Knapp Sigrid, Bertelmann Eckart, Hartmann Christian, Keipert Sigrid, Pleyer Uwe
Institut für Pharmazie, Humboldt Universität zu Berlin, Goethestr. 54, 13086 Berlin, Germany.
J Ocul Pharmacol Ther. 2003 Apr;19(2):181-92. doi: 10.1089/108076803321637717.
The efficacy of mycophenolate mofetil (MMF), a prodrug of mycophenolic acid (MPA), in high risk keratoplasties and ocular immune-mediated diseases has been shown in recent years. As peroral administration of MMF can cause various side effects, topical application should be considered. This study investigates the intraocular availability of MMF and MPA in the rabbit eye. An eye drop solution (MMF-CD; 1% MMF/10% hydroxypropyl-beta-cyclodextrin (HP-beta-CD)) or a 1% aqueous suspension (MMF-SP) was instilled into the lower cul-de-sac of the right eye of each rabbit. Rabbits (each group: n = 4) were put down after 30, 60 and 240 min. Aqueous humor, vitreous, cornea, sclera, conjunctiva, iris-ciliary-body, and plasma were isolated. Several extraction procedures were performed in order to quantify the drug by HPLC. The aqueous humor concentration of the active metabolite MPA was 24 microg/mL after 30 min for both preparations. The ratio of the MPA concentrations after 30, 60, and 240 min was 1 : 2 : 0.07 for MMF-CD and 1 : 0.6 : 0.04 for MMF-SP, respectively. MPA levels in the cornea were 90.78 / 56.90 / 4.08 x 10(-6) microg/microg for MMF-CD, whereas MMF-SP resulted in MPA levels of 102.65 / 31.18 / 2.59 x 10(-6) microg/microg at the three time points. As a high concentration of the active drug MPA in cornea and aqueous humor is desired, e.g. following corneal transplantation, the MMF/HP-beta-CD formulation could be an useful topical treatment. Furthermore, the present study shows that MMF-CD is superior to MMF-SP by increasing intraocular availability.
近年来已证实,麦考酚酸(MPA)的前体药物霉酚酸酯(MMF)在高风险角膜移植和眼部免疫介导疾病中具有疗效。由于口服MMF会引起各种副作用,因此应考虑局部应用。本研究调查了MMF和MPA在兔眼中的眼内可用性。将滴眼剂溶液(MMF-CD;1% MMF/10%羟丙基-β-环糊精(HP-β-CD))或1%水悬浮液(MMF-SP)滴入每只兔子右眼的下结膜囊。在30、60和240分钟后处死兔子(每组:n = 4)。分离房水、玻璃体、角膜、巩膜、结膜、虹膜睫状体和血浆。进行了几种提取程序以便通过高效液相色谱法对药物进行定量。两种制剂在30分钟后活性代谢物MPA的房水浓度均为24μg/mL。MMF-CD在30、60和240分钟后的MPA浓度比分别为1 : 2 : 0.07,MMF-SP的MPA浓度比分别为1 : 0.6 : 0.04。MMF-CD在角膜中的MPA水平在三个时间点分别为90.78 / 56.90 / 4.08×10⁻⁶μg/μg,而MMF-SP在三个时间点的MPA水平为102.65 / 31.18 / 2.59×10⁻⁶μg/μg。例如在角膜移植后,由于需要在角膜和房水中有高浓度的活性药物MPA,MMF/HP-β-CD制剂可能是一种有用的局部治疗方法。此外,本研究表明,MMF-CD通过提高眼内可用性优于MMF-SP。