Dipartimento di Scienze del Farmaco, Università degli Studi di Catania, Città Universitaria, Italy.
AAPS PharmSciTech. 2011 Jun;12(2):468-75. doi: 10.1208/s12249-011-9605-2. Epub 2011 Apr 9.
A series of amphiphilic ion pairs of erythromycin (ERY) with lipoamino acids (LAAs) were produced. The ion pairs were prepared by evaporation of a water/ethanol co-solution of the drug and LAA bearing an alkyl side chain of 10-16 carbon atoms. For the sake of comparison, equimolar physical mixtures were prepared by triturating ERY and the LAA in the absence of any solvent. FTIR spectroscopy confirmed the structure of ion pairs, while differential scanning calorimetry and powder X-ray diffractometry were used to assess the formation of new saline species. The solubility pattern of the coevaporates in different aqueous and organic solvents confirmed their amphiphilic properties. ERY-LAA ion pairs were submitted to an in vitro microbiological assay against different bacterial strains, both susceptible and resistant to macrolides. The presence of the LAA moiety was shown not altering the antibacterial spectrum of activity of the drug. These results can be the basis for a further evaluation of ERY-LAA ion pairs as a mean to improve the penetration of the drug inside bacterial cells and to optimize the loading of ERY in lipid-based nanocarriers.
制备了一系列红霉素(ERY)与脂氨基酸(LAAs)的双亲离子对。这些离子对是通过蒸发药物和具有 10-16 个碳原子烷基侧链的 LAAs 的水/乙醇共溶液来制备的。为了进行比较,通过在没有任何溶剂的情况下研磨 ERY 和 LAA 制备了等摩尔的物理混合物。傅里叶变换红外光谱(FTIR)证实了离子对的结构,而差示扫描量热法(DSC)和粉末 X 射线衍射法(PXRD)用于评估新盐物种的形成。共蒸发物在不同水相和有机相溶剂中的溶解度模式证实了它们的双亲性质。将 ERY-LAA 离子对进行了体外微生物测定,以评估其对不同细菌菌株的抗菌活性,这些细菌菌株对大环内酯类药物敏感和耐药。LAAs 部分的存在并没有改变药物的抗菌谱。这些结果可以作为进一步评估 ERY-LAA 离子对的基础,以提高药物在细菌细胞内的穿透性,并优化基于脂质的纳米载体中 ERY 的载药量。