Mori M, Nakamura Y, Shirai Y, Seto Y, Nakamura H, Makita H, Imasato Y
Pharmaceutical Research Laboratories, Dainippon Pharmaceutical Company, Ltd., Osaka, Japan.
J Pharm Sci. 1991 Sep;80(9):876-80. doi: 10.1002/jps.2600800915.
While bermoprofen [(+-)-10,11-dihydro-alpha,8-dimethyl-11- oxodibenz[b,f]oxepin-2-acetic acid], a new nonsteroidal antiinflammatory drug (NSAID), has potent antipyretic and analgesic activities with a short biological half-life, it shows ulcerogenic activity as a side-effect like other nonsteroidal anti-inflammatory drugs. A bermoprofen preparation was specially designed to prolong its duration of action and to reduce its side effect. Immediate-release granules (IRGs) were prepared by coating particles of Nonpareil 103 with bermoprofen. The IRGs were also coated by spraying a film solution composed of ethylcellulose and hydroxypropylmethylcellulose (3:2), and, thereby, three kinds of retard-release granules (RRGs) were obtained with the coating amounts of 1.5, 2.5, and 4%. Peak plasma bermoprofen levels were seen 0.5, 1, 2, and 3 h after single oral administrations of IRG, RRG(1.5%), RRG (2.5%), and RRG(4%), respectively, in rats. The potency order in ulcerogenic activity was RRG(1.5%) greater than IRG greater than RRG(2.5%) greater than RRG(4%) after a single oral dosage in rats. Then, IRG and RRG(4%) were mixed (in the ratio 3:7, which was calculated from their simulated plasma bermoprofen profiles) in order to get fast onset and long duration of antipyretic action. These mixed granules [i.e., the sustained-release granules (SRGs)] exhibited a falt plasma bermoprofen profile, and longer lasting antipyretic and lower ulcerogenic activities in rats in comparison with IRG or bermoprofen. From these results, it is suggested that a bermoprofen SRG preparation has more durable therapeutic activity and lower side-effects as a NSAID.
虽然新型非甾体抗炎药(NSAID)贝莫洛芬[(+-)-10,11-二氢-α,8-二甲基-11-氧代二苯并[b,f]氧杂环庚英-2-乙酸]具有强效的解热和镇痛活性且生物半衰期短,但它像其他非甾体抗炎药一样,会产生致溃疡活性这一副作用。专门设计了一种贝莫洛芬制剂来延长其作用持续时间并减少副作用。通过用贝莫洛芬包衣103号无核小丸颗粒制备速释颗粒(IRG)。还通过喷涂由乙基纤维素和羟丙基甲基纤维素(3:2)组成的薄膜溶液对IRG进行包衣,从而获得了包衣量分别为1.5%、2.5%和4%的三种缓释颗粒(RRG)。在大鼠单次口服IRG、RRG(1.5%)、RRG(2.5%)和RRG(4%)后,分别在0.5、1、2和3小时观察到血浆贝莫洛芬水平峰值。在大鼠单次口服给药后,致溃疡活性的强度顺序为RRG(1.5%)>IRG>RRG(2.5%)>RRG(4%)。然后,将IRG和RRG(4%)混合(比例为3:7,这是根据它们模拟的血浆贝莫洛芬曲线计算得出的),以实现快速起效和持久的解热作用。这些混合颗粒[即缓释颗粒(SRG)]呈现出平稳的血浆贝莫洛芬曲线,并且与IRG或贝莫洛芬相比,在大鼠中具有更持久的解热活性和更低的致溃疡活性。从这些结果表明,贝莫洛芬SRG制剂作为一种NSAID具有更持久的治疗活性和更低的副作用。