Improving Dissolution Rate of Carbamazepine-Glutaric Acid Cocrystal Through Solubilization by Excess Coformer

• Published in: Pharmaceutical research Vol. 35; no. 1; pp. 4 - 7
• Main Authors: Yamashita, Hiroyuki, Sun, Changquan Calvin
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.01.2018; Springer; Springer Nature B.V
• Subjects: Biochemistry; Biomedical and Life Sciences; Biomedical Engineering and Bioengineering; Biomedicine; Carbamazepine; Dissolution; Drug delivery; Fiber optics; Formulation and Manufacturing of Solid Dosage Forms; Hydrochloric acid; Intestine; Laboratories; Medical Law; pH effects; Pharmacology/Toxicology; Pharmacy; Potassium; Powder; Powders; Research Paper; Sodium; Solubility; Solubilization; Stainless steel; Viscosity; cocrystal; solubilization; dissolution; carbamazepine
• ISSN: 0724-8741; 1573-904X; 1573-904X
• DOI: 10.1007/s11095-017-2309-x

Purpose The use of soluble cocrystals is a promising strategy for delivering poorly soluble drugs. However, precipitation of poorly soluble crystal form during dissolution hinders the successful tablet development of cocrystals. This work was aimed to understand the mechanisms for improving dissolution performance of a soluble cocrystals by using excess coformer. Methods A highly soluble carbamazepine (CBZ) cocrystal with– glutaric acid (GLA) was studied. Impact of excess GLA on solubility and intrinsic dissolution rate (IDR) was assessed. Viscosity of GLA solutions was also measured. Solid form of powders and pellets was examined using powder X-ray diffractometry. IDRs of cocrystal and GLA mixtures in different ratios were measured to identify a suitable formulation for maintaining high dissolution rate of CBZ-GLA in an aqueous environment. Results IDR of CBZ-GLA in a pH 1.2 HCl solution was improved when GLA was present in the solution. Precipitation of CBZ·2H 2 O was eliminated when GLA concentration was ≥100 mg/mL. The improved IDR was accompanied by higher solubility of CBZ in GLA solution and increased solution viscosity. The trend in IDR profile matched well with the solubility profile normalized by solution viscosity. Mixture of cocrystal and GLA led to improved IDR in simulated intestinal fluid. Conclusions The excess GLA increased the aqueous solubility of CBZ·2H 2 O and, thereby, reduced the propensity to precipitation of CBZ·2H 2 O during dissolution by lowering the degree of supersaturation. This strategy allowed development of a CBZ-GLA formulation with a significantly enhanced dissolution rate than CBZ-GLA.