Sutananta W, Craig D Q, Newton J M
Centre for Materials Science, School of Pharmacy, University of London, UK.
J Pharm Pharmacol. 1995 May;47(5):355-9. doi: 10.1111/j.2042-7158.1995.tb05810.x.
The effects of preparation conditions on the release of theophylline from Gelucires 50/13 and 55/18 have been investigated. Samples were prepared by melting physical mixes under controlled conditions, followed by either slow or fast (ambient) cooling to the solid state. A rapid cooling rate was shown to result in a slower release rate for 2% w/w dispersions in Gelucire 55/18, with the slow- and fast-cooled systems resulting in drug release via a diffusion and a mixed diffusion/erosion mechanism, respectively. At higher drug loading (30% w/w), the cooling rate did not effect the release characteristics. The erosion of Gelucire 50/13 was found to be more rapid for slowly cooled samples. Viscosity measurements were used as a means of assessing the chemical stability of the Gelucires, with evidence being found for degradation of Gelucire 55/18 on storage following heat treatment, while Gelucire 50/13 appeared to be stable. The effects of storage on the dissolution profiles of ambiently cooled systems were studied, with drug release from both bases increasing on ageing for up to 180 days.
研究了制备条件对氨茶碱从Gelucire 50/13和55/18中释放的影响。通过在受控条件下熔融物理混合物来制备样品,随后进行缓慢或快速(环境温度)冷却至固态。结果表明,快速冷却速率会导致在Gelucire 55/18中2%w/w分散体的释放速率较慢,缓慢冷却和快速冷却的系统分别通过扩散和混合扩散/侵蚀机制实现药物释放。在较高载药量(30%w/w)下,冷却速率不影响释放特性。发现对于缓慢冷却的样品,Gelucire 50/13的侵蚀更快。粘度测量被用作评估Gelucire化学稳定性的一种方法,有证据表明热处理后储存时Gelucire 55/18会降解,而Gelucire 50/13似乎是稳定的。研究了储存对环境温度冷却系统溶出曲线的影响,两种基质的药物释放在老化长达180天时均增加。