Thumma Sridhar, Majumdar Soumyajit, Elsohly Mahmoud A, Gul Waseem, Repka Michael A
Department of Pharmaceutics, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, USA.
AAPS PharmSciTech. 2008;9(3):982-90. doi: 10.1208/s12249-008-9136-7. Epub 2008 Aug 28.
Preformulation studies were performed on a hemiglutarate ester prodrug of Delta(9)-tetrahydrocannabinol (THC-HG), to facilitate the development of stable formulations by hot-melt methods. The various studies performed included solid-state thermal characterization, pKa, logP, aqueous and pH dependent solubility, pH stability and effect of moisture, temperature and oxygen on solid-state stability. A hot-melt method was utilized to fabricate THC-HG incorporated poly (ethylene oxide) (PEO) matrices and the bioadhesive properties, release profiles and post-processing stability of these matrices were assessed as a function of the polymer molecular weight. The prodrug exhibited a T (g) close to 0 degrees C, indicating its amorphous nature. Thermogravimetric analysis revealed a rapid weight loss after 170 degrees C. The prodrug exhibited a seven-fold higher aqueous solubility as compared to the parent drug (THC). Also, the solubility of the compound increased with increasing pH, being maximum at pH 8. The prodrug exhibited a v-shaped pH-rate profile, with the degradation rate minimum between pH 3 and 4. The moisture uptake and drug degradation increased with an increase in relative humidity. Solid-state stability indicated that the prodrug was stable at -18 degrees C but demonstrated higher degradation at 4 degrees C, 25 degrees C and 40 degrees C (51.6%, 74.5% and 90.1%, respectively) at the end of 3-months. THC-HG was found to be sensitive to the presence of oxygen. The release of the active from the polymeric matrices decreased, while bioadhesion increased, with an increase in molecular weight of PEO.
对Δ⁹-四氢大麻酚半戊二酸酯前药(THC-HG)进行了处方前研究,以促进通过热熔法开发稳定的制剂。所进行的各种研究包括固态热表征、pKa、logP、水相和pH依赖性溶解度、pH稳定性以及水分、温度和氧气对固态稳定性的影响。采用热熔法制备了含THC-HG的聚环氧乙烷(PEO)基质,并评估了这些基质的生物粘附性能、释放曲线和后处理稳定性与聚合物分子量的关系。该前药的玻璃化转变温度(Tg)接近0℃,表明其为无定形性质。热重分析显示在170℃后重量迅速损失。与母体药物(THC)相比,该前药的水溶解度高7倍。此外,该化合物的溶解度随pH升高而增加,在pH 8时最大。该前药呈现出v形pH-速率曲线,在pH 3至4之间降解速率最低。吸湿和药物降解随相对湿度增加而增加。固态稳定性表明,该前药在-18℃下稳定,但在3个月结束时在4℃、25℃和40℃下表现出较高的降解(分别为51.6%、74.5%和90.1%)。发现THC-HG对氧气的存在敏感。随着PEO分子量的增加,活性成分从聚合物基质中的释放减少,而生物粘附性增加。