Solid state characterization, solubility, intrinsic dissolution and stability behavior of allopurinol hydrochloride salt
نویسندگان
چکیده
Since each solid form of an active pharmaceutical ingredient (API) can exhibit particular physicochemical properties, the objectives this work were to characterize and study solubility/stability properties allopurinol hydrochloride salt (ALO-HCl) for first time. ALO-HCl was obtained through unreported recrystallization process studied by X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC) thermogravimetric analysis (TGA). All characterization techniques effective differentiation from preferred (ALO). DSC TGA studies showed a solid-state conversion ALO upon HCl loss. Solubility dissolution tests that converts in aqueous media. Moreover, effect common ion decreased amount drug released during intrinsic assay medium. The stability partial after 6 months storage. results indicate comparative between crystalline forms APIs are great importance, as they contribute understanding aspects related quality medicines.
منابع مشابه
Solid state stability and solubility of triethylenetetramine dihydrochloride.
The API triethylenetetramine dihydrochloride used as an alternative treatment of Wilson's disease is sensitive to water and it exhibits polymorphism. As this may become an issue for the drug formulation, the physical stability has been studied by differential scanning calorimetry, high-pressure thermal analysis, dynamic vapor sorption, and X-ray diffraction as a function of temperature. In addi...
متن کاملStability of [(N-morpholine)metylene]daunorubicin hydrochloride in solid state.
The influence of temperature and relative air humidity on the stability of the novel derivative of daunorubicin: [(N-morpholine)metylene]daunorubicin hydrochloride was investigated. The process of degradation was studied by using high-performance liquid chromatography with ultraviolet (UV) detection. In dry air, the degradation of [(N-morpholine)metylene]daunorubicin hydrochloride was a first-o...
متن کاملEquilibrium solubility versus intrinsic dissolution: characterization of lamivudine, stavudine and zidovudine for BCS classification
Solubility and dissolution rate of drugs are of major importance in pre-formulation studies of pharmaceutical dosage forms. The solubility improvement allows the drugs to be potential biowaiver candidates and may be a good way to develop more dose-efficient formulations. Solubility behaviour of lamivudine, stavudine and zidovudine in individual solvents (under pH range of 1.2 to 7.5) was studie...
متن کاملPreparation, characterization, and dissolution studies of naproxen solid dispersions using polyethylene glycol 6000 and labrafil M2130
Naproxen is a poor water soluble, non-steroidal analgesic and anti-inflammatory drug. The enhancement of oral bioavailability of poor water soluble drugs remains one of the most challenging aspects of drug development. Although salt formation, solubilization and particle size reduction have commonly been used to increase dissolution rate and thereby oral absorption and bioavailability of low wa...
متن کاملSynthesis & Characterization of CaB4O7 Powder by Solid-State Reaction
The synthesis of calcium tetraborate was investigated in a temperature ranging from 800℃ to 900℃ using the solid-state reaction method. The synthesis was done using ammonium tetraborate tetrahydrate as the source of boron. At temperatures of 800 ℃ and 880 ℃, the mixed phases from different compounds were formed. At the optimum temperature of 840℃, the mixed phase was only composed of meta and t...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Drug Development and Industrial Pharmacy
سال: 2021
ISSN: ['0363-9045', '1520-5762']
DOI: https://doi.org/10.1080/03639045.2021.1934872