Department of Biotechnology and Life Sciences (DBSV), University of Insubria, Via J.H. Dunant 3, 21100 Varese, Italy.
Int J Mol Sci. 2022 Sep 5;23(17):10198. doi: 10.3390/ijms231710198.
Over the past 30 years, photodynamic therapy (PDT) has shown great development. In the clinical setting the few approved molecules belong almost exclusively to the porphyrin family; but in the scientific field, in recent years many researchers have been interested in other families of photosensitizers, among which BODIPY has shown particular interest. BODIPY is the acronym for 4,4-difluoro-4-bora-3a, 4a-diaza-s-indacene, and is a family of molecules well-known for their properties in the field of imaging. In order for these molecules to be used in PDT, a structural modification is necessary which involves the introduction of heavy atoms, such as bromine and iodine, in the beta positions of the pyrrole ring; this change favors the intersystem crossing, and increases the O yield. This mini review focused on a series of structural changes made to BODIPYs to further increase O production and bioavailability by improving cell targeting or photoactivity efficiency.
在过去的 30 年中,光动力疗法(PDT)取得了巨大的发展。在临床环境中,少数几种已批准的分子几乎完全属于卟啉家族;但在科学领域,近年来许多研究人员对其他光敏剂家族产生了兴趣,其中 BODIPY 引起了特别的关注。BODIPY 是 4,4-二氟-4-硼-3a,4a-二氮杂-s-茚满的缩写,是一类因其在成像领域的特性而广为人知的分子。为了将这些分子应用于 PDT,需要进行结构修饰,包括在吡咯环的β位引入重原子,如溴和碘;这种变化有利于系间窜跃,增加 O 的产量。这篇小型综述集中讨论了一系列对 BODIPY 进行的结构改变,旨在通过提高细胞靶向性或光活性效率来进一步提高 O 的产生和生物利用度。