Li Xin, Jiang Qingwei, Du Lina, Wang Chenyun, Chi Qiang
Department of Pharmacy, Chinese PLA General Hospital, China.
Pharmazie. 2012 Aug;67(8):695-700.
A novel osmotic pump tablet with ethyl cellulose (EC) and polyvinyl pyrrolidone (PVP) as the semipermeable membrane and isosorbide-5-mononitrate (5-ISMN) as the model drug was formulated in this study. Zero order release kinetics were attained by avoiding aging during storage. Drug release increased with an increase in the percentage of PVP K30 in the semipermeable membrane. However, drug release decreased with increased coating weight. Drug release rates decreased continuously for tablets coated with EC/PEG4000 and cellulose acetate (CA)/PEG4000. This tendency was more marked with longer storage time. However, there was little change in drug release rates for tablets with a semipermeable membrane of EC/PVP K30 at 6, 12 or 24 months. The weight loss test also validated the results mentioned above. The relative bioavailability of the osmotic-pump tablets against the reference formulation in single and multiple dose regimens was 116.7 and 106.5, respectively. This means that the bioavailability of osmotic pump tablets using PVP as the plasticiser was equal to that of the reference formulation. In general, 5-ISMN osmotic pump tablets with a semipermeable membrane composed of EC/PVP K30 may be useful in providing constant drug delivery with minimum fluctuations during longer storage time.
本研究制备了一种新型渗透泵片,以乙基纤维素(EC)和聚乙烯吡咯烷酮(PVP)作为半透膜,以5-单硝酸异山梨酯(5-ISMN)作为模型药物。通过避免储存期间的老化实现了零级释放动力学。药物释放随着半透膜中PVP K30百分比的增加而增加。然而,药物释放随着包衣重量的增加而降低。用EC/PEG4000和醋酸纤维素(CA)/PEG4000包衣的片剂的药物释放速率持续降低。这种趋势在储存时间延长时更为明显。然而,具有EC/PVP K30半透膜的片剂在6、12或24个月时药物释放速率几乎没有变化。失重试验也验证了上述结果。渗透泵片在单剂量和多剂量方案中相对于参比制剂的相对生物利用度分别为116.7和106.5。这意味着使用PVP作为增塑剂的渗透泵片的生物利用度与参比制剂相当。总体而言,具有由EC/PVP K30组成的半透膜的5-ISMN渗透泵片可能有助于在较长储存时间内提供恒定的药物递送,且波动最小。