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通过与β-环糊精络合提高盐酸多西环素的光稳定性。

Increasing doxycycline hyclate photostability by complexation with β-cyclodextrin.

作者信息

Kogawa Ana Carolina, Zoppi Ariana, Quevedo Mario Alfredo, Nunes Salgado Hérida Regina, Longhi Marcela Raquel

机构信息

Departamento de Fármacos e Medicamentos, Faculdade de Ciências Farmacêuticas UNESP, Araraquara, São Paulo, Brazil,

出版信息

AAPS PharmSciTech. 2014 Oct;15(5):1209-17. doi: 10.1208/s12249-014-0150-7. Epub 2014 Jun 3.

Abstract

Doxycycline hyclate (DOX) is a highly photosensitive drug, a feature that limits the stability of the corresponding dosage forms. The main objectives of this work were the preparation and characterization of an inclusion complex of DOX with β-cyclodextrin (βCD) and to investigate if this approach could improve the photostability of the drug. Guest-host interactions were investigated using nuclear magnetic resonance, which were afterwards combined with molecular modeling methods to study the complex formation and its three-dimensional structure was proposed. A freeze-drying method was applied to obtain the complex in the solid state, which was further confirmed by thermal and spectroscopic techniques. To evaluate the complexation effect on DOX integrity, the photostability of the inclusion complex was studied, with a significant decrease in the photodegradation of DOX being found in aqueous solution upon complexation. Finally, the photoprotection produced by the complexation was evaluated by means of an antimicrobial assay. Overall, the presented results suggest that the formulation of DOX complexed with βCD constitutes an interesting approach for the preparation of pharmaceutical dosage forms of DOX with enhanced stability properties.

摘要

盐酸多西环素(DOX)是一种对光高度敏感的药物,这一特性限制了相应剂型的稳定性。本研究的主要目的是制备DOX与β-环糊精(βCD)的包合物并对其进行表征,同时研究这种方法是否能够提高药物的光稳定性。利用核磁共振研究了客体-主体相互作用,随后结合分子建模方法研究了复合物的形成,并提出了其三维结构。采用冷冻干燥法获得固态复合物,通过热分析和光谱技术进一步证实。为评估包合作用对DOX完整性的影响,研究了包合物的光稳定性,发现包合后DOX在水溶液中的光降解显著降低。最后,通过抗菌试验评估了包合产生的光保护作用。总体而言,所呈现的结果表明,DOX与βCD复合的制剂是制备具有增强稳定性的DOX药物剂型的一种有趣方法。

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3
Quantification of doxycycline hyclate in tablets by HPLC-UV method.
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