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Starch

  • US 6,616,948 B2
  • Filed: 10/05/2001
  • Issued: 09/09/2003
  • Est. Priority Date: 10/06/2000
  • Status: Expired due to Fees
First Claim
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1. A process for the production of a starch that is pharmaceutically acceptable, especially for parenteral administration, for example by means of injection, to a mammal, especially a human, which comprisesa) starting from starch in solid form, especially particles, for example granules, and with an amylopectin content in excess of 85 percent by weight, expressed as dry weight of starch, b) subjecting said solid starch to washing(s) under conditions such that proteins, lipids and endotoxins surface-localized on the starch are dissolved whilst the starch remains undissolved, and separating the starch from the dissolved material, c) subjecting the starch and to a molecular weight reduction by acid hydrolysis such that a molecular weight distribution is obtained in which at least 80 percent by weight of the material lies within the range of 10-10000 kDa.

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