Magnetically responsive polymeric microparticles for oral delivery of protein drugs

Pharm Res. 2006 Mar;23(3):557-64. doi: 10.1007/s11095-005-9444-5. Epub 2006 Jan 1.

Abstract

Purpose: Protein drugs cannot be delivered efficiently through oral routes. To address this challenge, we evaluated the effect of prolonged gastrointestinal transit on the bioavailability of insulin carried by magnetically responsive microparticles in the presence of an external magnetic field.

Methods: Magnetite nanocrystals and insulin were coencapsulated into poly(lactide-co-glycolide) (PLGA) microparticles and their effects on hypoglycemia were evaluated in mice in the presence of a circumferentially applied external magnetic field.

Results: A single administration of 100 U/kg of insulin-magnetite-PLGA microparticles to fasted mice resulted in a reduction of blood glucose levels of up to 43.8% in the presence of an external magnetic field for 20 h (bioavailability = 2.77 +/- 0.46 and 0.87 +/- 0.29% based on glucose and ELISA assay, respectively), significantly higher than similarly dosed mice without a magnetic field (bioavailability = 0.66 +/- 0.56 and 0.30 +/- 0.06%, based on glucose and ELISA assay, respectively).

Conclusions: A substantially improved hypoglycemic effect was observed in mice that were orally administered with insulin-magnetite-PLGA microparticles in the presence of an external magnetic field, suggesting that magnetic force can be used to improve the efficiency of orally delivered protein therapeutics.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Blood Glucose / metabolism
  • Delayed-Action Preparations
  • Drug Carriers / administration & dosage
  • Drug Carriers / chemistry*
  • Electromagnetic Fields
  • Ferrosoferric Oxide / chemistry*
  • Gastrointestinal Transit
  • Hypoglycemia / blood
  • Hypoglycemia / drug therapy
  • Hypoglycemic Agents / administration & dosage
  • Hypoglycemic Agents / pharmacokinetics
  • Hypoglycemic Agents / therapeutic use
  • Insulin / administration & dosage
  • Insulin / pharmacokinetics
  • Insulin / therapeutic use
  • Intestinal Absorption
  • Lactic Acid / chemistry*
  • Mice
  • Mice, Inbred BALB C
  • Microspheres
  • Polyglycolic Acid / chemistry*
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Polymers / chemistry*
  • Proteins / administration & dosage*
  • Proteins / pharmacokinetics
  • Proteins / therapeutic use

Substances

  • Blood Glucose
  • Delayed-Action Preparations
  • Drug Carriers
  • Hypoglycemic Agents
  • Insulin
  • Polymers
  • Proteins
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Polyglycolic Acid
  • Lactic Acid
  • Ferrosoferric Oxide