A biocompatible system was developed that permits continuous release of biologicallyactive insulin from small polymer matrices. Powdered insulin particles were incorporated into an ethylene-vinyl acetate copolymer matrix. The presence of particulate insulin resulted in a matrixcomposed of tortuous channels and constricted pores through which release occurred. When aqueous release media permeated the matrix, the insulin dissolved and diffused slowly through this tortuous network. The large concentration of insulin within the matrix provided the driving force for release. Release kinetics from these insulin polymer matrices were enhanced by increasing the insulin solubility, the insulin powder particle size, the loading of insulin within the matrix, and the porosity of the matrix. Appropriate geometric design of the polymer matrix resulted in near-constant insulin release rates.
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Original Contribution|
June 01 1986
Controlled Release of Insulin From Polymer Matrices: In Vitro Kinetics Free
Larry Brown;
Larry Brown
Department of Applied Biological Sciences, Massachusetts Institute of Technology
Cambridge
Children's Hospital Medical Center, Department of Surgery
Boston
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Linda Siemer;
Linda Siemer
Department of Applied Biological Sciences, Massachusetts Institute of Technology
Cambridge
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Christina Munoz;
Christina Munoz
Children's Hospital Medical Center, Department of Surgery
Boston
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Robert Langer
Robert Langer
Whitaker College of Health Sciences, Technology and Management, Massachusetts Institute of Technology, and Harvard Medical School
Cambridge, Massachusetts
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Address reprint requests to Robert Langer, Department of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139.
Citation
Larry Brown, Linda Siemer, Christina Munoz, Robert Langer; Controlled Release of Insulin From Polymer Matrices: In Vitro Kinetics. Diabetes 1 June 1986; 35 (6): 684–691. https://doi.org/10.2337/diab.35.6.684
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