Li Chang-Jun, Zhu Jia-Bi, Yu Wang-Yang
Pharmaceutical Research Institute, China Pharmaceutical University, Nanjing 210009, China.
Yao Xue Xue Bao. 2008 Jun;43(6):652-6.
To prepare verapamil hydrochloride (VH) core-in-cup tablets with tri-layered tablet and four-layered tablet as core tablets, separately, which can provide biphasic release with double-pulsatile and multi-phasic release, core tablets were prepared by direct compression method, and core-in-cup tablets by dry-compression coated technology. The parameter, time-lag (T(lag)), was used to evaluate the influence of factors, such as the weight of the top cover layer, the amount of hydroxypropylmethylcellulose (HPMC), and the compression load on VH release. With the increase of the weight and HPMC amount of the top cover layer, the first lag time T(lag1) was prolonged. The second lag time T(lag2) of core-in-cup tablet with four-layered tablet as core tablet increased with the increasing amount of HPMC K100M. With the increase of compression load among the range (6 - 10 kg x cm(-2)), the two lag times were prolonged. Core-in-cup tablets with double-pulsatile and multi-phasic release released VH after the first lag time (4 -5 h), then kept sustained release for 12 h or 13 h, finally released rapidly. The drug in the core-in-cup tablet only released from the top cover layer. T(lag) is determined by the erosion rate of the inhibitor layers (the top cover layer and the sustained-release layer of the multi-layer core tablet).
分别以三层片和四层片为片芯制备盐酸维拉帕米(VH)杯包片,使其具有双脉冲双相释放和多相释放特性。片芯采用直接压片法制备,杯包片采用干压包衣技术制备。采用时滞(T(lag))参数评估顶覆层重量、羟丙基甲基纤维素(HPMC)用量和压片压力等因素对VH释放的影响。随着顶覆层重量和HPMC用量的增加,首次时滞时间T(lag1)延长。以四层片为片芯的杯包片的第二次时滞时间T(lag2)随着HPMC K100M用量的增加而延长。在6 - 10 kg·cm(-2)范围内,随着压片压力的增加,两个时滞时间均延长。具有双脉冲双相释放和多相释放特性的杯包片在首次时滞时间(4 - 5小时)后释放VH,然后持续释放12小时或13小时,最后快速释放。杯包片中的药物仅从顶覆层释放。T(lag)由抑制剂层(多层片芯的顶覆层和缓释层)的侵蚀速率决定。