Breda Susana A, Jimenez-Kairuz Alvaro F, Manzo Ruben H, Olivera María E
CONICET-Departamento de Farmacia, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Haya de la Torre y Medina Allende, Ciudad Universitaria (5000), Córdoba, Argentina.
Int J Pharm. 2009 Apr 17;371(1-2):106-13. doi: 10.1016/j.ijpharm.2008.12.026. Epub 2008 Dec 27.
The hydrochlorides of the 1:3 aluminum:norfloxacin and aluminum:ciprofloxacin complexes were characterized according to the Biopharmaceutics Classification System (BCS) premises in comparison with their parent compounds. The pH-solubility profiles of the complexes were experimentally determined at 25 and 37 degrees C in the range of pH 1-8 and compared to that of uncomplexed norfloxacin and ciprofloxacin. Both complexes are clearly more soluble than the antibiotics themselves, even at the lowest solubility pHs. The increase in solubility was ascribed to the species controlling solubility, which were analyzed in the solid phases at equilibrium at selected pHs. Additionally, permeability was set as low, based on data reported in the scientific literature regarding oral bioavailability, intestinal and cell cultures permeabilities and also considering the influence of stoichiometric amounts of aluminum. The complexes fulfill the BCS criterion to be classified as class 3 compounds (high solubility/low permeability). Instead, the active pharmaceutical ingredients (APIs) currently used in solid dosage forms, norfloxacin and ciprofloxacin hydrochloride, proved to be BCS class 4 (low solubility/low permeability). The solubility improvement turns the complexes as potential biowaiver candidates from the scientific point of view and may be a good way for developing more dose-efficient formulations. An immediate release tablet showing very rapid dissolution was obtained. Its dissolution profile was compared to that of the commercial ciprofloxacin hydrochloride tablets allowing to dissolution of the complete dose at a critical pH such as 6.8.
按照生物药剂学分类系统(BCS)的前提条件,对1:3铝与诺氟沙星及铝与环丙沙星配合物的盐酸盐进行了表征,并与它们的母体化合物进行了比较。在25℃和37℃下,于pH 1 - 8范围内通过实验测定了配合物的pH - 溶解度曲线,并与未配合的诺氟沙星和环丙沙星的曲线进行了比较。即使在最低溶解度pH值下,两种配合物的溶解度也明显高于抗生素本身。溶解度的增加归因于控制溶解度的物种,这些物种在选定pH值的平衡固相状态下进行了分析。此外,根据科学文献中关于口服生物利用度、肠道和细胞培养渗透率的数据,并考虑到铝的化学计量比的影响,设定渗透率较低。这些配合物符合BCS标准,可归类为3类化合物(高溶解度/低渗透率)。相反,目前固体剂型中使用的活性药物成分(API),即诺氟沙星和盐酸环丙沙星,被证明属于BCS 4类(低溶解度/低渗透率)。从科学角度来看,溶解度的提高使这些配合物成为潜在的生物豁免候选物,并且可能是开发更高效剂型的一个好方法。获得了一种溶出非常迅速的速释片剂。将其溶出曲线与市售盐酸环丙沙星片剂的溶出曲线进行了比较,后者在临界pH值如6.8时能使完整剂量溶解。