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多孔硅嵌入温敏水凝胶中,用于经鼻递送达治疗鼻窦炎的亲脂性药物。

Porous silicon embedded in a thermoresponsive hydrogel for intranasal delivery of lipophilic drugs to treat rhinosinusitis.

机构信息

School of Pharmacy, The University of Queensland, Queensland 4102, Australia.

Therapeutics Research Group, Diamantina Institute, University of Queensland, Brisbane, Queensland 4102, Australia.

出版信息

J Control Release. 2023 Nov;363:452-463. doi: 10.1016/j.jconrel.2023.09.045. Epub 2023 Oct 4.

Abstract

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).

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dda/11484479/3ac3aac5d808/nihms-2028867-f0001.jpg

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