I · DOI
- Cheng, 2005, Intranasal delivery of recombinant human growth hormone (somatropin) in sheep using chitosan-based powder formulations, Eur J Pharm Sci, 26, 9, 10.1016/j.ejps.2005.03.014 · DOI
- Illum, 2000, Transport of drugs from the nasal cavity to the central nervous system, Eur J Pharm Sci, 11, 1, 10.1016/S0928-0987(00)00087-7 · DOI · Paper page
- Illum, 2002, Intranasal delivery of morphine, J Pharmacol Exp Ther, 301, 391, 10.1124/jpet.301.1.391 · DOI
- Smith, 2004, Effect of chitosan on epithelial cell tight junctions, Pharm Res, 21, 43, 10.1023/B:PHAM.0000012150.60180.e3 · DOI
- Illum, 2002, Nasal drug delivery: new developments and strategies, Drug Discov Today, 7, 1184, 10.1016/S1359-6446(02)02529-1 · DOI
- Artursson, 1994, Effect of chitosan on the permeability of monolayers of intestinal epithelial cells (Caco-2), Pharm Res, 11, 1358, 10.1023/A:1018967116988 · DOI
- Dodane, 1999, Effect of chitosan on epithelial permeability and structure, Int J Pharm, 182, 21, 10.1016/S0378-5173(99)00030-7 · DOI
- Vllasaliu, 2010, Tight junction modulation by chitosan nanoparticles: comparison with chitosan solution, Int J Pharm, 400, 183, 10.1016/j.ijpharm.2010.08.020 · DOI
- Schipper, 1997, Chitosans as absorption enhancers for poorly absorbable drugs 2: mechanism of absorption enhancement, Pharm Res, 14, 923, 10.1023/A:1012160102740 · DOI
- Stenson, 1993, Regulation of paracellular permeability in Caco-2 cell monolayers by protein kinase C, Am J Physiol Gastrointest Liver Physiol, 265, 955, 10.1152/ajpgi.1993.265.5.G955 · DOI
- Fang, 2001, Interactions of phospholipid bilayer with chitosan: effect of molecular weight and pH, Biomacromolecules, 2, 1161, 10.1021/bm015548s · DOI
- Rinaudo, 1999, Solubilization of chitosan in strong acid medium, Int J Polym Anal Charact, 5, 267, 10.1080/10236669908009742 · DOI
- Fan, 2009, Preparation and structure of chitosan soluble in wide pH range, Carbohydr Polym, 78, 66, 10.1016/j.carbpol.2009.03.031 · DOI
- Pillai, 2009, Chitin and chitosan polymers: chemistry, solubility and fiber formation, Prog Polym Sci, 34, 641, 10.1016/j.progpolymsci.2009.04.001 · DOI
- Rinaudo, 1999, Influence of acetic acid concentration on the solubilization of chitosan, Polymer, 40, 7029, 10.1016/S0032-3861(99)00056-7 · DOI
- Van der Merwe, 2004, Trimethylated chitosan as polymeric absorption enhancer for improved peroral delivery of peptide drugs, Eur J Pharm Biopharm, 58, 225, 10.1016/j.ejpb.2004.03.023 · DOI
- Du, 2007, PEGylation of chitosan for improved solubility and fiber formation via electrospinning, Cellulose, 14, 543, 10.1007/s10570-007-9122-3 · DOI
- Bergström, 1992, Reduction of fibrinogen adsorption on PEG-coated polystyrene surfaces, J Biomed Mater Res, 26, 779, 10.1002/jbm.820260607 · DOI
- Cavalla, 2001, Adaptations and innovations in drug delivery, Drug News Perspect, 14, 495
- Tirelli, 2002, Poly(ethylene glycol) block copolymers, Rev Mol Biotechnol, 90, 3, 10.1016/S1389-0352(01)00057-5 · DOI
- Jevševar, 2010, PEGylation of therapeutic proteins, Biotechnol J, 5, 113, 10.1002/biot.200900218 · DOI · Paper page
- Thanou, 2000, Effect of degree of quaternization of N-trimethyl chitosan chloride for enhanced transport of hydrophilic compounds across intestinal Caco-2 cell monolayers, J Controlled Release, 64, 15, 10.1016/S0168-3659(99)00131-5 · DOI
- Snyman, 2003, Low molecular weight quaternised chitosan (I): synthesis and characterization, Pharmazie, 58, 705
- Amidi, 2006, Preparation and characterization of protein-loaded N-trimethyl chitosan nanoparticles as nasal delivery system, J Controlled Release, 111, 107, 10.1016/j.jconrel.2005.11.014 · DOI
- Philipp, 1996, Regioselective derivatization of cellulose. Routes of synthesis, effects on properties and areas of application, Polym News, 21, 155
- Bannikova, 2002, Hydrolysis of chitosan sulfate with an enzyme complex from Streptomyces kurssanovii, Appl Biochem Microbiol, 38, 413, 10.1023/A:1019904131791 · DOI
- Polnok, 2004, In vitro evaluation of intestinal absorption of desmopressin using drug-delivery systems based on superporous hydrogels, Int J Pharm, 269, 303, 10.1016/j.ijpharm.2003.09.022 · DOI
- Wongpanit, 2005, Preparation and characterization of microwave-treated carboxymethyl chitin and carboxymethyl chitosan films for potential use in wound care application, Macromol Biosci, 5, 1001, 10.1002/mabi.200500081 · DOI
- Richardson, 2003, Characterization of the substituent distribution in starch and cellulose derivatives, Anal Chim Acta, 497, 27, 10.1016/j.aca.2003.08.005 · DOI
- Yao, 2003, Synthesis and characterization of chitosan grafted oligo(L-lactic acid), Macromol Biosci, 3, 653, 10.1002/mabi.200350035 · DOI
- Shim, 2003, Preparation of poly(acrylic acid)–chitosan hydrogels by gamma irradiation and in vitro drug release, J Appl Polym Sci, 90, 3660, 10.1002/app.13120 · DOI
- Yazdani-Pedram, 1997, Homogeneous grafting reaction of vinyl pyrrolidone onto chitosan, J Appl Polym Sci, 63, 1321, 10.1002/(SICI)1097-4628(19970307)63:10<1321::AID-APP11>3.0.CO;2-7 · DOI
- Ngimhuang, 2004, Synthesis of a novel polymeric surfactant by reductive N-alkylation of chitosan with 3-O-dodecyl-glucose, Polymer, 45, 837, 10.1016/j.polymer.2003.11.034 · DOI
- Lee, 2004, Temperature/pH-sensitive comb-type graft hydrogels composed of chitosan and poly(N-isopropylacrylamide), J Appl Polym Sci, 92, 2612, 10.1002/app.20265 · DOI
- Muzzarelli, 1994, Solubility and structure of N-carboxymethylchitosan, Int J Biol Macromol, 4, 177, 10.1016/0141-8130(94)90048-5 · DOI
- Xiao Fei, 2001, Antibacterial action of chitosan and carboxymethylated chitosan, J Appl Polym Sci, 79, 1324, 10.1002/1097-4628(20010214)79:7<1324::AID-APP210>3.0.CO;2-L · DOI
- Ye, 2007, Effects of molecular structural parameters of carboxymethyl chitosan on the growth of fibroblasts in vitro, J Appl Polym Sci, 106, 3136, 10.1002/app.25967 · DOI
- Jayakumar, 2010, Novel carboxymethyl derivatives of chitin and chitosan materials and their biomedical applications, Prog Mater Sci, 55, 675, 10.1016/j.pmatsci.2010.03.001 · DOI
- Chen, 2003, Chemical characteristics of O-carboxymethyl chitosans related to the preparation conditions, Carbohydr Polym, 53, 355, 10.1016/S0144-8617(03)00051-1 · DOI
- Muzzarelli, 1988, Carboxymethylated chitins and chitosans, Carbohydr Polym, 8, 1, 10.1016/0144-8617(88)90032-X · DOI
- Snyman, 2002, The relationship between the absolute molecular weight and the degree of quaternization of N-trimethyl chitosan chloride, Carbohydr Polym, 50, 145, 10.1016/S0144-8617(02)00008-5 · DOI
- Domard, 1986, New method for the quaternization of chitosan, Int J Biol Macromol, 8, 105, 10.1016/0141-8130(86)90007-3 · DOI
- Mao, 2007, Characterization of chitosan and its derivatives using asymmetrical flow field-flow-fractionation: a comparison with traditional methods, J Pharm Biomed Anal, 45, 736, 10.1016/j.jpba.2007.08.012 · DOI
- Mourya, 2009, Trimethyl chitosan and its applications in drug delivery, J Mater Sci Mater Med, 20, 1057, 10.1007/s10856-008-3659-z · DOI
- Sieval, 1998, Preparation and NMR characterization of highly substituted N-trimethyl chitosan chloride, Carbohydr Polym, 36, 157, 10.1016/S0144-8617(98)00009-5 · DOI
- Kotzé, 1997, N-Trimethyl chitosan chloride as a potential absorption enhancer across mucosal surfaces: in vitro evaluation in intestinal epithelial cells (Caco-2), Pharm Res, 14, 1197, 10.1023/A:1012106907708 · DOI
- Kotzé, 1997, Chitosans for enhanced delivery of therapeutic peptides across intestinal epithelia: in vitro evaluation in Caco-2 cell monolayers, Int J Pharm, 159, 243, 10.1016/S0378-5173(97)00287-1 · DOI
- Verheul, 2008, Synthesis, characterization and in vitro biological properties of O-methyl free N,N,N-trimethylated chitosan, Biomaterials, 29, 3642, 10.1016/j.biomaterials.2008.05.026 · DOI
- Cano-Cebrian, 2005, Intestinal absorption enhancement via the paracellular route by fatty acids, chitosans and others: a target for drug delivery, Curr Drug Delivery, 2, 9, 10.2174/1567201052772834 · DOI
- Sajomsang, 2009, Quaternization of N-aryl chitosan derivatives: synthesis, characterization, and antibacterial activity, Carbohydr Res, 344, 2502, 10.1016/j.carres.2009.09.004 · DOI
- Zambito, 2006, Novel transmucosal absorption enhancers obtained by aminoalkylation of chitosan, Eur J Pharm Sci, 29, 460, 10.1016/j.ejps.2006.09.001 · DOI
- Holappa, 2004, Synthesis and characterization of chitosan N-betainates having various degrees of substitution, Macromolecules, 37, 2784, 10.1021/ma0358780 · DOI
- Bentley, 1998, Reductive amination using poly(ethylene glycol) acetaldehyde hydrate generated in situ: applications to chitosan and lysozyme, J Pharm Sci, 87, 1446, 10.1021/js980064w · DOI
- Muslim, 2001, Synthesis and bioactivities of poly(ethylene glycol)-chitosan hybrids, Carbohydr Polym, 46, 323, 10.1016/S0144-8617(00)00331-3 · DOI
- Park, 2003, Visualization of transfection of hepatocytes by galactosylated chitosan-graft-poly(ethylene glycol)/DNA complexes by confocal laser scanning microscopy, Int J Pharm, 257, 103, 10.1016/S0378-5173(03)00133-9 · DOI
- Mao, 2005, Synthesis, characterization and cytotoxicity of poly(ethylene glycol)-graft-trimethyl chitosan block copolymers, Biomaterials, 26, 6343, 10.1016/j.biomaterials.2005.03.036 · DOI
- Veronese, 2001, Peptide and protein PEGylation: a review of problems and solutions, Biomaterials, 22, 405, 10.1016/S0142-9612(00)00193-9 · DOI
- Veronese, 2005, PEGylation, successful approach to drug delivery, Drug Discov Today, 10, 1451, 10.1016/S1359-6446(05)03575-0 · DOI
- Harris, 2003, Effect of pegylation on pharmaceuticals, Nat Rev Drug Discov, 2, 214, 10.1038/nrd1033 · DOI · Paper page
- Ryan, 2008, Advances in PEGylation of important biotech molecules: delivery aspects, Exp Opin Drug Deliv, 5, 371, 10.1517/17425247.5.4.371 · DOI
- Kurita, 2001, Controlled functionalization of the polysaccharide chitin, Prog Polym Sci, 26, 1921, 10.1016/S0079-6700(01)00007-7 · DOI
- Ouchi, 1998, Aggregation phenomenon of PEG-grafted chitosan in aqueous solution, Polymer, 39, 5171, 10.1016/S0032-3861(97)10020-9 · DOI
- Hu, 2005, Preparation and characterization of poly(ethylene glycol)-g-chitosan with water-and organosolubility, Carbohydr Polym, 61, 472, 10.1016/j.carbpol.2005.06.022 · DOI
- Jeong, 2008, Preparation and spectroscopic characterization of methoxy poly(ethylene glycol)-grafted water-soluble chitosan, Carbohydr Res, 343, 282, 10.1016/j.carres.2007.10.025 · DOI
- Saito, 1997, Graft copolymers of poly(ethylene glycol) (PEG) and chitosan, Macromol Rapid Commun, 18, 547, 10.1002/marc.1997.030180703 · DOI
- Liu, 2006, Regioselective grafting of poly(ethylene glycol) onto chitosan and the properties of the resulting copolymers, Macromol Biosci, 6, 855, 10.1002/mabi.200600087 · DOI
- Gorochovceva, 2004, Synthesis and study of water-soluble chitosan-O-poly(ethylene glycol) graft copolymers, Eur Polym J, 40, 685, 10.1016/j.eurpolymj.2003.12.005 · DOI
- Makuska, 2006, Regioselective grafting of poly(ethylene glycol) onto chitosan through C-6 position of glucosamine units, Carbohydr Polym, 64, 319, 10.1016/j.carbpol.2005.12.006 · DOI
- Harris, 1984, Synthesis and characterization of poly(ethylene glycol) derivatives, J Polym Sci Polym Chem Ed, 22, 341, 10.1002/pol.1984.170220207 · DOI
- Sugimoto, 1998, Preparation and characterization of water-soluble chitin and chitosan derivatives, Carbohydr Polym, 36, 49, 10.1016/S0144-8617(97)00235-X · DOI
- Hu, 2008, PEGylated chitosan-based polymer micelle as an intracellular delivery carrier for anti-tumor targeting therapy, Eur J Pharm Biopharm, 70, 749, 10.1016/j.ejpb.2008.06.015 · DOI
- Casettari, 2010, Effect of PEGylation on the toxicity and permeability enhancement of chitosan, Biomacromolecules, 11, 2854, 10.1021/bm100522c · DOI
- Raviña, 2010, Hyaluronic acid/chitosan-g-poly(ethylene glycol) nanoparticles for gene therapy: an application for pDNA and siRNA delivery, Pharm Res, 27, 2544, 10.1007/s11095-010-0263-y · DOI
- Yoksan, 2004, Controlled hydrophobic/hydrophilic chitosan: colloidal phenomena and nanosphere formation, Colloid Polym Sci, 282, 337, 10.1007/s00396-003-0933-y · DOI
- Jang, 2003, Modification of low molecular water-soluble chitosan for pharmaceutical application, Bull Korean Chem Soc, 24, 1303, 10.5012/bkcs.2003.24.9.1303 · DOI
- Lin, 2011, Synthesis of lactobionic acid-grafted-pegylated-chitosan with enhanced HepG2 cells transfection, Carbohydr Polym, 83, 898, 10.1016/j.carbpol.2010.08.072 · DOI
- Tanuma, 2010, Preparation and characterization of PEG-cross-linked chitosan hydrogel films with controllable swelling and enzymatic degradation behavior, Carbohydr Polym, 80, 260, 10.1016/j.carbpol.2009.11.022 · DOI
- Kiuchi, 2008, Preparation and characterization of poly(ethylene glycol) crosslinked chitosan films, J Appl Polym Sci, 107, 3823, 10.1002/app.27546 · DOI
- Radhakumary, 2009, Chitosan-comb-graft-polyethylene glycol monomethacrylate-synthesis, characterization, and evaluation as a biomaterial for hemodialysis applications, J Appl Polym Sci, 114, 2873, 10.1002/app.30862 · DOI
- Wang, 2010, Folate-PEG coated cationic modified chitosan-cholesterol liposomes for tumor-targeted drug delivery, Biomaterials, 31, 4129, 10.1016/j.biomaterials.2010.01.089 · DOI
- Peng, 2010, Methoxy poly(ethylene glycol)-grafted-chitosan based microcapsules: synthesis, characterization and properties as a potential hydrophilic wall material for stabilization and controlled release of algal oil, J Food Eng, 101, 113, 10.1016/j.jfoodeng.2010.06.019 · DOI
- Cai, 2009, A facile route for regioselective conjugation of organo-soluble polymers onto chitosan, Macromol Biosci, 9, 256, 10.1002/mabi.200800153 · DOI
- Lebouc, 2005, Different ways for grafting ester derivatives of poly(ethylene glycol) onto chitosan: related characteristics and potential properties, Polymer, 46, 639, 10.1016/j.polymer.2004.11.104 · DOI
- Amiji, 1997, Synthesis of anionic poly(ethylene glycol) derivative for chitosan surface modification in blood-contacting applications, Carbohydr Polym, 32, 193, 10.1016/S0144-8617(97)00006-4 · DOI
- Deng, 2007, Investigation on the properties of methoxy poly(ethylene glycol)/chitosan graft co-polymers, J Biomater Sci Polym Ed, 18, 1575, 10.1163/156856207794761943 · DOI
- Dal Pozzo, 2000, Preparation and characterization of poly(ethylene glycol)-crosslinked reacetylated chitosans, Carbohydr Polym, 42, 201, 10.1016/S0144-8617(99)00134-4 · DOI
- Tao, 2004, α-Aldehyde terminally functional methacrylic polymers from living radical polymerization: application in protein conjugation “Pegylation”, J Am Chem Soc, 126, 13220, 10.1021/ja0456454 · DOI
- Jiang, 2006, Chitosan-g-PEG/DNA complexes deliver gene to the rat liver via intrabiliary and intraportal infusions, J Gene Med, 8, 477, 10.1002/jgm.868 · DOI
- Yoksan, 2008, Amphiphilic chitosan nanosphere: studies on formation, toxicity, and guest molecule incorporation, Bioorg Med Chem, 16, 2687, 10.1016/j.bmc.2007.11.037 · DOI
- Fangkangwanwong, 2006, One-pot synthesis in aqueous system for water-soluble chitosan-graft-poly(ethylene glycol) methyl ether, Biopolymers, 82, 580, 10.1002/bip.20511 · DOI
- Huang, 2006, Preparation of chitosan derivative with polyethylene glycol side chains for porous structure without specific processing technique, Int J Biol Macromol, 38, 191, 10.1016/j.ijbiomac.2006.02.008 · DOI
- Ohya, 2000, Preparation of PEG-grafted chitosan nanoparticles as peptide drug carriers, STP Pharm Sci, 10, 77
- Yang, 2008, Self-aggregated nanoparticles from methoxy poly(ethylene glycol)-modified chitosan: synthesis; characterization; aggregation and methotrexate release in vitro, Colloids Surf B, 61, 125, 10.1016/j.colsurfb.2007.07.012 · DOI
- Cai, 2009, pH-sensitive nanoparticles self-assembled from a novel class of biodegradable amphiphilic copolymers based on chitosan, J Mater Sci Mater Med, 20, 1315, 10.1007/s10856-008-3689-6 · DOI
- Shantha, 2002, Synthesis and characterization of chemically modified chitosan microspheres, Carbohydr Polym, 48, 247, 10.1016/S0144-8617(01)00244-2 · DOI
- Kong, 2010, Synthesis and characterization of a novel MPEG-chitosan diblock copolymer and self-assembly of nanoparticles, Carbohydr Polym, 79, 170, 10.1016/j.carbpol.2009.07.037 · DOI
- Gruškienė, 2009, Grafting of poly(ethylene glycol) to chitosan at C(6) position of glucosamine units via “click chemistry” reactions, Chemija, 20, 241
- Kulbokaite, 2009, N-Pegylation of chitosan via “click chemistry” reactions, React Funct Polym, 69, 771, 10.1016/j.reactfunctpolym.2009.06.010 · DOI
- Nishimura, 1991, Chemospecific manipulations of a rigid polysaccharide: syntheses of novel chitosan derivatives with excellent solubility in common organic solvents by regioselective chemical modifications, Macromolecules, 24, 4745, 10.1021/ma00017a003 · DOI
- Kulkarni, 2005, A novel method for the synthesis of the PEG-crosslinked chitosan with a pH-independent swelling behavior, Macromol Biosci, 5, 925, 10.1002/mabi.200500048 · DOI
- Kim, 2007, All-trans retinoic acid release from polyion-complex micelles of methoxy poly(ethylene glycol) grafted chitosan, J Appl Polym Sci, 105, 3246, 10.1002/app.26480 · DOI
- Yao, 2007, A series of novel chitosan derivatives: synthesis, characterization and micellar solubilization of paclitaxel, Carbohydr Polym, 68, 781, 10.1016/j.carbpol.2006.08.023 · DOI
- Wu, 2007, Water soluble complexes of chitosan-g-MPEG and hyaluronic acid, J Biomed Mater Res Part A, 80, 800, 10.1002/jbm.a.30972 · DOI
- Ganji, 2008, Synthesis and characterization of a new thermosensitive chitosan-PEG diblock copolymer, Carbohydr Polym, 74, 435, 10.1016/j.carbpol.2008.03.017 · DOI
- Zhang, 2008, PEG-grafted chitosan nanoparticles as an injectable carrier for sustained protein release, J Mater Sci Mater Med, 19, 3525, 10.1007/s10856-008-3500-8 · DOI
- Zhang, 2008, Nasal absorption enhancement of insulin using PEG-grafted chitosan nanoparticles, Eur J Pharm Biopharm, 68, 526, 10.1016/j.ejpb.2007.08.009 · DOI
- Yang, 2008, Novel polyion complex micelles for liver-targeted delivery of diammonium glycyrrhizinate: In vitro and in vivo characterization, J Biomed Mater Res Part A, 88, 140
- Wang, 2010, Nanoscaled polyion complex micelles for targeted delivery of recombinant hirudin to platelets based on cationic copolymer, Mol Pharmaceutics, 7, 718, 10.1021/mp900271r · DOI
- Chan, 2007, Synthesis and characterization of chitosan-g-poly(ethylene glycol)-folate as a non-viral carrier for tumor-targeted gene delivery, Biomaterials, 28, 540, 10.1016/j.biomaterials.2006.08.046 · DOI
- Mao, 2005, Uptake and transport of PEG-graft-trimethyl-chitosan copolymer–insulin nanocomplexes by epithelial cells, Pharm Res, 22, 2058, 10.1007/s11095-005-8175-y · DOI
- Sun, 2010, Bioadhesion and oral absorption of enoxaparin nanocomplexes, Int J Pharm, 386, 275, 10.1016/j.ijpharm.2009.11.025 · DOI
- Prego, 2006, Chitosan-PEG nanocapsules as new carriers for oral peptide delivery: effect of chitosan pegylation degree, J Controlled Release, 111, 299, 10.1016/j.jconrel.2005.12.015 · DOI
- Jiang, 2007, Immune stimulating activity of an atrophic rhinitis vaccine associated to pegylated chitosan microspheres in vitro, Polym Adv Technol, 18, 220, 10.1002/pat.861 · DOI
- Park, 2001, Galactosylated chitosan-graft-poly(ethylene glycol) as hepatocyte-targeting DNA carrier, J Controlled Release, 76, 349, 10.1016/S0168-3659(01)00448-5 · DOI
- Zhu, 2007, Synthesis and characterization of PEG modified N-trimethylaminoethylmethacrylate chitosan nanoparticles, Eur Polym J, 43, 2244, 10.1016/j.eurpolymj.2007.03.042 · DOI
- Jiang, 2008, Galactosylated poly(ethylene glycol)-chitosan-graft-polyethylenimine as a gene carrier for hepatocyte-targeting, J Controlled Release, 131, 150, 10.1016/j.jconrel.2008.07.029 · DOI
- Qu, 2009, PEG conjugated N-octyl-O-sulfate chitosan micelles for delivery of paclitaxel: in vitro characterization and in vivo evaluation, Eur J Pharm Sci, 37, 98, 10.1016/j.ejps.2009.01.004 · DOI
- Aktas, 2005, Development and brain delivery of chitosan-PEG nanoparticles functionalized with the monoclonal antibody OX26, Bioconjugate Chem, 16, 1503, 10.1021/bc050217o · DOI
- Zheng, 2010, Preparation and characterization of folate-poly(ethylene glycol)-grafted-trimethylchitosan for intracellular transport of protein through folate receptor-mediated endocytosis, J Biotechnol, 145, 47, 10.1016/j.jbiotec.2009.09.007 · DOI
- Huh, 2004, Supramolecular hydrogel formation based on inclusion complexation between poly(ethylene glycol)-modified chitosan and alpha-cyclodextrin, Macromol Biosci, 4, 92, 10.1002/mabi.200300037 · DOI
- Chang, 2007, Evaluation of chitosan-g-PEG copolymer for cell anti-adhesion application, J Med Biol Eng, 27, 41
- Zheng, 2010, Chitosan-g-MPEG-modified alginate/chitosan hydrogel microcapsules: a quantitative study of the effect of polymer architecture on the resistance to protein adsorption, Langmuir, 26, 17156, 10.1021/la1030203 · DOI
- Noh, 2010, Pegylated poly-l-arginine derivatives of chitosan for effective delivery of siRNA, J Controlled Release, 145, 159, 10.1016/j.jconrel.2010.04.005 · DOI
- Fernandez-Megia, 2007, Conjugation of bioactive ligands to PEG-grafted chitosan at the distal end of PEG, Biomacromolecules, 8, 833, 10.1021/bm060889x · DOI
- Li, 2009, Biodegradable MPEG-g-chitosan and methoxy poly(ethylene glycol)-b-poly([epsilon]-caprolactone) composite films: Part 1. Preparation and characterization, Carbohydr Polym, 79, 429, 10.1016/j.carbpol.2009.08.032 · DOI
- Jiang, 2004, Preparation and characterization of ibuprofen-loaded poly(lactide-co-glycolide)/poly(ethylene glycol)-g-chitosan electrospun membranes, J Biomater Sci Polym Ed, 15, 279, 10.1163/156856204322977184 · DOI
- Seo, 2009, Methotrexate-incorporated polymeric nanoparticles of methoxy poly(ethylene glycol)-grafted chitosan, Colloids Surf B, 69, 157, 10.1016/j.colsurfb.2008.10.020 · DOI
- Germershaus, 2008, Gene delivery using chitosan, trimethyl chitosan or polyethylenglycol-graft-trimethyl chitosan block copolymers: establishment of structure-activity relationships in vitro, J Controlled Release, 125, 145, 10.1016/j.jconrel.2007.10.013 · DOI
- Mao, 2006, Self-assembled polyelectrolyte nanocomplexes between chitosan derivatives and insulin, J Pharm Sci, 95, 1035, 10.1002/jps.20520 · DOI
- Zhong, 1999, Mechanical and cell interaction properties of PEG-modified chitosan, Proc First Joint BMES/EMBS Confer, 2, 779, 10.1109/IEMBS.1999.803934 · DOI
- Dong, 2008, Synthesis and properties of O-carboxymethyl chitosan/methoxy poly(ethylene glycol) graft copolymers, J Mater Sci Mater Med, 19, 869, 10.1007/s10856-007-3183-6 · DOI
- Gorochovceva, 2005, Chitosan-N-poly(ethylene glycol) brush copolymers: synthesis and adsorption on silica surface, Eur Polym J, 41, 2653, 10.1016/j.eurpolymj.2005.05.021 · DOI
- Zhang, 2009, Synthesis and properties of a novel methoxy poly(ethylene glycol)-modified galactosylated chitosan derivative, J Mater Sci Mater Med, 20, 673, 10.1007/s10856-008-3620-1 · DOI
- Wang, 2010, Construction of a novel cationic polymeric liposomes formed from PEGylated octadecyl-quaternized lysine modified chitosan/cholesterol for enhancing storage stability and cellular uptake efficiency, Biotechnol Bioeng, 106, 952, 10.1002/bit.22773 · DOI
- Wang, 2010, PLGA/polymeric liposome for targeted drug and gene co-delivery, Biomaterials, 31, 8741, 10.1016/j.biomaterials.2010.07.082 · DOI
- Opanasopit, 2006, Incorporation of camptothecin into N-phthaloyl chitosan-g-mPEG self-assembly micellar system, Eur J Pharm Biopharm, 64, 269, 10.1016/j.ejpb.2006.06.001 · DOI
- Opanasopit, 2007, Camptothecin-incorporating N-phthaloylchitosan-g-mPEG self-assembly micellar system: effect of degree of deacetylation, Colloids Surf B, 60, 117, 10.1016/j.colsurfb.2007.06.001 · DOI
- Opanasopit, 2007, N-Phthaloylchitosan-g-mPEG design for all-trans retinoic acid-loaded polymeric micelles, Eur J Pharm Sci, 30, 424, 10.1016/j.ejps.2007.01.002 · DOI
- El-Sherbiny, 2010, Biodegradable nano-micro carrier systems for sustained pulmonary drug delivery: (I) Self-assembled nanoparticles encapsulated in respirable/swellable semi-IPN microspheres, Int J Pharm, 395, 132, 10.1016/j.ijpharm.2010.05.032 · DOI
- El-Sherbiny, 2010, Swellable microparticles as carriers for sustained pulmonary drug delivery, J Pharm Sci, 99, 2343, 10.1002/jps.22003 · DOI
- Ngawhirunpat, 2009, Incorporation methods for cholic acid chitosan-g-mPEG self-assembly micellar system containing camptothecin, Colloids Surf B, 74, 253, 10.1016/j.colsurfb.2009.07.027 · DOI
- Sin, 2010, Chitosan-g-mPEG-supported palladium (0) catalyst for Suzuki cross-coupling reaction in water, J Mol Catal A Chem, 315, 99, 10.1016/j.molcata.2009.09.007 · DOI
- Liu, 2009, Synthesis and self-assembly of chitosan-based copolymer with a pair of hydrophobic/hydrophilic grafts of polycaprolactone and poly(ethylene glycol), Carbohydr Polym, 75, 401, 10.1016/j.carbpol.2008.07.038 · DOI
- Bae, 2009, Intracellular delivery of heparin complexed with chitosan-g-poly(ethylene glycol) for inducing apoptosis, Pharm Res, 26, 93, 10.1007/s11095-008-9713-1 · DOI
- Xu, 2009, Synthesis of biodegradable polycationic methoxy poly(ethylene glycol)-polyethylenimine-chitosan and its potential as gene carrier, Carbohydr Polym, 78, 46, 10.1016/j.carbpol.2009.04.019 · DOI
- Choochottiros, 2009, Amphiphilic chitosan nanospheres: factors to control nanosphere formation and its consequent pH responsive performance, Polymer, 50, 1877, 10.1016/j.polymer.2009.02.029 · DOI
- Lin, 2007, Synthesis of multifunctional chitosan with galactose as a targeting ligand for glycoprotein receptor, Carbohydr Polym, 67, 474, 10.1016/j.carbpol.2006.06.017 · DOI
200 of 235 shown
Cited by
Sorted by citations
Pardeshi, C. V., & Belgamwar, V. S. (2013) · Expert Opinion on Drug Delivery · doi:10.1517/17425247.2013.790887 · Cited by 482
Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment
Choukaife, H., Seyam, S., Alallam, B., Doolaanea, A. A., & Alfatama, M. (2022) · International Journal of Nanomedicine · doi:10.2147/ijn.s375229 · Cited by 127
Tamayol, A., Hassani Najafabadi, A., Mostafalu, P., Yetisen, A. K., Commotto, M., Aldhahri, M., Abdel-wahab, M. S., Najafabadi, Z. I., Latifi, S., Akbari, M., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-04749-8 · Cited by 115
Metadata
- Authors
- Casettari, L., Vllasaliu, D., Castagnino, E., Stolnik, S., Howdle, S., & Illum, L.
- Venue
- Progress in Polymer Science
- Publisher
- Elsevier BV
- Published
- 2012-05
- Volume
- 37
- Issue
- 5
- Pages
- 659-685
- ISSN
- 0079-6700
- Cited by
- 232
- References
- 2
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review