Design and optimization of metformin hydrophobic ion pairs for efficient encapsulation in polymeric drug carriers.
Ontology highlight
ABSTRACT: Loading small molecular weight hydrophilic drugs into polymeric carriers is a challenging task. Metformin hydrochloride (MET) is a highly soluble oral antidiabetic drug of small size and high cationic charge. Hydrophobic ion pairing (HIP) is an approach for reversible modulation of solubility and hydrophilicity of water-soluble drugs via complexation with oppositely charged molecules. Herein, we prepared MET ion pairs and carefully studied and characterized MET interaction with different ligands, with the aim of increasing MET lipophilicity and loading efficiency. HIP was successful using three hydrophilic anionic ligands; sodium dodecyl sulphate (SDS) Carbopol (CB) and tannic acid (TA). Electrostatic interaction and hydrogen bonding drove the complexation per spectroscopic and thermal stu
SUBMITTER: Abd-El Hafeez SI
PROVIDER: S-EPMC8986808 | biostudies-literature | 2022 Apr
REPOSITORIES: biostudies-literature
ACCESS DATA