School of Pharmacy, The University of Queensland, Queensland 4102, Australia.
Therapeutics Research Group, Diamantina Institute, University of Queensland, Brisbane, Queensland 4102, Australia.
J Control Release. 2023 Nov;363:452-463. doi: 10.1016/j.jconrel.2023.09.045. Epub 2023 Oct 4.
Intranasal delivery is the most preferred route of drug administration for treatment of a range of nasal conditions including chronic rhinosinusitis (CRS), caused by an infection and inflammation of the nasal mucosa. However, localised delivery of lipophilic drugs for persistent nasal inflammation is a challenge especially with traditional topical nasal sprays. In this study, a composite thermoresponsive hydrogel is developed and tuned to obtain desired rheological and physiochemical properties suitable for intranasal administration of lipophilic drugs. The composite is comprised of drug-loaded porous silicon (pSi) particles embedded in a poloxamer 407 (P407) hydrogel matrix. Mometasone Furoate (MF), a lipophilic corticosteroid (log P of 4.11), is used as the drug, which is loaded onto pSi particles at a loading capacity of 28 wt%. The MF-loaded pSi particles (MF@pSi) are incorporated into the P407-based thermoresponsive hydrogel (HG) matrix to form the composite hydrogel (MF@pSi-HG) with a final drug content ranging between 0.1 wt% to 0.5 wt%. Rheomechanical studies indicate that the MF@pSi component exerts a minimal impact on gelation temperature or strength of the hydrogel host. The in-vitro release of the MF payload from MF@pSi-HG shows a pronounced increase in the amount of drug released over 8 h (4.5 to 21-fold) in comparison to controls consisting of pure MF incorporated in hydrogel (MF@HG), indicating an improvement in kinetic solubility of MF upon loading into pSi. Ex-vivo toxicity studies conducted on human nasal mucosal tissue show no adverse effect from exposure to either pure HG or the MF@pSi-HG formulation, even at the highest drug content of 0.5 wt%. Experiments on human nasal mucosal tissue show the MF@pSi-HG formulation deposits a quantity of MF into the tissues within 8 h that is >19 times greater than the MF@HG control (194 ± 7 μg of MF/g of tissue vs. <10 μg of MF/g of tissue, respectively).
鼻腔给药是治疗多种鼻腔疾病(包括由鼻黏膜感染和炎症引起的慢性鼻-鼻窦炎(CRS))的首选药物给药途径。然而,对于持续的鼻腔炎症,亲脂性药物的局部递送是一个挑战,尤其是对于传统的局部鼻腔喷雾剂。在这项研究中,开发了一种复合温敏水凝胶,并对其进行了调整,以获得适合亲脂性药物鼻腔给药的所需流变学和物理化学性质。该复合材料由载药多孔硅(pSi)颗粒嵌入泊洛沙姆 407(P407)水凝胶基质组成。糠酸莫米松(MF),一种亲脂性皮质类固醇(log P 为 4.11),用作药物,其载药量为 28wt%。将糠酸莫米松负载的多孔硅颗粒(MF@pSi)掺入基于泊洛沙姆 407 的温敏水凝胶(HG)基质中,形成最终药物含量在 0.1wt%至 0.5wt%之间的复合水凝胶(MF@pSi-HG)。流变力学研究表明,MF@pSi 成分对凝胶温度或水凝胶基质的强度几乎没有影响。从 MF@pSi-HG 中释放 MF 有效载荷的体外释放表明,与包含在水凝胶中的纯 MF(MF@HG)相比,在 8 小时内释放的药物量明显增加(4.5 至 21 倍),表明 MF 负载到 pSi 中后,其动力学溶解度得到提高。在人鼻黏膜组织上进行的体外毒性研究表明,即使在药物含量最高(0.5wt%)的情况下,纯 HG 或 MF@pSi-HG 制剂也不会对组织造成任何不良影响。在人鼻黏膜组织上的实验表明,MF@pSi-HG 制剂在 8 小时内将 MF 沉积到组织中的量大于 MF@HG 对照物(194±7μg MF/g 组织与 10μg MF/g 组织相比)19 倍以上。