Department of Pharmacy, University of Greifswald, Greifswald, Germany.
Eur J Pharm Biopharm. 2013 Nov;85(3 Pt B):966-73. doi: 10.1016/j.ejpb.2013.06.004. Epub 2013 Jun 18.
The objective of the present study was to investigate if temperature can be utilized to accelerate drug release from Nuvaring®, a reservoir type intravaginal ring based on polyethylene vinyl acetate copolymer that releases a constant dose of contraceptive steroids over a duration of 3 weeks. The reciprocating holder apparatus (USP 7) was utilized to determine real-time and accelerated etonogestrel release from ring segments. It was demonstrated that drug release increased with increasing temperature which can be attributed to enhanced drug diffusion. An Arrhenius relationship of the zero-order release constants was established, indicating that temperature is a valid parameter to accelerate drug release from this dosage form and that the release mechanism is maintained under these accelerated test conditions. Accelerated release tests are particularly useful for routine quality control to assist during batch release of extended release formulations that typically release the active over several weeks, months or even years, since they can increase the product shelf life. The accelerated method should therefore be able to discriminate between formulations with different release characteristics that can result from normal manufacturing variance. In the case of Nuvaring®, it is well known that the process parameters during the extrusion process strongly influence the polymeric structure. These changes in the polymeric structure can affect the permeability which, in turn, is reflected in the release properties. Results from this study indicate that changes in the polymeric structure can lead to a different temperature dependence of the release rate, and as a consequence, the accelerated method can become less sensitive to detect changes in the release properties. When the accelerated method is utilized during batch release, it is therefore important to take this possible restriction into account and to evaluate the accelerated method with samples from non-conforming batches that are explicitly "out of specification" under real-time test conditions.
本研究的目的是考察温度是否可用于加速 Nuvaring®(一种基于聚乙烯醋酸乙烯酯共聚物的储库型阴道环)中药物的释放,Nuvaring® 在 3 周内持续释放恒定剂量的避孕甾体。采用往复式持器装置(USP7)测定环段中依托孕烯实时和加速释放。结果表明,药物释放随温度升高而增加,这归因于药物扩散增强。建立了零级释放常数的阿伦尼乌斯关系,表明温度是加速该剂型药物释放的有效参数,并且在这些加速测试条件下释放机制得以维持。加速释放试验对于常规质量控制特别有用,可协助延长释放制剂的批量放行,这些制剂通常在数周、数月甚至数年内释放活性成分,因为它们可以延长产品的保质期。因此,加速方法应该能够区分由于正常制造差异而导致的具有不同释放特征的配方。就 Nuvaring®而言,众所周知,挤出过程中的工艺参数会强烈影响聚合物结构。这些聚合物结构的变化会影响渗透性,进而反映在释放特性上。本研究结果表明,聚合物结构的变化会导致释放速率的温度依赖性不同,因此,加速方法对释放特性的变化可能变得不那么敏感。当在批量放行中使用加速方法时,因此必须考虑到这种可能的限制,并使用实时测试条件下明确“超出规格”的不合格批次的样品来评估加速方法。