Patent · US Active

Encapsulation of ultra-stable insulin analogues with polymer melts

US11583572B2 · kind B2 · utility

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1References
15Claims
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Assignee

Inventors

Key dates

Filing dateDec 23, 2016
Grant dateFeb 21, 2023
Priority date
Expiry dateAug 30, 2039

Classification

  • Technology area (CPC C)Chemistry; Metallurgy
  • CPC primaryC07K14/62
  • WIPO fieldPharmaceuticals
  • WIPO sectorChemistry

Abstract

An insulin composition comprises an insulin analogue and polymer blend. The insulin analogue contains cysteine substitutions at positions B4 and A10 (to form cystine B4-A10), and one or more additional substitutions selected from the group consisting of: a connecting domain of 5-11 amino acids between insulin A- and B domains; a non-beta-branched amino-acid substitution at position A8; a non-beta-branched acidic or polar side chain at position A14; a halogenic modification of PheB24 at the ortho position; and substitution of lysine at position B29 by Glu, Ala, Val, Ile, Leu, amino-propionic acid, amino-butryic acid, or Norleucine. The insulin analogue is compatible with a process of manufacture that includes one or more steps within the temperature range 90-120° C. The encapsulated insulin analogue may optionally contain free PEG or be PEGylated. The insulin analogue-encapsulated polymer blend may be cast as a microneedle patch for topical administration or as micropellets for subcutaneous injection.

Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.