Hoti Gjylije, Ferrero Riccardo, Caldera Fabrizio, Trotta Francesco, Corno Marta, Pantaleone Stefano, Desoky Mohamed M H, Brunella Valentina
Department of Chemistry, University of Torino, Via P. Giuria 7, 10125 Torino, Italy.
Polymers (Basel). 2023 Mar 20;15(6):1543. doi: 10.3390/polym15061543.
Melatonin is a neurohormone that ameliorates many health conditions when it is administered as a drug, but its drawbacks are its oral and intravenous fast release. To overcome the limitations associated with melatonin release, cyclodextrin-based nanosponges (CD-based NSs) can be used. Under their attractive properties, CD-based NSs are well-known to provide the sustained release of the drug. Green cyclodextrin (CD)-based molecularly imprinted nanosponges (MIP-NSs) are successfully synthesized by reacting β-Cyclodextrin (β-CD) or Methyl-β Cyclodextrin (M-βCD) with citric acid as a cross-linking agent at a 1:8 molar ratio, and melatonin is introduced as a template molecule. In addition, CD-based non-molecularly imprinted nanosponges (NIP-NSs) are synthesized following the same procedure as MIP-NSs without the presence of melatonin. The resulting polymers are characterized by CHNS-O Elemental, Fourier Transform Infrared Spectroscopy (FTIR), Thermogravimetric (TGA), Differential Scanning Calorimetry (DSC), Zeta Potential, and High-Performance Liquid Chromatography (HPLC-UV) analyses, etc. The encapsulation efficiencies are 60-90% for MIP-NSs and 20-40% for NIP-NSs, whereas melatonin loading capacities are 1-1.5% for MIP-NSs and 4-7% for NIP-NSs. A better-controlled drug release performance (pH = 7.4) for 24 h is displayed by the in vitro release study of MIP-NSs (30-50% released melatonin) than NIP-NSs (50-70% released melatonin) due to the different associations within the polymeric structure. Furthermore, a computational study, through the static simulations in the gas phase at a Geometry Frequency Non-covalent interactions (GFN2 level), is performed to support the inclusion complex between βCD and melatonin with the automatic energy exploration performed by Conformer-Rotamer Ensemble Sampling Tool (CREST). A total of 58% of the CD/melatonin interactions are dominated by weak forces. CD-based MIP-NSs and CD-based NIP-NSs are mixed with cream formulations for enhancing and sustaining the melatonin delivery into the skin. The efficiency of cream formulations is determined by stability, spreadability, viscosity, and pH. This development of a new skin formulation, based on an imprinting approach, will be of the utmost importance in future research at improving skin permeation through transdermal delivery, associated with narrow therapeutic windows or low bioavailability of drugs with various health benefits.
褪黑素是一种神经激素,作为药物使用时可改善多种健康状况,但其缺点是口服和静脉注射时释放速度快。为克服与褪黑素释放相关的局限性,可使用基于环糊精的纳米海绵(CD基纳米海绵)。基于其吸引人的特性,众所周知,CD基纳米海绵可实现药物的缓释。通过使β-环糊精(β-CD)或甲基-β-环糊精(M-βCD)与柠檬酸作为交联剂以1:8的摩尔比反应,成功合成了绿色基于环糊精的分子印迹纳米海绵(MIP-NSs),并引入褪黑素作为模板分子。此外,按照与MIP-NSs相同的程序合成基于CD的非分子印迹纳米海绵(NIP-NSs),但不存在褪黑素。通过CHNS-O元素分析、傅里叶变换红外光谱(FTIR)、热重分析(TGA)、差示扫描量热法(DSC)、zeta电位和高效液相色谱(HPLC-UV)分析等对所得聚合物进行表征。MIP-NSs的包封效率为60-90%,NIP-NSs的包封效率为20-40%,而MIP-NSs的褪黑素负载量为1-1.5%,NIP-NSs的褪黑素负载量为4-7%。由于聚合物结构内的不同缔合作用,MIP-NSs的体外释放研究(30-50%的褪黑素释放)显示出比NIP-NSs(50-70%的褪黑素释放)在24小时内具有更好控制的药物释放性能(pH = 7.4)。此外,通过在几何频率非共价相互作用(GFN2水平)的气相中进行静态模拟进行了一项计算研究,以支持β-CD与褪黑素之间的包合络合物,通过构象异构体-旋转异构体集合采样工具(CREST)进行自动能量探索。总共58%的CD/褪黑素相互作用由弱力主导。基于CD的MIP-NSs和基于CD的NIP-NSs与乳膏配方混合,以增强和维持褪黑素向皮肤的递送。乳膏配方的效率由稳定性、铺展性、粘度和pH值决定。这种基于印迹方法的新型皮肤配方的开发,对于未来通过透皮给药改善皮肤渗透的研究至关重要,这与治疗窗窄或具有各种健康益处的药物的低生物利用度相关。