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半固体制剂中光敏剂用于微生物光动力灭活

Use of Photosensitizers in Semisolid Formulations for Microbial Photodynamic Inactivation.

作者信息

González-Delgado José A, Kennedy Patrick J, Ferreira Marta, Tomé João P C, Sarmento Bruno

机构信息

Inovapotek, Pharmaceutical Research & Development , Edifício Inovar e Crescer, Salas 23 e 39, Rua Alfredo Allen, 455/461, 4200-135 Porto, Portugal.

QOPNA and Department of Chemistry, University of Aveiro , 3810-193 Aveiro, Portugal.

出版信息

J Med Chem. 2016 May 26;59(10):4428-42. doi: 10.1021/acs.jmedchem.5b01129. Epub 2015 Dec 1.

Abstract

Semisolid formulations, such as gels, creams and ointments, have recently contributed to the progression of photodynamic therapy (PDT) and microbial photodynamic inactivation (PDI) in clinical applications. The most important challenges facing this field are the physicochemical properties of photosensitizers (PSs), optimal drug release profiles, and the photosensitivity of surrounding tissues. By further integration of nanotechnology with semisolid formulations, very promising pharmaceuticals have been generated against several dermatological diseases (PDT) and (antibiotic-resistant) pathogenic microorganisms (PDI). This review focuses on the different PSs and their associated semisolid formulations currently found in both the market and clinical trials that are used in PDT/PDI. Special emphasis is placed on the advantages that the semisolid formulations bring to drug delivery in PDI. Lastly, some potential considerations for improvement in this field are also discussed.

摘要

半固体制剂,如凝胶、乳膏和软膏,最近在光动力疗法(PDT)和微生物光动力灭活(PDI)的临床应用进展中发挥了作用。该领域面临的最重要挑战是光敏剂(PSs)的物理化学性质、最佳药物释放曲线以及周围组织的光敏性。通过将纳米技术与半固体制剂进一步整合,已经开发出了针对几种皮肤病(PDT)和(耐抗生素)致病微生物(PDI)的非常有前景的药物。本综述重点关注目前在市场和临床试验中用于PDT/PDI的不同PSs及其相关的半固体制剂。特别强调了半固体制剂在PDI药物递送方面带来的优势。最后,还讨论了该领域改进的一些潜在考虑因素。

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