Polymer Nanocoating of Amorphous Drugs for Improving Stability, Dissolution, Powder Flow, and Tabletability: The Case of Chitosan-Coated Indomethacin
Overview
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As a result of its higher molecular mobility, the surface of an amorphous drug can grow crystals much more rapidly than the bulk, causing poor stability and slow dissolution of drug products. We show that a nanocoating of chitosan (a pharmaceutically acceptable polymer) can be deposited on the surface of amorphous indomethacin by electrostatic deposition, leading to significant improvement of physical stability, wetting by aqueous media, dissolution rate, powder flow, and tabletability. The coating condition was chosen so that the positively charged polymer deposits on the negatively charged drug. Chitosan coating is superior to gelatin coating with respect to stability against crystallization and agglomeration of coated particles.
Bookwala M, Wildfong P Pharm Res. 2023; 40(12):2963-2981.
PMID: 37389801 DOI: 10.1007/s11095-023-03547-4.
Nguyen H, Van Duong T, Taylor L Int J Pharm. 2023; 642:123139.
PMID: 37311499 PMC: 10390825. DOI: 10.1016/j.ijpharm.2023.123139.
A concise summary of powder processing methodologies for flow enhancement.
Shah D, Moravkar K, Jha D, Lonkar V, Amin P, Chalikwar S Heliyon. 2023; 9(6):e16498.
PMID: 37292344 PMC: 10245010. DOI: 10.1016/j.heliyon.2023.e16498.
Yao X, Neusaenger A, Yu L Pharmaceutics. 2021; 13(8).
PMID: 34452231 PMC: 8401805. DOI: 10.3390/pharmaceutics13081271.
Gui Y, McCann E, Yao X, Li Y, Jones K, Yu L Mol Pharm. 2021; 18(3):1364-1372.
PMID: 33522821 PMC: 7927142. DOI: 10.1021/acs.molpharmaceut.0c01180.