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Chitosan Chemistry: Relevance to the Biomedical Sciences
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“Chitosan is a natural, biodegradable, biocompatible, and non-toxic biopolymer obtained from chitin deacetylation that is sourced from the exo-skeleton of crustaceans (Muzzarelli and Muzzarelli, 2005; Lizardi-Mendoza et al., 2016).”
From GRAS, plant- and animal-derived compounds as alternatives to conventional fungicides for the control of postharvest diseases of fresh horticultural produce (2016) · cites this paper as Muzzarelli and Muzzarelli, 2005
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Isolation of lysozyme on chitosan
Muzzarelli, R. A. A., Barontini, G., & Rochetti, R. (1978) · Biotechnology and Bioengineering · doi:10.1002/bit.260200107 · Cited by 34
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Items 301–400 of 475
Amamou, O., Kefil, S., Denis, J.-P., Boubaker, T., & Cardinal, S. (2024) · Molecules · doi:10.3390/molecules29132962 · Cited by 15
“Due to its remarkable properties, including its non-toxicity, biocompatibility, biodegrad-ability, and antimicrobial properties, chitosan has become an important research topic [2–5].”
BackgroundGonzález, J. A., & Villalobos, J. R. V. (2023) · Pharmaceuticals · doi:10.3390/ph16101503 · Cited by 15
“Chitosan, a chitin-derived linear cationic polysaccharide, is a natural, hydrophilic, non-allergenic, biocompatible, non-toxic and biodegradable product obtained from chitin of cuttlebone [112,113].”
BackgroundSohi, A. N., Naderi-Manesh, H., Soleimani, M., Mirzaei, S., Delbari, M., & Dodel, M. (2018) · Polymer Science Series A · doi:10.1134/s0965545x18040077 · Cited by 15
Volod’ko, A. V., Давыдова, В. Н., Nedashkovskaya, O. I., Terentieva, N. A., Chusovitin, E. A., Galkin, N. G., & Yermak, I. M. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.05.215 · Cited by 16
DNA gel particles: An overview
Morán, M. C., Vinardell, M. P., Infante, M. R., Miguel, M. G., & Lindman, B. (2013) · Advances in Colloid and Interface Science · doi:10.1016/j.cis.2013.09.002 · Cited by 22
“4 Biocompatible polymers are widely used in drug delivery and tissue engineering, where they form a variety structures, through either chemical cross-linking or physical association, that range from nanoparticles to macroscopic scaffolds [10-15].”
BackgroundChitin based polyurethanes using hydroxyl terminated polybutadiene. Part I: molecular engineering.
Zia, K., Mahmood, K., Zuber, M., Jamil, T., & Shafiq, M. (2013) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2013.04.069 · Cited by 15
Sagheer, F. A. A., Khalil, K., & Ibrahim, E. I. (2013) · doi:10.1016/j.eurpolymj.2013.03.010 · Cited by 15
Petrova, V., Nud’ga, L. A., Bochek, A. M., Yudin, V., Gofman, I., Elokhovskii, V., & Dobrovol’skaya, I. (2012) · Polymer Science Series A · doi:10.1134/s0965545x1203008x · Cited by 15
Baimark, Y., Niamsa, N., Morakot, N., Threeprom, J., & Srisuwan, Y. (2007) · doi:10.1080/10236660701636108 · Cited by 15
“Chitosan is a biopolymer that has received great deal of attention in a variety of applications because of its biodegradability and biocompatibility.([1,2]) Because of its excellent film-forming property, chitosan can be used effectively as a film-forming material to carry active ingredients such as minerals or vitami…”
BackgroundApplication of low molecular weight chitosan in animal nutrition, husbandry, and health: A review
Boamah, P., Onumah, J., Agolisi, M. H., & Idan, F. (2023) · Carbohydrate Polymer Technologies and Applications · doi:10.1016/j.carpta.2023.100329 · Cited by 15
Antunes, J., Gonçalves, R., & Barbosa, M. (2016) · Research & Reviews Journal of Material Sciences · doi:10.4172/2321-6212.1000153 · Cited by 15
“Chitin is abundant in Nature (primary structural component of the exoskeleton of shrimps, crabs and lobster and squid pens as an equivalent to collagen, and present in lesser amounts in cell walls of some fungi and yeast and in plants as the equivalent of cellulose) [20,54,56-58].”
BackgroundPreparation and characterization of chitosanates loaded with Brazilian red propolis extract
Nascimento, T. G. D., Nascimento, N. M. D., Ribeiro, A., de Almeida, C. P., dos Santos, J. I. Z., Basílio-Júnior, I. D., Calheiros-Silva, F. G., Lira, G. M., Escodro, P. B., Porto, I. C. C. D. M., et al. (2021) · Journal of Thermal Analysis and Calorimetry · doi:10.1007/s10973-021-11060-2 · Cited by 14
Novel nanoparticle materials for drug/food delivery-polysaccharides
Chen, L., Liu, X., & Wong, K.-H. (2016) · Physical Sciences Reviews · doi:10.1515/psr-2016-0053 · Cited by 14
“Chitosan is produced industrially by alkali treatment to hydrolyze the amino-acetyl groups of chitin with the degree of deacetylation (%DD) in range 60–100%[117, 118].”
Synthesis and characterization of chitosan/cloisite 30B film for controlled release of ofloxacin
Sahoo, D., & Nayak, P. (2012) · doi:10.1002/app.34595 · Cited by 14
Preparation and Swelling Behavior of Chitosan/Poly(N-2-Aminoethyl Acrylamide) Composite Hydrogels
Drăgan, E., & Perju, M. (2010) · Soft Materials · doi:10.1080/15394451003598536 · Cited by 14
Victor, R. D. S., Santos, A. M. D. C., de Sousa, B. V., Neves, G. D. A., Santana, L. N. D. L., & Menezes, R. R. (2020) · Materials · doi:10.3390/ma13214995 · Cited by 260
Qi, P., Ning, Z., & Zhang, X. (2023) · IET Nanobiotechnology · doi:10.1049/nbt2.12103 · Cited by 13
Future direction of wound dressing research: Evidence From the bibliometric analysis
Ho, Y., Sharmin, A. A., Islam, M. T., & Halim, A. F. (2022) · Journal of Industrial Textiles · doi:10.1177/15280837221130518 · Cited by 13
Preparation and characterization of chloridazon-loaded alginate/chitosan nanocapsules.
Babaei, S., Kahrizi, D., Nosratti, I., Karimi, N., Arkan, E., & Tahir, M. (2022) · Cellular and Molecular Biology · doi:10.14715/cmb/2022.68.3.5 · Cited by 13
“chitosan are natural amino polysaccharides with unique structures, multidimensional properties, highly advanced functions and wide applications in biomedical and other industrial fields (27, 28).”
BackgroundMarks, J. A., Fox, S. C., & Edgar, K. J. (2016) · Cellulose · doi:10.1007/s10570-016-0929-7 · Cited by 12
Mithun, U., Vishalakshi, B., & Karthika, J. (2016) · Iranian polymer journal · doi:10.1007/s13726-016-0425-9 · Cited by 13
“Chitosan (Cts), a partially deacetylated derivative of Chitin, is a highly useful material for pharmaceutical and nonpharmaceutical applications [1].”
BackgroundDing, W., Wu, M. N., Liang, M.-K., Ni, H., & Li, Y. (2015) · doi:10.1080/00032719.2014.991965 · Cited by 13
Chitosan-Based Macromolecular Biomaterials for the Regeneration of Chondroskeletal and Nerve Tissue
Guerra, G., Barbani, N., Gagliardi, M., Rosellini, E., & Cristallini, C. (2011) · International Journal of Carbohydrate Chemistry · doi:10.1155/2011/303708 · Cited by 13
“Muzzarelli thoroughly reviewed the researches made on CHI and its derivatives as biomaterials [13].”
BackgroundChitosan Microparticles Prepared by the Simple Emulsification-Diffusion Method
Kotsaeng, N., Karnchanajindanun, J., & Baimark, Y. (2010) · doi:10.1080/02726351003702574 · Cited by 13
Ozerin, A., Perov, N., Zelenetskii, A., Akopova, T., Ozerina, L., Kechek'yan, A., Surin, N., Vladimirov, L., & Yulovskaya, V. (2009) · doi:10.1134/s1995078009050103 · Cited by 13
Radiation Grafting of Biopolymers and Synthetic Polymers
Pino-Ramos, V. H., Melendez‐Ortiz, H. I., Ramos‐Ballesteros, A., & Bucio, E. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-810462-0.00006-5 · Cited by 18
Effect of Chitosan Molecular Weights on Characteristics of Silk Fibroin/Chitosan Blend Films
Baimark, Y., Srihanam, P., & Srisuwan, Y. (2009) · doi:10.3923/crc.2009.8.14 · Cited by 13
Xu, Y., Gan, K., Liang, S.-Y., Liu, H.-T., & Wang, Q.-H. (2021) · Water · doi:10.3390/w13040513 · Cited by 12
“Chitin turns into chitosan when the deacetylation degree (DD) is over 50% [17], and then becomes soluble in water [18].”
BackgroundSanuja, R. G., Kalutharage, N. K., & Cumaranatunga, P. (2017) · doi:10.4038/sljas.v22i1.7516 · Cited by 12
Burova, T., Grinberg, N., Dubovik, A., Olenichenko, E. A., Orlov, V., & Grinberg, V. (2017) · doi:10.1016/j.polymer.2016.11.049 · Cited by 12
Hydrodynamic behavior of quaternized chitosan at acidic and neutral pH
Yevlampieva, N., Gubarev, A., Gorshkova, M., Okrugin, B., & Ryumtsev, E. (2015) · Journal of polymer research · doi:10.1007/s10965-015-0802-7 · Cited by 12
“Insertion of the charged quaternary ammonium moieties onto the chitosan chain is a possibility to improve its solubility in a wide pH range [1].”
BackgroundFormation of Concentric Multilayers in a Chitosan Hydrogel Inspired by Liesegang Ring Phenomena
Li, B.-Q., Gao, Y.-S., Feng, Y.-J., Ma, B., Zhu, R., & Zhou, Y. (2011) · Journal of Biomaterials Science. Polymer Edition · doi:10.1163/092050610x538425 · Cited by 12
Chitosan-based drug delivery systems in cancer therapeutics
Padhi, S., Behera, A., Hasnain, M. S., & Nayak, A. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819336-5.00011-x · Cited by 12
Singh, B. K., & Dutta, P. K. (2015) · Springer series on polymer and composite materials · doi:10.1007/978-81-322-2511-9_7 · Cited by 17
Chitosan-Based Beads for Controlled Release of Proteins
Dash, M., Piras, A., & Chiellini, F. (2009) · doi:10.1007/978-88-470-1104-5_10 · Cited by 12
“In addition, it has good adhesion properties [2], ability to coagulate, and immuno stimulating activity [ 3 ].”
BackgroundUtilization of By-Products in the Fish Industry
Kristbergsson, K., & Arason, S. (2007) · doi:10.1007/978-0-387-35766-9_12 · Cited by 12
“This will lead to very highly priced products for medical applications in the area of tissue engineering ( Murugan and Ramakrishna, 2006 ) and bone repair (Samdancioglu et al., 2006).”
BackgroundGelation in solutions of low deacetylated chitosan initiated by high shear stresses.
Lipatova, I., Yusova, A., Losev, N., & Indeikin, E. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.07.164 · Cited by 11
Hepatoprotective effect of chitosan-caffeic acid conjugate against ethanol-treated mice.
Park, S.-Y., Ahn, G., Um, J., Han, E., Ahn, C.-B., Yoon, N., & Je, J.-Y. (2017) · Experimental and Toxicological Pathology · doi:10.1016/j.etp.2017.05.009 · Cited by 11
Tan, E., Karakuş, S., Soylu, G. S. P., Birer, Ö., Zengin, Y., & Kilislioglu, A. (2017) · Ultrasonics sonochemistry · doi:10.1016/j.ultsonch.2016.08.027 · Cited by 11
Application of Raman Spectroscopy for Evaluation of Chemical Changes in Dibutyrylchitin Fibres
Biniaś, D., Biniaś, W., & Janicki, J. (2016) · doi:10.5604/12303666.1207842 · Cited by 11
“It can also be found in insects, as well as in some microorganisms and fungi [1, 2].”
BackgroundPodorozhko, E., Lunev, I. A., Ryabev, A. N., Kil'deeva, N., & Lozinsky, V. (2015) · Colloid Journal · doi:10.1134/s1061933x1502012x · Cited by 11
Altered enzymatic activity of lysozymes bound to variously sulfated chitosans
Wang, H.-W., Yuan, L., Zhao, T., Huang, H., Chen, H., & Wu, D. (2012) · Chinese Journal of Polymer Science · doi:10.1007/s10118-012-1181-8 · Cited by 11
Kipper, M. (2020) · Encyclopedia of Biophysics · doi:10.1007/978-3-642-35943-9_690-1 · Cited by 11
Zhang, S.-P., Li, S.-Y., Ma, J., Xiong, F., & Qu, S. (2013) · Journal of Nanomaterials · doi:10.1155/2013/751236 · Cited by 11
Polysaccharide Based Nanoparticles
Khan, W., Abtew, E., Modani, S., & Domb, A. (2018) · Israel Journal of Chemistry · doi:10.1002/ijch.201800051 · Cited by 10
Chitosan Coating on Silica-Modified Polymethyl Methacrylate for Dental Applications
Więckiewicz, M., Wolf, E., Walczak, K., Meissner, H., & Boening, K. (2017) · doi:10.3390/coatings7100168 · Cited by 10
“As a chemoattractant, chitosan can activate macrophages and neutrophils, stimulate fibroblasts and other human cells, capture growth factors, induce the production of cytokines, and promote angiogenesis [5,6].”
BackgroundNikonorov, V. V., Ivanov, R., Kil'deeva, N., & Lozinskiĭ, V. I. (2011) · doi:10.1134/s0965545x1112011x · Cited by 10
PVA engineered microcapsules for targeted delivery of camptothecin to HeLa cells
Galbiati, A., della Rocca, B. M., Tabolacci, C., Beninati, S., Desideri, A., & Paradossi, G. (2011) · doi:10.1016/j.msec.2011.07.010 · Cited by 10
Nanocosmetics: future perspective
Morganti, P., Chen, H.-D., & Morganti, G. (2020) · Nanocosmetics · doi:10.1016/b978-0-12-822286-7.00020-6 · Cited by 10
Encapsulation of Bacillus subtilis in Chitosan Gel Beads for Eco-Friendly Crop Protection
Krastev, V., Stoyanova, N., Valcheva, I., Draganova, D., Spasova, M., & Stoilova, O. (2025) · Gels · doi:10.3390/gels11040302 · Cited by 9
Fatty acid-modified chitosan and nanoencapsulation of essential oils: A snapshot of applications.
Abdulsalam, R., Ijabadeniyi, O., & Sabiu, S. (2024) · Carbohydrate Research · doi:10.1016/j.carres.2024.109196 · Cited by 9
Kalantarian, G., Ziamajidi, N., Abbasalipourkabir, R., Mahjub, R., Goodarzi, M., Saidijam, M., Asl, S. S., & Jamshidi, M. (2019) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp-2019-0147 · Cited by 9
“Chitins are characterized as white, non-elastic, hard, nitrogenous polysaccharides that have been estimated to be synthesized at approximately 1 billion tons annually [15], [16].”
BackgroundChitosan Applications on Pharmaceutical Sciences: A Review
Nieva, C. A. B., Villegas, M., Cid, A., Romero, A. I., & Bermúdez, J. M. (2019) · Drug Delivery Letters · doi:10.2174/2210303109666190404143906 · Cited by 9
Drug-release system of microchannel transport used in minimally invasive surgery for hemostasis
Huang, H., Liu, H.-H., Zhou, H., Liang, Z.-L., Song, D., Zhang, Y., Huang, W., Zhao, X., Wu, B., Ye, G.-D., et al. (2019) · Drug Design, Development and Therapy · doi:10.2147/dddt.s180842 · Cited by 9
“The hemostasis results for the test drugs are shown in Figure 6.(40,41) A small amount of blood flowed when the muscle was cut.”
BackgroundAydınoğlu, D., & Ünal, M. (2019) · International Journal of Polymeric Materials · doi:10.1080/00914037.2018.1525545 · Cited by 9
Dye removal from wastewater using shrimp chitosan as an eco-friendly adsorbent
Fat'hi, M., & Ahmadi, A. (2016) · doi:10.4103/2277-9183.190645 · Cited by 9
Modification of the chitosan structure and properties using high-energy chemistry methods
Demina, T., Gil'man, A. B., Akopova, T. A., & Zelenetskii, A. (2014) · High Energy Chemistry · doi:10.1134/s0018143914050063 · Cited by 9
Chitin based polyurethanes using hydroxyl terminated polybutadiene, Part II: morphological studies.
Zia, K., Qureshi, N., Mujahid, M., Mahmood, K., & Zuber, M. (2013) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2013.04.042 · Cited by 9
Niamsa, N., Puntumchai, A., Sutthikhum, V., Srisuwan, Y., & Baimark, Y. (2008) · doi:10.1002/app.28117 · Cited by 9
Functional properties of chitin and chitosan-based polymer materials
Maleki, G., & Milani, J. (2020) · doi:10.1016/b978-0-12-817966-6.00006-6 · Cited by 9
Passive and Interactive Dressing Materials
Davis, J., & McLister, A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803762-1.00004-7 · Cited by 9
Applications, Uses and By-products from Cephalopods
Kouéta, N., Viala, H., & Bihan, E. L. (2014) · doi:10.1007/978-94-017-8648-5_8 · Cited by 9
Roldo, M., & Fatouros, D. (2011) · Studies in mechanobiology, tissue engineering and biomaterials · doi:10.1007/8415_2010_55 · Cited by 9
Energetics and mechanism of complexation between β-lactoglobulin and oligochitosan
Grinberg, V., Burova, T., Grinberg, N., Tikhonov, V., Dubovik, A., Orlov, V., Plashchina, I., Usov, A., & Khokhlov, A. (2022) · Food Hydrocolloids · doi:10.1016/j.foodhyd.2022.108021 · Cited by 8
Tan, T., Bakar, N. H. H. A., Bakar, M. A., & Talib, N. N. A. (2021) · Journal of Polymers and the Environment · doi:10.1007/s10924-021-02164-9 · Cited by 8
“However, due to its high molecular weight (105–106) [14, 15], low solubility in water [16] and high solution viscosity [17], the usage of CS in extensive applications, such as wastewater treatment [18], food [19] and biomedicine [20] is scarce.”
BackgroundReview article- Role of Chitosan in Wound Healing - a Review of the Recent Advances
Gokarneshan, N. (2017) · doi:10.19080/gjarm.2017.04.555637 · Cited by 8
Podorozhko, E., Ul'yabaeva, G. R., Kil'deeva, N., Tikhonov, V., Antonov, Y., Zhuravleva, I., & Lozinsky, V. (2016) · Colloid Journal · doi:10.1134/s1061933x16010130 · Cited by 8
Formation of concentric multi-layer chitosan hydrogel loaded with isoniazid.
Li, B.-Q., Gao, Y.-S., Feng, Y.-J., Ma, B., Zhu, R., & Zhou, Y. (2011) · Journal of Controlled Release · doi:10.1016/j.jconrel.2011.08.113 · Cited by 8
Grinberg, V., Burova, T., Grinberg, N., Dubovik, A., Tur, D., Usov, A. I., Papkov, V., & Khokhlov, A. (2011) · Langmuir · doi:10.1021/la200785g · Cited by 8
Karnchanajindanun, J., Srisa-ard, M., Srihanam, P., & Baimark, Y. (2010) · doi:10.4236/ns.2010.210131 · Cited by 8
“Chitosan is a copolymer of 2-glucosamine and Nacetyl-2-glucosamine prepared by alkaline deacetylation of chitin that has received great attention for its possible uses in medical, pharmaceutical and metal ion treatment applications because of its biodegradability, biocompatibility and high concentration of amine funct…”
BackgroundPreparation and structure of chitosan-silica organic-inorganic hybrid films
Tyukova, I. S., Suvorova, A., Okuneva, A. I., & Shishkin, E. (2010) · doi:10.1134/s1560090410090071 · Cited by 8
Mendez‐Alpuche, A. A., Ríos-Soberanis, C. R., Rodriguez-Laviada, J., Pérez-Pacheco, E., & Zaldívar-Rae, J. (2020) · ChemistrySelect · doi:10.1002/slct.202000085 · Cited by 7
Chitosan as Anticancer Compound and Nanoparticulate Matrix for Cancer Therapeutics
Nawaz, A., & Wong, T. W. (2020) · Wiley eBooks · doi:10.1002/9781119143802.ch73 · Cited by 12
Features of сhitosan interaction with copper(II) and cobalt(II) tetrasulfophthalocyanines
Lebedeva, N., Gubarev, Y. A., Yurina, E., Vyugin, A. I., & Lipatova, I. (2017) · Russian journal of general chemistry · doi:10.1134/s1070363217100139 · Cited by 7
Exposure of chitosan to UV/ozone: Structural information and antibacterial activity
Guirguis, O., El-Bassyouni, G., Esawy, M., Abdelkader, N., Mahmoud, H. A., Mostafa, H. M., & Abdel-Zaher, N. (2016) · doi:10.7324/japs.2016.601217 · Cited by 7
Yulianti, E., Saputri, R. D., Sudaryanto, S., Jodi, H., & Salam, R. (2013) · Jurnal Kimia dan Kemasan · doi:10.24817/jkk.v35i2.1877 · Cited by 7
Hattori, K., & Yoshida, T. (2012) · doi:10.1002/pola.26262 · Cited by 7
INVESTIGATION OF CHITOSAN FOR DECORPORATION OF 60Co IN THE RAT
Levitskaia, T., Creim, J., Curry, T. L., Luders, T., Morris, J. E., Sinkov, S., Woodstock, A., & Thrall, K. (2009) · Health Physics · doi:10.1097/01.hp.0000346798.82764.d7 · Cited by 7
“…internally deposited 60Co. Chitosan is non-toxic and its use in the medical and pharmaceutical fields is currently being investigated (Uragami and Tokura 2006; Muzzarelli and Muzzarelli 2005; Kumar et al. 2004), thus there is a potential for rapid distribution in the event of a nuclear emergency.”
BackgroundPhysical and chemical modification of biopolymers and biocomposites
Ganie, S. A., Ali, A., Mir, T., & Li, Q. (2021) · doi:10.1016/b978-0-12-819988-6.00016-1 · Cited by 7
Essawy, A., Hefni, H., & el-Nggar, A. (2019) · Sustainable Polymer Composites and Nanocomposites · doi:10.1007/978-3-030-05399-4_5 · Cited by 7
Functionalization of Polymer Materials for Medical Applications Using Chitosan Nanolayers
Zemljič, L. F., Bračič, M., Ristić, T., Šauperl, O., Strnad, S., & Peršin, Z. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813932-5.00009-1 · Cited by 8
A novel approach to 1,2,3-triazole grafted chitosans via modified Wolff’s cyclocondensation
Zhang, Z.-X., Wang, Z.-K., Mu, H.-L., Wang, X., Li, Y.-H., Yan, J.-L., & Wang, Z. (2018) · doi:10.1016/j.eurpolymj.2017.11.047 · Cited by 7
Investigating Swelling and Bending Response of pH-Sensitive Chitosan-Based Hydrogels
Mehr, J. A., & Hatami-Marbini, H. (2025) · Macromol · doi:10.3390/macromol5040057 · Cited by 6
“Its unique cationic nature enables the formation of interpenetrating networks with negatively charged polyanions, while its demonstrated biocompatibility and non-toxicity make it highly suitable for medical applications [20].”
Deng, H., Yu, W., Fan, Z., Xue, J.-F., Gu, Y., Tang, X., Zhou, X., & Yu, N. (2025) · Talanta: The International Journal of Pure and Applied Analytical Chemistry · doi:10.1016/j.talanta.2025.128883 · Cited by 6
(Minakov), Д. (. В. (. М., (Vereshchagin), А. (. Л. (. В., (Morozhenko), Ю. (. В. (. М., & (Bazarnova), Н. (. Г. (. Б. (2019) · chemistry of plant raw material · doi:10.14258/jcprm.2019014368 · Cited by 6
Scope of Electrospun Chitosan Nanofibrous Web for its Potential Application in Water Filtration
Gadkari, R., Ali, W., Das, A., & Alagirusamy, R. (2017) · doi:10.1002/9781119364849.ch16 · Cited by 6
Preparation of anticoagulant polyvinylidene fluoride hollow fiber hemodialysis membranes
Zhang, Q., Lu, X., Yang, S., Zhang, Q., & Zhao, L. (2016) · Biomedizinische Technik/Biomedical Engineering · doi:10.1515/bmt-2015-0149 · Cited by 6
“The positive facets of excellent biocompatibility and admirable biodegradability with ecological safety and low toxicity with versatile biological activities such as antimicrobial activity and low immunogenicity have provided ample opportunities for further development [8, 12, 13, 20, 21, 25].”
BackgroundSTRUCTURAL RESEARCH OF THERMOSENSITIVE CHITOSAN-COLLAGEN GELS CONTAINING ALP
Skwarczyńska, A., Biniaś, D., & Modrzejewska, Z. (2016) · doi:10.15259/pcacd.21.19 · Cited by 6
“These forms may be in the shape of hydrogels, dried forms (through lyophilization, by atomization method or in supercritical conditions), or matrixes woven from fibres created for instance by the method of electrospinning [6-11].”
MethodPolysaccharidic binders for the conception of an insulating agro-composite
Mati-Baouche, N., de Baynast, H., Sun, S., Lebert, A., Petit, E., & Michaud, P. (2015) · doi:10.1016/j.compositesa.2015.08.006 · Cited by 6
Timashev, P., Demina, T., Minaev, N., Bardakova, K. N., Koroleva, A., Kufelt, O., Chichkov, B., Panchenko, V., Akopova, T. A., & Bagratashvili, V. (2015) · High Energy Chemistry · doi:10.1134/s0018143915040177 · Cited by 6
Chitosan as an Advanced Healthcare Material
Jardine, M., & Sayed, S. (2014) · doi:10.1002/9781118774052.ch5 · Cited by 6
Bochek, A. M., Zabivalova, N. M., Lavrent'ev, V. K., Abalov, I. V., & Gofman, I. (2011) · doi:10.1134/s1070427211090199 · Cited by 6
Zhou, Z.-Y., Huang, H.-T., Xu, P.-H., Fan, L.-H., Yu, J.-H., & Huang, J. (2009) · doi:10.1002/app.29432 · Cited by 6
Surface Treatments of Titanium with Antibacterial Agents for Implant Applications
Milošev, I. (2016) · doi:10.1007/978-3-319-31849-3_1 · Cited by 6
Natural bioresorbable polymers
Paul, W., & Sharma, C. P. (2008) · doi:10.1533/9781845695033.2.67 · Cited by 6
Osiriphun, S., Jirarattanarangsri, W., & Laokuldilok, T. (2025) · Food Chemistry Advances · doi:10.1016/j.focha.2025.101178 · Cited by 5
Amjed, N., Bhatti, I., Simon, L., Hafiz, I., Akram, N., Zia, K., & Rasheed, T. (2024) · Materials Chemistry and Physics · doi:10.1016/j.matchemphys.2024.128982 · Cited by 5
Studies on Chitosan, Chitin and Chitooligosaccharides and Their Biomedical Properties
Ibram, A. (2021) · European Journal of Medicine and Natural Sciences · doi:10.26417/805xka61j · Cited by 5
Begum, E., Bhavani, K., Kumari, S., Devi, S., Gowripriya, C., & Shenbagarathai, R. (2018) · Journal of Polymers and the Environment · doi:10.1007/s10924-017-1020-7 · Cited by 5
Chitosan Composites: Preparation and Applications in Removing Water Pollutants
Ganjali, M., Rezapour, M., Faridbod, F., & Norouzi, P. (2017) · Handbook of Composites from Renewable Materials · doi:10.1002/9781119441632.ch124 · Cited by 5
Metadata
- Authors
- Muzzarelli, R. A. A., & Muzzarelli, C.
- Affiliations
- Marche Polytechnic University (IT)
- Venue
- Advances in Polymer Science
- Publisher
- Springer-Verlag
- Published
- 2005-11-16
- Pages
- 151-209
- OpenAlex
- W2486270894
- Cited by
- 555
- References
- 290
- Citations by year
- 2026: 5 · 2025: 17 · 2024: 22 · 2023: 22 · 2022: 18 · 2021: 28 · 2020: 33 · 2019: 39 · 2018: 26 · 2017: 39 · 2016: 45 · 2015: 33 · 2014: 35 · 2013: 42 · 2012: 38
- FWCI
- 53.63
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- Springer eBooks (publishedVersion)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Physical Sciences › Materials Science › Biomaterials › Nanocomposite Films for Food Packaging
- Physical Sciences › Materials Science › Biomaterials › Hydrogels: synthesis, properties, applications
- Keywords
- chitosan, chitin, drug delivery, drug carriers, biocompatibility, biodegradability, wound healing, coagulation, immunostimulation, chitin nanoparticles, nanofibrils, bandages, nutraceuticals, cosmetics
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