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脂质体包合改善牛至中迷迭香酸和香芹酚的溶解和稳定性

Liposomal Incorporation to Improve Dissolution and Stability of Rosmarinic Acid and Carvacrol Extracted from Oregano ( L.).

机构信息

Department of Analytical and Toxicological Chemistry, Lithuanian University of Health Sciences, Medical Academy, Sukileliu pr. 13 LT-50162, Kaunas, Lithuania.

Institute of Pharmaceutical Technologies, Medical Academy, Lithuanian University of Health Sciences, Eiveniu 4, LT-50161 Kaunas, Lithuania.

出版信息

Biomed Res Int. 2018 Jul 24;2018:6147315. doi: 10.1155/2018/6147315. eCollection 2018.

Abstract

The potential antimicrobial benefit of high levels of rosmarinic acid (RA) and carvacrol (CA) in oregano ( L.) extract has been limited until now by poor bioavailability arising from the low aqueous-phase solubility and slow dissolution behaviour of the lyophilized extract (E). To address this issue, various ratios of phospholipon 90H (P90H) and 1,2-dimyristoyl--glycero-3-phospho-(1'-rac-glycerol), sodium salt (DMPG) were sonicated, yielding four empty liposomes (L1, L2, L3, and L90). After an initial selection process, Turkish oregano extract was internalized into the more promising candidates. Each empty liposome, extract-loaded liposome (LE1, LE2, and LE3), and freeze-dried control (E) was assessed in terms of structure, composition, RA and CA dissolution profile, storage stability, and, when relevant, zeta potential. Empty liposome L1, which was prepared using P90H and DMPG in a 1:1 ratio, displayed the most convenient encapsulation traits among the four unloaded types. Loaded liposome LE1, obtained by combining oregano extract and L1 in a 1:1 ratio, proved superior as a vehicle to deliver RA & CA when compared against control freeze-dried E and test liposomes LE2 and LE3. Dissolution profiles of the active compounds RA and CA in loaded liposomes were determined using a semi-automated dissolution tester. The basket method was applied using artificial gastric juice without pepsin (AGJ, 50rpm, 500mL). The pH value was maintained at 1.5 (37 ± 0.5°C). Aliquots (5ml) were manually extracted from parallel dissolution vessels at 1, 3, 5, 7, 10, 15, 20, 25, 30, 45, and 60-minute time points. Dissolution tests, run to completion on LE1, showed that approximately 99% of loaded CA and 88% of RA had been released. Shorter dissolution times were also noted in using LE1. In particular, the release profile of CA and RA had levelled off after only 25 minutes, respectively, depicting an impressive 3.0-3.3 and 2.3-2.6 rate increase compared to the freeze-dried control extract. The improved dispersibility of RA and CA in the form of LE1 was supported by particle size and zeta potential measurements of the liposome, yielding 234.3nm and -30.9mV, respectively. The polydispersity index value was 0.35, indicating a reasonable particle size distribution. To study storage stability, liposomes were stored (4°C, 6 months) in amber coloured glass containers (4 oz.). Each container held 30 capsules, which were stored according to the ICH guidelines prescribed for long-term storage (25°C ± 2°C; 60% ± 5% RH). Triplicate samples were withdrawn after 0, 3, 6, 9, and 12 months for analysis. Lastly, LE1 displayed good storage stability. The results imply that RA and CA can be conveniently and routinely delivered via oral and mucosal routes by first internalizing oregano extracts into appropriately engineered liposomes.

摘要

罗丝玛丽酸(RA)和香芹酚(CA)在牛至( L.)提取物中具有潜在的抗菌益处,但由于冻干提取物(E)的水相溶解度低和溶解速度慢,其生物利用度一直受到限制。为了解决这个问题,我们对不同比例的磷脂酰胆碱 90H(P90H)和 1,2-二肉豆蔻酰基--甘油-3-磷酸-(1'-rac-甘油),钠盐(DMPG)进行了超声处理,得到了四种空脂质体(L1、L2、L3 和 L90)。经过初步筛选,土耳其牛至提取物被内化到更有前途的候选物中。每个空脂质体、载药脂质体(LE1、LE2 和 LE3)和冷冻干燥对照物(E)在结构、组成、RA 和 CA 溶解曲线、储存稳定性以及相关的情况下,进行了 Zeta 电位评估。用 P90H 和 DMPG 以 1:1 的比例制备的空脂质体 L1 在四种未负载的类型中显示出最方便的包封特性。通过将牛至提取物和 L1 以 1:1 的比例组合制备的负载脂质体 LE1 被证明是一种更好的输送 RA 和 CA 的载体,与对照冷冻干燥 E 和测试脂质体 LE2 和 LE3 相比。使用半自动溶解测试仪测定活性化合物 RA 和 CA 在负载脂质体中的溶解曲线。采用 basket 法,使用不含胃蛋白酶的人工胃液(AGJ,50rpm,500mL)。pH 值保持在 1.5(37±0.5°C)。在 1、3、5、7、10、15、20、25、30、45 和 60 分钟时间点,从平行溶解容器中手动提取 5ml 等分试样。对 LE1 进行的溶解试验表明,大约 99%的负载 CA 和 88%的 RA 已经释放。使用 LE1 也记录到较短的溶解时间。特别是 CA 和 RA 的释放曲线在 25 分钟后趋于平稳,分别显示出令人印象深刻的 3.0-3.3 和 2.3-2.6 速率增加,与冷冻干燥对照提取物相比。LE1 中 RA 和 CA 的分散性得到改善,这得到了脂质体粒径和 Zeta 电位测量的支持,分别为 234.3nm 和-30.9mV。多分散指数值为 0.35,表明粒径分布合理。为了研究储存稳定性,将脂质体(4°C,6 个月)储存在琥珀色玻璃容器(4 盎司)中。每个容器中装有 30 个胶囊,根据 ICH 规定的长期储存(25°C±2°C;60%±5%RH)储存。在 0、3、6、9 和 12 个月后,每个容器中取出 3 个样品进行分析。最后,LE1 显示出良好的储存稳定性。结果表明,RA 和 CA 可以通过首先将牛至提取物内化到适当设计的脂质体中,方便且常规地通过口服和粘膜途径输送。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8477/6081540/c5ff4614a2cd/BMRI2018-6147315.001.jpg

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