journal article·2014-08-13Open access

Formation of Liquid-Crystalline Structures in the Bile Salt–Chitosan System and Triggered Release from Lamellar Phase Bile Salt–Chitosan Capsules

Kristian J. Tangso, Seth Lindberg, Patrick G. Hartley, Robert Knott, Patrick Spicer, Ben J. Boyd

Abstract

Nanostructured capsules comprised of the anionic bile salt, sodium taurodeoxycholate (STDC), and the biocompatible cationic polymer, chitosan, were prepared to assess their potential as novel tailored release nanomaterials. For comparison, a previously studied system, sodium dodecyl sulfate (SDS), and polydiallyldimethylammonium chloride (polyDADMAC) was also investigated. Crossed-polarizing light microscopy (CPLM) and small-angle X-ray scattering (SAXS) identified the presence of lamellar and hexagonal phase at the surfactant-polymer interface of the respective systems. The hydrophobic and electrostatic interactions between the oppositely charged components were studied by varying temperature and salt concentration, respectively, and were found to influence the liquid-crystalline nanostructure formed. The hexagonal phase persisted at high temperatures, however the lamellar phase structure was lost above ca. 45 °C. Both mesophases were found to dissociate upon addition of 4% NaCl solution. The rate of release of the model hydrophilic drug, Rhodamine B (RhB), from the lamellar phase significantly increased in response to changes in the solution conditions studied, suggesting that modulating the drug release from these bile salt-chitosan capsules is readily achieved. In contrast, release from the hexagonal phase capsules had no appreciable response to the stimuli applied. These findings provide a platform for these oppositely charged surfactant and polymer systems to function as stimuli-responsive or sustained-release drug delivery systems.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Surfactants and Colloidal Systems · Proteins in Food Systems · Food Chemistry and Fat Analysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Drug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University (Parkville Campus), 381 Royal Parade, Parkville, Victoria 3052, Australia

The Procter and Gamble Company, Corporate Engineering Technical Laboratories Building, Cincinnati, Ohio 45069, United States

Commonwealth Scientific and Industrial Research Organization, Bag 10, Clayton South, VIC 3169, Australia

Bragg Institute, Australian Nuclear Science and Technology Organization, Menai, NSW 2234, Australia

School of Chemical Engineering, University of New South Wales, Sydney, NSW 2052, Australia

References (61)

Show source-provided references
1. Goddard E. · J. Am. Oil Chem. Soc. · 1977 · 54 · 56110.1007/BF03027636 ↗
2. Goddard E. D. · J. Colloid Interface Sci. · 1976 · 55 · 7310.1016/0021-9797(76)90010-2 ↗
3. Wang Y. · Phys. Chem. Chem. Phys. · 2011 · 13 · 478210.1039/c0cp02287j ↗
4. Johnston A. P. R. · Curr. Opin. Colloid Interface Sci. · 2006 · 11 · 20310.1016/j.cocis.2006.05.001 ↗
5. Hössel · Int. J. Cosmet. Sci. · 2000 · 22 · 110.1046/j.1467-2494.2000.00003.x ↗
6. Morán M. C. · Biomacromolecules · 2007 · 8 · 388610.1021/bm700850z ↗
7. Hsu W.-L. · Langmuir · 2006 · 22 · 752110.1021/la060862z ↗
8. Rosa M. · Colloids Surf., A · 2007 · 301 · 36110.1016/j.colsurfa.2006.12.082 ↗
9. Fong W.-K. · J. Controlled Release · 2009 · 135 · 21810.1016/j.jconrel.2009.01.009 ↗
10. Phan S. · Int. J. Pharm. · 2011 · 421 · 17610.1016/j.ijpharm.2011.09.022 ↗
11. Lee K. W. Y. · Int. J. Pharm. · 2009 · 365 · 19010.1016/j.ijpharm.2008.08.022 ↗
12. Harada A. · Polymer Bull. · 1984 · 11 · 17510.1007/BF00258026 ↗
13. Nizri G. · Langmuir · 2004 · 20 · 438010.1021/la0364441 ↗
14. Yeh F. · J. Am. Chem. Soc. · 1996 · 118 · 661510.1021/ja960298m ↗
15. Svensson A. · J. Phys. Chem. B · 2006 · 110 · 1033210.1021/jp057402j ↗
16. Thalberg K. · J. Phys. Chem. · 1991 · 95 · 337010.1021/j100161a073 ↗
17. Chu B. · Macromolecules · 1995 · 28 · 844710.1021/ma00128a071 ↗
18. Chronakis I. S. · Macromolecules · 2001 · 34 · 500510.1021/ma000609k ↗
19. Zhou S. · Langmuir · 2004 · 20 · 848210.1021/la049142n ↗
20. Zhou S. · Macromolecules · 1998 · 31 · 815710.1021/ma9810058 ↗
21. Kogej K. · Langmuir · 2002 · 18 · 879910.1021/la025998l ↗
22. Starodubtsev S. G. · Langmuir · 2004 · 20 · 659910.1021/la049541i ↗
23. Loyen K. · Langmuir · 1995 · 11 · 105310.1021/la00004a002 ↗
24. Thongngam M. · Langmuir · 2004 · 21 · 7910.1021/la048711o ↗
25. Sokolov E. · J. Phys. Chem. B · 1998 · 102 · 709110.1021/jp9809686 ↗
26. Merta J. · Macromolecules · 2001 · 34 · 293710.1021/ma001793c ↗
27. Janiak J. · Langmuir · 2012 · 28 · 1653610.1021/la303938k ↗
28. Alatorre-Meda M. · Colloids Surf., A · 2009 · 339 · 14510.1016/j.colsurfa.2009.02.014 ↗
29. Bronich T. K. · Colloids Surf., B · 1999 · 16 · 24310.1016/S0927-7765(99)00075-2 ↗
30. Leonard M. J. · Macromolecules · 2003 · 36 · 954910.1021/ma034352c ↗
31. Bilalov A. · Soft Matter · 2011 · 7 · 73010.1039/C0SM00650E ↗
32. Miguel M. G. · Colloid Surface Physicochem Eng. Aspect · 2003 · 228 · 4310.1016/S0927-7757(03)00334-0 ↗
33. Amar-Yuli I. · Soft Matter · 2011 · 7 · 816210.1039/c1sm05612c ↗
34. Admirand W. H. · J. Clin. Investig. · 1968 · 47 · 104310.1172/JCI105794 ↗
35. Marques E. F. · Langmuir · 2000 · 16 · 517810.1021/la9912803 ↗
36. Hirano S. · 1990 · 28310.1007/978-1-4899-0768-4_28 ↗
37. Hoogstraate J. A. J. · Pharm. Sci. Technol. Today · 1998 · 1 · 30910.1016/S1461-5347(98)00076-5 ↗
38. Harris D. · J. Pharm. Sci. · 1992 · 81 · 110.1002/jps.2600810102 ↗
39. Mironov A. V. · J. Phys. Chem. B · 2001 · 105 · 561210.1021/jp002187m ↗
40. Sokolov E. L. · Langmuir · 1996 · 12 · 622910.1021/la960274t ↗
41. Bakeev K. N. · Macromolecules · 1996 · 29 · 132010.1021/ma9511311 ↗
42. Tangso K. J. · J. Phys. Chem. B · 2013 · 117 · 1020310.1021/jp403840m ↗
43. Rosevear F. B. · J. Am. Oil Chem. Soc. · 1954 · 31 · 62810.1007/BF02545595 ↗
44. Kirby N. M. · J. Appl. Crystallogr. · 2013 · 46 · 167010.1107/S002188981302774X ↗
45. Hyde, S.Handbook of Appled Surface and Colloid Chemistry;John Wiley & Sons: 2001; p299–332.
46. Babak V. G. · Polym. Bull. · 2000 · 45 · 7710.1007/s002890070059 ↗
47. Higuchi W. I. · J. Pharm. Sci. · 1967 · 56 · 31510.1002/jps.2600560302 ↗
48. Zabara A. · ChemComm · 2014 · 50 · 2642
49. Lameiro M. H. · J. Biotechnol. · 2006 · 126 · 15210.1016/j.jbiotec.2006.04.030 ↗
50. Lameiro M. H. · Int. J. Pharm. · 2006 · 312 · 11910.1016/j.ijpharm.2006.01.006 ↗
51. Thongngam M. · Food Hydrocolloids · 2005 · 19 · 81310.1016/j.foodhyd.2004.11.001 ↗
52. Youssry M. · Phys. Chem. Chem. Phys. · 2008 · 10 · 688010.1039/b809582e ↗
53. Kratohvil J. P. · Can. J. Biochem. · 1968 · 46 · 94510.1139/o68-141 ↗
54. Israelachvili J. N. · J. Chem. Soc., Faraday Trans. 2 · 1976 · 72 · 152510.1039/f29767201525 ↗
55. Thalberg K. · J. Phys. Chem. · 1991 · 95 · 600410.1021/j100168a053 ↗
56. Abraham A. · Soft Matter · 2009 · 5 · 371810.1039/b903158h ↗
57. Pojják K. · Langmuir · 2011 · 27 · 913910.1021/la2021353 ↗
58. Mironov A. V. · Macromolecules · 1998 · 31 · 769810.1021/ma971816w ↗
59. Yu L. X. · Int. J. Pharm. · 1996 · 140 · 11110.1016/0378-5173(96)04592-9 ↗
60. Ritschel W. A. · Methods Find. Exp. Clin. Pharmacol. · 1991 · 13 · 313
61. Squier C. A. · J. Investig. Dermatol. · 1985 · 84 · 17610.1111/1523-1747.ep12264711 ↗