Kasai M, Hatano S, Kitagawa M, Yoshimi A, Nishimura K, Mori N, Sakai A, Sugihara T
Research Laboratories, Kyoto Pharmaceutical Industries, Ltd., Japan.
Chem Pharm Bull (Tokyo). 1999 Aug;47(8):1081-8. doi: 10.1248/cpb.47.1081.
Ceftizoxime (CZX), a parenteral cephalosporin, has potent and broad antibacterial activity. To improve its oral absorption, we synthesized a series of monofunctional and bifunctional prodrugs of CZX. In rabbits, urinary recovery after oral administration of CZX was improved by esterification of the carboxyl group at the C-4 position with various lipophilic moieties (monofunctional prodrugs), and was further increased by introduction of a hydrophilic L-alanine to the amino group on the thiazole ring at the C-7 position (bifunctional prodrugs). Least-squares analysis showed good parabolic correlations between log P and urinary recovery for monofunctional and bifunctional prodrugs, respectively. AS-924, a bifunctional prodrug with a pivaloyloxymethyl and L-alanyl moiety had the best balance of lipophilicity and water-solubility for oral absorption among the prodrugs synthesized.
头孢唑肟(CZX)是一种肠胃外使用的头孢菌素,具有强大且广泛的抗菌活性。为提高其口服吸收效果,我们合成了一系列CZX的单功能和双功能前药。在兔子身上,通过用各种亲脂性基团酯化C-4位的羧基(单功能前药),口服CZX后的尿液回收率得到提高,并且通过在C-7位噻唑环上的氨基引入亲水性L-丙氨酸(双功能前药),回收率进一步提高。最小二乘法分析表明,单功能和双功能前药的log P与尿液回收率之间分别呈现良好的抛物线相关性。AS-924是一种具有新戊酰氧基甲基和L-丙氨酰部分的双功能前药,在所合成的前药中,其在口服吸收的亲脂性和水溶性方面具有最佳平衡。