Skip to Content
Merck
  • Synthesis and characterization of neutral and anionic cellulosic amphiphiles.

Synthesis and characterization of neutral and anionic cellulosic amphiphiles.

Carbohydrate polymers (2014-09-27)
Haoyu Liu, Kevin J Edgar
ABSTRACT

Polymer design and selection are crucial to the development of amorphous solid dispersions (ASD) for solubilization of otherwise poorly water-soluble drugs. The matrix polymer is required to interact strongly at the molecular level with the drug to prevent recrystallization, but must also be able to release the drug at an adequate rate upon entering the absorptive portion of the digestive tract. Herein we report versatile syntheses of a non-ionic, water-soluble cellulosic polymer family, cellulose trioxodecanoates, containing a hydrophilic oligo(ethylene oxide) side chain. This series of cellulose derivatives is designed for both adequate stabilization of amorphous drugs with high crystallization tendency, and timely release of those drugs. Alternatively, these polymers can be rendered anionic by also appending a pH-responsive ω-carboxyalkanoate group. Detailed structural information and structure-property relationship characterization of these amphiphilic polymers are described, which will permit evaluation of these materials as ASD polymers for enhancement of drug solubility and bioavailability.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
4-(Dimethylamino)pyridine solution, 0.5 M in THF
Supelco
Dimethylformamide, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Sodium hydroxide, ultra dry, powder or crystals, 99.99% trace metals basis
Sigma-Aldrich
Lithium chloride, BioUltra, Molecular Biology, anhydrous, ≥99.0% (AT)
Sigma-Aldrich
CDI, ≥97.0% (T)
Supelco
Sodium hydroxide solution, 49-51% in water, eluent for IC
Sigma-Aldrich
Sodium hydroxide solution, BioUltra, Molecular Biology, 10 M in H2O
Sigma-Aldrich
CDI, reagent grade
Sigma-Aldrich
Oxalyl chloride, ReagentPlus®, ≥99%
Sigma-Aldrich
N,N-Dimethylformamide, anhydrous, 99.8%
Sigma-Aldrich
Phthalic anhydride, ReagentPlus®, 99%
Sigma-Aldrich
Propionic anhydride, ≥99%
Sigma-Aldrich
Lithium chloride, AnhydroBeads, −10 mesh, 99.998% trace metals basis
Sigma-Aldrich
Phthalic anhydride, ACS reagent, ≥99%
Sigma-Aldrich
Propionic anhydride, 97%
Sigma-Aldrich
Lithium chloride, AnhydroBeads, −10 mesh, ≥99.9% trace metals basis
Sigma-Aldrich
Lithium chloride, powder, ≥99.98% trace metals basis
Supelco
Lithium chloride solution, 1 M in ethanol
Sigma-Aldrich
Lithium chloride, BioXtra, ≥99.0% (titration)
Sigma-Aldrich
Lithium chloride solution, 8 M, Molecular Biology, ≥99%
Sigma-Aldrich
N,N-Dimethylformamide, Molecular Biology, ≥99%
Sigma-Aldrich
3-Ethyl-2,4-pentanedione, mixture of tautomers, 98%
Sigma-Aldrich
Oxalyl chloride solution, 2.0 M in methylene chloride
Sigma-Aldrich
N,N-Dimethylformamide, ACS reagent, ≥99.8%
Sigma-Aldrich
Propionic anhydride, purum, ≥96.0% (NT)
Sigma-Aldrich
Lithium chloride, Molecular Biology, ≥99%
Sigma-Aldrich
Sodium hydroxide, BioUltra, suitable for luminescence, ≥98.0% (T), pellets
Lithium chloride solution, 2 M in ethanol
Valaciclovir impurity G, European Pharmacopoeia (EP) Reference Standard
USP
Valacyclovir Related Compound G, United States Pharmacopeia (USP) Reference Standard