209
Views
7
CrossRef citations to date
0
Altmetric
Research Article

Fabrication of chitosan–polyacrylic acid complexes as polymeric osmogents for swellable micro/nanoporous osmotic pumps

, , , &
Pages 926-933 | Received 10 Aug 2010, Accepted 19 Dec 2010, Published online: 21 Mar 2011

References

  • Malaterre V, Ogorka J, Loggia N, Gurny R. (2009). Oral osmotically driven systems: 30 years of development and clinical use. Eur J Pharm Biopharm, 73:311–323.
  • Theeuwes F. (1975). Elementary osmotic pump. J Pharm Sci, 64:1987–1991.
  • Theeuwes F, Swanson D, Wong P, Bonsen P, Place V, Heimlich K et al. (1983). Elementary osmotic pump for indomethacin. J Pharm Sci, 72:253–258.
  • Sinchaipanid N, Pongwai S, Limsuwan P, Mitrevej A. (2003). Design of salbutamol EOP tablets from pharmacokinetics parameters. Pharm Dev Technol, 8:135–142.
  • Shokri J, Ahmadi P, Rashidi P, Shahsavari M, Rajabi-Siahboomi A, Nokhodchi A. (2008). Swellable elementary osmotic pump (SEOP): an effective device for delivery of poorly water-soluble drugs. Eur J Pharm Biopharm, 68:289–297.
  • Swanson DR, Barclay BL, Wong PS, Theeuwes F. (1987). Nifedipine gastrointestinal therapeutic system. Am J Med, 83:3–9.
  • Liu L, Ku J, Khang G, Lee B, Rhee JM, Lee HB. (2000). Nifedipine controlled delivery by sandwiched osmotic tablet system. J Control Release, 68:145–156.
  • Malaterre V, Ogorka J, Loggia N, Gurny R. (2009). Approach to design push–pull osmotic pumps. Int J Pharm, 376:56–62.
  • Zentner GM, McClelland GA, Sutton SC. (1991). Controlled porosity solubility- and resin-modulated osmotic drug delivery systems for release of diltiazem hydrochloride. J Control Release, 16:237–244.
  • Zentner GM, Rork GS, Himmelstein KJ. (1985). The controlled porosity osmotic pump. J Control Release, 1:269–282.
  • Tuntikulwattana S, Mitrevej A, Kerdcharoen T, Williams DB, Sinchaipanid N. (2010). Development and optimization of micro/nanoporous osmotic pump tablets. AAPS Pharmscitech, 11:924–935.
  • Herbig SM, Cardinal JR, Korsmeyer RW, Smith KL. (1995). Asymmetric-membrane tablet coatings for osmotic drug delivery. J Control Release, 35:127–136.
  • Thombre AG, Cardinal JR, DeNoto AR, Herbig SM, Smith KL. (1999). Asymmetric membrane capsules for osmotic drug delivery. I. Development of a manufacturing process. J Control Release, 57:55–64.
  • Thombre AG, Cardinal JR, DeNoto AR, Gibbes DC. (1999). Asymmetric membrane capsules for osmotic drug delivery II. In vitro and in vivo drug release performance. J Control Release, 57:65–73.
  • Thombre AG, Appel LE, Chidlaw MB, Daugherity PD, Dumont F, Evans LA et al. (2004). Osmotic drug delivery using swellable-core technology. J Control Release, 94:75–89.
  • Liu L, Che B. (2006). Preparation of monolithic osmotic pump system by coating the indented core tablet. Eur J Pharm Biopharm, 64:180–184.
  • Okimoto K, Tokunaga Y, Ibuki R, Irie T, Uekama K, Rajewski RA et al. (2004). Applicability of (SBE)7m-beta-CD in controlled-porosity osmotic pump tablets (OPTs). Int J Pharm, 286:81–88.
  • Verma RK, Krishna DM, Garg S. (2002). Formulation aspects in the development of osmotically controlled oral drug delivery systems. J Control Release, 79:7–27.
  • Liu H, Yang XG, Nie SF, Wei LL, Zhou LL, Liu H et al. (2007). Chitosan-based controlled porosity osmotic pump for colon-specific delivery system: screening of formulation variables and in vitro investigation. Int J Pharm, 332:115–124.
  • Prabakaran D, Singh P, Kanaujia P, Jaganathan KS, Rawat A, Vyas SP. (2004). Modified push–pull osmotic system for simultaneous delivery of theophylline and salbutamol: development and in vitro characterization. Int J Pharm, 284:95–108.
  • Lee JW, Kim SY, Kim SS, Lee YM, Lee KH, Kim SJ. (1999). Synthesis and characteristics of interpenetrating polymer network hydrogel composed of chitosan and poly(acrylic acid). J Appl Polym Sci, 73:113–120.
  • Bae YH, Kim SW. (1993). Hydrogel delivery systems based on polymer blends, block co-polymers or interpenetrating networks. Adv Drug Deliver Rev, 11:109–135.
  • Wang H, Li W, Lu Y, Wang Z. (1997). Studies on chitosan and poly(acrylic acid) interpolymer complex. I. Preparation, structure, pH-sensitivity, and salt sensitivity of complex-forming poly(acrylic acid):chitosan semi-interpenetrating polymer network. J Appl Polym Sci, 65:1445–1450.
  • Wang H, Li W, Lu Y, Wang Z, Zhong W. (1996). Studies on chitosan and poly(acrylic acid) interpolymer complex. II. Solution behaviors of the mixture of water-soluble chitosan and poly(acrylic acid). J Appl Polym Sci, 61:2221–2224.
  • Nge TT, Yamaguchi M, Hori N, Takemura A, Ono H. (2002). Synthesis and characterization of chitosan/poly(acrylic acid) polyelectrolyte complex. J Appl Polym Sci, 83:1025–1035.
  • Ahn JS, Choi HK, Cho CS. (2001). A novel mucoadhesive polymer prepared by template polymerization of acrylic acid in the presence of chitosan. Biomaterials, 22:923–928.
  • Ahn JS, Choi HK, Chun MK, Ryu JM, Jung JH, Kim YU et al. (2002). Release of triamcinolone acetonide from mucoadhesive polymer composed of chitosan and poly(acrylic acid) in vitro. Biomaterials, 23:1411–1416.
  • De la Torre PM, Torrado S, Torrado S. (2003). Interpolymer complexes of poly(acrylic acid) and chitosan: influence of the ionic hydrogel-forming medium. Biomaterials, 24:1459–1468.
  • De la Torre PM, Enobakhare Y, Torrado G, Torrado S. (2003). Release of amoxicillin from polyionic complexes of chitosan and poly(acrylic acid). Study of polymer/polymer and polymer/drug interactions within the network structure. Biomaterials, 24:1499–1506.
  • Torrado S, Prada P, de la Torre PM, Torrado S. (2004). Chitosan–poly(acrylic) acid polyionic complex: in vivo study to demonstrate prolonged gastric retention. Biomaterials, 25:917–923.
  • Rossi S, Sandri G, Ferrari F, Bonferoni MC, Caramella C. (2003). Buccal delivery of acyclovir from films based on chitosan and polyacrylic acid. Pharm Dev Technol, 8:199–208.
  • Hu Y, Jiang X, Ding Y, Ge H, Yuan Y, Yang C. (2002). Synthesis and characterization of chitosan–poly(acrylic acid) nanoparticles. Biomaterials, 23:3193–3201.
  • De la Torre PM, Torrado G, Torrado S. (2004). Poly(acrylic acid) chitosan interpolymer complexes for stomach controlled antibiotic delivery. J Biomed Mater Res, 72B:191–197.
  • Illum L. (1998). Chitosan and its use as a pharmaceutical excipient. Pharm Res, 15:1326–1331.
  • US Department of Health and Human Service Food and Drug Administration Center for Drug Evaluation and Research (CDER). (1997). Guidance for Industry: Modified Release Solid Oral Dosage Forms: SUPAC-MR: Chemistry, Manufacturing and Controls, In vitro Dissolution Testing and In vivo Bioequivalence Documentation (September 1997). Available at: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM070640.pdf. Accessed on July 9, 2010.
  • Moharram MA, Balloomal LS, El-Gendy HM. (1996). Infrared study of the complexation of poly(acrylic acid) with poly(acrylamide). J Appl Polym Sci, 59:987–990.
  • Wu Y, Guo J, Yang W, Wang C, Fu S. (2006). Preparation and characterization of chitosan–poly(acrylic acid) polymer magnetic microspheres. Polymer, 47:5287–5294.
  • Risbud MV, Hardikar AA, Bhat SV, Bhonde RR. (2000). pH-sensitive freeze-dried chitosan–polyvinyl pyrrolidone hydrogels as controlled release system for antibiotic delivery. J Control Release, 68:23–30.
  • Shin HS, Kim SY, Lee YM. (1997). Indomethacin release behaviors from pH and thermoresponsive poly(vinyl alcohol) and poly(acrylic acid) IPN hydrogels for site-specific drug delivery. J Appl Polym Sci, 65:685–693.
  • Takka S. (2003). Propranolol hydrochloride–anionic polymer binding interaction. Farmaco, 58:1051–1056.
  • Siemoneit U, Schmitt C, Alvarez-Lorenzo C, Luzardo A, Otero-Espinar F, Concheiro A et al. (2006). Acrylic/cyclodextrin hydrogels with enhanced drug loading and sustained release capability. Int J Pharm, 312:66–74.
  • Rigo MV, Allemandi DA, Manzo RH. (2006). Swellable drug–polyelectrolyte matrices (SDPM) of alginic acid characterization and delivery properties. Int J Pharm, 322:36–43.
  • Costa P, Sousa Lobo JM. (2001). Modeling and comparison of dissolution profiles. Eur J Pharm Sci, 13: 123–133.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.