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. 2005 Oct 24;6(3):E487–E494. doi: 10.1208/pt060361

Preparation, in vitro release, in vivo absorption and biocompatibility studies of insulin-loaded microspheres in rabbits

Feirong Kang 1, Jagdish Singh 1,
PMCID: PMC2750395  PMID: 16354009

Abstract

The purpose of this study was to develop a single-dose insulin delivery system based on poly (lactide-co-glycolide) (PLGA) microspheres to provide basal insulin level for a prolonged period. Insulin-loaded PLGA microspheres were prepared by water-in-oil-in-water double emulsion (batch A) and solid-in0oil-in-water emulsion (batch B) methods. Microspheres were characterized for physical characteristics and in vitro release. In vivo absorption of insulin and biocompatibility of insulin-loaded PLGA microspheres were performed in diabetic New Zealand white rabbits. Light and transmission electron microscopy were performed on the skin tissues excised from microspheres injected sites in order to study the biocompatibility. The burst release of insulin was high (47%) from batch B and low (5%) from batch A. Therefore, we mixed microspheres of batch A and B in ratio of 3∶ w/w, which produced desirable in vitro release profile. In vivo absorption study showed that insulin-loaded microspheres provided a serum insulin level of 20–40 μU/ml up to 40 days. Biocompatibility study provided evidence of normal inflammatory and foreign body reactions, which were characterized by the presence of macrophages, fibroblasts and foreign body giant cells. Neither necrosis nor tissue damage was identified. At the end of 12 weeks, no distinct histological differences were observed in comparison to the control tissue samples. In conclusion, insulin-loaded PLGA microspheres controlled the in vivo absorption of insulin to maintain the basal insulin level for longer period and the delivery system was biocompatible.

Keywords: PLGA, microspheres, insulin, in vivo absorption, biocompatibility

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References

  • 1.Steil CF. Diatetes mellitus. In: DiPiro JT, Talbert RL, Yee GC, editors. Pharmacotherapy: A pathophysiologic approach. 4th ed. Stamford, CT: Appleton & Lange; 1999. pp. 1219–1243. [Google Scholar]
  • 2.Galloway JA, Chance RE. Improving insulin therapy: achievements and challenges. Horm Metab Res. 1994;26:591–598. doi: 10.1055/s-2007-1001766. [DOI] [PubMed] [Google Scholar]
  • 3.White J, Campbell RD. Diabetes mellitus. In: Herfindal ET, Gourly DR, editors. Textbook of therapeutics: drug and disease management. Baltimore, MD: Williams & Wilkins; 1996. pp. 357–386. [Google Scholar]
  • 4.Riddle MC. Timely initiation of basal insulin. Am J Med. 2004;116:3S–9S. doi: 10.1016/j.amjmed.2003.12.003. [DOI] [PubMed] [Google Scholar]
  • 5.LeRoith D, Levetan CS, Hirsch IB, Riddle MC. Type 2 diabetes: the role of basal insulin therapy. J Fam Pract. 2004;53:215–222. [PubMed] [Google Scholar]
  • 6.Jiang G, Qiu W, DeLuca PP. Preparation and in vitro/in vivo evaluation of insulin-loaded poly(acryloyl-hydroxyethyl starch)-PLGA composite microspheres. Pharm Res. 2003;20:452–459. doi: 10.1023/A:1022668507748. [DOI] [PubMed] [Google Scholar]
  • 7.Ziats NP, Miller KM, Anderson JM. In vitro and in vivo interactions of cells with biomaterials. Biomaterials. 1988;9:5–13. doi: 10.1016/0142-9612(88)90063-4. [DOI] [PubMed] [Google Scholar]
  • 8.Athanasiou KA, Niederauer GG, Agrawal CM. Sterilization, toxicity, biocompatibility and clinical applications of poly lactic acid/polyglycolic acid copolymers. Biomaterials. 1996;17:93–102. doi: 10.1016/0142-9612(96)85754-1. [DOI] [PubMed] [Google Scholar]
  • 9.Anderson JM, Shive MS. Biodegradation and biocompatibility of PLA and PLGA microspheres. Adv Drug Deliv Rev. 1997;28:5–24. doi: 10.1016/S0169-409X(97)00048-3. [DOI] [PubMed] [Google Scholar]
  • 10.Pariente JL, Kim BS, Atala A. In vitro biocompatibility assessment of naturally derived and synthetic biomaterials using normal human urothelial cells. J Biomed Mater Res. 2001;55:33–39. doi: 10.1002/1097-4636(200104)55:1<33::AID-JBM50>3.0.CO;2-7. [DOI] [PubMed] [Google Scholar]
  • 11.Ike O, Shimizu Y, Wada R, Hyon SH, Ikada Y. Controlled cisplatin delivery system using poly(D,L-lactic acid) Biomaterials. 1992;13:230–234. doi: 10.1016/0142-9612(92)90189-U. [DOI] [PubMed] [Google Scholar]
  • 12.Smith PK, Krohn RI, Hermanson GT, et al. Measurement of protein using bicinchoninic acid. Anal Biochem. 1985;150:76–85. doi: 10.1016/0003-2697(85)90442-7. [DOI] [PubMed] [Google Scholar]
  • 13.Trinder P. Determination of blood glucose using an oxidase-peroxidase system with a non-carcinogenic chromogen. J Clin Pathol. 1969;22:158–161. doi: 10.1136/jcp.22.2.158. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Morgan CR, Lazarow A. Immunoassay of insulin using a two-antibody system. Proc Soc Exp Biol Med. 1962;110:29–32. doi: 10.3181/00379727-110-27411. [DOI] [PubMed] [Google Scholar]
  • 15.Ravivarapu HB, Burton K, DeLuca PP. Polymer and microsphere blending to alter the release of a peptide from PLGA microspheres. Eur J Pharm Biopharm. 2000;50:263–270. doi: 10.1016/S0939-6411(00)00099-0. [DOI] [PubMed] [Google Scholar]
  • 16.Takenaga M, Yamaguchi Y, Kitagawa A, Ogawa Y, Mizushima Y, Igarashi R. A novel insulin formulation can keep providing steady levels of insulin for much longer periods in-vivo. J Pharm Pharmacol. 2002;54:1189–1194. doi: 10.1211/002235702320402026. [DOI] [PubMed] [Google Scholar]

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