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      Preparation and characterization of poly(D,L-lactide-co-glycolide) microspheres for controlled release of human growth hormone

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      AAPS PharmSciTech
      American Association of Pharmaceutical Scientists (AAPS)

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          Abstract

          The purpose of this research was to assess the physicochemical properties of a controlled release formulation of recombinant human growth hormone (rHGH) encapsulated in poly(D,L-lactide-co-glycolide) (PLGA) composite microspheres. rHGH was loaded in poly(acryloyl hydroxyethyl) starch (acHES) microparticles, and then the protein-containing microparticles were encapsulated in the PLGA matrix by a solvent extraction/evaporation method. rHGH-loaded PLGA microspheres were also prepared using mannitol without the starch hydrogel microparticle microspheres for comparison. The detection of secondary structure changes in protein was investigated by using a Fourier Transfer Infrared (FTIR) technique. The composite microspheres were spherical in shape (44.6 +/- 2.47 microm), and the PLGA-mannitol microspheres were 39.7 +/- 2.50 microm. Drug-loading efficiency varied from 93.2% to 104%. The composite microspheres showed higher overall drug release than the PLGA/mannitol microspheres. FTIR analyses indicated good stability and structural integrity of HGH localized in the microspheres. The PLGA-acHES composite microsphere system could be useful for the controlled delivery of protein drugs.

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          [13] Resolution-enhanced fourier transform infrared spectroscopy of enzymes

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            On Protein Denaturation in Aqueous−Organic Mixtures but Not in Pure Organic Solvents

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              A month-long effect from a single injection of microencapsulated human growth hormone.

              An injectable sustained-release form of human growth hormone (hGH) was developed by stabilizing and encapsulating the protein, without altering its integrity, into biodegradable microspheres using a novel cryogenic process. A single injection of microspheres in monkeys resulted in elevated serum levels of recombinant hGH (rhGH) for more than one month. Insulin-like growth factor-I (IGF-I) and its binding protein IGFBP-3, both of which are induced by hGH, were also elevated for four weeks by the rhGH containing microspheres to a level greater than that induced by the same amount of rhGH administered by daily injections. These results show that, by using appropriate methods of stabilization and encapsulation, the advantages of sustained-release formulations previously demonstrated for low-molecular-weight drugs can now be extended to protein therapeutics.
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                Author and article information

                Journal
                AAPS PharmSciTech
                AAPS PharmSciTech
                American Association of Pharmaceutical Scientists (AAPS)
                1530-9932
                June 2003
                June 2003
                : 4
                : 2
                : 147-156
                Article
                10.1208/pt040228
                2750591
                12916910
                86c8b750-4162-4970-835e-b3eb127977e3
                © 2003
                History

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