4.8 Article

Substituted Polyesters by Thiol-Ene Modification: Rapid Diversification for Therapeutic Protein Stabilization

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 139, Issue 3, Pages 1145-1154

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b10776

Keywords

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Funding

  1. National Science Foundation (NSF) [CHE-1507735]
  2. NSF [CHE-1049904, DGE-1144087]
  3. MRSEC Program of the NSF [DMR 1121053]
  4. Christopher S. Foote Graduate Research Fellowship in Organic Chemistry
  5. NIH Chemistry-Biology Interface Training Fellowship [T32-GM-008496]
  6. UCLA Graduate Division
  7. Direct For Mathematical & Physical Scien
  8. Division Of Chemistry [1507735] Funding Source: National Science Foundation

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Many proteins, especially those used as therapeutics, are unstable to storage and shipping temperatures, leading to increased costs in research and industry. Therefore, the design and synthesis of novel stabilizers is an important area of investigation. Herein we report new degradable polymers that stabilize proteins to environmental stressors such as refrigeration and elevated temperature. Specifically, polycaprolactones with different pendant groups were synthesized and surveyed for their ability to stabilize an important therapeutic protein to storage and shipping conditions. Ring-opening polymerization (ROP) of an allyl-substituted caprolactone monomer was carried out using the organocatalyst 1,5,7-triazabicyclo[4.4.0]-dec-5-ene (TBD) to yield a well-defined, alkene-substituted degradable polymer, which was used as a common backbone to control for the degree of polymerization. Relevant side chains such as trehalose, lactose, glucose, carboxybetaine, and oligo(ethylene glycol) were installed via postpolymerization thiol-ene reactions. These degradable polymers were then employed as excipients for the stabilization of the therapeutic protein granulocyte colony-stimulating factor (G-CSF) against storage at 4 degrees C and shipping temperatures of 60 degrees C. The best stabilization was observed using the trehalose- and zwitterion-substituted polyesters. Both the trehalose- and carboxybetaine-substituted pCL were further investigated with regard to molecular weight dependence, and it was found that the molecular weight was minimally important for stabilization to refrigeration, but critical for G-CSF stabilization at elevated temperatures. Both high performing zwitterionic and trehalose polyesters were also degraded, and the polymers and degradation products were shown to be noncytotoxic. This work provides potential biocompatible polymers for stabilization of the important therapeutic G-CSF, as well as a general platform for the future discovery of new polymeric protein stabilizers.

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