Issue

Vol. 34 No. 5 (2022): Vol 34 Issue 5, 2022

Copyright (c) 2022 AJC

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Cross-Linked Ionic Polysaccharides: Insights from the Structure to Stimuli-Sensitive Drug Delivery System Applications: A Mini Review

https://doi.org/10.14233/ajchem.2022.23722
Tuhin Ghosh
Department of Chemistry (UG & PG), Durgapur Government College, Durgapur-713214, India
Suman Mukherjee
Department of Zoology (UG & PG), Bidhannagar College, EB-2, Sector-1, Salt Lake City, Kolkata-700064, India

Corresponding Author(s) : Tuhin Ghosh

tuhinghoshbuchem@gmail.com

Asian Journal of Chemistry, Vol. 34 No. 5 (2022): Vol 34 Issue 5, 2022

Abstract

The review provides an insight regarding the state of the art of cross-linked ionic polysaccharides, which are a part of common drug delivery systems, which are involved in the regulation of release of drug in specific required sites. The changes in pH, ion concentration, wavelength, redox potential, temperature, electric and magnetic field intensity are the stimuli sensitive functions, which play a major roles. Due to their high reproducibility and better characterization from natural resources, the polysaccharides remains as a point of interest for compiling many stimuli-responsive drug delivery systems. The hydrogel networks are formed from ready cross-linking of ionic polysaccharides, subject to control of internal and external variables. These hydrogel networks become operative for drug release on-off through complex mechanisms. The polysaccharide-based drug delivery systems are now responsive to different hybrids, composites and grafted polymers with a broad range of stimuli functions.

Keywords

Ionic polysaccharides Ionic polysaccharides Chitosan Chitosan Carboxymethyl cellulose Carboxymethyl cellulose Heparin Heparin Stimuli sensitive Stimuli sensitive Drug delivery system Drug delivery system
Ghosh, T., & Mukherjee, S. (2022). Cross-Linked Ionic Polysaccharides: Insights from the Structure to Stimuli-Sensitive Drug Delivery System Applications: A Mini Review. Asian Journal of Chemistry, 34(5), 1066–1072. https://doi.org/10.14233/ajchem.2022.23722
Download Citation
Endnote/Zotero/Mendeley (RIS)
BibTeX
References
  1. W.B. Wang, J.X. Xu and A.Q. Wang, Express Polym. Lett., 5, 385 (2011); https://doi.org/10.3144/expresspolymlett.2011.38
  2. F. Maestrelli, M. Garcia-Fuentes, P. Mura and M.J. Alonso, Eur. J. Pharm. Biopharm., 63, 79 (2006); https://doi.org/10.1016/j.ejpb.2005.12.006
  3. C. Pinto Reis, R.J. Neufeld, A.J. Ribeiro and F. Veiga, Nanomedicine, 2, 8 (2006); https://doi.org/10.1016/j.nano.2005.12.003
  4. L. Illum, J. Pharm. Sci., 96, 473 (2007); https://doi.org/10.1002/jps.20718
  5. A. Rubinstein, Drug Dev. Res., 50, 435 (2000); https://doi.org/10.1002/1098-2299(200007/08)50:3/4<435::AID-DDR26>3.0.CO;2-5
  6. J.W. Lee, J.H. Park and J.R. Robinson, J. Pharm. Sci., 89, 850 (2000); https://doi.org/10.1002/1520-6017(200007)89:7<850::AID-JPS2>3.0.CO;2-G
  7. V.R. Sinha and R. Kumria, Int. J. Pharm., 224, 19 (2001); https://doi.org/10.1016/S0378-5173(01)00720 7
  8. Y.K. Lee and D.J. Mooney, Prog. Polym. Sci., 37, 106 (2012); https://doi.org/10.1016/j.progpolymsci.2011.06.003
  9. D.R. Sahoo and T. Biswal, SN Appl. Sci., 3, 30 (2021); https://doi.org/10.1007/s42452-020-04096-w
  10. Y. Freile-Pelegrín and E. Murano, Bioresour. Technol., 96, 295 (2005); https://doi.org/10.1016/j.biortech.2004.04.010
  11. H. Sjöberg, S. Persson and N. Caram-Lelham, J. Control. Release, 59, 391 (1999); https://doi.org/10.1016/S0168-3659(99)00013-9
  12. J. Liu, S. Lin, L. Li and E. Liu, Int. J. Pharm., 298, 117 (2005); https://doi.org/10.1016/j.ijpharm.2005.04.006
  13. E. Amici, A.H. Clark, V. Normand and N.B. Johnson, Biomacromolecules, 3, 466 (2002); https://doi.org/10.1021/bm010157z
  14. W.J. Frith, Adv. Colloid Interf., 161, 48 (2010); https://doi.org/10.1016/j.cis.2009.08.001
  15. N. Yamaguchi, L. Zhang, B.-S. Chae, C.S. Palla, E.M. Furst and K.L. Kiick, J. Am. Chem. Soc., 129, 3040 (2007); https://doi.org/10.1021/ja0680358
  16. S.H. Kim and K.L. Kiick, Macromol. Rapid Commun., 31, 1231 (2010); https://doi.org/10.1002/marc.201000130
  17. P. Calvo, C. Remunan-Lopez, J.L. Vila-Jato and M.J. Alonso, J. Appl. Polym. Sci., 63, 125 (1997); https://doi.org/10.1002/(SICI)1097-4628(19970103)63:1<125::AID-APP13>3.0.CO;2-4
  18. P. Calvo, C. Remuñan-López, J.L. Vila-Jato and M.J. Alonso, Pharm. Res., 14, 1431 (1997); https://doi.org/10.1023/A:1012128907225
  19. D. Jain and R. Banerjee, J. Biomed. Mater. Res., 86B, 105 (2008); https://doi.org/10.1002/jbm.b.30994
  20. M. Amidi, S.G. Romeijn, G. Borchard, H.E. Junginger, W.E. Hennink and W. Jiskoot, J. Control. Release, 111, 107 (2006); https://doi.org/10.1016/j.jconrel.2005.11.014
  21. Z.R. Cui, R.J. Mumper, J. Control. Release, 75, 409 (2001). https://doi.org/10.1016/S0168 3659(01)00407-2
  22. Y. Chen, V.J. Mohanraj and J.E. Parkin, Lett. Pept. Sci., 10, 621 (2003); https://doi.org/10.1007/s10989 004-2433-4
  23. B. Sarmento, D. Ferreira, F. Veiga and A. Ribeiro, Carbohydr. Polym., 66, 1 (2006); https://doi.org/10.1016/j.carbpol.2006.02.008
  24. B. Sarmento, D.C. Ferreira, L. Jorgensen and M. van de Weert, Eur. J. Pharm. Biopharm., 65, 10 (2007); https://doi.org/10.1016/j.ejpb.2006.09.005
  25. T. Li, X.W. Shi, Y.M. Du and Y.F. Tang, J. Biomed. Mater. Res., 83A, 383 (2007); https://doi.org/10.1002/jbm.a.31322
  26. I.T. Norton, D.M. Goodall, S.A. Frangou, E.R. Morris and D.A. Rees, J. Mol. Biol., 175, 371 (1984); https://doi.org/10.1016/0022-2836(84)90354-1
  27. E.R. Morris, K. Nishinari and M. Rinaudo, Food Hydrocoll., 28, 373 (2012); https://doi.org/10.1016/j.foodhyd.2012.01.004
  28. E. Favre and S. Girard, Eur. Polym. J., 37, 1527 (2001); https://doi.org/10.1016/S0014-3057(01)00024-6
  29. S. Gorgieva and V. Kokol, Carbohydr. Polym., 85, 664 (2011); https://doi.org/10.1016/j.carbpol.2011.03.037
  30. C. Chang, B. Duan, J. Cai and L. Zhang, Eur. Polym. J., 46, 92 (2010); https://doi.org/10.1016/j.eurpolymj.2009.04.033
  31. M. Hamcerencu, J. Desbrieres, M. Popa and G. Riess, Carbohydr. Polym., 89, 438 (2012); https://doi.org/10.1016/j.carbpol.2012.03.026
  32. C. Alvarez-Lorenzo, A. Concheiro, A.S. Dubovik, N.V. Grinberg, T.V. Burova and V.Y. Grinberg, J. Control. Release, 102, 629 (2005); https://doi.org/10.1016/j.jconrel.2004.10.021
  33. S. Ekici, J. Mater. Sci., 46, 2843 (2011); https://doi.org/10.1007/s10853-010-5158-0
  34. M. Hamcerencu, M. Popa, J. Desbrieres and G. Riess, Macromol. Symp., 297, 114 (2010); https://doi.org/10.1002/masy.200900100
  35. R.C. Mundargi, N.B. Shelke, V.R. Babu, P. Patel, V. Rangaswamy and T.M. Aminabhavi, J. Appl. Polym. Sci., 116, 1832 (2010); https://doi.org/10.1002/app.31551
  36. M. Hamcerencu, J. Desbrieres, A. Khoukh, M. Popa and G. Riess, Polym. Int., 60, 1527 (2011); https://doi.org/10.1002/pi.3113
  37. A.C. Lima, W. Song, B. Blanco-Fernandez, C. Alvarez-Lorenzo and J.F. Mano, Pharm. Res., 28, 1294 (2011); https://doi.org/10.1007/s11095-011-0380-2
  38. H.K. Ju, S.Y. Kim and Y.M. Lee, Polymer, 42, 6851 (2001); https://doi.org/10.1016/S0032 3861(01)00143-4
  39. H.K. Ju, S.Y. Kim, S.J. Kim and Y.M. Lee, J. Appl. Polym. Sci., 83, 1128 (2002); https://doi.org/10.1002/app.10137
  40. M.R. de Moura, F. Ahmad Aouada, S.L. Favaro, E. Radovanovic, A. Forti Rubira and E.C. Muniz, Mater. Sci. Eng. C, 29, 2319 (2009); https://doi.org/10.1016/j.msec.2009.05.022
  41. J. Shi, N.M. Alves and J.F. Mano, J. Biomed. Mater. Res. B Appl. Biomater., 84, 595 (2007); https://doi.org/10.1002/jbm.b.30907
  42. J. Shi, L. Liu, X. Sun, S. Cao and J.F. Mano, Macromol. Biosci., 8, 260 (2008); https://doi.org/10.1002/mabi.200700177
  43. C. Ding, L. Zhao, F. Liu, J. Cheng, J. Gu, S. Dan, C. Liu, X. Qu and Z. Yang, Biomacromolecules, 11, 1043 (2010); https://doi.org/10.1021/bm1000179
  44. L. Zhao, L. Zhu, F. Liu, C. Liu, Q. Shan-Dan, Q. Wang, C. Zhang, J. Li, J. Liu, X. Qu and Z. Yang, Int. J. Pharm., 410, 83 (2011); https://doi.org/10.1016/j.ijpharm.2011.03.034
  45. L.A. Wells, M.A. Brook and H. Sheardown, Macromol. Biosci., 11, 988 (2011); https://doi.org/10.1002/mabi.201100001
  46. L.A. Wells and H. Sheardown, Eur. J. Pharm. Biopharm., 79, 304 (2011); https://doi.org/10.1016/j.ejpb.2011.03.023
  47. P.V. Kulkarni, J. Keshavayya and V.H. Kulkarni, Polym. Adv. Technol., 18, 814 (2007); https://doi.org/10.1002/pat.940
  48. R. Barreiro-Iglesias, R. Coronilla, A. Concheiro and C. Alvarez-Lorenzo, Eur. J. Pharm. Sci., 24, 77 (2005); https://doi.org/10.1016/j.ejps.2004.09.013
  49. X.Z. Shu and K.J. Zhu, Eur. J. Pharm. Biopharm., 54, 235 (2002); https://doi.org/10.1016/S0939-6411(02)00052-8
  50. A.V. Nand, D.R. Rohindra, J.R. Khurma, e-Polymers, 7, 33 (2007); https://doi.org/10.1515/epoly.2007.7.1.402
  51. Q. Wang, Z. Dong, Y. Du and J.F. Kennedy, Carbohydr. Polym., 69, 336 (2007); https://doi.org/10.1016/j.carbpol.2006.10.014
  52. L. Chen, Z. Tian and Y. Du, Biomaterial s, 25, 3725 (2004); https://doi.org/10.1016/j.biomaterials.2003.09.100
  53. O.S. Lawal, M. Yoshimura, R. Fukae and K. Nishinari, Colloid Polym. Sci., 289, 1261 (2011); https://doi.org/10.1007/s00396-011-2458-0
  54. A. Kikuchi, M. Kawabuchi, M. Sugihara, Y. Sakurai and T. Okano, J. Control. Release, 47, 21 (1997); https://doi.org/10.1016/S0168-3659(96)01612-4
  55. S.N. Pawar and K.J. Edgar, Biomaterials, 33, 3279 (2012); https://doi.org/10.1016/j.biomaterials.2012.01.007
  56. A. Kikuchi and T. Okano, Adv. Drug Deliv. Rev., 54, 53 (2002); https://doi.org/10.1016/S0169-409X(01)00243-5
  57. T.M. Aminabhavi, S.A. Agnihotri and B.V.K. Naidu, J. Appl. Polym. Sci., 94, 2057 (2004); https://doi.org/10.1002/app.21139
  58. J.P. Preetha, K. Karthika, N.R. Rekha and K. Elshafie, J. Chem. Pharm. Res., 2, 528 (2010).
  59. Y. Nobuhiko, O. Teruo and S. Yasuhisa, J. Control. Release, 22, 105 (1992); https://doi.org/10.1016/0168-3659(92)90195-W
  60. S.H. Yu, S.J. Wu, D.W. Tang, Y.C. Ho, F.L. Mi, T.H. Kuo and H.M. Sung, Carbohydr. Polym., 87, 531 (2012); https://doi.org/10.1016/j.carbpol.2011.08.015
  61. L. Gao, J. Fei, J. Zhao, W. Cui, Y. Cui and J. Li, Chem. Eur. J., 18, 3185 (2012); https://doi.org/10.1002/chem.201103584
  62. H. Zheng, Y. Rao, Y. Yin, X. Xiong, P. Xu and B. Lu, Carbohydr. Polym., 83, 1952 (2011); https://doi.org/10.1016/j.carbpol.2010.10.069
Read More
Author biographies is not available.
Download
PDF
Statistic
Read Counter : 0 Download : 0