Hooper Mark W, He Liang
MedCryst Therapeutics Ltd, Centre for Innovation & Enterprise, Oxford University Begbroke Science Park, Oxford, OX5 1PF, UK.
PharmHe, Chertsey, UK.
J Pain Res. 2022 Jun 29;15:1825-1835. doi: 10.2147/JPR.S367536. eCollection 2022.
Gout is caused by crystals of monosodium urate (MSU) in the joints. Topical nonsteroidal anti-inflammatory drug products (NSAIDs) are often the first-choice immediate treatment. This study examined the effect of commercially available and newly developed transdermal NSAID products on the solubility of MSU in a physiologically relevant system, alongside the efficacy of transdermal NSAID delivery.
Drug permeability of 7 commercially available topical NSAID products, alongside 3 newly developed "Gout Buster" products, was evaluated in vitro using pig's ear skin in Franz diffusion cells. The standard Franz cell experimental protocol was adapted to include assessment of MSU solubility in phosphate buffered saline for each product. Some materials were also tested via direct solubility studies.
The amount of drug delivered transdermally varied significantly between different formulations, with the best ibuprofen delivery being ~5 times higher than the lowest, and best diclofenac delivery being ~3.5 times higher than the lowest. Changes in formulations and the drug concentration in the product both affected the amount of drug delivered. Overall ibuprofen permeation was higher than diclofenac. The commercially available products showed little or no effect on the MSU solubility (99-103% vs control). The Gout Buster products showed significant improvement in the MSU solubility after permeation through skin (120-126%). Increased sodium levels reduced the solubility of MSU in direct solubility studies.
In these trials, the Gout Buster products showed significantly improved permeation of both ibuprofen and diclofenac over the commercial products at similar drug concentrations, and showed significant improvement for MSU solubility. Increased sodium levels reduced the solubility of MSU and could cause more crystallisation in vivo. Therefore, topical NSAID products with the Gout Buster formulation may have the best likelihood of both reducing inflammation and helping re-dissolve the MSU crystals that cause gout.
痛风是由关节中的尿酸单钠(MSU)晶体引起的。局部用非甾体抗炎药产品(NSAIDs)通常是首选的即时治疗药物。本研究考察了市售和新开发的透皮NSAIDs产品在生理相关体系中对MSU溶解度的影响,以及透皮NSAIDs给药的疗效。
使用猪耳皮肤在Franz扩散池中体外评估7种市售局部用NSAIDs产品以及3种新开发的“痛风克星”产品的药物渗透性。对标准Franz细胞实验方案进行调整,以评估每种产品在磷酸盐缓冲盐水中MSU的溶解度。一些材料还通过直接溶解度研究进行了测试。
不同制剂经皮给药的药物量差异显著,布洛芬的最佳给药量比最低给药量高约5倍,双氯芬酸的最佳给药量比最低给药量高约3.5倍。制剂变化和产品中的药物浓度均影响给药量。总体而言,布洛芬的渗透率高于双氯芬酸。市售产品对MSU溶解度几乎没有影响(与对照相比为99 - 103%)。“痛风克星”产品在透过皮肤渗透后,MSU溶解度有显著提高(120 - 126%)。在直接溶解度研究中,钠水平升高会降低MSU的溶解度。
在这些试验中,“痛风克星”产品在相似药物浓度下,布洛芬和双氯芬酸的渗透均比市售产品有显著改善,且MSU溶解度有显著提高。钠水平升高会降低MSU的溶解度,并可能在体内导致更多结晶。因此,具有“痛风克星”制剂的局部用NSAIDs产品最有可能既减轻炎症又有助于重新溶解导致痛风的MSU晶体。