Yong Chul Soon, Choi Young-Kwon, Kim Yong-Il, Park Byung-Joo, Quan Qi-Zhe, Rhee Jong-Dal, Kim Chong-Kook, Choi Han-Gon
College of Pharmacy, Yeungnam University, 214-1, Dae-Dong, Gyongsan 712-749, Korea.
Arch Pharm Res. 2003 Feb;26(2):162-7. doi: 10.1007/BF02976664.
Liquid suppository systems composed of poloxamers and bioadhesive polymers were easy to administer to the anus and mucoadhesive to the rectal tissues without leakage after the dose. However, a liquid suppository containing diclofenac sodium could not be developed using bioadhesive polymers, since the drug was precipitated in this preparation. To develop a liquid suppository system using sodium chloride instead of bioadhesive polymers, the physicochemical properties such as gelation temperature, gel strength and bioadhesive force of various formulations composed of diclofenac sodium, poloxamers and sodium chloride were investigated. Furthermore, the pharmacokinetic study of diclofenac sodium delivered by the liquid suppository was performed. Diclofenac sodium significantly increased the gelation temperature and weakened the gel strength and bioadhesive force, while sodium chloride did the opposite. The liquid suppositories with less than 1.0% of sodium chloride, in which the drug was not precipitated, were inserted into the rectum without difficulty and leakage. Furthermore, liquid suppository gave significantly higher initial plasma concentrations and faster Tmax of diclofenac sodium than did solid suppository, indicating that drug from liquid suppository could be absorbed faster than that from solid one in rats. Our results suggested that a thermosensitive liquid suppository system with sodium chloride and poloxamers was a more physically stable, convenient and effective rectal dosage form for diclofenac sodium.
由泊洛沙姆和生物粘附性聚合物组成的液体栓剂系统易于给药至肛门,且在给药后能粘膜粘附于直肠组织而无泄漏。然而,由于药物在该制剂中沉淀,无法使用生物粘附性聚合物开发含双氯芬酸钠的液体栓剂。为了开发一种使用氯化钠而非生物粘附性聚合物的液体栓剂系统,研究了由双氯芬酸钠、泊洛沙姆和氯化钠组成的各种制剂的理化性质,如胶凝温度、凝胶强度和生物粘附力。此外,还对液体栓剂递送的双氯芬酸钠进行了药代动力学研究。双氯芬酸钠显著提高了胶凝温度,削弱了凝胶强度和生物粘附力,而氯化钠则起相反作用。氯化钠含量低于1.0%且药物未沉淀的液体栓剂可顺利插入直肠且无泄漏。此外,液体栓剂给予的双氯芬酸钠初始血浆浓度显著高于固体栓剂,且达峰时间更快,表明在大鼠中液体栓剂中的药物比固体栓剂中的药物吸收更快。我们的结果表明,含氯化钠和泊洛沙姆的热敏性液体栓剂系统是一种更物理稳定、方便且有效的双氯芬酸钠直肠剂型。