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. 2004 Sep 1;6(3):65–71. doi: 10.1208/aapsj060324

Morphology and buoyancy of oil-entrapped calcium pectinate gel beads

Pornsak Sriamornsak 1,, Nartaya Thirawong 1, Satit Puttipipatkhachorn 2
PMCID: PMC2751249  PMID: 15760109

Abstract

A new emulsion-gelation method to prepare oil-entrapped calcium pectinate gel (CaPG) beads capable of floating in the gastric condition was designed and tested. The gel beads containing edible oil were prepared by either being gently mixed or homogenized an oil phase and a water phase containing pectin, and then extruded into calcium chloride solution with gentle agitation at room temperature. The gel beads formed were then separated, washed with distilled water, and dried at 37°C for 12 hours. A model of the emulsion-gelation process to illustrate the formation of oil-entrapped CaPG beads was proposed. The effect of selected factors, such as type of oil, percentage of oil, and type of pectin on morphology and floating properties was investigated. The oil-entrapped calcium pectinate gel beads floated if a sufficient amount of oil was used. Scanning electron photomicrographs demonstrated very small pores, ranging between 5 and 40 μm, dispersed all over the beads. The type and percentage of oil play an important role in controlling the floating of oil-entrapped CaPG beads. The results suggested that oil-entrapped CaPG beads were promising as a carrier for intragastric floating drug delivery.

Keywords: calcium pectinate, pectin, oil, emulsion, gel beads, floating, gastro-retentive

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References

  • 1.Moes AJ. Gastroretentive dosage forms. Crit Rev Ther Drug Carrier Syst. 1993;10:143–195. [PubMed] [Google Scholar]
  • 2.Singh BM, Kim KH. Floating drug delivery systems: an approach to oral controlled drug delivery via gastric retention. J Control Release. 2000;63:235–239. doi: 10.1016/S0168-3659(99)00204-7. [DOI] [PubMed] [Google Scholar]
  • 3.Cooreman MP, Krausgrill P, Hengels KJ. Local gastric and serum amoxycillin concentrations after different oral application forms. Antimicrob Agents Chemother. 1993;37:1506–1509. doi: 10.1128/AAC.37.7.1506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Streubel A, Siepmann J, Bodmeier R. Floating microparticles based on low density foam powder. Int J Pharm. 2002;241:279–292. doi: 10.1016/S0378-5173(02)00241-7. [DOI] [PubMed] [Google Scholar]
  • 5.Rouge N, Buri P, Doelker E. Drug absorption sites in the gastrointestinal tract and dosage forms for site-specific delivery. Int J Pharm. 1996;136:117–139. doi: 10.1016/0378-5173(96)85200-8. [DOI] [Google Scholar]
  • 6.Akiyama Y, Nagahara N. Novel formulation approaches to oral mucoadhesive drug delivery systems. In: Mathiowitz E, Chickering DE, Lehr CM, editors. Bioadhesive Drug Delivery Systems Fundamentals: Novel Approaches and Development. New York, NY: Marcel Dekker; 1999. pp. 477–505. [Google Scholar]
  • 7.Joseph NJ, Lakshmi S, Jayakrishnan A. A floating-type oral dosage form for piroxicam based on hollow polycarbonate microspheres: in vitro and in vivo evaluation in rabbits. J Control Release. 2002;79:71–79. doi: 10.1016/S0168-3659(01)00507-7. [DOI] [PubMed] [Google Scholar]
  • 8.Chien YW. Oral drug delivery. In: Chien YW, editor. Novel Drug Delivery System. New York, NY: Marcel Dekker; 1992. pp. 139–196. [Google Scholar]
  • 9.Thanoo BC, Sunny MC, Jayakrishnan A. Oral sustained-release drug delivery systems using polycarbonate microspheres capable of floating on the gastric fluid. J Pharm Pharmacol. 1993;45:21–24. doi: 10.1111/j.2042-7158.1993.tb03672.x. [DOI] [PubMed] [Google Scholar]
  • 10.Iannuccelli V, Coppi G, Bernabel MT, Cameroni R. Air compartment multiple-unit system for prolonged gastric residence. Part I: Formulation study. Int J Pharm. 1998;174:47–54. doi: 10.1016/S0378-5173(98)00229-4. [DOI] [Google Scholar]
  • 11.Desai S, Bolton S. A floating controlled release drug delivery system: in-vitro—in-vivo evaluation. Pharm Res. 1993;10:1321–1325. doi: 10.1023/A:1018921830385. [DOI] [PubMed] [Google Scholar]
  • 12.Rolin C. Pectin. In: Whistler RL, Benliller JN, editors. Industrial Gums: Polysaccharides and Their Derivatives. New York, NY: Academic Press; 1993. pp. 257–293. [Google Scholar]
  • 13.Leroux J, Langendorff V, Schick G, Vaishnav V, Mazoyer J. Emulsion stabilizing properties of pectin. Food Hydrocolloids. 2003;17:455–462. doi: 10.1016/S0268-005X(03)00027-4. [DOI] [Google Scholar]
  • 14.Schols HA, Voragen AGJ. Complex pectin: structure elucidation using enzymes. In: Visser J, Voragen AGJ, editors. Progress in Biotechnology: Pectin and Pectinases. Amsterdam, The Netherlands: Elsevier; 1996. pp. 3–19. [Google Scholar]
  • 15.Sriamornsak P, Nunthanid J. Calcium pectinate gel beads for controlled release drug delivery. I. Preparation and in-vitro release studies. Int J Pharm. 1998;160:207–212. doi: 10.1016/S0378-5173(97)00310-4. [DOI] [Google Scholar]
  • 16.Sriamornsak P, Nunthanid J. Calcium pectinate gel beads for controlled release drug delivery. II. Effect of formulation and processing variables on drug release. J Microencapsul. 1999;16:303–313. doi: 10.1080/026520499289031. [DOI] [PubMed] [Google Scholar]
  • 17.Sriamornsak P. Effect of calcium concentration, hardening agent and drying condition on release characteristics of oral proteins from calcium pectinate gel beads. Eur J Pharm Sci. 1999;8:221–227. doi: 10.1016/S0928-0987(99)00010-X. [DOI] [PubMed] [Google Scholar]
  • 18.Sriamornsak P, Thirawong N. Use of back-scattered electron imaging as a tool for examination matrix structure of calcium pectinate. Int J Pharm. 2003;267:151–156. doi: 10.1016/j.ijpharm.2003.08.005. [DOI] [PubMed] [Google Scholar]
  • 19.Garti N, Reichman D. Hydrocolloids as food emulsifiers and stabilizers. Food Structure. 1993;12:411–426. [Google Scholar]
  • 20.Friberg SE, Goubran RF, Kayali IH. Emulsion stability. In: Larsson K, Friberg SE, editors. Food Ennilsions. New York, NY: Marcel Dekker; 1990. pp. 1–6. [Google Scholar]

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