Lauriola Carolina, Di Muzio Laura, Paolicelli Patrizia, Casadei Maria Antonietta, Sergi Claudia, Tirillò Jacopo, Carriero Vito Cosimo, Adrover Alessandra
Dipartimento di Ingegneria Chimica, Materiali e Ambiente, Sapienza Univerisità di Roma, 00184 Rome, Italy.
Dipartimento di Chimica e Tecnologia del Farmaco, Sapienza Università di Roma, 00185 Rome, Italy.
Pharmaceutics. 2024 Sep 27;16(10):1256. doi: 10.3390/pharmaceutics16101256.
In this work, five different dextran-based cryogels for controlled drug release are investigated. Vitamin B12 was used as a model drug for in vitro release tests. Two different drug-loading procedures were adopted, leading to very different drug release curves. Indeed, a fast Fickian release was observed when freeze-dried samples of DEXPEGMA and DEXPEGMA were infused with the drug after cryogel formation. On the contrary, a slowed highly non-Fickian behavior arises when the drug is loaded before the low-temperature crosslinking step, leading to the cryogel formation. The non-Fickian drug release, observed for all the five different dextran-based cryogels investigated, is actually due to the cryoconcentration phenomenon, modeled with a two-step release process. The proposed transport model accurately predicts experimental release curves characterized by a long lag time, confirming that dextran-based cryogels are suitable for controlled release.
在这项工作中,研究了五种不同的基于葡聚糖的用于控释的冷冻凝胶。维生素B12用作体外释放试验的模型药物。采用了两种不同的载药程序,导致了非常不同的药物释放曲线。事实上,当DEXPEGMA和DEXPEGMA的冻干样品在冷冻凝胶形成后注入药物时,观察到快速的菲克扩散释放。相反,当药物在低温交联步骤之前加载,导致冷冻凝胶形成时,会出现缓慢的高度非菲克行为。在所研究的所有五种不同的基于葡聚糖的冷冻凝胶中观察到的非菲克药物释放,实际上是由于冷冻浓缩现象,用两步释放过程进行建模。所提出的传输模型准确地预测了具有长滞后时间特征的实验释放曲线,证实了基于葡聚糖的冷冻凝胶适用于控释。