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设计、研制和鉴定多塞平口腔黏附膜用于治疗牙痛。

Design, development and characterization of buccal bioadhesive films of Doxepin for treatment of odontalgia.

机构信息

a Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy , University of Granada , Granada , Spain.

出版信息

Drug Deliv. 2015;22(6):869-76. doi: 10.3109/10717544.2014.896958. Epub 2014 Mar 27.

DOI:10.3109/10717544.2014.896958
PMID:24670096
Abstract

Tricyclic antidepressants, as doxepin hydrochloride (DH), may have analgesic local effect due to its biochemical mechanism of action. Delivery of DH directly to the oral cavity could be an interesting alternative for toothache due to its analgesic local effect. One problem associated with the mucosal administration routes is the short residence time of the dosage form on the mucosal membranes. In this sense, we have developed new doxepin mucoadhesive films able of reducing pain and increasing the effectiveness of treatment. For this purpose, we tested three different polymers: chitosan, sodium hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (SCMC) in film elaboration. The results obtained show that all films are hydrophilic matrices that absorb water when placed in an aqueous media. All the films hydrated very quickly, reaching high percentage of swelling after just few minutes (5 min for SCMC, 2 min for HPMC and 30 min for chitosan). Moreover, the SCMC and HPMC films were dissolved whereas chitosan was not dissolved. Dissolution also leads to viscous liquids with a higher retention time over mucosal surfaces what may lead to adhesive interactions. In vitro permeation studies showed that for all the formulations studied, SCMC (19.91%), HPMC (69.5%) and chitosan (24.17%), the percentage of drug permeated increased compared to the drug solution (8.26%). Specifically the HPMC film presents greater amounts of doxepin permeated (49.27 ± 4.47 µg/cm(2)).

摘要

三环类抗抑郁药,如盐酸多塞平(DH),可能因其生化作用机制而具有局部镇痛作用。DH 直接递送到口腔可能是治疗牙痛的一种有趣的替代方法,因为它具有局部镇痛作用。粘膜给药途径的一个问题是剂型在粘膜上的停留时间短。从这个意义上说,我们开发了新的具有镇痛作用的多塞平粘膜粘附膜,能够减轻疼痛并提高治疗效果。为此,我们测试了三种不同的聚合物:壳聚糖、羟丙基甲基纤维素(HPMC)和羧甲基纤维素钠(SCMC)在薄膜中的应用。结果表明,所有的薄膜都是亲水性基质,在水介质中会吸收水分。所有的薄膜都很快水化,在短短几分钟内(SCMC 为 5 分钟,HPMC 为 2 分钟,壳聚糖为 30 分钟)达到高的溶胀率。此外,SCMC 和 HPMC 薄膜溶解,而壳聚糖不溶解。溶解也会导致粘性液体在粘膜表面停留时间延长,从而导致粘附相互作用。体外渗透研究表明,对于所有研究的制剂,SCMC(19.91%)、HPMC(69.5%)和壳聚糖(24.17%),与药物溶液(8.26%)相比,药物渗透的百分比增加。特别是 HPMC 膜具有更大的多塞平渗透量(49.27 ± 4.47 µg/cm(2))。

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