Since borneol is a water-insoluble bicyclic monoterpene alcohol which could be soluble in some organic solvents, it is possible for using as matrix former of solvent removal-based in situ forming matrix (ISM) formulation. In this study, borneol was dissolved in organic solvents of ISM including N-methyl pyrrolidone (NMP), dimethyl sulfoxide (DMSO), 2-pyrrolidone (PYR), and using ethanol as a controlled solvent. Borneol precipitates (B precipitate) and intact borneol (intact B) were characterized by infrared spectroscopy (IR), powder X-ray diffractometry (PXRD), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). Moreover, the behavior of borneol solutions after injection into phosphate buffer pH 6.8 was also investigated which borneol in DMSO and NMP exhibited faster matrix formation. All B precipitates showed similar peaks of function groups in IR spectra as intact B. They exhibited a degradation temperature less than intact B whereas the melting temperature of all B precipitates was rather higher than intact B. The crystallinity of B precipitates was decreased as compared with intact B in which B precipitate from DMSO exhibited the lowest crystallinity change. Thus, DMSO was considered as the most suitable solvent for borneol-ISM whereas NMP and PYR also showed the potential. These obtained data of physicochemical characteristics are useful for developing borneol-based ISM formulation using a solvent-removal technique.
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