将芦荟叶粘液和柠檬油作为潜在的渗透增强剂,利用纳米囊状凝胶增加洛诺昔康的透皮给药。

IF 0.7 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pakistan journal of pharmaceutical sciences Pub Date : 2024-05-01
Gopinath Subramaniyan, Shaik Rubina, Bachu Venkata Ramana, A Meriton Stanley, Devasena Srinivasan
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引用次数: 0

摘要

现有工作的目标是利用柠檬油(LO)和芦荟叶粘液(AVLM)作为渗透增强剂,制作含有洛诺昔康(LXM)凝胶的基质透皮贴片,以促进 LXM 在皮肤上的跨膜运输,并测试其体内镇痛效果。为此,使用 Design Expert® 11 按照 CCD 设计制作了九种配方。反应因子则为 Q1d(Y1)、Q2d(Y2)和 Q3d,即 LXM 在第 1、2 和 3 天的渗透率。选择 AVLM 浓度(X1)和柠檬油(X2)作为自变量。在大鼠身上测试了优化贴片的皮肤敏感反应和镇痛活性。结果表明,通过使用 AVLM 和 LO 作为渗透增强剂,基质系统的 LXM 长效(零阶)释放率分别为 24.15%(24 小时)、49.00%(48 小时)和 69.45%(针对所需的镇痛资产进行了优化)。经确定,含有 3 毫升 AVLM 和 LO 作为渗透增强剂的 LTDP-8 配方是最佳配方。鉴于它能够持续地通过皮肤给药 LXM,同时产生可耐受的镇痛效果。研究得出结论,人工透皮 LXM 给药系统是口服途径的合适替代品。
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Aloe vera leaf mucilage and lemon oil as potential penetration-enhancing agents to increase lornoxicam transdermal administration using nano vesicular gel.

The goal of the existing work was to create matrix transdermal patches with lornoxicam (LXM) gel using lemon oil (LO) and Aloe vera leaves mucilage (AVLM) as penetration enhancers to boost LXM transport crossways the skin and test its in vivo analgesic effects. Nine formulas were produced for this purpose using Design Expert® 11 in line with CCD design. The response factors, on the other hand, were Q1d (Y1), Q2d (Y2) and Q3d, or LXM permeation at days 1, 2 and 3. The AVLM concentration (X1) and lemon oil (X2) were selected as independent variables. The optimized patch's skin sensitivity response and analgesic activity were tested on rats. The results exhibited that a matrix system with prolonged (zero-order) LXM release of 24.15% (@24h), 49.00% (@48h) and 69.45% (optimized for the needed analgesic asset by using AVLM and LO as penetration enhancers. It was resolute that the formulation known as LTDP-8, which contains 3mL of AVLM and LO as permeability enhancers, is the best one. In light of its ability to administer LXM across the skin sustainably while producing a tolerable analgesic effect. The study concludes that the artificial transdermal LXM delivery system is a suitable substitution for the oral route.

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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
211
审稿时长
4.5 months
期刊介绍: Pakistan Journal of Pharmaceutical Sciences (PJPS) is a peer reviewed multi-disciplinary pharmaceutical sciences journal. The PJPS had its origin in 1988 from the Faculty of Pharmacy, University of Karachi as a biannual journal, frequency converted as quarterly in 2005, and now PJPS is being published as bi-monthly from January 2013. PJPS covers Biological, Pharmaceutical and Medicinal Research (Drug Delivery, Pharmacy Management, Molecular Biology, Biochemical, Pharmacology, Pharmacokinetics, Phytochemical, Bio-analytical, Therapeutics, Biotechnology and research on nano particles.
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