Meyvis T K, De Smedt S C, Van Oostveldt P, Demeester J
Laboratory of General Biochemistry and Physical Pharmacy, University of Gent, Belgium.
Pharm Res. 1999 Aug;16(8):1153-62. doi: 10.1023/a:1011924909138.
This review introduces the basics of fluorescence recovery after photobleaching (FRAP) from a theoretical and an instrumentational approach. The most interesting and innovative applications with a pharmaceutical point of view are briefly discussed and possible future applications are suggested. These future applications include research on the mobility of macromolecular drugs in macro- or microscopic pharmaceutical dosage forms, mobility, and binding of antitumor drugs in tumor tissue, intracellular trafficking of gene complexes and mobility of drugs in membranes prior to transmembrane penetration. The paper is also intended to be an introductory guideline to those who would like to get involved in FRAP related experimental techniques. Therefore, comprehensive details on different setups and data analysis are given, as well as a brief outline of the problems that may be encountered when performing FRAP. Overall, this review shows the great potential of FRAP in pharmaceutical research. This is complemented by our own results illustrating the possibility of performing FRAP in microscopic dosage forms (microspheres) using a high resolution variant of FRAP.
本综述从理论和仪器方法的角度介绍了光漂白后荧光恢复(FRAP)的基础知识。简要讨论了从药学角度来看最有趣和最具创新性的应用,并提出了可能的未来应用。这些未来应用包括对大分子药物在宏观或微观药物剂型中的流动性、抗肿瘤药物在肿瘤组织中的流动性和结合、基因复合物的细胞内运输以及药物在跨膜渗透之前在膜中的流动性的研究。本文还旨在为那些希望参与FRAP相关实验技术的人员提供入门指南。因此,给出了不同设置和数据分析的详细信息,以及进行FRAP时可能遇到的问题的简要概述。总体而言,本综述展示了FRAP在药学研究中的巨大潜力。我们自己的结果补充了这一点,这些结果说明了使用FRAP的高分辨率变体在微观剂型(微球)中进行FRAP的可能性。