Loading of Propranolol-H⁺ onto SP Sephadex C-25 Studied by Isothermal Calorimetry and Spectroscopy

References

1. 1.↵
   1. Halder A.,
   2. Sa B.

   Sustained release of propranolol hydrochloride based on ion-exchange resin entrapped within polystyrene microcapsules. J. Microencapsul. 2006, 23(8),899–911.

   OpenUrlPubMed
2. 2.↵
   1. Raghunathan Y.,
   2. Amsel L.,
   3. Hinsvark O. ,
   4. Bryant W.

   Sustained-release drug delivery system. I: Coated ion-exchange resin system for phenylpropanolamine and other drugs. J. Pharm. Sci. 1981, 70 (4),379–384.

   OpenUrlCrossRefPubMedWeb of Science
3. 3.↵
   1. Sriwongjanya M.,
   2. Bodmeier R.

   Effect of ion exchange resins on the drug release from matrix tablets. Eur. J. Pharm. Biopharm. 1998,46(3), 321–327.

   OpenUrlPubMed
4. 4.↵
   1. Atyabi F.,
   2. Sharma H. L.,
   3. Mohammad H. A. H.,
   4. Fell J. T.

   Controlled drug release from coated floating ion exchange resin beads. J. Controlled Release. 1996, 42 (1),25–28.

   OpenUrl
5. 5.↵
   1. Agarwal R.,
   2. Mittal R.,
   3. Singh A.

   Studies of ion-exchange resin complex of chloroquine phosphate. Drug Dev. Ind. Pharm. 2000, 26 (7),773–776.

   OpenUrlPubMed
6. 6.↵
   1. Bess W. S.,
   2. Kulkarni N.,
   3. Ambike S. H.,
   4. Ramsay M. P.

   Fast dissolving orally consumable films containing an Ion exchange resin as a taste masking agent. U.S. Patent 2006/0204559 A1, 2006.
7. 7.↵
   1. Gao R.,
   2. Shao Z. J. ,
   3. Fan A.,
   4. C.-L.,
   5. Witchey-Lakshmanan L. C.,
   6. Stewart D. C.

   “Taste masking of oral quinolone liquid preparations using ion exchange resins,” U.S. Patent 2000, 614523, 12 7, 2000.
8. 8.↵
   1. Bouchard E. F. ,
   2. Friedman I. J. ,
   3. Taylor R. J.

   Vitamin B12 products. U.S. Patent 2830933, 19580415, April 15, 1958.
9. 9.↵
   1. Akkaramongkolporn P.,
   2. Terada K. ,
   3. Yonemochi E.

   Molecular properties of propranolol hydrochloride prepared as drug-resin complexes. Drug Dev. Ind. Pharm., 2001,27 (4),359–364.

   OpenUrlPubMed
10. 10.↵
    1. Anand V. ,
    2. Kandarapu R. ,
    3. Garg S.

    Ion exchange resins: carrying drug delivery forward. Drug Discovery Today, 2001, 6 (>17), 905–914.

    OpenUrlPubMed
11. 11.↵
    The United States Pharmacopeia 29, United States Pharmacopeial Convention, Rockville, Md., 2006.
12. 12.↵
    SP Sephadex™ Technical Data Sheet. Amersham Biosciences, www.aemershambioscience.com (accessed June 21, 2007).
13. 13.↵
    1. Zeiss D. ,
    2. Bauer-Brandl A.

    Ion exchange resins as excipients for drug delivery: Issues for reproducible drug loading. Open Drug Delivery Journal, 2007, 1, 60–67.

    OpenUrl
14. 14.↵
    1. Abdekhodaie M. J. ,
    2. Wu X. Y.

    Drug loading onto ion-exchange microspheres: Modeling study and experimental verification. Biomaterials 2006, 27(>19), 3652–3662.

    OpenUrlPubMed
15. 15.↵
    1. Boyd G. E. ,
    2. Schubert J. ,
    3. Adamson A. W.

    The exchange adsorption of ions from aqueous solutions by organic zeolites. I. Ion-exchange equilibria. J. Am. Chem. Soc., 1947, 69 (11), 2818–2829.

    OpenUrlPubMed
16. 16.↵
    1. Johns W. H.,
    2. Bates T. R.

    Quantification of the binding tendencies of cholestyramine. I. Effect of structure and added electrolytes on the binding of unconjugated and conjugated bile-salt anions. J. Pharm. Sci., 1969, 58 (2),179–183.

    OpenUrlCrossRefPubMedWeb of Science
17. 17.↵
    1. Misak N. Z.

    Adsorption isotherms in ion exchange reactions. Further treatments and remarks on the application of the Langmuir isotherm,. Colloids and Surfaces, A: Physicochemical and Engineering Aspects 1995, 97 (2),128–140.

    OpenUrl
18. 18.↵
    1. Boudy V.,
    2. Voute N. ,
    3. Pradeau D. ,
    4. Chaumeil J. C.

    Adsorption of an ionizable drug onto microspheres: experimental and modeling studies. Int. J. Pharm, 2002, 239 (1),13–22.

    OpenUrlPubMed
19. 19.↵
    1. Langmuir I.

    The adsorption of gases on plane surfaces of glass, mica, and platinum. J. Am. Chem. Soc., 1918 40 (9), 1361–1403.

    OpenUrlCrossRef
20. 20.↵
    1. Zeiss D. ,
    2. Bauer-Brandl A.

    Isothermal calorimetry (ITC) method to study drug/ion exchanger interaction. J. Therm. Anal. Calorim., 2006 83 (2), 309–312.

    OpenUrl
21. 21.↵
    1. Liu Z.,
    2. Cheung R.,
    3. Wu X. Y. ,
    4. Ballinger J. R. ,
    5. Bendayan R. ,
    6. Rauth A. M.

    A study of doxorubicin loading onto and the release from sulfopropyl dextran ion exchange microspheres. J. Controlled Release 2001, 77 (3),213–224.

    OpenUrlCrossRefPubMedWeb of Science
22. 22.↵
    Rohm and Haas; Amberlite™ IRP69 technical data sheet, www.rohmhaas.com/markets/pharmaceutical.html (accessed May 2, 2007).
23. 23.↵
    1. Ritger P. L. ,
    2. Peppas N. A.

    A simple equation for description of solute release. I. Fickian and non-Fickian release from non-swellable devices in the form of slabs, spheres, cylinders or disks. J. Controlled Release, 1987 5 (1), 23–36.

    OpenUrlCrossRef
24. 24.↵
    1. Peppas N. A.,
    2. Sahlin J. J.

    A simple equation for the description of solute release. III. Coupling of diffusion and relaxation. Int. J. Pharm. 1989, 57 (2),169–172.

    OpenUrl