All Issue

2025 Vol.57, Issue 6 Preview Page

Review

30 December 2025. pp. 25-40
Abstract
References
1

Teleanu, D. M., Niculescu, A. G., Lungu, II, Radu, C. I., Vladacenco, O., Roza, E., Costachescu, B., Grumezescu, A. M., & Teleanu, R. I. (2022). An overview of oxidative stress, neuroinflammation, and neurodegenerative diseases. International Journal of Molecular Sciences, 23(11), 5938.

10.3390/ijms2311593835682615PMC9180653
2

Plascencia-Villa, G., & Perry, G. (2023). Roles of oxidative stress in synaptic dysfunction and neuronal cell death in Alzheimer’s disease. Antioxidants, 12(8), 1628.

10.3390/antiox1208162837627623PMC10451948
3

Toader, C., Tataru, C. P., Munteanu, O., Serban, M., Covache-Busuioc, R. A., Ciurea, A. V., & Enyedi, M. (2024). Decoding neurodegeneration: A review of molecular mechanisms and therapeutic advances in Alzheimer’s, Parkinson’s, and ALS. International Journal of Molecular Sciences, 25(23), 12613.

10.3390/ijms25231261339684324PMC11641752
4

Rust, R., Yin, H., Achon Buil, B., Sagare, A. P., & Kisler, K. (2025). The blood–brain barrier: A help and a hindrance. Brain, 148(7), 2262-2282.

10.1093/brain/awaf06839969549PMC12233556
5

Noori, A., Arango, I., Byrd, W. E., & Amin, N. (2024). Multi-objective generative AI for designing novel brain-targeting small molecules. arXiv preprint arXiv:2407.00004.

6

Qiao, L., Du, X., Wang, H., Wang, Z., Gao, S., & Zhao, C. Q. (2024). Research progress on the strategies for crossing the blood–brain barrier. Molecular Pharmaceutics, 21(10), 4786-4803.

10.1021/acs.molpharmaceut.4c00447
7

Sharma, S., & Dang, S. (2023). Nanocarrier-based drug delivery to brain: Interventions of surface modification. Current Neuropharmacology, 21(3), 517-535.

10.2174/1570159X2066622070612141235794771PMC10207924
8

Ali, T., Klein, A. N., McDonald, K., Johansson, L., Mukherjee, P. G., Hallbeck, M., Doh-Ura, K., Schatzl, H. M., & Gilch, S. (2023). Cellulose ether treatment inhibits amyloid beta aggregation, neuroinflammation and cognitive deficits in transgenic mouse model of Alzheimer’s disease. Journal of Neuroinflammation, 20(1), 177.

10.1186/s12974-023-02858-y37507761PMC10375631
9

Nishiyama, Y., Langan, P., & Chanzy, H. (2002). Crystal structure and hydrogen-bonding system in cellulose Iβ from synchrotron X-ray and neutron fiber diffraction. Journal of the American Chemical Society, 124(31), 9074-9082.

10.1021/ja0257319
10

Tanaka, Y., Li, Q., Hatakeyama, M., & Kitaoka, T. (2024). Synthesis and structural design of microspheres comprising cellulose nanofibers and artificial lignin polymer by enzyme-mediated Pickering emulsion templating. RSC Sustainability, 2(5), 1580-1589.

10.1039/D4SU00067F
11

Won, T., Goh, M., Lim, C., Moon, J., Lee, K., Park, J., Chung, K., Kim, Y., Lee, S., Hong, H., & Gwon, K. (2025). Recent progress in cellulose nanofibril hydrogels for biomedical applications. Polymers, 17(17), 2272.

10.3390/polym1717227240942190PMC12430530
12

Bhandari, J., Mishra, H., Mishra, P. K., Wimmer, R., Ahmad, F. J., & Talegaonkar, S. (2017). Cellulose nanofiber aerogel as a promising biomaterial for customized oral drug delivery. International Journal of Nanomedicine, 12, 2021-2031.

10.2147/IJN.S12431828352172PMC5359002
13

Nordenström, M. (2020). Colloidal interactions and arrested dynamics of cellulose nanofibrils (Publication Number 2020:52) [Doctoral thesis, comprehensive summary, KTH Royal Institute of Technology]. DiVA. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-284491

14

Tamo, A. K. (2024). Nanocellulose-based hydrogels as versatile materials with interesting functional properties for tissue engineering applications. Journal of Materials Chemistry B, 12(32), 7692-7759.

10.1039/D4TB00397G
15

Malandain, N., Sanz-Fraile, H., Farre, R., Otero, J., Roig, A., & Laromaine, A. (2023). Cell-laden 3D hydrogels of type I collagen incorporating bacterial nanocellulose fibers. ACS Applied Bio Materials, 6(9), 3638-3647.

10.1021/acsabm.3c0012637669535PMC10521014
16

Bacha, E. G., Demsash, H. D., Shumi, L. D., & Debesa, B. E. (2022). Investigation on reinforcement effects of nanocellulose on the mechanical properties, water absorption capacity, biodegradability, optical properties, and thermal stability of a polyvinyl alcohol nanocomposite film. Advances in Polymer Technology, 2022, 6947591.

10.1155/2022/6947591
17

Kang, J., & Yun, S. I. (2022). Double-network hydrogel films based on cellulose derivatives and κ-carrageenan with enhanced mechanical strength and superabsorbent properties. Gels, 9(1), 20.

10.3390/gels901002036661788PMC9858413
18

Pajorova, J., Skogberg, A., Hadraba, D., Broz, A., Travnickova, M., Zikmundova, M., Honkanen, M., Hannula, M., Lahtinen, P., Tomkova, M., Bacakova, L., & Kallio, P. (2020). Cellulose mesh with charged nanocellulose coatings as a promising carrier of skin and stem cells for regenerative applications. Biomacromolecules, 21(12), 4857-4870.

10.1021/acs.biomac.0c01097
19

Huo, Y., Liu, Y., Xia, M., Du, H., Lin, Z., Li, B., & Liu, H. (2022). Nanocellulose-based composite materials used in drug delivery systems. Polymers, 14(13), 2648.

10.3390/polym1413264835808693PMC9268916
20

Saito, T., & Isogai, A. (2004). TEMPO-mediated oxidation of native cellulose. The effect of oxidation conditions on chemical and crystal structures of the water-insoluble fractions. Biomacromolecules, 5(5), 1983-1989.

10.1021/bm0497769
21

De France, K. J., Hoare, T., & Cranston, E. D. (2017). Review of hydrogels and aerogels containing nanocellulose. Chemistry of Materials, 29(11), 4609-4631.

10.1021/acs.chemmater.7b00531
22

Lungare, S., Bowen, J., & Badhan, R. (2016). Development and evaluation of a novel intranasal spray for the delivery of amantadine. Journal of Pharmaceutical Sciences, 105(3), 1209-1220.

10.1016/j.xphs.2015.12.016
23

Koo, J., Lim, C., & Oh, K. T. (2024). Recent advances in intranasal administration for brain-targeting delivery: A comprehensive review of lipid-based nanoparticles and stimuli-responsive gel formulations. International Journal of Nanomedicine, 19, 1767-1807.

10.2147/IJN.S43918138414526PMC10898487
24

Tuladhar, A., Obermeyer, J. M., Payne, S. L., Siu, R. C. W., Zand, S., Morshead, C. M., & Shoichet, M. S. (2020). Injectable hydrogel enables local and sustained co-delivery to the brain: Two clinically approved biomolecules, cyclosporine and erythropoietin, accelerate functional recovery in rat model of stroke. Biomaterials, 235, 119794.

10.1016/j.biomaterials.2020.119794
25

Hong, L. T. A., Kim, Y. M., Park, H. H., Hwang, D. H., Cui, Y., Lee, E. M., Yahn, S., Lee, J. K., Song, S. C., & Kim, B. G. (2017). An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling. Nature Communications, 8(1), 533.

10.1038/s41467-017-00583-828912446PMC5599609
26

Bittleman, K. R., Dong, S., Roman, M., & Lee, Y. W. (2018). Folic acid-conjugated cellulose nanocrystals show high folate-receptor binding affinity and uptake by KB and breast cancer cells. ACS Omega, 3(10), 13952-13959.

10.1021/acsomega.8b0161930411055PMC6217680
27

Fam, S. Y., Chee, C. F., Yong, C. Y., Ho, K. L., Mariatulqabtiah, A. R., & Tan, W. S. (2020). Stealth coating of nanoparticles in drug-delivery systems. Nanomaterials, 10(4), 787.

10.3390/nano1004078732325941PMC7221919
28

Zhang, Y., Chen, H., Li, R., Sterling, K., & Song, W. (2023). Amyloid beta-based therapy for Alzheimer’s disease: Challenges, successes and future. Signal Transduction and Targeted Therapy, 8(1), 248.

10.1038/s41392-023-01484-737386015PMC10310781
29

Aguilera, G., Berry, C. C., West, R. M., Gonzalez-Monterrubio, E., Angulo-Molina, A., Arias-Carrion, O., & Mendez-Rojas, M. A. (2019). Carboxymethyl cellulose coated magnetic nanoparticles transport across a human lung microvascular endothelial cell model of the blood-brain barrier. Nanoscale Advances, 1(2), 671-685.

10.1039/C8NA00010G
30

Bi, C., Wang, A., Chu, Y., Liu, S., Mu, H., Liu, W., Wu, Z., Sun, K., & Li, Y. (2016). Intranasal delivery of rotigotine to the brain with lactoferrin-modified PEG-PLGA nanoparticles for Parkinson’s disease treatment. International Journal of Nanomedicine, 11, 6547-6559.

10.2147/IJN.S12093927994458PMC5153272
31

Zuccato, C., Valenza, M., & Cattaneo, E. (2010). Molecular mechanisms and potential therapeutical targets in Huntington’s disease. Physiological Reviews, 90(3), 905-981.

10.1152/physrev.00041.2009
32

Tong, H., Yang, T., Xu, S., Li, X., Liu, L., Zhou, G., Yang, S., Yin, S., Li, X. J., & Li, S. (2024). Huntington’s disease: Complex pathogenesis and therapeutic strategies. International Journal of Molecular Sciences, 25(7), 3845.

10.3390/ijms2507384538612657PMC11011923
33

Sarkar, S., Davies, J. E., Huang, Z., Tunnacliffe, A., & Rubinsztein, D. C. (2007). Trehalose, a novel mTOR-independent autophagy enhancer, accelerates the clearance of mutant huntingtin and alpha-synuclein. Journal of Biological Chemistry, 282(8), 5641-5652.

10.1074/jbc.M609532200
34

Im, J., Kim, S., Jeong, Y. H., Kim, W., Lee, D., Lee, W. S., Chang, Y. T., Kim, K. T., & Chung, S. K. (2013). Preparation and evaluation of BBB-permeable trehalose derivatives as potential therapeutic agents for Huntington’s disease. MedChemComm, 4(2), 310-316.

10.1039/C2MD20112G
35

Debnath, K., Pradhan, N., Singh, B. K., Jana, N. R., & Jana, N. R. (2017). Poly(trehalose) nanoparticles prevent amyloid aggregation and suppress polyglutamine aggregation in a Huntington’s disease model mouse. ACS Applied Materials & Interface, 9(28), 24126-24139.

10.1021/acsami.7b06510
36

Mendonca, M. C. P., Kont, A., Aburto, M. R., Cryan, J. F., & O’Driscoll, C. M. (2021). Advances in the design of (nano)formulations for delivery of antisense oligonucleotides and small interfering RNA: Focus on the central nervous system. Molecular Pharmaceutics, 18(4), 1491-1506.

10.1021/acs.molpharmaceut.0c0123833734715PMC8824433
37

Lopez-Pingarron, L., Almeida, H., Soria-Aznar, M., Reyes-Gonzales, M. C., Terron, M. P., & Garcia, J. J. (2023). Role of oxidative stress on the etiology and pathophysiology of amyotrophic lateral sclerosis (ALS) and its relation with the enteric nervous system. Current Issues in Molecular Biology, 45(4), 3315-3332.

10.3390/cimb4504021737185741PMC10136958
38

Zhang, W., Xiao, D., Mao, Q., & Xia, H. (2023). Role of neuroinflammation in neurodegeneration development. Signal Transduction and Targeted Therapy, 8(1), 267.

10.1038/s41392-023-01486-537433768PMC10336149
39

Gao, Z., Qiu, R., Dave, D. R., Chandravanshi, P., Soares, G. P., Smith, C. S., Ortega, J. A., Palmer, L. C., Alvarez, Z., & Stupp, S. I. (2025). Supramolecular copolymerization of glycopeptide amphiphiles and amyloid peptides improves neuron survival. Journal of the American Chemical Society, 147(21), 17710-17724.

10.1021/jacs.5c00105
40

Cheng, K. C., Huang, C. F., Wei, Y., & Hsu, S. H. (2019). Novel chitosan-cellulose nanofiber self-healing hydrogels to correlate self-healing properties of hydrogels with neural regeneration effects. NPG Asia Materials, 11, 25.

10.1038/s41427-019-0124-z
41

Wu, D., Chen, Q., Chen, X., Han, F., Chen, Z., & Wang, Y. (2023). The blood-brain barrier: Structure, regulation, and drug delivery. Signal Transduction and Targeted Therapy, 8(1), 217.

10.1038/s41392-023-01481-w37231000PMC10212980
42

Juhairiyah, F., & de Lange, E. C. M. (2021). Understanding drug delivery to the brain using liposome-based strategies: Studies that provide mechanistic insights are essential. The AAPS Journal, 23(6), 114.

10.1208/s12248-021-00648-z34713363PMC8553706
43

Cavaletti, G., Cassetti, A., Canta, A., Galbiati, S., Gilardini, A., Oggioni, N., Rodriguez-Menendez, V., Fasano, A., Liuzzi, G. M., Fattler, U., Ries, S., Nieland, J., Riccio, P., & Haas, H. (2009). Cationic liposomes target sites of acute neuroinflammation in experimental autoimmune encephalomyelitis. Molecular Pharmaceutics, 6(5), 1363-1370.

10.1021/mp8001478
44

Shen, S., Wu, Y., Liu, Y., & Wu, D. (2017). High drug-loading nanomedicines: Progress, current status, and prospects. International Journal of Nanomedicine, 12, 4085-4109.

10.2147/IJN.S13278028615938PMC5459982
45

Lee, M. K. (2020). Liposomes for enhanced bioavailability of water-insoluble drugs: In vivo evidence and recent approaches. Pharmaceutics, 12(3), 264.

10.3390/pharmaceutics1203026432183185PMC7151102
46

Pawlik, M., Laskowski, J. S., & Ansari, A. (2003). Effect of carboxymethyl cellulose and ionic strength on stability of mineral suspensions in potash ore flotation systems. Journal of Colloid and Interface Science, 260(2), 251-258.

10.1016/S0021-9797(02)00225-4
47

Curtis, C., Toghani, D., Wong, B., & Nance, E. (2018). Colloidal stability as a determinant of nanoparticle behavior in the brain. Colloids and Surfaces B: Biointerfaces, 170, 673-682.

10.1016/j.colsurfb.2018.06.05029986264PMC6664798
48

Nowak, M., Brown, T. D., Graham, A., Helgeson, M. E., & Mitragotri, S. (2020). Size, shape, and flexibility influence nanoparticle transport across brain endothelium under flow. Bioengineering & Translational Medicine, 5(2), e10153.

10.1002/btm2.1015332440560PMC7237148
49

Li, H., Dai, W. N., Xiao, L., Sun, L., & He, L. Y. (2023). Biopolymer-based nanosystems: Potential novel carriers for kidney drug delivery. Pharmaceutics, 15(8), 2150.

10.3390/pharmaceutics1508215037631364PMC10459991
50

Vital, N., Ventura, C., Kranendonk, M., Silva, M. J., & Louro, H. (2022). Toxicological assessment of cellulose nanomaterials: Oral exposure. Nanomaterials, 12(19), 3375.

10.3390/nano1219337536234501PMC9565252
51

Sanchez-Salvador, J. L., Xu, H. Y., Balea, A., Negro, C., & Blanco, A. (2023). Nanocellulose from a colloidal material perspective. Frontiers in Materials, 10, 1231404.

10.3389/fmats.2023.1231404
52

Foote, C. A., Soares, R. N., Ramirez-Perez, F. I., Ghiarone, T., Aroor, A., Manrique-Acevedo, C., Padilla, J., & Martinez-Lemus, L. (2022). Endothelial glycocalyx. Comprehensive Physiology, 12(4), 3781-3811.

10.1002/cphy.c21002935997082PMC10214841
53

Kholousi Adab, F., Mehdi Yaghoobi, M., & Gharechahi, J. (2024). Enhanced crystalline cellulose degradation by a novel metagenome-derived cellulase enzyme. Scientific Reports, 14(1), 8560.

10.1038/s41598-024-59256-438609443PMC11014956
54

Erdal, N. B., & Hakkarainen, M. (2022). Degradation of cellulose derivatives in laboratory, man-made, and natural environments. Biomacromolecules, 23(7), 2713-2729.

10.1021/acs.biomac.2c0033635763720PMC9277587
55

Sola, R. J., & Griebenow, K. (2009). Effects of glycosylation on the stability of protein pharmaceuticals. Journal of Pharmaceutical Sciences, 98(4), 1223-1245.

10.1002/jps.2150418661536PMC2649977
56

Miller, D. S., Bauer, B., & Hartz, A. M. (2008). Modulation of P-glycoprotein at the blood-brain barrier: Opportunities to improve central nervous system pharmacotherapy. Pharmacological Reviews, 60(2), 196-209.

10.1124/pr.107.0710918560012PMC2634288
57

Malmo, J., Sandvig, A., Varum, K. M., & Strand, S. P. (2013). Nanoparticle mediated P-glycoprotein silencing for improved drug delivery across the blood-brain barrier: A siRNA-chitosan approach. PLoS One, 8(1), e54182.

10.1371/journal.pone.005418223372682PMC3553124
58

Zhang, K., Geissler, A., Chen, X., Rosenfeldt, S., Yang, Y., Forster, S., & Muller-Plathe, F. (2015). Polymeric flower-like microparticles from self-assembled cellulose stearoyl esters. ACS Macro Letters, 4(2), 214-219.

10.1021/mz500788e
59

Song, Y., Zhang, L., Gan, W., Zhou, J., & Zhang, L. (2011). Self-assembled micelles based on hydrophobically modified quaternized cellulose for drug delivery. Colloids and Surfaces B: Biointerfaces, 83(2), 313-320.

10.1016/j.colsurfb.2010.11.039
60

Zuppolini, S., Maya, I. C., Diodato, L., Guarino, V., Borriello, A., & Ambrosio, L. (2020). Self-associating cellulose-graft-poly(epsilon-caprolactone) to design nanoparticles for drug release. Materials Science and Engineering: C, 108, 110385.

10.1016/j.msec.2019.110385
61

Guo, Y., Wang, X., Shen, Z., Shu, X., & Sun, R. (2013). Preparation of cellulose-graft-poly(varepsilon-caprolactone) nanomicelles by homogeneous ROP in ionic liquid. Carbohydrate Polymers, 92(1), 77-83.

10.1016/j.carbpol.2012.09.058
62

Zhang, F., Islam, M. S., Berry, R. M., & Tam, K. C. (2019). β-Cyclodextrin-functionalized cellulose nanocrystals and their interactions with surfactants. ACS Omega, 4(1), 2102-2110.

10.1021/acsomega.8b0253431459458PMC6648498
63

Liu, T., Chen, Y. Y., Wang, Y. Q., Wang, X. P., & Zheng, J. K. (2025). β-Cyclodextrin/cationic-cellulose/naringenin complex-stabilized Pickering lemon emulsions with enhanced bioavailability. Food Hydrocolloids, 166, 111294.

10.1016/j.foodhyd.2025.111294
Information
  • Publisher :Korea Technical Association of The Pulp and Paper Industry
  • Publisher(Ko) :한국펄프종이공학회
  • Journal Title :Journal of Korea TAPPI
  • Journal Title(Ko) :펄프종이기술
  • Volume : 57
  • No :6
  • Pages :25-40
  • Received Date : 2025-12-01
  • Revised Date : 2025-12-04
  • Accepted Date : 2025-12-05