Bajwa Gurjit S, Hoebler Katrin, Sammon Chris, Timmins Peter, Melia Colin D
Formulation Insights, School of Pharmacy, University of Nottingham, NG7 2RD UK.
J Pharm Sci. 2006 Oct;95(10):2145-57. doi: 10.1002/jps.20656.
A real-time confocal fluorescence imaging method has been developed which allows the critical early stages of gel layer formation in hydroxypropylmethylcellulose (HPMC) matrices to be examined. Congo Red, a fluorophore whose fluorescence is selectively intensified when bound to beta-D-glucopyranosyl sequences, has allowed mapping of hydrated polymer regions within the emerging gel layer, and revealed for the first time, the microstructural sequence of polymer hydration during development of the early gel layer. Liquid penetration and swelling can be examined in unprecedented detail. The earliest images revealed an initial phase of liquid ingress into the tablet pore network, followed by the progressive formation of a coherent gel layer by outward columnar swelling and coalescence of hydrated HPMC particles. Salts can markedly affect HPMC matrix behaviour. Gel layer growth in 0.1-0.5 M NaCl was progressively suppressed until at 0.75 M, particles clearly failed to coalesce into a gel layer, although with considerable polymer swelling. The failure to form a limiting diffusion barrier resulted in enhanced liquid penetration of the core, and the swelling of particles that did not coalesce culminated in surface disintegration. This provides direct evidence of physical mechanisms that contribute to salts accelerating drug release from HPMC matrices.
已开发出一种实时共聚焦荧光成像方法,该方法可用于研究羟丙基甲基纤维素(HPMC)基质中凝胶层形成的关键早期阶段。刚果红是一种荧光团,当其与β-D-吡喃葡萄糖基序列结合时,荧光会选择性增强,它可对正在形成的凝胶层内的水合聚合物区域进行映射,并首次揭示了早期凝胶层形成过程中聚合物水合的微观结构序列。液体渗透和溶胀可以以前所未有的细节进行研究。最早的图像显示,液体最初进入片剂孔隙网络,随后通过水合HPMC颗粒向外柱状溶胀和聚结逐渐形成连贯的凝胶层。盐会显著影响HPMC基质的行为。在0.1 - 0.5 M NaCl中凝胶层的生长逐渐受到抑制,直到在0.75 M时,颗粒明显无法聚结成凝胶层,尽管聚合物有相当大的溶胀。无法形成限制扩散屏障导致核心液体渗透增强,未聚结颗粒的溶胀最终导致表面崩解。这为盐加速药物从HPMC基质中释放的物理机制提供了直接证据。