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用于褪黑素时空释放的刺激响应性纳米胶囊:预防胃部炎症

Stimuli-Responsive Nanocapsules for the Spatiotemporal Release of Melatonin: Protection against Gastric Inflammation.

作者信息

Pramanik Sumit Kumar, Pal Uttam, Choudhary Preety, Singh Harwinder, Reiter Russel J, Ethirajan Anitha, Swarnakar Snehasikta, Das Amitava

机构信息

CSIR-Central Salt and Marine Chemicals Research Institute, Bhavnagar, Gujarat 364 002, India.

Chemical Sciences Division, Saha Institute of Nuclear Physics, Kolkata, West Bengal 700 064, India.

出版信息

ACS Appl Bio Mater. 2019 Dec 16;2(12):5218-5226. doi: 10.1021/acsabm.9b00236. Epub 2019 May 8.

Abstract

Melatonin is a secretory product of the pineal gland that regulates circadian rhythm. It is also well-known for its anti-inflammatory and antioxidant properties against the damaging influences of reactive oxygen species. To improve its therapeutic efficacy, a new formulation with melatonin loaded in a stimuli-responsive polymeric nanocapsule has been prepared following an inverse mini-emulsion technique. The colloidal stability of the melatonin-loaded nanocapsules (MNCs) is studied using dynamic light scattering, while the morphology of these MNCs is characterized using various electron microscopies. These MNCs have an inner diameter of 80-120 nm with a cell wall thickness of 29 ± 11 nm. The emission band maximum for melatonin appears at 350 nm following excitation at 305 nm (quantum yield, Φ = 0.13). The self-quenching nature of the entrapped melatonin molecules inside the nanocapsules attributes to a lower Φ value for the MNCs. The controlled release of melatonin from MNCs in an condition is achieved by inducing a rupture of the polymeric backbone through maintaining a certain media pH (∼2.0-4.0) as an external stimulus, and this accounts for a significant enhancement in its characteristic luminescence. The H,K-ATPase, an integral membrane protein, maintains this specific pH range in the interior of the gastrointestinal tract. This methodology is adopted for developing an efficient drug delivery process in the gastric environment. A significant improvement in the AGS cell survival under oxidative stress conditions is observed during preincubation with MNCs compared to free melatonin. In a murine model of the stress-induced gastric ulcer, MNCs outperformed free melatonin in terms of drug efficacy. The value for the gastric ulcer index is reduced from ∼30 to ∼15 by free melatonin and from ∼30 to ∼8 by MNCs treatments, respectively. Such formulation could be a step forward for developing more efficient melatonin-based gastroprotective supplements.

摘要

褪黑素是松果体分泌的一种产物,可调节昼夜节律。它还因其对活性氧损伤影响的抗炎和抗氧化特性而广为人知。为提高其治疗效果,采用反相微乳液技术制备了一种载有褪黑素的刺激响应性聚合物纳米胶囊新制剂。使用动态光散射研究了载褪黑素纳米胶囊(MNCs)的胶体稳定性,同时使用各种电子显微镜对这些MNCs的形态进行了表征。这些MNCs的内径为80 - 120 nm,细胞壁厚度为29±11 nm。在305 nm激发后,褪黑素的发射带最大值出现在350 nm(量子产率,Φ = 0.13)。纳米胶囊内包封的褪黑素分子的自猝灭特性导致MNCs的Φ值较低。通过维持一定的介质pH(约2.0 - 4.0)作为外部刺激诱导聚合物主链断裂,实现了MNCs中褪黑素在特定条件下的控释,这导致其特征发光显著增强。H,K - ATP酶是一种整合膜蛋白,可维持胃肠道内部的这种特定pH范围。该方法用于在胃环境中开发高效的药物递送过程。与游离褪黑素相比,在与MNCs预孵育期间观察到氧化应激条件下AGS细胞存活率有显著提高。在应激诱导的胃溃疡小鼠模型中,MNCs在药物疗效方面优于游离褪黑素。游离褪黑素使胃溃疡指数值从约30降至约15,而MNCs处理使其从约30降至约8。这种制剂可能是开发更有效的基于褪黑素的胃保护补充剂的一个进步。

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