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负载美洛昔康-薄荷油纳米乳剂的冻干复合物用于牙周疼痛

Lyophilized Composite Loaded with Meloxicam-Peppermint oil Nanoemulsion for Periodontal Pain.

作者信息

Sindi Amal M, Hosny Khaled M, Alharbi Waleed S

机构信息

Department of Oral Diagnostic Sciences, Faculty of Dentistry, King Abdulaziz University, Jeddah 21589, Saudi Arabia.

Department of Pharmaceutics, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.

出版信息

Polymers (Basel). 2021 Jul 14;13(14):2317. doi: 10.3390/polym13142317.

Abstract

Maintaining oral health helps to prevent periodontal inflammation and pain, which can progress into more detrimental issues if left untreated. Meloxicam (MX) is a commonly used analgesic for periodontal pain, but it can have adverse gastrointestinal effects and poor solubility. Therefore, this study aimed to enhance the solubility of MX by developing a self-nanoemulsifying drug delivery system (SNEDDS). Considering the anti-ulcer activity of peppermint oil (PO), it was added in a mixture with medium-chain triglyceride (MCT) to the MX-loaded SNEDDS formulation (MX-PO-SNEDDS). After optimization, MX-PO-SNEDDS exhibited a PO:MCT ratio of 1.78:1, surfactant mixture HLB value of 14, and MX:oil mix ratio of 1:15, a particle size of 47 ± 3 nm, stability index of 85 ± 4%, ex vivo J of 4 ± 0.6 μg/cmmin, and ulcer index of 1 ± 0.25 %. Then, orally flash disintegrating lyophilized composites (MX-SNELCs) were prepared using the optimized MX-PO-SNEDDs. Results reveal that MX-SNELCs had a wetting time of 4 ± 1 s and disintegration time of 3 ± 1 s with a high in vitro MX release of 91% by the end of 60 min. The results of pharmacokinetic studies in human volunteers further demonstrated that, compared to a marketed MX tablets, MX-SNELCs provided a higher C, T, and AUC and a relatively greater bioavailability of 152.97 %. The successfully developed MX-SNELCs were found to be a better alternative than the conventional tablet dosage form, thus indicating their potential for further development in a clinically acceptable strategy for managing periodontal pain.

摘要

保持口腔健康有助于预防牙周炎症和疼痛,如果不加以治疗,这些问题可能会发展成更严重的问题。美洛昔康(MX)是一种常用的治疗牙周疼痛的镇痛药,但它可能会产生不良的胃肠道影响且溶解度不佳。因此,本研究旨在通过开发一种自纳米乳化药物递送系统(SNEDDS)来提高MX的溶解度。考虑到薄荷油(PO)的抗溃疡活性,将其与中链甘油三酯(MCT)混合添加到载MX的SNEDDS制剂(MX-PO-SNEDDS)中。优化后,MX-PO-SNEDDS的PO:MCT比例为1.78:1,表面活性剂混合物的亲水亲油平衡值(HLB值)为14,MX:油混合比例为1:15,粒径为47±3纳米,稳定性指数为85±4%,体外渗透量J为4±0.6微克/平方厘米·分钟,溃疡指数为1±0.25%。然后,使用优化后的MX-PO-SNEDDs制备口服速崩冻干复合物(MX-SNELCs)。结果显示,MX-SNELCs的润湿时间为4±1秒,崩解时间为3±1秒,在60分钟结束时体外MX释放率高达91%。在人类志愿者中进行的药代动力学研究结果进一步表明,与市售的MX片剂相比,MX-SNELCs具有更高的血药浓度(C)、达峰时间(T)和曲线下面积(AUC),相对生物利用度更高,为152.97%。已成功开发的MX-SNELCs被发现是比传统片剂剂型更好的替代品,因此表明它们在临床上可接受的牙周疼痛管理策略中具有进一步开发的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73df/8309367/73b4852abacb/polymers-13-02317-g001.jpg

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