Zecchi Riccardo, Trevisani Marcello, Pittelli Maria, Pedretti Pamela, Manni Maria Elena, Pieraccini Giuseppe, Pioselli Barbara, Amadei Francesco, Moneti Gloriano, Catinella Silvia
Centro di servizi di spettrometria di massa (CISM), University of Florence, Italy.
Chiesi Farmaceutici SpA, Corporate Preclinical R&D-FABER Project Group, Florence, Italy.
Eur J Mass Spectrom (Chichester). 2013;19(6):475-82. doi: 10.1255/ejms.1254.
During the last decade, significant technological improvements in mass spectrometry have had a great impact on drug discovery. The development of matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI-IMS) has set a new frontier for the study of the distribution of endogenous and exogenous molecules present within a tissue. MALDI-IMS is a surface sampling technique that allows not only the detection of multiple analytes but also gives the spatial distribution of those analytes. Active compounds for pulmonary disease need an optimal and well-studied delivery into the lungs, in order to assure distribution with greater penetration into the peripheral or the alveolar region of the lung to maximize the therapeutic effects. IMS is very useful in the field of drug discovery, showing drug delivery and distribution in the body and organs. In this study, we present a comparison between two different ways of carrying out pulmonary drug administration: inhalation of a nebulized aerosol of aqueous drug solutions and intratracheal administration, which is much simpler, not expensive and commonly used during in vivo screening. Tiotropium bromide is a long-acting anticholinergic medicine used for maintenance treatment of chronic obstructive pulmonary disease. In the present work, tiotropium was administered by nebulization and by intratracheal instillation to guinea pigs at doses able to induce significant anti-bronchoconstrictive activity. Lung samples were dissected, frozen, cryosectioned and coated with matrix (α-hydroxy-cinnamic acid). IMS analyses were performed using a MALDI-LTQ-Orbitrap XL. Using this technique we were able to compare different distributions of the drug depending on the method of administration.
在过去十年中,质谱技术的重大改进对药物研发产生了巨大影响。基质辅助激光解吸/电离成像质谱(MALDI-IMS)的发展为研究组织内源性和外源性分子的分布开辟了新领域。MALDI-IMS是一种表面采样技术,不仅能检测多种分析物,还能给出这些分析物的空间分布。治疗肺部疾病的活性化合物需要以最佳且经过充分研究的方式递送至肺部,以确保药物在肺部外周或肺泡区域的分布更深入,从而使治疗效果最大化。IMS在药物研发领域非常有用,可显示药物在体内和器官中的递送及分布情况。在本研究中,我们比较了两种不同的肺部给药方式:吸入雾化的水性药物溶液和气溶胶以及气管内给药,后者更为简单、成本低廉且常用于体内筛选。噻托溴铵是一种长效抗胆碱能药物,用于慢性阻塞性肺疾病的维持治疗。在本研究中,将噻托溴铵以能够诱导显著抗支气管收缩活性的剂量通过雾化和气溶胶吸入的方式给予豚鼠。解剖肺部样本,冷冻、进行冷冻切片并涂覆基质(α-羟基肉桂酸)。使用MALDI-LTQ-Orbitrap XL进行IMS分析。利用该技术,我们能够根据给药方式比较药物的不同分布情况。