老年用含地氯雷他定的羟丙基甲基纤维素口服分散膜:配方和评价。

Aya Yahya Fayez Al-Oran, Evrim Yenilmez
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引用次数: 0

摘要

背景:口条在形状、大小和厚度上都与邮票的薄条非常相似。该条被设计用于放置在舌头或任何口腔粘膜组织上,这些组织在与唾液接触后立即变湿并水合。地氯雷他定是众所周知的第二代抗组胺药之一,已被研究为能有效缓解过敏性鼻腔和皮肤症状。目的:研制崩解时间快、机械强度适中的地氯雷他定口服分散膜(ODF),用于治疗老年患者的过敏症状,以提高依从性和方便性。方法:采用溶剂浇铸法,以羟丙基甲基纤维素(HPMC)为成膜聚合物。聚乙二醇400(PEG 400)和甘油(Gly)用作增塑剂,柠檬酸(CA)用作唾液刺激剂。使用扫描电子显微镜评估所得薄膜的崩解时间、耐折叠性、表面pH、重量变化、厚度、表面形态、药物含量、含量均匀性、水分损失、水分吸收以及使用DSC和FT-IR的药物-赋形剂相容性。结果:所有选定的薄膜在不到14秒内开始崩解。所选择的最佳薄膜表现出良好的机械性能,耐折性值大于100。获得了所选薄膜中重量、厚度和药物含量的均匀性。表面pH值在正常范围内(6.4-6.8),薄膜表面光滑,DSC和FT-IR证实了药物与辅料的相容性。通过使用常规溶出试验装置模拟口腔生理条件,对最佳薄膜配方进行溶出试验。超过87%的药物在第4分钟释放。结论:采用溶剂浇铸法成功地制备了地氯雷他定口服分散膜,以改善药物在口腔中的崩解/溶出,从而提高患者的依从性和有效的治疗效果。
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Hydroxypropyl Methylcellulose Orodispersible Film Containing Desloratadine for Geriatric Use: Formulation and Evaluation.

Background: Oral strip is very similar to thin strip of postage stamp in shape, size and thickness. The strip is designed to be placed on the tongue or any oral mucosal tissue which immediately gets wet and hydrated after being in contact with the saliva. Desloratadine is one of the better- known second-generation antihistamines that has been studied for being effective in relieving the allergic nasal and skin symptoms.

Objective: The aim of this study is to develop desloratadine orodispersible film (ODF) with fast disintegration time and suitable mechanical strength to treat allergic symptoms in geriatric patients in order to increase compliance and convenience.

Methods: Solvent casting method using hydroxypropyl methylcellulose (HPMC) as the film forming polymer was applied. Polyethylene glycol 400 (PEG 400) and glycerol (Gly) were used as the plasticizers and citric acid (CA) was used as saliva stimulating agent. The resultant films were evaluated for disintegration time, folding endurance, surface pH, weight variation, thickness, surface morphology using scanning electron microscopy, drug content, content uniformity, moisture loss, moisture uptake, and drug-excipient compatibility using DSC and FT-IR.

Results: All the selected films started to disintegrate in less than 14 seconds. Selected optimum films exhibited good mechanical properties with a folding endurance value greater than 100. The uniformity in weight, thickness, and drug content in the selected films was obtained. Surface pH was within the normal range (6.4 - 6.8). A smooth surface of the films was obtained and drugexcipient compatibility was proved using DSC and FT-IR. The dissolution test was done for optimum film formulations by simulating the oral cavity physiological conditions using the conventional dissolution test apparatus. More than 87% of the drug was released by the 4th minute.

Conclusion: Orodispersible film of desloratadine was successfully prepared by solvent casting method in order to improve the disintegration/dissolution of the drug in oral cavity and hence better patient compliance and effective therapy.

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